395 results on '"Ata, B."'
Search Results
2. Can endometrial compaction predict live birth rates in assisted reproductive technology cycles? A systematic review and meta-analysis
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Turkgeldi, E., Yildiz, S, Kalafat, E., Keles, I., Ata, B., and Bozdag, G.
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- 2023
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3. The HERA (Hyper-response Risk Assessment) Delphi consensus for the management of hyper-responders in in vitro fertilization
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Feferkorn, I., Santos-Ribeiro, S., Ubaldi, F. M., Velasco, J. G., Ata, B., Blockeel, C., Conforti, A., Esteves, S. C., Fatemi, H. M., Gianaroli, L., Grynberg, M., Humaidan, P., Lainas, G.T, La Marca, A., Craig, L. B., Lathi, R., Norman, R. J., Orvieto, R., Paulson, R., Pellicer, A., Polyzos, N. P., Roque, M., Sunkara, S. K., Tan, S. L., Urman, B., Venetis, C., Weissman, A., Yarali, H., and Dahan, M. H.
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- 2023
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4. Ongoing pregnancy rates in single euploid frozen embryo transfers remain unaffected by female age: a retrospective study
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Lawrenz, B., Kalafat, E., Ata, B., Gallego, R. Del, Melado, L., Bayram, A., Elkhatib, I., and Fatemi, H.
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- 2024
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5. Correction to: The HERA (Hyper‑response Risk Assessment) Delphi consensus for the management of hyper‑responders in in vitro fertilization
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Feferkorn, I., Santos‑Ribeiro, S., Ubaldi, F. M., Velasco, J. G., Ata, B., Blockeel, C., Conforti, A., Esteves, S. C., Fatemi, H. M., Gianaroli, L., Grynberg, M., Humaidan, P., Lainas, G. T, La Marca, A., Craig, L. B., Lathi, R., Norman, R. J., Orvieto, R., Paulson, R., Pellicer, A., Polyzos, N. P., Roque, M., Sunkara, S. K., Tan, S. L., Urman, B., Venetis, C., Weissman, A., Yarali, H., and Dahan, M. H.
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- 2024
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6. Cortico-hippocampal networks carry information about characters and their relationships in an extended narrative
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Karagoz, Ata B., Morse, Sarah J., and Reagh, Zachariah M.
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- 2023
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7. Undetected, natural conception pregnancies in luteal phase stimulations—case series and review of literature.
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Lawrenz, B, Ata, B, Kalafat, E, Gallego, R Del, Selim, S, Edades, J, and Fatemi, H
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LUTEAL phase , *CORPUS luteum , *INDUCED ovulation , *MENSTRUATION , *OVARIAN hyperstimulation syndrome , *ECTOPIC pregnancy - Abstract
STUDY QUESTION What is the risk of an undetected natural conception pregnancy during luteal phase ovarian stimulation, and how does it impact the pregnancy's course? SUMMARY ANSWER The risk for an undetected, natural conception pregnancy in luteal phase ovarian stimulation is low and it appears that ovarian stimulation is unlikely to harm the pregnancy. WHAT IS KNOWN ALREADY Random start ovarian stimulation appears to be similarly effective as early follicular stimulation start; and it allows ovarian stimulation to be started independent of the cycle day and throughout the cycle, in accordance with the patients' and clinics' schedule as long as there is no intention of a fresh embryo transfer in the same cycle. Starting ovarian stimulation in the luteal phase bears the possibility of an—at the timepoint of stimulation start—undetected, natural conception pregnancy that has already occurred. There is scarce data on the incidence of this event as well as on the possible implications of ovarian stimulation on the course of an existing pregnancy. STUDY DESIGN, SIZE, DURATION This retrospective observational study, performed between June 2017 and January 2024, analyzed luteal phase stimulations, in which a natural conception pregnancy was detected during the ovarian stimulation treatment for IVF/ICSI. Luteal phase stimulation was defined as ovarian stimulation started after ovulation and before the next expected menstrual bleeding, with a serum progesterone (P4) level of >1.5 ng/ml on the day of stimulation start or 1 day before. PARTICIPANTS/MATERIALS, SETTING, METHODS Women who underwent a luteal phase ovarian stimulation in a tertiary referral ART center. MAIN RESULTS AND THE ROLE OF CHANCE A total of 488 luteal phase stimulation cycles were included in the analysis. Luteal phase stimulation was only started after a negative serum hCG measurement on the day or 1 day before commencement of ovarian stimulation. Ten patients (2.1%) had an undetected natural conception pregnancy at the time of luteal phase stimulation start. Eight of these patients underwent an ovarian stimulation in a GnRH-antagonist protocol and two in a progestin-primed stimulation protocol (PPOS). Recombinant FSH was used as stimulation medication for all patients, the patients with a PPOS protocol received additional recombinant LH. One pregnancy (0.2%) was detected after the oocyte retrieval, the other nine pregnancies were detected either due to persistent high serum progesterone levels or due to an increasing progesterone level after an initial decrease before oocyte retrieval. In the cycles with an undetected natural conception pregnancy, the median number of stimulation days was 8 days (range: 6–11 days) and median serum hCG at detection of pregnancy was 59 IU hCG (range: 14.91–183.1). From 10 patients with a pregnancy, three patients delivered a healthy baby, two patients had ongoing pregnancies at the time of summarizing the data, three patients had biochemical pregnancies (patient age: 30, 39, and 42 years), one patient had an ectopic pregnancy which required a salpingectomy, and one patient (age: 34 years) had an early pregnancy loss. LIMITATIONS, REASONS FOR CAUTION The retrospective study design and the small sample size can limit the accuracy of the estimates. WIDER IMPLICATIONS OF THE FINDINGS Overall, there is a small risk of undetected natural conception pregnancies when luteal phase stimulation is undertaken. It appears that there are no adverse effects through either direct effect on the embryo or indirectly through a detrimental effect on the corpus luteum function on the pregnancy in our cohort. STUDY FUNDING/COMPETING INTEREST(S) This study did not receive funding. The authors declare that there is no conflict of interest. TRIAL REGISTRATION NUMBER N/A. [ABSTRACT FROM AUTHOR]
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- 2024
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8. Conventional IVF revisited: Is ICSI better for non-male factor infertility? Randomized controlled double blind study
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Isikoglu, M., Avci, A., Kendirci Ceviren, A, Aydınuraz, B, and Ata, B
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- 2021
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9. Do women with severely diminished ovarian reserve undergoing modified natural‐cycle in‐vitro fertilization benefit from earlier trigger at smaller follicle size?
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Lawrenz, B., Kalafat, E., Ata, B., Melado, L., Del Gallego, R., Elkhatib, I., and Fatemi, H.
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OVARIAN reserve ,INDUCED ovulation ,MENSTRUAL cycle ,OVUM ,OVULATION - Abstract
Objective: To evaluate whether trigger and oocyte collection at a smaller follicle size decreases the risk of premature ovulation while maintaining the reproductive potential of oocytes in women with a severely diminished ovarian reserve undergoing modified natural‐cycle in‐vitro fertilization. Methods: This was a retrospective cohort study including women who had at least one unsuccessful cycle (due to no response) of conventional ovarian stimulation with a high dosage of gonadotropins and subsequently underwent a modified natural cycle with a solitary growing follicle (i.e. only one follicle > 10 mm at the time of trigger). The association between follicle size at trigger and various cycle outcomes was tested using regression analyses. Results: A total of 160 ovarian stimulation cycles from 110 patients were included in the analysis. Oocyte pick‐up (OPU) was performed in 153 cycles and 7 cycles were canceled due to premature ovulation. Patients who received their trigger at smaller follicle sizes (≤ 15 mm) had significantly lower rates of premature ovulation and thus higher rates of OPU (98.9% vs 90.8%; odds ratio, 9.56 (95% CI, 1.58–182.9); P = 0.039) compared with those who received their trigger at larger follicle sizes (> 15 mm). On multivariable analysis, smaller follicle sizes at trigger (> 10 to 13 mm, > 13 to 15 mm, > 15 mm to 17 mm) were not associated significantly with a lower rate of cumulus–oocyte complex (COC) retrieval, metaphase‐II (MII) oocytes or blastulation when compared to the > 17‐mm group. On sensitivity analysis including only the first cycle of each couple, the maturity rate among those with COC retrieval was highest in follicle sizes > 15 to 17 mm (92.3%) and > 13 to 15 mm (91.7%), followed by > 10 to 13 mm (85.7%) and lowest in the > 17‐mm group (58.8%). During the study period, five euploid blastocysts developed from 48 fertilized MII oocytes with follicle sizes of 12 mm (n = 3), 14 mm (n = 1) and 16 mm (n = 1) at trigger. Of those, four were transferred and resulted in two live births, both of which developed from follicles with a size at trigger of 12 mm. Conclusions: The ideal follicle size for triggering oocyte maturation may be smaller in women with a severely diminished ovarian reserve managed on a modified natural cycle when compared to conventional cut‐offs. The risk of OPU cancellation was significantly higher in women triggered at follicle size > 15 mm and the yield of mature oocytes was not adversely affected in women triggered at follicle size > 13 to 15 mm compared with > 15 to 17 mm. Waiting for follicles to reach sizes > 17mm may be detrimental to achieving optimal outcome. © 2024 International Society of Ultrasound in Obstetrics and Gynecology. [ABSTRACT FROM AUTHOR]
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- 2024
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10. Evidence for shallow cognitive maps in schizophrenia
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Karagoz, Ata B., primary, Moran, Erin K., additional, Barch, Deanna M., additional, Kool, Wouter, additional, and Reagh, Zachariah M., additional
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- 2024
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11. Do women with severely diminished ovarian reserve undergoing modified natural cycles benefit from earlier trigger at smaller follicle size?
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Lawrenz, B., primary, Kalafat, E., additional, Ata, B., additional, Melado, L., additional, Del Gallego, R., additional, Elkhatib, I., additional, and Fatemi, H., additional
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- 2024
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12. Correction to: The HERA (Hyper‑response Risk Assessment) Delphi consensus for the management of hyper‑responders in in vitro fertilization
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Feferkorn, I., primary, Santos‑Ribeiro, S., additional, Ubaldi, F. M., additional, Velasco, J. G., additional, Ata, B., additional, Blockeel, C., additional, Conforti, A., additional, Esteves, S. C., additional, Fatemi, H. M., additional, Gianaroli, L., additional, Grynberg, M., additional, Humaidan, P., additional, Lainas, G. T, additional, La Marca, A., additional, Craig, L. B., additional, Lathi, R., additional, Norman, R. J., additional, Orvieto, R., additional, Paulson, R., additional, Pellicer, A., additional, Polyzos, N. P., additional, Roque, M., additional, Sunkara, S. K., additional, Tan, S. L., additional, Urman, B., additional, Venetis, C., additional, Weissman, A., additional, Yarali, H., additional, and Dahan, M. H., additional
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- 2023
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13. The construction and use of cognitive maps in model-based control.
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Karagoz, Ata B., primary, Reagh, Zachariah M., additional, and Kool, Wouter, additional
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- 2023
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14. Evidence-based and experience-based medicine, which comes first: the chicken or the egg?
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Ata, B, primary and Saridogan, E, additional
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- 2023
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15. O-203 Unexplained infertility: diagnosis by exclusion
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Ata, B, primary, Bhattacharya, S, additional, Bosch, E, additional, Costello, M, additional, Dos Santos-Ribeiro, S, additional, Gersak, K, additional, Homburg, R, additional, Le Clef, N, additional, Mincheva, M, additional, Norman, R, additional, Piltonen, T, additional, Scicluna, D, additional, Somers, S, additional, Sunkara, S K, additional, Verhoeve, H, additional, and Romualdi, D, additional
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- 2023
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16. P-777 Can endometrial compaction predict live birth/ongoing pregnancy rates in assisted reproductive technology cycles? A systematic review and meta-analysis
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Turkgeldi, E, primary, Kalafat, E, additional, Yildiz, S, additional, Keles, I, additional, Ata, B, additional, and Bozdag, G, additional
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- 2023
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17. The Construction and Use of Cognitive Maps in Model-Based Control.
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Karagoz, Ata B., Reagh, Zachariah M., and Kool, Wouter
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When making decisions, we sometimes rely on habit and at other times plan toward goals. Planning requires the construction and use of an internal representation of the environment, a cognitive map. How are these maps constructed, and howdo they guide goal-directed decisions? We coupled a sequential decision-making task with a behavioral representational similarity analysis approach to examine how relationships between choice options change when people build a cognitive map of the task structure. We found that participants who encoded stronger higher-order relationships among choice options showed increased planning and better performance. These higher-order relationships were more strongly encoded among objects encountered in high-reward contexts, indicating a role for motivation during cognitive map construction. In contrast, lower-order relationships such as simple visual co-occurrence of objects did not predict goal-directed planning. These results show that the construction of cognitive maps is an active process, with motivation dictating the degree to which higher-order relationships are encoded and used for planning. [ABSTRACT FROM AUTHOR]
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- 2024
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18. Are systemic progesterone levels in true natural cycle euploid frozen embryo transfers with luteal phase support predictive for ongoing pregnancy rates?
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Lawrenz, B, primary, Ata, B, additional, Kalafat, E, additional, Melado, L, additional, ElKhatib, I, additional, Del Gallego, R, additional, and Fatemi, H, additional
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- 2023
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19. Generalization of cognitive maps across space and time
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Sherrill, Katherine R, primary, Molitor, Robert J, additional, Karagoz, Ata B, additional, Atyam, Manasa, additional, Mack, Michael L, additional, and Preston, Alison R, additional
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- 2023
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20. The HERA (Hyper-response Risk Assessment) Delphi consensus definition of hyper-responders for in-vitro fertilization
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Feferkorn, Ido, primary, Ata, B., additional, Esteves, S. C., additional, La Marca, A., additional, Paulson, R., additional, Blockeel, C., additional, Conforti, A., additional, Fatemi, H. M., additional, Humaidan, P., additional, Lainas, G. T., additional, Mol, B. W., additional, Norman, R. J., additional, Orvieto, R., additional, Polyzos, N. P., additional, Santos-Ribeiro, S., additional, Sunkara, S. K., additional, Tan, S. L., additional, Ubaldi, F. M., additional, Urman, B., additional, Velasco, J. G., additional, Weissman, A., additional, Yarali, H., additional, and Dahan, M. H., additional
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- 2023
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21. Mind the gap: deciphering the role of anti-Müllerian hormone in follicular development—from animal studies toward clinical application
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Fraire-Zamora, JJ, Sharma, K, Ammar, OF, Massarotti, C, Ali, ZE, Telfer, EE, Williams, S, Ata, B, and Liperis, G
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fertility ,Reproductive Medicine ,ESHRE Journal Club ,oogenesis ,Rehabilitation ,AMH ,Obstetrics and Gynecology ,atresia ,follicle development - Abstract
Anti-Müllerian hormone (AMH) is produced by granulosa cells during follicular development where it inhibits the transition from primordial to primary follicles. It also regulates the FSH sensitivity of early antral stages during dominant follicle selection (Broer et al., 2014). The inhibitory effect of AMH on primordial follicle activation has been described in several mammals (Durlinger et al., 2002; Nilsson et al., 2007; Yang et al., 2017) and has been considered the main mechanism maintaining the pool of primordial follicles from early exhaustion (Moolhuijsen and Visser, 2020). Other than the established role of AMH as an inhibitory molecule on follicle activation and the regulation of FSH sensitivity, it is important to decipher if AMH has any other functions. The December edition of the ESHRE Journal Club discussed a basic science research paper by Zhou et al. (2022), in which an additional role of AMH was suggested, as the results showed experimental evidence of AMH-induced atresia in murine preantral follicles. Zhou et al. used transgenic mice to determine the number of follicles in mice lacking the AMH gene (Amh−/−) and observed that these animals had less primordial follicles but more primary, secondary and small antral follicles compared to wild type mice. The authors observed that this difference was due to a higher survival ratio of primordial follicles transitioning into primary follicles. Mice that overexpress AMH had higher rates of follicle atresia as evidenced by apoptosis markers and empty primordial follicles, thus leading the authors to conclude that the role of AMH is not to maintain the ovarian reserve but rather to prevent the antral follicle pool becoming too large through AMH-induced atresia of preantral follicles. If these findings can be generalized to humans, they would represent a paradigm shift on the role of AMH and possibly affect clinical practice. The Journal Club discussion focused on the different implications of AMH-induced atresia both in biological and clinical contexts. These included the importance of AMH concentration levels, the role of FSH in rescuing follicles from AMH-induced atresia, the variation of AMH levels during ovarian suppression in humans, and the translation of the findings into clinical practice.
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- 2023
22. Generalization of cognitive maps across space and time
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Katherine R Sherrill, Robert J Molitor, Ata B Karagoz, Manasa Atyam, Michael L Mack, and Alison R Preston
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Cellular and Molecular Neuroscience ,Cognitive Neuroscience - Abstract
Prominent theories posit that associative memory structures, known as cognitive maps, support flexible generalization of knowledge across cognitive domains. Here, we evince a representational account of cognitive map flexibility by quantifying how spatial knowledge formed one day was used predictively in a temporal sequence task 24 hours later, biasing both behavior and neural response. Participants learned novel object locations in distinct virtual environments. After learning, hippocampus and ventromedial prefrontal cortex (vmPFC) represented a cognitive map, wherein neural patterns became more similar for same-environment objects and more discriminable for different-environment objects. Twenty-four hours later, participants rated their preference for objects from spatial learning; objects were presented in sequential triplets from either the same or different environments. We found that preference response times were slower when participants transitioned between same- and different-environment triplets. Furthermore, hippocampal spatial map coherence tracked behavioral slowing at the implicit sequence transitions. At transitions, predictive reinstatement of virtual environments decreased in anterior parahippocampal cortex. In the absence of such predictive reinstatement after sequence transitions, hippocampus and vmPFC responses increased, accompanied by hippocampal-vmPFC functional decoupling that predicted individuals’ behavioral slowing after a transition. Collectively, these findings reveal how expectations derived from spatial experience generalize to support temporal prediction.
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- 2023
23. Evidence-based guideline: unexplained infertility.
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Infertility, The Guideline Group on Unexplained, Romualdi, D, Ata, B, Bhattacharya, S, Bosch, E, Costello, M, Gersak, K, Homburg, R, Mincheva, M, Norman, R J, Piltonen, T, Santos-Ribeiro, S Dos, Scicluna, D, Somers, S, Sunkara, S K, Verhoeve, H R, and Clef, N Le
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INFERTILITY ,URINARY incontinence ,MALE reproductive organs ,INDUCED ovulation ,MONETARY incentives ,STOCK options ,MEDICAL writing - Abstract
STUDY QUESTION What is the recommended management for couples presenting with unexplained infertility (UI), based on the best available evidence in the literature? SUMMARY ANSWER The evidence-based guideline on UI makes 52 recommendations on the definition, diagnosis, and treatment of UI. WHAT IS KNOWN ALREADY UI is diagnosed in the absence of any abnormalities of the female and male reproductive systems after 'standard' investigations. However, a consensual standardization of the diagnostic work-up is still lacking. The management of UI is traditionally empirical. The efficacy, safety, costs, and risks of treatment options have not been subjected to robust evaluation. STUDY DESIGN, SIZE, DURATION The guideline was developed according to the structured methodology for ESHRE guidelines. Following formulation of key questions by a group of experts, literature searches, and assessments were undertaken. Papers written in English and published up to 24 October 2022 were evaluated. PARTICIPANTS/MATERIALS, SETTING, METHODS Based on the available evidence, recommendations were formulated and discussed until consensus was reached within the guideline development group (GDG). Following stakeholder review of an initial draft, the final version was approved by the GDG and the ESHRE Executive Committee. MAIN RESULTS AND THE ROLE OF CHANCE This guideline aims to help clinicians provide the best care for couples with UI. As UI is a diagnosis of exclusion, the guideline outlined the basic diagnostic procedures that couples should/could undergo during an infertility work-up, and explored the need for additional tests. The first-line treatment for couples with UI was deemed to be IUI in combination with ovarian stimulation. The place of additional and alternative options for treatment of UI was also evaluated. The GDG made 52 recommendations on diagnosis and treatment for couples with UI. The GDG formulated 40 evidence-based recommendations—of which 29 were formulated as strong recommendations and 11 as weak—10 good practice points and two research only recommendations. Of the evidence-based recommendations, none were supported by high-quality evidence, one by moderate-quality evidence, nine by low-quality evidence, and 31 by very low-quality evidence. To support future research in UI, a list of research recommendations was provided. LIMITATIONS, REASONS FOR CAUTION Most additional diagnostic tests and interventions in couples with UI have not been subjected to robust evaluation. For a large proportion of these tests and treatments, evidence was very limited and of very low quality. More evidence is required, and the results of future studies may result in the current recommendations being revised. WIDER IMPLICATIONS OF THE FINDINGS The guideline provides clinicians with clear advice on best practice in the care of couples with UI, based on the best evidence currently available. In addition, a list of research recommendations is provided to stimulate further studies in the field. The full guideline and a patient leaflet are available in www.eshre.eu/guideline/UI. STUDY FUNDING/COMPETING INTEREST(S) The guideline was developed by ESHRE, who funded the guideline meetings, literature searches, and dissemination of the guideline in collaboration with the Monash University led Australian NHMRC Centre of Research Excellence in Women's Health in Reproductive Life (CREWHIRL). The guideline group members did not receive any financial incentives; all work was provided voluntarily. D.R. reports honoraria from IBSA and Novo Nordisk. B.A. reports speakers' fees from Merck, Gedeon Richter, Organon and Intas Pharma; is part of the advisory board for Organon Turkey and president of the Turkish Society of Reproductive Medicine. S.B. reports speakers' fees from Merck, Organon, Ferring, the Ostetric and Gynaecological Society of Singapore and the Taiwanese Society for Reproductive Medicine; editor and contributing author, Reproductive Medicine for the MRCOG, Cambridge University Press; is part of the METAFOR and CAPE trials data monitoring committee. E.B. reports research grants from Roche diagnostics, Gedeon Richter and IBSA; speaker's fees from Merck, Ferring, MSD, Roche Diagnostics, Gedeon Richter, IBSA; E.B. is also a part of an Advisory Board of Ferring Pharmaceuticals, MSD, Roche Diagnostics, IBSA, Merck, Abbott and Gedeon Richter. M.M. reports consulting fees from Mojo Fertility Ltd. R.J.N. reports research grant from Australian National Health and Medical Research Council (NHMRC); consulting fees from Flinders Fertility Adelaide, VinMec Hospital Hanoi Vietnam; speaker's fees from Merck Australia, Cadilla Pharma India, Ferring Australia; chair clinical advisory committee Westmead Fertility and research institute MyDuc Hospital Vietnam. T.P. is a part of the Research Council of Finland and reports research grants from Roche Diagnostics, Novo Nordics and Sigrid Juselius foundation; consulting fees from Roche Diagnostics and organon; speaker's fees from Gedeon Richter, Roche, Exeltis, Organon, Ferring and Korento patient organization; is a part of NFOG, AE-PCOS society and several Finnish associations. S.S.R. reports research grants from Roche Diagnostics, Organon, Theramex; consulting fees from Ferring Pharmaceuticals, MSD and Organon; speaker's fees from Ferring Pharmaceuticals, MSD/Organon, Besins, Theramex, Gedeon Richter; travel support from Gedeon Richter; S.S.R. is part of the Data Safety Monitoring Board of TTRANSPORT and deputy of the ESHRE Special Interest Group on Safety and Quality in ART; stock or stock options from IVI Lisboa, Clínica de Reprodução assistida Lda; equipment/medical writing/gifts from Roche Diagnostics and Ferring Pharmaceuticals. S.K.S. reports speakers' fees from Merck, Ferring, MSD, Pharmasure. HRV reports consulting and travel fees from Ferring Pharmaceuticals. The other authors have nothing to disclose. DISCLAIMER This guideline represents the views of ESHRE, which were achieved after careful consideration of the scientific evidence available at the time of preparation. In the absence of scientific evidence on certain aspects, a consensus between the relevant ESHRE stakeholders has been obtained. Adherence to these clinical practice guidelines does not guarantee a successful or specific outcome, nor does it establish a standard of care. Clinical practice guidelines do not replace the need for application of clinical judgment to each individual presentation, nor variations based on locality and facility type. ESHRE makes no warranty, express or implied, regarding the clinical practice guidelines and specifically excludes any warranties of merchantability and fitness for a particular use or purpose. (Full disclaimer available at www.eshre.eu/guidelines.) [ABSTRACT FROM AUTHOR]
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- 2023
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24. SARS-CoV-2, fertility and assisted reproduction
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Ata, B. (Baris), Vermeulen, N. (Nathalie), Mocanu, E. (Edgar), Gianaroli, L. (Luca), Lundin, K. (Kersti), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), Veiga, A. (Anna), Ata, B. (Baris), Vermeulen, N. (Nathalie), Mocanu, E. (Edgar), Gianaroli, L. (Luca), Lundin, K. (Kersti), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), and Veiga, A. (Anna)
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Background: In 2020, SARS-CoV-2 and the COVID-19 pandemic had a huge impact on the access to and provision of ART treatments. Gradually, knowledge of the virus and its transmission has become available, allowing ART activities to resume. Still, questions on the impact of the virus on human gametes and fertility remain. Objective and rationale: This article summarizes published data, aiming to clarify the impact of SARS-CoV-2 and the COVID-19 disease on human fertility and assisted reproduction, as well as the impact of vaccination, and from this, provide answers to questions that are relevant for people contemplating pregnancy and for health care professionals. Search methods: PUBMED/MEDLINE and the WHO COVID-19 database were searched from inception to 5 October 2022 with search terms focusing on ‘SARS-CoV-2’ and gametes, embryos, reproductive function, fertility and ART. Non-English studies and papers published prior to 2020 were excluded, as well as reviews and non-peer reviewed publications. Full papers were assessed for relevance and quality, where feasible. Outcomes: From the 148 papers included, the following observations were made. The SARS-CoV-2-binding proteins, angiotensin-converting enzyme 2 (ACE2) and type II transmembrane serine protease (TMPRSS2), are expressed in the testis, but co-expression remains to be proven. There is some evidence of SARS-CoV-2 RNA in the ejaculate of COVID-19 patients with severe disease, but not in those with mild/moderate disease. SARS-CoV-2 infection can impair spermatogenesis, but this seems to resolve after one spermatogenic cycle. Testosterone levels seem to be lower during and after COVID-19, but long-term data are lacking; disease severity may be associated with testosterone levels. COVID-19 cannot be considered a sexually transmitted disease. There is no co-expression of ACE2 and TMPRSS2 in the myometrium, uterus, ovaries or fallopian tubes. Oocytes seem to have the receptors and protease machinery to be susce
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- 2022
25. Infantile or hypoplastic uterus? A proposal for a modification to the ESHRE/ESGE classification of female genital tract congenital abnormalities
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Küçük, T, primary and Ata, B, additional
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- 2022
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26. Clinical severity of SARS‐CoV ‐2 infection among vaccinated and unvaccinated pregnancies during the Omicron wave
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Birol Ilter, P., primary, Prasad, S., additional, Berkkan, M., additional, Mutlu, M. A., additional, Tekin, A. B., additional, Celik, E., additional, Ata, B., additional, Turgal, M., additional, Yildiz, S., additional, Turkgeldi, E., additional, O'Brien, P., additional, von Dadelszen, P., additional, Magee, L. A., additional, Kalafat, E., additional, Tug, N., additional, and Khalil, A., additional
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- 2022
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27. The role of corifollitropin alfa in controlled ovarian stimulation for IVF in combination with GnRH antagonist
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Seyhan A and Ata B
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Gynecology and obstetrics ,RG1-991 - Abstract
Ayse Seyhan, Baris AtaDivision of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology, McGill University, Montreal, QC, CanadaAbstract: Corifollitropin alfa is a synthetic recombinant follicle-stimulating hormone (rFSH) molecule containing a hybrid beta subunit, which provides a plasma half-life of ∼65 hours while maintaining its pharmocodynamic activity. A single injection of corifollitropin alfa can replace daily FSH injections for the first week of ovarian stimulation for in vitro fertilization. Stimulation can be continued with daily FSH injections if the need arises. To date, more than 2500 anticipated normoresponder women have participated in clinical trials with corifollitropin alfa. It is noteworthy that one-third of women did not require additional gonadotropin injections and reached human chorionic gonadotropin criterion on day 8. The optimal corifollitropin dose has been calculated to be 100 µg for women with a body weight ≤ 60 kg and 150 µg for women with a body weight >60 kg, respectively. Combination of corifollitropin with daily gonadotropin-releasing hormone antagonist injections starting on stimulation day 5 seems to yield similar or significantly higher numbers of oocytes and good quality embryos, as well as similar ongoing pregnancy rates compared with women stimulated with daily rFSH injections. Stimulation characteristics, embryology, and clinical outcomes seem consistent with repeated corifollitropin-stimulated assisted reproductive technologies cycles. Multiple pregnancy or ovarian hyperstimulation syndrome rates with corifollitropin were not increased over daily FSH regimen. The corifollitropin alfa molecule does not seem to be immunogenic and does not induce neutralizing antibody formation. Drug hypersensitivity and injection-site reactions are not increased. Incidence and nature of adverse events and serious adverse events are similar to daily FSH injections. Current trials do not provide information regarding use of corifollitropin alfa in anticipated hyper- and poor responders to gonadotropin stimulation. Although corifollitropin alfa is unlikely to be teratogenic, at the moment data on congenital malformations is missing.Keywords: follicle-stimulating hormone, long acting, controlled ovarian hyperstimulation, in vitro fertilization, assisted reproduction
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- 2011
28. General gynecology
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Salfelder A., Lueken R. P., Bormann C., Gallinat A., Moeller C. P., Busche D., Nugent W., Krueger E., Nugent A., Caglar G., Tasci Y., Kayikcioglu F., Haberal A., Hasskamp Th., Krichbaum M., Aka N., Köse G., Sabah G., Sayharman E. S., Kumru P., Aka N., Karaca K., Köse G., Kumru P., Sayharman E. S., Haydardedeoglu B., Simsek E., Kilicdag E., Tarim E., Bagis T., Dede F. S., Dilbaz B., Dede H., Ilhan A. K., Haberal A., Dede F. S., Dilbaz B., Oral S., Erten A., Ilhan A. K., Haberal A., Ertas I. E., Kahyaoglu S., Turgay I., Tug M., Kalyoncu S., Batioglu S., Zorlu G., Arici C., Akar M. E., Ari E. S., Ari E., Erbay O. U., Caliskan M. O., Akar M. E., Simsek M., Taskm O., Gümüs Il., Turhan N. O., Arikan G., Giuliani A., Kelekci S., Yorgancioglu Z., Yilmaz B., Yasar L., Savan K., Sonmez S., Kart C., Vural M., Tanriverdi H. A., Cinar E., Barut A., Özbay K., Yardim T., Demir B., Kilinc N., Gul T., Erden A. C., Turgay I., Kahyaoglu S., Kokanali M. K., Batioglu S., Haydardedeoglu B., Simsek E., Kilicdag E. B., Tarim E., Aslan E., Bagis T., Seval M., Taskin S., Özmen B., Kahraman K., Yarci A., Tasci T., Unlü C., Taskin S., Seval M., Özmen B., Kahraman K., Gözükücük M., Kurt S., Unlü C., Taskin S., Özmen B., Bozaci E. A., Seval M., Ortac F., Yasar L., Sönmez A. S., Zebitay A. G., Gezer N., Yazicioglu H. F., Mehmetoglu G., Dede F. S., Dilbaz B., Kocak M., Dede H., Haberal A., Erten A., Ilhan A. K., Algül Y. L., Erden A. C., Yasar L., Zebitay A. G., Ozcan J., Duman O., Sonmez S., Yazicioglu F., Sensoy Y., Koc S., Cebi Z., Yasar L., Zebitay A. G., Özcan J., Duman O., Sönmez S., Yazicioglu F., Sensoy Y., Cebi Z., Zebitay A. G., Yasar L., Özcan J., Duman O., Sönmez S., Yazicioglu F., Sensoy Y., Koc S., Cebi Z., Zebitay A. G., Yasar L., Özcan J., Duman O., Sönmez S., Yazicioglu F., Sensoy Y., Cebi Z., Simsek M., Mendilcioglu I., Özekinci M., Ulukus M., Ulukus E. C., Seval Y., Cinar O., Zheng W., Arici A., Erkan L., Soylu F., Tatli O., Ozkent V., Dilbaz B., Ilhan A. K., Oral S., Dede H., Dogan A. R., Gün I., Erdemoglu E., Sargin H., Kamaci M., Dede F. S., Erten A., Sendag F., Akman L., Yucebilgin S., Karadadas N., Oztekin K., Bilgin O., Topuz S., Cigerli E., Iyibozkurt C. A., Akhan E. S., Saygili H., Berkman S., Bezircioglu I., Karakaya E., Baran N., Baloglu A., Aydin C., Hizli N., Cetinkaya B., Kavas A., Baloglu A., Cukurova K., Köksal A., Yetimalar H., Yildiz A., Ivit H., Keklik A., Pinar F., Aka N., Köse G., Tosun N., Kumru P., Tuncel T., Boynukalin K., Salman M. C., Ozyuncu O., Bozdag G., Ayhan A., Ates U., Usta T., Seyhan A., Ata B., Sidal B., Guler O. T., Salman M. C., Bozdag G., Ozyuncu O., Esin S., Ozyuncu O., Salman M. C., Bozdag G., Guven S., Gürban A., Gürban G., Özen S., Kirecci A., Özkesici B., Yücel S., Süer N., Erdemoglu E., Gün I., Sargin H., Erdemoglu C. E., Kamaci M., Akhan S. E., Citil I., Topuz S., Iyibozkurt C., Kesim M. D., Atis A., Aydin Y., Özpak D., Tashan F., Zeteroglu S., Kolusari A., Altunay H., Sahin H. G., Kamaci M., Kayikcioglu F., Erol O., Sarici S., Haberal A., Dingiloglu B. S., Güngör T., Özdal B., Cavkaytar S., Bilge Ü., Mollamahmutoglu L., Toprak Konca M., Özsoy S., Hekim N., Özel E., Senates M., Yener C., Göker N., Caliskan E., Filiz T., Yucesoy G., Coskun E., Vural B., Corakci A., Narin M. A., Caliskan E., Kayikcioglu F., Haberal A., Meydanli M. M., Kamaci M., Sahin H. G., Kolusari A., Yildizbas B., Bolluk G., Ates U., Usta T., Ata B., Seyhan A., Ozdemir B., Sidal B., Ünlü B. S., Aytan H., Evsen S., Tapisiz Ö L., Zergeroglu S., Zeteroglu S., Sahin H. G., Guler A., Kolusari A., Kamaci M., Altay M. M., Can A., Ungormus A., Polat A., and Haberal A.
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- 2005
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29. Are live birth rate and obstetric outcomes different between immediate and delayed embryo transfers following a freeze-all cycle? A retrospective study combined with a meta-analysis
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Yildiz, S., Turkgeldi, E., Kalafat, Erkan, Gokyer, D., Keles, I., Ata, B., and OpenMETU
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- 2021
30. P–691 How predictive is endometrial thickness for live birth after fresh and frozen-thawed embryo transfer when no cut-off is employed?
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Turkgeldi, E, primary, Shakerian, B, additional, Yildiz, S, additional, Keles, I, additional, and Ata, B, additional
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- 2021
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31. P–692 Are live birth rate and obstetric outcomes different between immediate and delayed embryo transfers following a freeze-all cycle? A retrospective study combined with a meta-analysis
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Yildiz, S, primary, Turkgeldi, E, additional, Kalafat, E, additional, Gokyer, D, additional, Keles, I, additional, and Ata, B, additional
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- 2021
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32. P–709 Dual stimulation in-vitro-maturation (Duostim IVM) for overcoming oocyte maturation arrest, resulting in embryo transfer and livebirth
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Hatirnaz, S, primary, Hatirnaz, E, additional, Dahan, M, additional, Ata, B, additional, Basbug, A, additional, Hatirnaz, K, additional, and Tan, S, additional
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- 2021
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33. O-036 COVID-19, vertical transmission and ART pregnancy outcomes
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Ata, B, primary
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- 2021
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34. P–342 Are blastulation and clinical pregnancy rates in women with endometriomas different than those without?
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Kantarci, R, primary, Gule. Cekic, S, additional, Türkgeldi, E, additional, Yildiz, S, additional, Keles, I, additional, and Ata, B, additional
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- 2021
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35. The calm after the storm:re-starting ART treatments safely in the wake of the COVID-19 pandemic
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T. E. (The ESHRE COVID-19 Working Group), Gianaroli, L. (Luca), Ata, B. (Baris), Lundin, K. (Kersti), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), Vermeulen, N. (Nathalie), Veiga, A. (Anna), and Mocanu, E. (Edgar)
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medically assisted reproduction ,coronavirus disease 2019 ,IVF ,SARS-CoV-2 ,pandemic ,COVID-19 ,triage ,ART services ,testing ,severe acute respiratory syndrome coronavirus 2 - Abstract
The coronavirus disease 2019 (COVID-19) pandemic created a significant impact on medically assisted reproduction (MAR) services. ESHRE decided to mobilize resources in order to collect, analyse, monitor, prepare and disseminate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) knowledge specifically related to ART and early pregnancy. This article presents the impact of the SARS-CoV-2 pandemic focusing on reproductive healthcare. It details the rationale behind the guidance prepared to support MAR services in organizing and managing the re-start of treatments or in case of any future wave of COVID-19 disease. The guidance includes information on patient selection and informed consent, staff and patient triage and testing, adaptation of ART services, treatment planning and code of conduct. The initiatives detailed in this article are not necessarily COVID-specific and such action plans could be applied effectively to manage similar emergency situations in different areas of medicine, in the future.
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- 2021
36. Dual stimulation in-vitro-maturation (Duostim IVM) for overcoming oocyte maturation arrest, resulting in embryo transfer and livebirth
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Hatirnaz, S., Hatirnaz, E., Dahan, M., Ata, B., Basbug, A., Hatirnaz, K., Tan, S., and [Belirlenecek]
- Abstract
[Abstract Not Available] WOS:000672766502132
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- 2021
37. Outcomes of SARS-CoV-2 infected pregnancies after medically assisted reproduction
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T. E. (The ESHRE COVID-19 Working Group), Ata, B. (Baris), Gianaroli, L. (Luca), Lundin, K. (Kersti), Mcheik, S. (Saria), Mocanu, E. (Edgar), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), Vermeulen, N. (Nathalie), Veiga, A. (Anna), T. E. (The ESHRE COVID-19 Working Group), Ata, B. (Baris), Gianaroli, L. (Luca), Lundin, K. (Kersti), Mcheik, S. (Saria), Mocanu, E. (Edgar), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), Vermeulen, N. (Nathalie), and Veiga, A. (Anna)
- Abstract
Study question: What is the impact of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection on the outcome of a pregnancy after medically assisted reproduction (MAR)? Summary answer: Our results suggest that MAR pregnancies are not differentially affected by SARS-CoV-2 infection compared to spontaneous pregnancies. What is known already: Information on the effects of coronavirus disease 2019 (COVID-19) on pregnancy after MAR is scarce when women get infected during MAR or early pregnancy, even though such information is vital for informing women seeking pregnancy. Study design, size, duration: Data from SARS-CoV-2 affected MAR pregnancies were collected between May 2020 and June 2021 through a voluntary data collection, organised by the European Society of Human Reproduction and Embryology (ESHRE). Participants/materials, setting, methods: All ESHRE members were invited to participate to an online data collection for SARS-CoV-2-infected MAR pregnancies. Main results and the role of chance: The dataset includes 80 cases from 32 countries, including 67 live births, 10 miscarriages, 2 stillbirths and 1 maternal death. An additional 25pregnancies were ongoing at the time of writing. Limitations, reasons for caution: An international data registry based on voluntary contribution can be subject to selective reporting with possible risks of over- or under-estimation. Wider implications of the findings: The current data can be used to guide clinical decisions in the care of women pregnant after MAR, in the context of the COVID-19 pandemic. Study funding/competing interest(s): The authors acknowledge the support of ESHRE for the data registry and meetings. J.S.T. reports grants or contracts from Sigrid Juselius Foundation, EU and Helsinki University Hospital Funds, outside the scope of the current work. The other authors declare that they have no conflict of interest.
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- 2021
38. Obstetric outcomes of IVF trichorionic triamniotic triplets which are spontaneously or electively reduced to twins
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Ata, B., Rasillo, L. J., Sukhdeo, S., Son, W. Y., Tan, S. L., and Dahan, M. H.
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- 2011
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39. Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease
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Ridker PM, Everett BM, Thuren T, MacFadyen JG, Chang WH, Ballantyne C, Fonseca F, Nicolau J, Koenig W, Anker SD, Kastelein JJP, Cornel JH, Pais P, Pella D, Genest J, Cifkova R, Lorenzatti A, Forster T, Kobalava Z, Vida-Simiti L, Flather M, Shimokawa H, Ogawa H, Dellborg M, Rossi PRF, Troquay RPT, Libby P, Glynn RJ, Novo S, Krum H, Varigos J, Siostrzonek P, Sinnaeve P, Gotcheva N, Yong H, Urina-Triana M, Milicic D, Vettus R, Manolis AJ, Wyss F, Sigurdsson A, Fucili A, Veze I, Petrauskiene B, Salvador L, Klemsdal TO, Medina F, Budaj A, Otasevic P, Lainscak M, Seung KB, Commerford P, Donath M, Hwang JJ, Kultursay H, Bilazarian S, East C, Forgosh L, Harris B, Ligueros M, Bohula E, Charmarthi B, Cheng S, Chou S, Danik J, McMahon G, Maron B, Ning M, Olenchock B, Pande R, Perlstein T, Pradhan A, Rost N, Singhal A, Taqueti V, Wei N, Burris H, Cioffi A, Dalseg AM, Ghosh N, Gralow J, Mayer T, Rugo H, Fowler V, Limaye AP, Cosgrove S, Levine D, Lopes R, Scott J, Hilkert R, Tamesby G, Mickel C, Manning B, Woelcke J, Tan M, Manfreda S, Ponce T, Kam J, Saini R, Banker K, Salko T, Nandy P, Tawfik R, O’Neil G, Manne S, Jirvankar P, Lal S, Nema D, Jose J, Collins R, Bailey K, Blumenthal R, Colhoun H, Gersh B, Abreu M, Actis MV, Aiub J, Aiub F, Albisu J, Alvarisqueta A, Avalos V, Barreto M, Berli MA, Blumberg C, Bocanera M, Botta C, Bowen L, Budassi N, Buhlman S, Westberg JC, Carabajal T, Caruso G, Casala J, Cendali G, Coloma G, Berra FC, Cuneo C, Degennaro N, Dellasa M, Diaz M, Dos Santos P, Espinosa V, Facello A, Facello M, Farias E, Fernandez AA, Ferrari V, Pacora FF, Flores GS, Franco M, Gabito A, Viola HG, Garcia F, Garcia Duran R, Garcia Pinna J, Glenny J, Godoy Sanchez M, Grosse A, Guzman P, Hasbani E, Hominal M, Ibañez J, Jure H, Jure D, Vico ML, Liniado G, Luciardi H, Luquez H, Maehara G, Maffei L, Majul C, Mallagray M, Marinaro S, Martinez J, Massaccesi R, De Los Milagros Had M, Azize GM, Montana O, Montenegro E, Morell Y, Muntaner J, Navarrete S, Olmedo M, Paganini M, Paz S, Perez Manghi F, Piskorz D, Polato C, Recoaro R, Romano A, Salinger M, Sanchez A, Saravia MA, Sarjanovich R, Scaro G, Schiavi LB, Soler J, Tinnirello V, Tomassi A, Valle M, Vallejo MA, Venturini C, Marcela Wenetz LM, Yossen M, Zaidman C, Zalazar L, Zangroniz P, Amerena J, Brady L, Colquhoun D, Eccleston D, Ferreira-Jardim A, French J, Jayasinghe R, Mcintosh C, Ord M, Plotz M, Purnell P, Roberts-Thomson P, Schultz C, Shanahan T, Tan R, Taverner P, Turner F, Vibert J, Vorster M, William M, Youssef G, Bergler-Klein J, Brath H, Brodmann M, Fliesser-Goerzer E, Haider K, Heeren G, Hiden C, Mandic L, Paulweber B, Ploechl A, Prenner A, Steringer-Mascherbauer R, Strohner-Kaestenbauer H, Barbato E, Bouvy C, Briké C, Charlier F, Cools F, De Knijf K, De Wolf L, Delforge M, Deweerdt N, Gits F, Goffinet C, Hermans K, Hollanders G, Mestdagh I, Pirenne B, Servaes V, Simons N, Tahon S, Theunissen E, Van Genechten G, Vervoort G, Vissers C, Vranckx P, Vrolix M, Abib E Jr, Abrantes J, Araujo Fonseca M, Barbosa E, Barroso W, Barroso A, Bodanese L, Botelho R, Costa Amorim R, Da Costa F, Da Silva A, Da Silva O Jr, Da Silva D Jr, Ferreira Dos Santos T, Dos Santos F, Dos Santos A, Duda N, Feitosa G, Felario Junior GA, Ferraz R, Filho P, Fonseca A, Wanderley FF, Freitas E, Fucci F, Marengo Garcia De Carvalho L, Hernandez M, Hettwer Magedanz E, Julião K, Kormann A, Lameira A, Lima F, Lino E, Maia L, Manenti E, Marchi AL, Fischer SM, Michalaros Y, Moraes J Jr, Moreira L, Pagnan M, Pesce F, Pinheiro L, Rassi S, Reis G, Reis H, Resende I, Roel A, Ruschel K, Saporito W, Saraiva JF, Seroqui M, Silva R, Unterkircher B, Vicente C, Vieira N, Xavier JP, Zucchetti C, Angelova I, Dimitrov G, Genova D, Gospodinov K, Goudev A, Grigorova V, Hristova K, Makedonska JJ, Katova T, Kostov K, Lazov P, Manov E, Manukov I, Manukov D, Milanova M, Kabakchieva VM, Petrov D, Petrusheva T, Pramatarova I, Raev D, Runev N, Sirakova-Taseva A, Tisheva-Gospodinova S, Todorova A, Tzekova M, Yakovova S, Yanev T, Abulencia K, Arora S, Baker A, Bata IR, Beaudry M, Belle Isle J, Bilodeau N, Boivin MC, Bolduc H, Bourgeois S, Brons S, Cantor W, Chaussé I, Chhabra A, Chouinard G, Cleveland T, Dattani D, Deslongchamps F, Diodati J, Drouin K, Duchesne L, Fontaine S, d'Amours DG, Gervais B, Gosselin G, Graham J, Grover A, Gupta A, Haldane H, Hartleib M, Hickey L, Huynh T, Johnston J, Julien VE, Lachance P, Lake J, Lamontagne C, Lauzon C, Lepage S, Maheux K, Manyari D, Martin E, McPherson C, Mehta S, Michaud N, Kouz SM, Murphy G, OKeefe D, Otis R, Ouimet F, Pandey S, Peck C, Perkins L, Richert L, Robbins K, Robinson S, Cabau JR, Ross B, Roy C, Roy M, Roy A, Rupka D, Affaki GS, Saunders K, Savard D, Soucy D, St Amour E, Thiessen S, Vertes G, Vezina M, Vincelli G, Weisnagel SJ, Zadra R, Chen J, Chen Y, Dong X, Feng Y, Feng Z, Fu G, Han B, Hao Y, He Y, He Z, Hong T, Jia Z, Jiang T, Jiang J, Jiang X, Ke Y, Li Y, Li Z, Li W, Li X, Liu P, Liu Y, Liu B, Liu S, Liu L, Lu Z, Lv Y, Ma C, Ma G, Peng L, Qing L, Ren L, Sang X, Song M, Sun Z, Wang J, Wang Y, Wei J, Wu W, Wu J, Xu H, Yan J, Yang P, Yang K, Yao Z, Yaoqing H, Yuan Z, Zhai Z, Zhang J, Zhang Y, Zhao R, Zhou H, Accini Mendoza JL, Aparicio CV, Castillo T, Chaverra I, Conrado Y, Coronel J, Cotes C, Cuentas I, Cuervo A, Dussan MA, Echeverria L, Hernandez E, Ibarra J, Isaza D, Jimenez D, Lopez P, Manzur F, Mejia I, Mendoza Y, Molina DI, Patino JM, Rodriguez D, Rodriguez LM, Rodriguez SM, Sanchez Vallejo G, Luz Serrano H, Sotomayor A, Urina M, Vesga B, Yupanqui H, Akrap B, Busic N, Ciglenecki N, Cmrecnjak J, Fucak E, Gabor M, Jeric M, Jutrisa N, Kordic K, Planinc I, Popovic Z, Radeljic V, Sesto I, Sutalo K, Tusek S, Belohlavek J, Budkova J, Busak L, Capova L, Cech V, Cermak O, Coufalova Z, Cyprian R, Dedek V, Dedkova S, Ferkl R, Hanak P, Hanustiakova A, Homza M, Horackova K, Houra M, Iveta H, Kaiserova L, Kala P, Karel I, Kellnerova I, Koleckar P, Kreckova M, Krupicka J, Lorenc Z, Machova V, Malik J, Masarikova L, Matyasek I, Mikus M, Mikusova T, Ondrasik J, Otava M, Palubova L, Pavlickova L, Peterka M, Petrova I, Pokorna B, Povolny P, Radvan M, Reznakova S, Rickova Z, Roszkowska P, Rotreklova M, Samkova D, Skalicka H, Slechticka A, Sternthal P, Telekes P, Tesak M, Vesely P, Vesely J, Vins P, Vitovec M, Vodnansky P, Zidova M, Keba E, Laane E, Pool T, Randvee L, Ratnik E, Reimand M, Reinmets S, Rivis L, Siemann M, Stern M, Toom M, Vahula V, Apel T, Axthelm C, Ayasse D, Ayasse M, Baar M, Baeumer A, Bagi ES, Becker B, Binder A, Blankenberg S, Braun P, Johansen BB, Contzen C, Delfonso F, Denecke C, Dengler T, Donaubauer T, Eichinger G, Englmann E, Erhard M, Faghih M, Foerster A, Frankenstein L, Fuchs R, Furch G, Gaeb-Strasas B, Germann H, Giese C, Goette A, Gravenhorst-Muenter U, Haege R, Haenel T, Hagemann D, Hagenow A, Hanefeld M, Heider J, Heisters J, Hennig D, Hielscher S, Himpel-Boenninghoff A, Holscher A, Hornig M, Jeserich M, Kaczmarek N, Kanitz S, Kara YD, Khariouzov A, Kiefer R, Kiroglu K, Klamm M, Klein C, 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B, Mbulaiteye A, Mcalister R, Mccoy C, Mccrary D Jr, Mccullough-O'Brien H, Mcdonald M, Mcgill J, Mcgrew F, Mckenzie C, Mclaurin B, Mclellan BA, Mcneil D, Mcneill R, Mehrle A, Melbie K, Melliza T, Messina T, Meyer R, Michel K, Mikdadi G, Miller C, Miller R, Miller A, Miller G, Miller W, Mitchell J, Moats DJR, Mody F, Moffat J, Molk B, Molter D, Monroe T, Montero H, Montgomery R, Mookherjee D, Moran J, Moriarty P, Morrison J, Morton D, Moshayedi P, Mosley J, Moustafa M, Munshi K, Murray A, Mustafa J, Nadar V, Naidu R, Nalley J, Navy S, Neil L, Neutel JM, Niblack P, Nicely V, Nicolai M, Nijmeh G, Nikas A, Nikyar A, Nixon S, Norman L, Noto G, Nour K, Nugent A, Ocman B, Odegard A, Olsen S, Ortiz-Carrasquillo R, Ossino N, Paez H, Palchick B, Paliwal Y, Pannell R, Parfait V, Partridge J, Patel B, Patel R, Patel M, Patel S, Paysor C, Pena A, Pereira S, Perez M, Perez A, Perkins H, Perry B, Peters P, Phillippi C, Phillips A, Phillips A, Piacente R, Pintado M, Pish R, Pitt W, Poling T, Pomposini D, Poock J, Potts J, Poudrier R, Prior J, Pritchard C, Purighalla R, Quddusi K, Quinones J, Quinton D, Radin M, Radojcsics B, Rajput B, Rama B, Ramos M, Rauch R, Raynes K, Reber AM, Reddy J, Reeves M, Reilly K, Renaud K, Resnick H, Reyes R, Richardson M, Riethof M, Riser J, Rodero M, Rodriguez Araya E, Roper L, Rozeman P, Ruder D, Runquist L, Sack G, Saint-Jacques H, Salfity M, Sall N, Sam K, Samal A, Sanchez D, Santiago J Jr, Savignano C, Saylor R, Scheffel M, Schifferdecker B, Schindler E, Schneider P, Schneider R, Schnitzler R, Schrager B, Schwartz A, Scott R, Seals A, Shah AV, Shah A, Shatsky K, Shayani S, Shealy N, Sheets L, Shelley J, Shepard P, Shetty S, Silver K, Simon M, Singh K, Singh N, Sizemore BC, Skatrud L, Slayton C, Slimak V, Sloane G, Smallwood B, Smith P, Smith M, Smith T, Smith G, Smith B, Smith W, Smith M, Smith J, Smith J, Soca Y, Sofley C, Sopko K, Sosa-Padilla M, Sotolongo R, Sprinkle B, Srivastava S, Starzec M, Steinhoff J, Stelly L, Stinson J, Stoddard M, Stoltz S, Stone B, Stover T, Strain J, Strugatsky S, Stys T, Suleman A, Sullivan P, Tamez W, Tandon N, Teltser M, Terry PS, Terry K, Tessmar C, Thekkoott D, Thomas D, Thomas DM, Thompson E, Thompson J, Thornton A, Tjaden T, Tobias C, Topper J, Tran A, Treasure C, Trenkamp P, Trevino M, Tsou L, Tuholske C, Uy W, Vahtel M, Vaid B, Valenzuela M, Vance A, Vandam J, Vanhecke T, Vanness WC III, Vargas R, Vaz S, Vazquez Tanus J, Veerina K, Vega J, Vento A, Vijay N, Voelker F, Vogt E, Vold D, Vora K, Wade RD, Wadell C, Waksman R, Walker K, Walker K, Wallace K, Warren M, Washam M, Watson B, Webel R, Wells T, West M, Whitaker J, White J, White C, White A, White A, Wilhoit G, Wilkins M, Willingham K, Wilson S, Wilson V, Wise J, Woodall S, Woods A, Wright J, Wu J, Xu ZJ, Yarows S, Young A, Younis L, Zarate J, Zebrack J, Zhang W, Zieve F, Zineldine A, Ridker, P. M., Everett, B. M., Thuren, T., Macfadyen, J. G., Chang, W. H., Ballantyne, C., FONSECA E PIRES, CARLOS EDUARDO, Nicolau, J., Koenig, W., Anker, S. D., Kastelein, J. J. P., Cornel, J. H., Pais, P., Pella, D., Genest, J., Cifkova, R., Lorenzatti, A., Forster, T., Kobalava, Z., Vida-Simiti, L., Flather, M., Shimokawa, H., Ogawa, H., Dellborg, M., Rossi, P. R. F., Troquay, R. P. T., Libby, P., Glynn R., J, CANTOS Trial, Group, Perrone, Filardi, P, ACS - Amsterdam Cardiovascular Sciences, Vascular Medicine, ACS - Pulmonary hypertension & thrombosis, and ACS - Atherosclerosis & ischemic syndromes
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0301 basic medicine ,030204 cardiovascular system & hematology ,law.invention ,0302 clinical medicine ,c-reactive protein ,Randomized controlled trial ,law ,Cardiovascular Disease ,middle aged ,double-blind method ,antibodies ,Myocardial infarction ,humans ,Stroke ,interleukin-1beta ,biology ,Antibodies, Monoclonal ,drug ,General Medicine ,Lipid ,Aged ,anti-inflammatory agents ,monoclonal ,humanized ,atherosclerosis ,cardiovascular diseases ,dose-response relationship ,female ,incidence ,infections ,lipids ,male ,myocardial infarction ,neutropenia ,secondary prevention ,stroke ,Anti-Inflammatory Agent ,aged ,Editorial ,Atherosclerosi ,Monoclonal ,Human ,medicine.drug ,medicine.medical_specialty ,Neutropenia ,Antibodies, Monoclonal, Humanized ,Infections ,Placebo ,antibodies, monoclonal ,dose-response relationship, drug ,infection ,medicine (all) ,03 medical and health sciences ,Internal medicine ,medicine ,Dose-Response Relationship, Drug ,business.industry ,Antiinflammatory Therapy, Canakinumab, for Atherosclerotic Disease ,C-reactive protein ,medicine.disease ,Surgery ,Canakinumab ,030104 developmental biology ,biology.protein ,business - Abstract
Background: Experimental and clinical data suggest that reducing inflammation without affecting lipid levels may reduce the risk of cardiovascular disease. Yet, the inflammatory hypothesis of atherothrombosis has remained unproved. Methods: We conducted a randomized, double-blind trial of canakinumab, a therapeutic monoclonal antibody targeting interleukin-1β, involving 10,061 patients with previous myocardial infarction and a high-sensitivity C-reactive protein level of 2 mg or more per liter. The trial compared three doses of canakinumab (50 mg, 150 mg, and 300 mg, administered subcutaneously every 3 months) with placebo. The primary efficacy end point was nonfatal myocardial infarction, nonfatal stroke, or cardiovascular death. RESULTS: At 48 months, the median reduction from baseline in the high-sensitivity C-reactive protein level was 26 percentage points greater in the group that received the 50-mg dose of canakinumab, 37 percentage points greater in the 150-mg group, and 41 percentage points greater in the 300-mg group than in the placebo group. Canakinumab did not reduce lipid levels from baseline. At a median follow-up of 3.7 years, the incidence rate for the primary end point was 4.50 events per 100 person-years in the placebo group, 4.11 events per 100 person-years in the 50-mg group, 3.86 events per 100 person-years in the 150-mg group, and 3.90 events per 100 person-years in the 300-mg group. The hazard ratios as compared with placebo were as follows: in the 50-mg group, 0.93 (95% confidence interval [CI], 0.80 to 1.07; P = 0.30); in the 150-mg group, 0.85 (95% CI, 0.74 to 0.98; P = 0.021); and in the 300-mg group, 0.86 (95% CI, 0.75 to 0.99; P = 0.031). The 150-mg dose, but not the other doses, met the prespecified multiplicity-adjusted threshold for statistical significance for the primary end point and the secondary end point that additionally included hospitalization for unstable angina that led to urgent revascularization (hazard ratio vs. placebo, 0.83; 95% CI, 0.73 to 0.95; P = 0.005). Canakinumab was associated with a higher incidence of fatal infection than was placebo. There was no significant difference in all-cause mortality (hazard ratio for all canakinumab doses vs. placebo, 0.94; 95% CI, 0.83 to 1.06; P = 0.31). Conclusions: Antiinflammatory therapy targeting the interleukin-1β innate immunity pathway with canakinumab at a dose of 150 mg every 3 months led to a significantly lower rate of recurrent cardiovascular events than placebo, independent of lipid-level lowering. (Funded by Novartis; CANTOS ClinicalTrials.gov number, NCT01327846.)
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- 2017
40. Failure-to-rescue and interprovider comparisons after elective abdominal aortic aneurysm repair: La incapacidad para prevenir la muerte y otras comparaciones entre diferentes proveedores después de la reparación electiva de un aneurisma de aorta abdominal
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Sinha, S., Ozdemir, Ata B., Khalid, U., Karthikesalingam, A., Poloniecki, J. D., Thompson, M. M., and Holt, P. J. E.
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- 2014
41. BRD9-containing non-canonical BAF complexes safeguard cell identity and prevent reprogramming
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Sevinç, Kenan, primary, Sevinç, Gülben Gürhan, additional, Cavga, Ayşe Derya, additional, Philpott, Martin, additional, Kelekçi, Simge, additional, Can, Hazal, additional, Cribbs, Adam P., additional, Ayar, Enes Sefa, additional, Arabacı, Dilşad H., additional, Dunford, James E., additional, Demir, Ata B., additional, Sigua, Logan H., additional, Qi, Jun, additional, Oppermann, Udo, additional, and Onder, Tamer T., additional
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- 2021
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42. A picture of medically assisted reproduction activities during the COVID-19 pandemic in Europe
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The ESHRE COVID-19 Working Group, . (), Vermeulen, N. (Nathalie), Ata, B. (Baris), Gianaroli, L. (Luca), Lundin, K. (Kersti), Mocanu, E. (Edgar), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), Veiga, A. (Anna), The ESHRE COVID-19 Working Group, . (), Vermeulen, N. (Nathalie), Ata, B. (Baris), Gianaroli, L. (Luca), Lundin, K. (Kersti), Mocanu, E. (Edgar), Rautakallio-Hokkanen, S. (Satu), Tapanainen, J. S. (Juha S.), and Veiga, A. (Anna)
- Abstract
Study question: How did coronavirus disease 2019 (COVID-19) impact on medically assisted reproduction (MAR) services in Europe during the COVID-19 pandemic (March to May 2020)? Summary answer: MAR services, and hence treatments for infertile couples, were stopped in most European countries for a mean of 7 weeks. What is known already: With the outbreak of COVID-19 in Europe, non-urgent medical care was reduced by local authorities to preserve health resources and maintain social distancing. Furthermore, ESHRE and other societies recommended to postpone ART pregnancies as of 14 March 2020. Study design, size, duration: A structured questionnaire was distributed in April among the ESHRE Committee of National Representatives, followed by further information collection through email. Participants/materials, setting, methods: The information was collected through the questionnaire and afterwards summarised and aligned with data from the European Centre for Disease Control on the number of COVID-19 cases per country. Main results and the role of chance: By aligning the data for each country with respective epidemiological data, we show a large variation in the time and the phase in the epidemic in the curve when MAR/ART treatments were suspended and restarted. Similarly, the duration of interruption varied. Fertility preservation treatments and patient supportive care for patients remained available during the pandemic. Large scale data: N/A Limitations, reasons for caution: Data collection was prone to misinterpretation of the questions and replies, and required further follow-up to check the accuracy. Some representatives reported that they, themselves, were not always aware of the situation throughout the country or reported difficulties with providing single generalised replies, for instance when there were regional differences within their country. Wider implications of the findings: The current article provides a basis for further research of the different
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- 2020
43. Maternal fetal medicine-perinatology
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Tekcan, C., Naki, M. M., Özcan, N., Cebi, M., Kanadikirik, F., Has, R., Aydoadu, M., Frenz, J. P., Schröder, W., Dede, F. S., Kovalak, E. E., Gelisen, O., Dede, H., Sariisik, B., Haberal, A., Caliskan, E., Turkoz, E., Corakci, A., Ozeren, S., Yucesoy, I., Terzioglu, N., Köhler, W., Feige, A., Atad, J., Auslender, R., Bardicef, M., Calderon, I., Leron, E., Abramovici, H., Ertas, I. F., Kahyaoglu, S., Turgay, M., Sut, N., Yilmaz, B., Ozel, M., Danisman, N., Kocak, I., Üstün, C., Bese, E., Ingec, M., Borekci, B., Yilmaz, M., Kadanali, S., Ingec, M., Kadanali, S., Erdogan, F., Kumtepe, Y., Gümüs, I. I., Turhan, N. O., Tamburaci, E., Gunduz, O., Akar, M., Simsek, M., Zorlu, G., Ingec, M., Borekci, B., Kadanali, S., Balci, O., Gezginc, K., Acar, A., Akyürek, C., Kocak, I., Üstün, C., Bese, E., Biri, A., Guler, I., Himmetoglu, O., Karaoguz, M. Y., Balci, Sevim, Tanriverdi, H. A., Usal, D., Cinar, E., Barut, A., Pilanci, B., Imren, A., Öztekin, D., Kurt, S., Tinar, S., Canoruc, N., Kale, A., Kale, E., Yalinkaya, A., Akdeniz, N., Gol, M., Tuna, B., Guclu, S., Altunyurt, S., Demir, N., Biri, A., Ciftci, B., Senol, E., Haznedarohlu, S., Gucuyener, K., Gursoy, R., Kahyaoglu, S., Turgay, I., Gocmen, M., Yilmaz, B., Neslihanoglu, R., Danisman, N., Kahyaoglu, S., Turgay, I., Gocmen, M., Yilmaz, B., Ozel, M., Danisman, N., Kahyaoglu, S., Turgay, I., Kokanali, M. K., Kunt, C., Yapar, E. G., Taskin, S., Yarci, A., Bozaci, E. A., Atabekoglu, C., Söylemez, F., Taskin, S., Seval, M., Bozaci, E. A., Özmen, B., Mammadova, S., Unlü, C., Seval, M., Taskin, S., Özmen, B., Güleryüz, D., Sahincioglu, Ö., Unlü, C., Öztürk, N., Yalvac, S., Caliskan, E., Erten, A., Dölen, I., Haberal, A., Gul, A., Cebeci, A., Gedikbasi, A., Erol, O., Ceylan, Y., Tekirdag, A. I., Onan, M. A., Turp, A., Kurdoglu, M., Gunaydin, G., Kurdoglu, Z., Guler, I., Erdem, A., Himmetoglu, O., Tulumbaci, O., Onan, M. A., Turkoglu, S., Kurdoglu, M., Boyaci, B., Tiras, M. B., Kurdoglu, Z., Gunaydin, G., Kadayifci, O., Demir, S. C., Ürünsak, I. F., Özgünen, T., Evrüke, I. C., Demir, S. C., Evrüke, I. C., Özgünen, T., Kadayifci, O., Güzel, A. B., Urünsak, I. F., Uckuyu, A., Ozcimen, E. E., Nisanoglu, O., Yanik, F., Akgun, S., Kuscu, E., Sayin, N. C., Canda, M. T., Ahmet, N., Kurt, I., Varol, F. G., Erkanli, S., Caliskan, K., Bagis, T., Kilicdag, E., Tarim, E., Kuscu, E., Tutuncu, L., Ardic, N., Mungen, E., Ergur, A. R., Yergok, Y. Z., Cölcimen, N., Sahin, H. G., Kamaci, M., Bezircioglu, I., Bicer, M., Uysal, D., Yigit, S., Baloglu, A., Bezircioglu, I., Bicer, M., Karci, L., Ozder, F., Baloglu, A., Has, R., Yüksel, A., Büyükkurt, S., Tatli, B., Kalelioglu, I., Kesim, M. D., Aydin, Y., Atis, A., Gezer, A., Erkan, S., Simsek, Y., Kahraman, N., Uludag, S., Altinok, T., Kale, A., Erdemoglu, M., Akdeniz, N., Ozcan, Y., Yalinkaya, A., Köse, G., Tuncel, T., Aka, N., Kumru, P., Güven, M. A., Ciragil, P., Tutuncu, L., Ozdemir, E., Mungen, E., Ergur, A. R., Yergok, Y. Z., Güven, M. A., Aktan, E., Bozkurt, K., Güven, M. A., Kilinc, M., Ekerbicer, H., Güven, M. A., Ceylaner, S., Ceylaner, G., Gul, D., Ertas, E., Güven, M. A., Ceylaner, S., Batukan, C., Ozbek, A., Demirpolat, G., Uzel, M., Basaran, A., Bozdag, G., Dagdelen, S., Gürlek, A., Beksac, S., Arici, Özkan A., Isparta, T., Dikis, F. C., Civas, S. B., Ispahi, C., Kalelioalu, I. K., Has, R., Yüksel, A., Gilbaz, E., Ibrahimoglu, L., Ermis, H., Yildirim, A., Dane, B., Yayla, M., Dane, C., Özek, M., Kalelioglu, I. K., Has, R., Yüksel, A., Gilbaz, E., Ibrahimoglu, L., Ermis, H., Yildirim, A., Dane, B., Yayla, M., Cem, Dane, Salih, Dural, Dane, C., Yayla, M., Dane, B., Cetin, A., Kiray, M., Dane, B., Yayla, M., Dane, C., Ataoglu, E., Döventas, Y., Delier, H., Has, R., Kalelioglu, I., Büyükkurt, S., Has, R., Kalelioglu, I. K., Yüksel, A., Gilbaz, E., Ibrahimoglu, L., Ermis, H., Yildirim, A., Has, R., Kalelioglu, I. K., Yüksel, A., Gilbaz, E., Ibrahimoglu, L., Ermis, H., Yildirim, A., Yildiz, A., Köksal, A., Celik, N., Yetimalar, H., Keklik, A., Ivit, H., Cukurova, K., Hizli, D., Dilbaz, S., Acer, N., Deveci, S., Dilbaz, B., Haberal, A., Cukurova, K., Köksal, A., Yilmaz, S., Ivit, H., Yildiz, A., Yetimalar, H., Keklik, A., Bicer, Bulbul M., Karakaya, E., Pehlivan, M., Baloglu, A., Caliskan, E., Doger, E., Duman, C., Turker, G., Ozeren, S., Yucesoy, I., Caliskan, E., Doger, E., Cakiroglu, Y., Corakci, A., Ozeren, S., Caliskan, E., Turkoz, E., Ozeren, S., Corakci, A., Ozkan, S., Yucesoy, I., Caliskan, E., Cakiroglu, Y., Dundar, D., Doger, E., Caliskan, S., Ozeren, S., Cukurova, K., Köksal, A., Ivit, H., Yetimalar, H., Yildiz, A., Keklik, A., Aksakalli, V., Cukurova, K., Köksal, A., Önal, G., Yildiz, A., Ivit, H., Keklik, A., Yetimalar, H., Kesim, M. D., Demirkaya, B. Ö., Atis, A., Yavuz, M., Bozkurt, T., Ozyuncu, O., Bozdag, G., Salman, M. C., Durukan, T., Beksac, S., Onderoglu, L., Deren, O., Ayhan, A., Tufekci, C., Karalök, H., Ilter, E., Cil, L., Karalök, A. E., Akyol, H., Kesim, M. D., Demirkaya, B. Ö., Atis, A., Oruc, Ö., Ekin, M., Ülku, M., Caglar, P., Demirel, C., Güngör, T., Mollamahmutoglu, L., Usta, T., Özdemir, B., Ates, U., Numanoglu, N., Seyhan, A., Sidal, B., Akdeniz, N., Kale, A., Erdemoglu, M., Ozcan, Y., Yalinkaya, A., Ozdemir, B., Numanoglu, N., Usta, T., Ortakuz, S., Seyhan, A., Sidal, B., Seyhan, A., Numanoglu, N., Usta, T., Ortakuz, S., Öztarhan, A., Özdemir, B., Dogan, O., Ilbaz, S., Kovalak, E. E., Tarcan, A., Sariisik, B., Sivaslioglu, A., Haberal, A., Cinar, E., Tanriverdi, H. A., Akbulut, V., Sade, H., Barut, A., Dede, A., Özel, M., Günaydin, S., Ertas, E., Danisman, N., Mollamahmutoglu, L., Ates, U., Seyhan, A., Atmaca, U., Ortakuz, S., Ata, B., Akar, S., Sidal, B., Tanriverdi, H. A., Akbulut, V., Usal, D., Cinar, E., Barut, A., Vural, B., Özkan, S., Costur, P., Dalcik, H., Filiz, S., Yücesoy, I., Erdemoglu, E., Kolusari, A., Sahin, H. G., Kamaci, M., Sahin, A. V., Vural, B., Özkan, S., Tas, A., Dalcik, C., Dalcik, H., Yücesoy, G., Unlubilgin, E., Caliskan, E., Demir, B., Dilbaz, S., Sonmezer, M., Haberal, A., Erdem, M., Turp, A., Gunaydin, G., Erdem, A., Sade, H., Tanriverdi, H. A., Gezer, S., Bayar, Ü., Barut, A., Demir, B., Demir, F., Yayla, M., Api, O., Aygün, E., Kars, B., Cengizoglu, B., Bulut, S., Turan, C., Unal, O., Api, O., Ünal, O., Karageyim, Y. K., Balcik, O., Kara, Ö., Dogance, U., Akil, A., Api, M., Balsak, D., Avci, M. E., Elveren, B., Hanhan, M., Kayhan, K., Tinar, S., Ispahi, C., Mollamahmutoglu, L., Güngör, T., Özdal, B., Cavkaytar, S., Özat, M., Demirel, C., Aksakal, O., Caliskan, E., Unlubilgin, E., Cakiroglu, Y., Dilbaz, B., Dilbaz, S., Dilbaz, S., Caliskan, E., Dilbaz, B., Ozdas, E., Filiz, T., Haberal, A., Asian, E., Tarim, E., Kilicdag, E., Haydardedeoglu, B., Kuscu, E., Asian, E., Kilicdag, E., Simsek, E., Bolat, F., Haydardedeoglu, B., Ocak, S., Zeteroglu, S., Deveci, A., Gungoren, A., Borazan, E., Hakverdi, A., Zeteroglu, S., Ocak, S., Deveci, A., Gungoren, A., Andi, A., and Hakverdi, A.
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- 2005
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44. Endocrinology and reproductive medicine
- Author
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Mardi A., Rahimi G., Amani M., Mashoufi M., Kheirkhah M., Ghaffari Novin M., Pierovi T., Soleimani Rad J., Vanlioglu F., Karaman Y., Bingol B., Tavmergen E., Akdogan A., Akman A., Levi R., Tavmergen Goker EN., Ates U., Seyhan A., Atmaca U., Ortakuz S., Ata B., Akar S., Usta T., Özdemir B., Sidal B., Yoldemir T., Gee A., Sutherland P., Bowman M., Fraser I. S., Haydardedeoglu B., Bagis T., Kilicdag E. B., Simsek E., Aslan E., Zeyneloglu H. B., Kahyaoglu S., Turgay I., Ertas E., Yilmaz B., Var T., Batioglu S., Muftuoglu K., Tekcan C., Naki M. M., Uysal A., Güzin K., Yücel N., Kanadikirik F., Kelekci S., Savan K., Kalyoncu S., Gokturk U., Oral H., Mollamahmutoglu L., Ertas I. E., Mollamahmutoglu L., Kahveci S., Dogan M., Mollamahmutoglu L., Isik A., Saygili U., Gol M., Koyuncuoglu M., Uslu T., Erten O., Ciftci B., Biri A., Bozkurt N., Karabacak O., Himmetoglu O., Amir Jannati N., Nouri M., Hascalik S., Celik O., Parlakpinar H., Mizrak B., Ozsahin M., Önder C., Gezginc K., Colakoglu M., Demir S. C., Cetin M. T., Kadayifci O., Güzel A. B., Polat I., Yildirim G., Özdemir A., Tekirdag Ali I., Kizkin S., Engin-Ustun Y., Ustun Y., Ozcan C., Serbest S., Ozisik H. I., Ergenoglu M., Goker E. N. T., Uckuyu A., Ozcimen E. E., Nisanoglu O., Onal C., Akgun S., Koc S., Cebi Z., Sönmez S., Yasar L., Küpelioglu L., Bilecan S., Aygün M., Zebitay A. G., Dursun P., Ötegen Ü., Bozdag G., Yarali H., Demirci F., Mun S., Eraydin E., Sadik S., Sipahi C., Bayol Ü., Sarikaya S., Garipoglu Dalgin E., Delilbasi L., Gursoy R., Engin-Ustun Y., Meydanli M. M., Atmaca R., Kafkasli A., Canda M. T., Kucuk M., Bagriyanik H. A., Ozyurt D., Canda T., Güven M. A., Tamsoy S., Kaymak O., Ozkale D., Okyay R. E., Neslihanoglu R., Mollamahmutoglu L., Basaran A., Gultekin M., Saygili Yilmaz E., Esinler I., Bayer U., Gunalp S., Aksu T., Gultekin M., Leventerler H., Taga S., Cetin T., Solmaz S., Dikmen N., Karalök H., Ilter E., Tufekci C., Yilmaz S., Karalök A. E., Batur O., Kilicdag E., Haydardedeoglu B., Tarim E., Api M., Gültekin E., Görgen H., Cetin A., Yayla M., Özkilic T., Arikan I., Abali R., Arikan D., Bozkurt S., Demir B., Gunalp S., Erden A. C., Özcan J., Yazicioglu F., and Demirbas R.
- Published
- 2005
- Full Text
- View/download PDF
45. Increase in the number of retrieved oocytes in the second treatment cycle of a poor responder is independent from the change in the stimulation protocol: O-115
- Author
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Alatas, C., Yakin, K., Oktem, O., Ata, B., Ayhan, C., and Urman, B.
- Published
- 2012
46. Placenta/birthweight ratio and perinatal outcome: a retrospective cohort analysis
- Author
-
Shehata, F, Levin, I, Shrim, A, Ata, B, Weisz, B, Gamzu, R, and Almog, B
- Published
- 2011
- Full Text
- View/download PDF
47. O-060 Effect of hyaluronan-enriched transfer medium on take home baby rate after day 3 and day 5 embryo transfers: a prospective randomized study
- Author
-
Balaban, B., Yakin, K., Ata, B., Isiklar, A., and Urman, B.
- Published
- 2011
48. O-027 Prospective assessment of the impact of laparoscopic excision of endometrioma on ovarian reserve; gentle surgery can benefit the ovary
- Author
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Kasapoglu, I., Ata, B., Ozerkan, K., Uncu, Y., Celik, N., and Uncu, G.
- Published
- 2011
49. Luteal phase empirical low molecular weight heparin administration in patients with failed ICSI embryo transfer cycles: a randomized open-labeled pilot trial
- Author
-
Urman, B, Ata, B, Yakin, K, Alatas, C, Aksoy, S, Mercan, R, and Balaban, B
- Published
- 2009
50. A randomized controlled study of human Day 3 embryo cryopreservation by slow freezing or vitrification: vitrification is associated with higher survival, metabolism and blastocyst formation†
- Author
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Balaban, B., Urman, B., Ata, B., Isiklar, A., Larman, M.G., Hamilton, R., and Gardner, D.K.
- Published
- 2008
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