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1,889 results on '"Porro, G."'

9. Treatment and outcome of the Dutch Childhood Craniopharyngioma Cohort study; first results after centralization of care

Author

MS Radiotherapie, Cancer, MS Oogheelkunde, Brain, Endocrinologie patientenzorg, PMC Medisch specialisten, Neurochirurgen, Child Health, Van Schaik, J, Schouten-van Meeteren, A Y N, Vos-Kerkhof, E, Janssens, G O, Porro, G L, Fiocco, M, Bakker, B, Tissing, W J E, Hoving, E W, van Santen, H M, MS Radiotherapie, Cancer, MS Oogheelkunde, Brain, Endocrinologie patientenzorg, PMC Medisch specialisten, Neurochirurgen, Child Health, Van Schaik, J, Schouten-van Meeteren, A Y N, Vos-Kerkhof, E, Janssens, G O, Porro, G L, Fiocco, M, Bakker, B, Tissing, W J E, Hoving, E W, and van Santen, H M

Published
2023

10. Fluorescence sensing and intravascular microdialysis for personalised medicine: The case of immunosuppressants in transplanted patients (Conference Presentation)

Author

Baldini, F., primary, Tombelli, S., additional, Trono, C., additional, Berneschi, S., additional, Giannetti, A., additional, Bernini, R., additional, Persichetti, G., additional, Testa, G., additional, Orellana, G., additional, Salis, F., additional, Weber, S., additional, Luppa, P. B., additional, Porro, G., additional, Quartu, G., additional, Schubert, M. B., additional, Berner, M., additional, Becker, H., additional, Gärtner, C., additional, and O'Connell, M. T., additional

Published
2023
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22. Minimally invasive fetal surgery for myelomeningocele: Preliminary report from a single center

Author

Carrabba, G, Macchini, F, Fabietti, I, Schisano, L, Meccariello, G, Campanella, R, Bertani, G, Locatelli, M, Boito, S, Porro, G, Gabetta, L, Picciolini, O, Cinnante, C, Triulzi, F, Ciralli, F, Mosca, F, Lapa, D, Leva, E, Rampini, P, Persico, N, Carrabba G., Macchini F., Fabietti I., Schisano L., Meccariello G., Campanella R., Bertani G., Locatelli M., Boito S., Porro G. A., Gabetta L., Picciolini O., Cinnante C., Triulzi F., Ciralli F., Mosca F., Lapa D. A., Leva E., Rampini P., Persico N., Carrabba, G, Macchini, F, Fabietti, I, Schisano, L, Meccariello, G, Campanella, R, Bertani, G, Locatelli, M, Boito, S, Porro, G, Gabetta, L, Picciolini, O, Cinnante, C, Triulzi, F, Ciralli, F, Mosca, F, Lapa, D, Leva, E, Rampini, P, Persico, N, Carrabba G., Macchini F., Fabietti I., Schisano L., Meccariello G., Campanella R., Bertani G., Locatelli M., Boito S., Porro G. A., Gabetta L., Picciolini O., Cinnante C., Triulzi F., Ciralli F., Mosca F., Lapa D. A., Leva E., Rampini P., and Persico N.

Abstract

OBJECTIVE Recent trials have shown the safety and benefits of fetoscopic treatment of myelomeningocele (MMC). The authors' aim was to report their preliminary results of prenatal fetoscopic treatment of MMC using a biocellulose patch, focusing on neurological outcomes, fetal and maternal complications, neonatal CSF leakage, postnatal hydrocephalus, and radiological outcomes. METHODS Preoperative assessment included clinical examination, ultrasound imaging, and MRI of the fetus. Patients underwent purely fetoscopic in utero MMC repair, followed by postoperative in utero and postnatal MRI. All participants received multidisciplinary follow-up. RESULTS Five pregnant women carrying fetuses affected by MMC signed informed consent for the fetoscopic treatment of the defect. The mean MMC size was 30.4 mm (range 19-49 mm). Defect locations were L1 (2 cases), L5 (2 cases), and L4 (1 case). Hindbrain herniation and ventriculomegaly were documented in all cases. The mean gestational age at surgery was 28.2 weeks (range 27.8-28.8 weeks). Fetoscopic repair was performed in all cases. The mean gestational age at delivery was 33.9 weeks (range 29.3-37.4 weeks). After surgery, reversal of hindbrain herniation was documented in all cases. Three newborns developed signs of hydrocephalus requiring CSF diversion. Neurological outcomes in terms of motor level were favorable in all cases, but a premature newborn died due to CSF infection and sepsis. CONCLUSIONS The authors' preliminary results suggest that fetoscopic treatment of MMC is feasible, reproducible, and safe for mothers and their babies. Neurological outcomes were favorable and similar to those in the available literature. As known, prematurity was the greatest complication.

Published
2019

31. Autologous haematopoietic stem cell transplantation without CD34+ cell selection in refractory Crohn's disease

Author

Cassinotti, A., Annaloro, C., Ardizzone, S., Onida, F., Della Volpe, A., Clerici, M., Usardi, P., Greco, S., Maconi, G., Porro, G.. Bianchi, and Deliliers, G. Lambertenghi

Subjects
Autografts -- Methods, Autografts -- Research, CD4 lymphocytes -- Identification and classification, CD4 lymphocytes -- Research, Crohn's disease -- Care and treatment, Hematopoietic stem cells -- Transplantation, Hematopoietic stem cells -- Usage, Hematopoietic stem cells -- Research, Health
Published
2008

33. Clinical-Cytological-Grading and phenotyping in patients with chronic rhinosinusitis with nasal polyps: the relevance in clinical practice

Author

Gelardi, M., Porro, G., Quaranta, V., Quaranta, N., Cassano, M., Ciprandi, G., Luigi, Alonzi, Arturo Arnone Caruso, Francesco, Barbara, Michele, Barbara, Paolo, Castelnuovo, Giovanna, Ciancio, Ciofalo, Andrea, Michele, Curatolo, Nicola De Candia, Carlo De Luca, Valentina De Robertis, Valentina Di Benedetto, Valeria, Fiore, Lucia, Iannuzzi, Clara, Imperatore, Cristiano, Lingua, Giuseppe, Lombardo, Alberto, Macchi, Michela, Mancini, Alessandro Maselli del Giudice, Patrizia, Mola, Mario, Notargiacomo, Antonio, Palma, Piero, Pecoraro, Giuseppe, Pellitteri, Krizia, Piccininni, Massimo, Rinaldi, and Valentina, Rossi. Study Group On CRSwNP I.

Subjects
Pulmonary and Respiratory Medicine, Adult, Male, Allergy, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, real-world, cytological phenotype, Chronic rhinosinusitis, lcsh:Medicine, Comorbidity, chronic rhinosinusitis with nasal polyps, Nasal Polyps, Internal medicine, clinical-cytological-grading, Eosinophilic, Outcome Assessment, Health Care, medicine, Hypersensitivity, Prevalence, Humans, Nasal polyps, Sinusitis, Grading (tumors), Asthma, Retrospective Studies, Aspirin, business.industry, lcsh:R, Cell Biology, Middle Aged, medicine.disease, asthma, comorbidity, Clinical Practice, Cross-Sectional Studies, Phenotype, Italy, Chronic Disease, Female, Cardiology and Cardiovascular Medicine, business
Abstract

Chronic rhinosinusitis (CRS) includes two main phenotypes: without nasal polyps (CRSsNP) and with nasal polyps (CRSwNP). CRSwNP may be associated with comorbidity, mainly concerning asthma, aspirin intolerance, and allergy. CRSwNP patients may also be evaluated by clinical-cytological grading (CCG). The current study investigated the prevalence and characteristics of the different CCG and phenotypes in CRSwNP outpatients examined in clinical practice. This retrospective cross-sectional study enrolled 791 consecutive CRSwNP outpatients (424 males, mean age 48.8 years). In the total population, asthma was a common comorbidity (30.8%) as well as aspirin intolerance (24.8%), and allergy (50.8%). As concerns CCG-grading, 210 (26.5%) outpatients had low-grade, 366 (46.3%) medium, and 215 (27.2%) high. As regards cytological phenotypes, 87 (11%) had neutrophilic type, 371 (46.3%) eosinophilic, 112 (14.2%) mast cell, and 221 (27.9%) mixed. High-grade CCG was significantly associated with more frequent asthma, aspirin intolerance, allergy, recurrent surgery, and mixed cytological phenotype. Low-grade CCG was characterized by fewer comorbidities and operations, and neutrophilic phenotype. Therefore, the present study confirmed that CCG is a useful tool in the management of outpatients with CRSwNP. CRSwNP is frequently associated with asthma, aspirin intolerance, and allergy comorbidity. High-grade CCG is frequently characterized by a mixed cytological phenotype, thus, by more severe progress. These real-world outcomes underline that CRSwNP deserves adequate attention for careful management and optimal identification of the best-tailored therapy; CCG and cytological phenotyping could be fruitful tools in clinical practice. Asthma and aspirin intolerance should be adequately investigated in all CRS patients.

Published
2020

43. Bowel ultrasound in assessment of Crohn's disease and detection of related small bowel strictures: A prospective comparative study versus X ray and intraoperative findings. (Original Article)

Author

Parente, F., Maconi, G., Bollani, S., Anderloni, A., Sampietro, G., Cristaldi, M., Franceschelli, N., Bianco, R., Taschieri, A.M., and Porro, G. Bianchi

Subjects
Intestines, Crohn's disease -- Diagnosis, Health, Diagnosis
Abstract

Background and aim: Despite the fact that bowel ultrasound (US) has recently been proved to be useful in the assessment of bowel diseases, uncertainty persists as to its diagnostic role [...]

Published
2002

44. The vascularity of internal fistulae in Crohn's disease: An in vivo power Doppler ultrasonography assessment. (Original Article)

Author

Maconi, G., Sampietro, G.M., Russo, A., Bollani, S., Cristaldi, M., Parente, F., Dottorini, F., and Porro, G. Bianchi

Subjects
Doppler ultrasonography -- Evaluation, Fistula, Intestinal -- Diagnosis -- Complications and side effects, Crohn's disease -- Complications and side effects -- Diagnosis, Health
Abstract

Aim: To evaluate the efficacy of power Doppler sonography (US) in depicting internal fistulae and their vascularity, and to study the characteristics of blood flow within the fistula wall. Patients [...]

Published
2002

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