Výsledky vyhledávání - "Alessandro, Cicognani"

Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14-year follow-up

Autor: Monia Gennari, Annarita Armaroli, I. Cecconi, Luciano Merlini, Saverio Gnudi, Elisabetta Malaspina, Emilio Franzoni, Alessandra Ferlini, Beril Talim, Alessandro Cicognani

Publikováno v: Muscle & Nerve. 45:796-802

Introduction: Corticosteroid treatment is the standard of care in Duchenne muscular dystrophy (DMD), but the optimal age to initiate treatment and dosage pattern remain a matter of discussion. Methods: We performed a long-term study of alternate-day

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::43924f0a6f76da828d13af887bca88a1
https://doi.org/10.1002/mus.23272

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Psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening: comparison between parents' and children's perceptions

Autor: Laura Nardi, Veronica Conti, Franco D'Alberton, Ilaria Bettocchi, Alessandro Cicognani, Graziana D'Addabbo, Sara Monti, Milva Orquidea Bal, Alessandra Cassio, Nicoletta Bisacchi

Publikováno v: European Journal of Endocrinology. 164:269-276

ObjectiveTo compare the psychological adjustment and behaviour of congenital hypothyroidism (CH) children and their parents with a control group.Study designA cross-sectional study was carried out with 84 CH subjects diagnosed by neonatal screening (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27a31cd32fa7e8178e4e51289fe6d3e2
https://doi.org/10.1530/eje-10-0761

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High Rate of Regression From Micro-Macroalbuminuria to Normoalbuminuria in Children and Adolescents With Type 1 Diabetes Treated or Not With Enalapril

Autor: Stefano Gualandi, Alessandro Cicognani, Giulio Maltoni, Mirella Scipione, Alessandra Rollo, Claudia Balsamo, Stefano Zucchini, Silvana Salardi

Publikováno v: Diabetes Care

OBJECTIVE To evaluate the frequency of normalization, the persistence of remission, and the impact on normalization of glycemic control and lipid profile, we analyzed data from a retrospective observational cohort study of type 1 diabetic children an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62dcd54cffcca1f9df69f2bc2c375f45
http://europepmc.org/articles/PMC3024361

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Long-term Clinical Significance of Thyroid Autoimmunity in Children with Celiac Disease

Autor: Barbara Bigucci, Angela Miniaci, Alessandro Cicognani, Alessandra Cassio, Milva Orquidea Bal, Giampaolo Ricci, Veronica Conti, Federico Baronio

Publikováno v: The Journal of Pediatrics. 156:292-295

Objective To evaluate the long-term outcome of thyroid function and autoimmunity in a large series of children with celiac disease. Study design This longitudinal, retrospective study (duration of follow-up, 8.9 ± 4.0 years) was conducted at the Ped

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ced3ef10ffafcd17b8ecfee3dc30fea
https://doi.org/10.1016/j.jpeds.2009.08.047

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Ginecomastia: classificazione e terapia

Autor: Federico Baronio, Alessandro Cicognani

Publikováno v: L'Endocrinologo. 10:66-73

La ginecomastia vera, una proliferazione benigna del tessuto ghiandolare mammario maschile, e condizione clinica di comune riscontro. La prevalenza in alcuni periodi della vita e tale da essere considerata quasi un fenomeno fisiologico, come nel neon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::76f471fd1bde42007dcde6071cc94bb9
https://doi.org/10.1007/bf03344652

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17β-Hydroxysteroid dehydrogenase-3 deficiency: From pregnancy to adolescence

Autor: Lucia Giordani, Annalisa Nicoletti, Gi Baroncelli, Rita Fischetto, Antonio Balsamo, D Concolino, Monia Gennari, Giuseppe Chiumello, Mc Maggio, Gianni Russo, Luciano Cavallo, Silvano Bertelloni, Alessandro Cicognani, Maurizio Delvecchio, Maria Felicia Faienza, Olaf Hiort

Publikováno v: Journal of Endocrinological Investigation. 32:666-670

OBJECTIVE: Aim of this study is to report on basal clinical phenotype and follow up after diagnosis, of patients with 17beta-hydroxysteroid-dehydrogenase type 3 (17beta-HSD3) deficiency in Italy. SETTING: Pediatric Endocrine Departments, University H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c67f5d08e4006f8de8ea66ee898fe78
https://doi.org/10.1007/bf03345738

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A novelPRKAR1Amutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations

Autor: Alessandro Cicognani, Monia Gennari, Constantine A. Stratakis, Piero Pirazzoli, Anelia Hovarth

Publikováno v: Clinical Endocrinology. 69:751-755

Summary Context Carney complex (CNC) is an autosomal dominant multiple endocrine neoplasia syndrome (OMIM 160980). About 70% of cases are familiar; most have mutations of the PRKAR1A gene on chromosome 17q22–24. There is little phenotype–genotype

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e34d54ca044eaf57363b41e9b9305f1
https://doi.org/10.1111/j.1365-2265.2008.03286.x

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Quality of life, psychological adjustment and metabolic control in youths with type 1 diabetes: a study with self- and parent-report questionnaires

Autor: Franco D'Alberton, Alessandro Cicognani, Silvana Salardi, Giulio Maltoni, Stefano Zucchini, Nicoletta Bisacchi, Laura Nardi, Daniela Elleri

Publikováno v: Pediatric Diabetes. 9:496-503

Nardi L, Zucchini S, D’Alberton F, Salardi S, Maltoni G, Bisacchi N,Elleri D, Cicognani A. Quality of life, psychological adjustment andmetabolic control in youths with type 1 diabetes: a study with self- andparent-report questionnaires.Pediatric D

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26c2bd09314ad814ca5fa000ea92aa5b
https://doi.org/10.1111/j.1399-5448.2008.00414.x

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Hearing loss in Turner syndrome: Results of a multicentric study

Autor: C Bergonzoni, Francesca Mencarelli, M Rosano, R. Bergamaschi, Laura Mazzanti, F Messina, Alessandro Cicognani, Emanuela Scarano, Lorenzo Iughetti

Publikováno v: Scopus-Elsevier

The purpose of this article was to evaluate otological diseases in 173 patients (pts) with Turner syndrome (TS). STUDY DESIGN: One hundred and seventy-three pts, mean chronological age (CA) 12+/-6.2 yr. Patients were submitted to different therapies:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c03e85345fec3cbe4c20b07a66350b6
https://doi.org/10.1007/bf03349257

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