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32 results on '"Ibba, Anastasia"'

2. Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study

Author

Tromp, Tycho R., Hartgers, Merel L., Hovingh, G. Kees, Vallejo-Vaz, Antonio J., Ray, Kausik K., Soran, Handrean, Freiberger, Tomas, Bertolini, Stefano A., Harada-Shiba, Mariko, Pang, Jing, Watts, Gerald F., Greber-Platzer, Susanne, Mäser, Martin, Stulnig, Thomas M., Ebenbichler, Christoph F., Bin Thani, Khalid, Cassiman, David, Descamps, Olivier S., Rymen, Daisy, Witters, Peter, Santos, Raul D., Brunham, Liam R., Francis, Gordon A., Genest, Jacques, Hegele, Robert A., Kennedy, Brooke A., Ruel, Isabelle, Sherman, Mark H., Jiang, Long, Wang, Luya, Reiner, Željko, Blaha, Vladimir, Ceska, Richard, Dvorakova, Jana, Dlouhy, Lubomir, Horak, Pavel, Soska, Vladimir, Tichy, Lukas, Urbanek, Robin, Vaverkova, Helena, Vrablik, Michal, Zemek, Stanislav, Zlatohlavek, Lukas, Emil, Sameh, Naguib, Tarek, Reda, Ashraf, Béliard, Sophie, Bruckert, Eric, Gallo, Antonio, Elisaf, Moses S., Kolovou, Genovefa, Cohen, Hofit, Durst, Ronen, Dann, Eldad J., Elis, Avishay, Hussein, Osama, Leitersdorf, Eran, Schurr, Daniel, Setia, Nitika, Verma, Ishwar C., Alareedh, Mohammed D., Al-Khnifsawi, Mutaz, Abdalsahib Al-Zamili, Ali F., Rhadi, Sabah H., Shaghee, Foaad K., Arca, Marcello, Averna, Maurizio, Bartuli, Andrea, Bucci, Marco, Buonuomo, Paola S., Calabrò, Paolo, Calandra, Sebastiano, Casula, Manuela, Catapano, Alberico L., Cefalù, Angelo B., Cicero, Arrigo F.G., D'Addato, Sergio, D'Erasmo, Laura, Di Costanzo, Alessia, Fasano, Tommaso, Gazzotti, Marta, Giammanco, Antonina, Iannuzzo, Gabriella, Ibba, Anastasia, Negri, Emanuele A., Pasta, Andrea, Pavanello, Chiara, Pisciotta, Livia, Rabacchi, Claudio, Ripoli, Carlo, Sampietro, Tiziana, Sbrana, Francesco, Sileo, Fulvio, Suppressa, Patrizia, Tarugi, Patrizia, Trenti, Chiara, Zenti, Maria G., Hori, Mika, Ayesh, Mahmoud H., Azar, Sami T., Bitar, Fadi F., Fahed, Akl C., Moubarak, Elie M., Nemer, Georges, Nawawi, Hapizah M., Madriz, Ramón, Mehta, Roopa, Cupido, Arjen J., Defesche, Joep C., Reijman, M. Doortje, Roeters-van Lennep, Jeanine E., Stroes, Erik S.G., Wiegman, Albert, Zuurbier, Linda, Al-Waili, Khalid, Sadiq, Fouzia, Chlebus, Krzysztof, Bourbon, Mafalda, Gaspar, Isabel M., Lalic, Katarina S., Ezhov, Marat V., Susekov, Andrey V., Groselj, Urh, Charng, Min-Ji, Khovidhunkit, Weerapan, Aktan, Melih, Altunkeser, Bulent B., Demircioglu, Sinan, Kose, Melis, Gokce, Cumali, Ilhan, Osman, Kayikcioglu, Meral, Kaynar, Leyla G., Kuku, Irfan, Kurtoglu, Erdal, Okutan, Harika, Ozcebe, Osman I., Pekkolay, Zafer, Sag, Saim, Salcioglu, Osman Z., Temizhan, Ahmet, Yenercag, Mustafa, Yilmaz, Mehmet, Yilmaz Yasar, Hamiyet, Mitchenko, Olena, Lyons, Alexander R.M., Stevens, Christophe A.T., Brothers, Julie A., Hudgins, Lisa C., Nguyen, Christina, Alieva, Rano, Shek, Aleksandr, Do, Doan-Loi, Kim, Ngoc-Thanh, Le, Hong-An, Le, Thanh-Tung, Nguyen, Mai-Ngoc T., Truong, Thanh-Huong, Blom, Dirk J., Raal, Frederick J., Cuchel, Marina, Tromp, Tycho R, Hartgers, Merel L, Hovingh, G Kees, Vallejo-Vaz, Antonio J, Ray, Kausik K, Bertolini, Stefano, Blom, Dirk J, and Raal, Frederick J

Published
2022
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4. Isolated Growth Hormone Deficiency.

Author

Ibba, Anastasia, Guzzetti, Chiara, Sanfilippo, Lavinia, and Loche, Sandro

Subjects
*GROWTH of children, *PITUITARY hormones, *SOMATOTROPIN, *IDIOPATHIC diseases, *INJECTIONS
Abstract

Growth hormone deficiency (GHD) is the most frequent pituitary hormone deficiency in childhood, with an incidence of 1 in 4000–10,000 live births. GHD can be congenital (genetic or due to hypothalamic/pituitary abnormalities) or acquired and can be isolated (IGHD) or associated with other pituitary hormone deficiencies, but most cases are idiopathic. GH stimulation testing is commonly used in the diagnostic workup of GHD, except for some clinical conditions that do not require GH stimulation tests for the diagnosis. Children with GHD receive replacement therapy with daily injections of recombinant human GH (rhGH). RhGH therapy is effective in increasing short-term height gain and adult height in patients with GHD. The safety of long term GH therapy has been confirmed in many large international studies. Recently, long-acting weekly GH formulations have been introduced, showing good efficacy and safety profiles. [ABSTRACT FROM AUTHOR]

Published
2024
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5. Central Precocious Puberty in Italian Boys: Data From a Large Nationwide Cohort.

Author

Cassio, Alessandra, Marescotti, Gloria, Aversa, Tommaso, Salerno, Mariacarolina, Tornese, Gianluca, Stancampiano, Marianna, Tuli, Gerdi, Faienza, Maria Felicia, Cavarzere, Paolo, Fava, Daniela, Parpagnoli, Maria, Bruzzi, Patrizia, Ibba, Anastasia, Calcaterra, Valeria, Mameli, Chiara, Grandone, Anna, Cherubini, Valentino, Assirelli, Valentina, Franchina, Francesca, and Capalbo, Donatella

Subjects
PRECOCIOUS puberty, ITALIANS, MAGNETIC resonance imaging, GONADOTROPIN releasing hormone, AGE, BODY mass index
Abstract

Context There are only a few nationwide studies on boys with central precocious puberty (CPP) and the last Italian study is a case series of 45 boys that dates back to 2000. Objective We aimed to evaluate the causes of CPP in boys diagnosed during the last 2 decades in Italy and the relative frequency of forms with associated central nervous system (CNS) abnormalities on magnetic resonance imaging (MRI) compared to idiopathic ones. Methods We performed a national multicenter retrospective study collecting data from 193 otherwise normal healthy boys with a diagnosis of CPP. Based on MRI findings, the patients were divided into: Group 1, no CNS abnormalities; Group 2, mild abnormalities (incidental findings) unrelated to CPP; and Group 3, causal pathological CNS abnormalities. Results The MRI findings show normal findings in 86%, mild abnormalities (incidental findings) in 8.3%, and causal pathological CNS abnormalities in 5.7% of the cases. In Group 3, we found a higher proportion of patients with chronological age at diagnosis < 7 years (P =.00001) and body mass index greater than +2 SDS (P <.01). Gonadotropin-releasing hormone analogue therapy was started in 183/193 subjects. The final height appeared in the range of the target height in all groups and in 9 patients in whom the therapy was not started. Conclusion In our study on a large nationwide cohort of boys referred for precocious puberty signs, the percentage of forms associated with CNS abnormalities was one of the lowest reported in the literature. [ABSTRACT FROM AUTHOR]

Published
2024
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6. Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features

Author

Bartuli, Andrea, Bucci, Marco, Buonuomo, Paola Sabrina, Calabrò, Paolo, Casula, Manuela, Cefalù, Angelo Baldassare, Cicero, Arrigo, D'Addato, Sergio, D'Erasmo, Laura, Fasano, Tommaso, Iannuzzo, Gabriella, Ibba, Anastasia, Negri, Emanuele A., Pasta, Andrea, Pavanello, Chiara, Pisciotta, Livia, Rabacchi, Claudio, Ripoli, Carlo, Sampietro, Tiziana, Sbrana, Francesco, Sileo, Fulvio, Suppressa, Patrizia, Trenti, Chiara, Zenti, Maria Grazia, Bertolini, Stefano, Calandra, Sebastiano, Arca, Marcello, Averna, Maurizio, Catapano, Alberico L., and Tarugi, Patrizia

Published
2020
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10. Growth Hormone Deficiency in the Transition Age

Author

Loche, Sandro, primary, Di Iorgi, Natascia, additional, Patti, Giuseppa, additional, Noli, Serena, additional, Giaccardi, Marta, additional, Olivieri, Irene, additional, Ibba, Anastasia, additional, and Maghnie, Mohamad, additional

Published
2018
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16. Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features

Author

Bertolini, Stefano, primary, Calandra, Sebastiano, additional, Arca, Marcello, additional, Averna, Maurizio, additional, Catapano, Alberico L., additional, Tarugi, Patrizia, additional, Bartuli, Andrea, additional, Bucci, Marco, additional, Buonuomo, Paola Sabrina, additional, Calabrò, Paolo, additional, Casula, Manuela, additional, Cefalù, Angelo Baldassare, additional, Cicero, Arrigo, additional, D'Addato, Sergio, additional, D'Erasmo, Laura, additional, Fasano, Tommaso, additional, Iannuzzo, Gabriella, additional, Ibba, Anastasia, additional, Negri, Emanuele A., additional, Pasta, Andrea, additional, Pavanello, Chiara, additional, Pisciotta, Livia, additional, Rabacchi, Claudio, additional, Ripoli, Carlo, additional, Sampietro, Tiziana, additional, Sbrana, Francesco, additional, Sileo, Fulvio, additional, Suppressa, Patrizia, additional, Trenti, Chiara, additional, and Zenti, Maria Grazia, additional

Published
2020
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17. IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal

Author

Ibba, Anastasia, primary, Corrias, Francesca, additional, Guzzetti, Chiara, additional, Casula, Letizia, additional, Salerno, Mariacarolina, additional, di Iorgi, Natascia, additional, Tornese, Gianluca, additional, Patti, Giuseppa, additional, Radetti, Giorgio, additional, Maghnie, Mohamad, additional, Cappa, Marco, additional, and Loche, Sandro, additional

Published
2020
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18. Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging “Mismatch Pattern”

Author

Bianco, Deborah, primary, Napoli, Flavia, additional, Morana, Giovanni, additional, Pistorio, Angela, additional, Allegri, Anna Elsa Maria, additional, Fava, Daniela, additional, Schiavone, Maurizio, additional, Thiabat, Hanan F, additional, Crocco, Marco, additional, Camia, Tiziana, additional, Lezzi, Marilea, additional, Calandrino, Andrea, additional, Tortora, Domenico, additional, Severino, Mariasavina, additional, Patti, Giuseppa, additional, Ibba, Anastasia, additional, Rossi, Andrea, additional, Di Iorgi, Natascia, additional, and Maghnie, Mohamad, additional

Published
2020
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21. Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency

Author

Patti, Giuseppa, primary, Noli, Serena, additional, Capalbo, Donatella, additional, Allegri, Anna Maria Elsa, additional, Napoli, Flavia, additional, Cappa, Marco, additional, Ubertini, Grazia Maria, additional, Gallizia, Annalisa, additional, Notarnicola, Sara, additional, Ibba, Anastasia, additional, Crocco, Marco, additional, Parodi, Stefano, additional, Salerno, Mariacarolina, additional, Loche, Sandro, additional, Garré, Maria Luisa, additional, Tornari, Elena, additional, Maghnie, Mohamad, additional, and Di Iorgi, Natascia, additional

Published
2019
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25. Next-Generation Sequencing Identifies Different Genetic Defects in 2 Patients with Primary Adrenal Insufficiency and Gonadotropin-Independent Precocious Puberty

Author

Guzzetti, Chiara, primary, Bizzarri, Carla, additional, Pisaneschi, Elisa, additional, Mucciolo, Mafalda, additional, Bellacchio, Emanuele, additional, Ibba, Anastasia, additional, Casula, Letizia, additional, Novelli, Antonio, additional, Loche, Sandro, additional, and Cappa, Marco, additional

Published
2018
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26. Cut-off limits of the peak GH response to stimulation tests for the diagnosis of GH deficiency in children and adolescents: study in patients with organic GHD

Author

Guzzetti, Chiara, primary, Ibba, Anastasia, additional, Pilia, Sabrina, additional, Beltrami, Nadia, additional, Di Iorgi, Natascia, additional, Rollo, Alessandra, additional, Fratangeli, Nadia, additional, Radetti, Giorgio, additional, Zucchini, Stefano, additional, Maghnie, Mohamad, additional, Cappa, Marco, additional, and Loche, Sandro, additional

Published
2016
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29. Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

Author

Ghizzoni, Lucia, primary, Cappa, Marco, additional, Vottero, Alessandra, additional, Ubertini, Graziamaria, additional, Carta, Daniela, additional, Di Iorgi, Natascia, additional, Gasco, Valentina, additional, Marchesi, Maddalena, additional, Raggi, Vera, additional, Ibba, Anastasia, additional, Napoli, Flavia, additional, Massimi, Arianna, additional, Maghnie, Mohamad, additional, Loche, Sandro, additional, and Porzio, Ottavia, additional

Published
2011
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30. The role of FTOgenotype on eating behavior in obese Sardinian children and adolescents

Author

Ibba, Anastasia, Pilia, Sabrina, Zavattari, Patrizia, Loche, Alberto, Guzzetti, Chiara, Casini, Maria Rosaria, Minerba, Luigi, and Loche, Sandro

Abstract

AbstractAim:We aimed to study the influence of the fat mass and obesity-associated (FTO) gene on eating behavior in 412 obese Sardinian children and adolescents. Genome-wide association studies (GWAS) have identified several susceptibility loci for obesity. Among these, the polymorphisms in the intron 1 of the FTOgene has been found associated to weight gain and obesity in various populations.Methods: All obese patients were genotyped for the FTOsingle nucleotide polimorphysm (SNP) rs9939609. In all subjects we evaluated eating behavior using the Child Eating Behaviour Questionnaire (CEBQ).Results:We found no differences in eating behavior according to the genotype, either in the entire cohort, or when subjects were subdivided into four different age groups.Conclusions: FTOgenotype is associated with body mass index but does not influence eating behavior in a selected cohort of obese children from the isolated genetic population of Sardinia.

Published
2013
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31. IGF-I for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal

Author

Anastasia, Ibba, Corrias, Francesca, Chiara, Guzzetti, Letizia, Casula, Mariacarolina, Salerno, Natascia di Iorgi, Tornese, Gianluca, Giuseppa, Patti, Giorgio, Radetti, Mohamad, Maghnie, Marco, Cappa, Sandro, Loche, Ibba, Anastasia, Corrias, Francesca, Guzzetti, Chiara, Casula, Letizia, Salerno, Mariacarolina, di Iorgi, Natascia, Tornese, Gianluca, Patti, Giuseppa, Radetti, Giorgio, Maghnie, Mohamad, Cappa, Marco, and Loche, Sandro

Subjects
growth hormone deficiency, short stature, children, adolescent, insulin-like growth factor-I, adolescents
Abstract

A number of studies have evaluated the role of IGF-I measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate the accuracy and the best cut-off of IGF-I SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two children and adolescents with GHD [(63 organic/genetic (OGHD), 79 idiopathic (IGHD)] and 658 short non-GHD children (median age 10.4 y) were included in the analysis. The two groups were subdivided according to age (G1

Published
2020

32. Accuracy and limitations of the growth hormone (GH) releasing hormone-arginine retesting in young adults with childhood-onset GH deficiency

Author

Flavia Napoli, Anna Allegri, Serena Noli, Annalisa Gallizia, Elena Tornari, Mariacarolina Salerno, Donatella Capalbo, Sandro Loche, Natascia Di Iorgi, Giuseppa Patti, Stefano Parodi, Anastasia Ibba, Maria Luisa Garrè, Grazia Maria Ubertini, Marco Crocco, Sara Notarnicola, Mohamad Maghnie, Marco Cappa, Patti, Giuseppa, Noli, Serena, Capalbo, Donatella, Allegri, Anna Maria Elsa, Napoli, Flavia, Cappa, Marco, Ubertini, Grazia Maria, Gallizia, Annalisa, Notarnicola, Sara, Ibba, Anastasia, Crocco, Marco, Parodi, Stefano, Salerno, Mariacarolina, Loche, Sandro, Garré, Maria Luisa, Tornari, Elena, Maghnie, Mohamad, and Di Iorgi, Natascia

Subjects
0301 basic medicine, medicine.medical_specialty, Arginine, Endocrinology, Diabetes and Metabolism, Brain tumors, GH deficiency, GHRH-arg, Transition, Young adults, 030209 endocrinology & metabolism, lcsh:Diseases of the endocrine glands. Clinical endocrinology, 03 medical and health sciences, Endocrinology, 0302 clinical medicine, Internal medicine, medicine, Young adult, Original Research, lcsh:RC648-665, business.industry, Insulin tolerance test, Growth hormone secretion, 030104 developmental biology, Etiology, GH deficiency, GHRH-arg, brain tumors, transition, young adults, IGHD, business, GH Deficiency, Hormone
Abstract

Background: Re-testing for GH secretion is needed to confirm the diagnosis of GH deficiency (GHD) after adult height achievement in childhood-onset GHD (COGHD).Aim: To define the cut-off of GH peak after retesting with GH-releasing hormone plus arginine (GHRHarg) in the diagnosis of permanent GHD in COGHD of different etiology.Patients and methods: Eighty-eight COGHD (median age 17.2 y), 29 idiopathic GHD (IGHD), 44 cancer survivors (TGHD) and 15 congenital GHD (CGHD) were enrolled in the study; 54 had isolated GHD (iGHD) and 34 had multiple pituitary hormone deficiencies (MPHD). All were tested with insulin tolerance test (ITT) and GHRHarg. IGHD with a GH response to ITT >= 6 mu g/L were considered true negatives and served as the control group, and patients with a GH response = 6 mu g/L and 42 with GH peak = 6 mu g/L. ROC analysis based on the etiology indicated the best diagnostic accuracy for peak GH cutoffs after GHRHarg of 25.3 mu g/L in CGHD, 15.7 in TGHD, and 13.8 in MPHD, and for IGF-1 SDS at -2.1 in CGHD, -1.5 in TGHD, and -1.9 in MPHD.Conclusions: Our findings indicate that the best cut-off for GH peak after retesting with GHRHarg changes according to the etiology of GHD during the transition age. Based on these results the diagnostic accuracy of GHRHarg remains questionable.

Published
2019

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