Zobrazeno 1 - 10
of 207
pro vyhledávání: '"Giuseppe, Chiumello"'
Autor:
Giuseppe Chiumello, Emanuela Scarano, Graziano Grugni, Marco Cappa, Nella Augusta Greggio, Claudia Brufani, L. Ragusa, Andrea Corrias, S. Di Candia, Danilo Fintini, Alessandro Salvatoni, A. Crinò, Adriana Franzese, Sarah Bocchini, Laura Mazzanti, G. Trifirò, Maurizio Delvecchio
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 26:842-847
Background and aims Prader–Willi syndrome (PWS) is characterized by a high incidence of altered glucose metabolism (AGM). However, epidemiological data on impaired fasting glucose (IFG), impaired glucose tolerance (IGT) and type 2 diabetes mellitus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9104b37cd56c582b0e4d17447c927263
https://doi.org/10.1016/j.numecd.2016.05.010
https://doi.org/10.1016/j.numecd.2016.05.010
Autor:
Claudio Pagano, S. Di Candia, Giuseppe Chiumello, Luigi Gargantini, Roberto Vettor, A. Crinò, Alessandro Sartorio, Marco Cappa, Giorgio Bedogni, S. Spera, Andrea Corrias, Graziano Grugni, Lorenzo Iughetti, Paolo Brambilla, Alessandro Salvatoni, L. Ragusa
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 23:1134-1140
Prader-Willi syndrome (PWS), the most common genetic cause of obesity, is characterized by elevated morbility and mortality in all ages. In this context, non-obese PWS children showed low frequency of metabolic syndrome (MetS), while a comparable pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bffcc0fca26b4d6f452e8c76fd7e5d1
https://doi.org/10.1016/j.numecd.2012.11.006
https://doi.org/10.1016/j.numecd.2012.11.006
Autor:
Laura Fugazzola, Carlo Corbetta, I. Zamproni, Giuseppe Chiumello, Maria Cristina Vigone, Giovanna Weber, Francesca Cortinovis, Luca Persani, Sarah Rabbiosi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 98:1395-1402
Context: In recent years changes in screening strategies for congenital hypothyroidism (CH) led to an increased detection of mild forms of CH, associated with eutopic thyroid gland. Objectives: We aimed to determine the clinical evolution of CH with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf3ca71dc1f90de647044644300c4d31
https://doi.org/10.1210/jc.2012-3174
https://doi.org/10.1210/jc.2012-3174
Autor:
P. Chiabotto, Isped, Benedetta Mariani, Lorenzo Iughetti, Giuseppe Chiumello, Alessandro Mussa, Antonino Crinò, Simeone Andrulli, S. Spera, Stefania Di Candia, Alessandro Salvatoni, A. Luce, Clotilde De Medici, Graziano Grugni, Luigi Gargantini, Andrea Corrias, Diabetology (Siedp), L. Ragusa, Luciano Beccaria, Anna Cogliardi
Publikováno v:
Clinical Endocrinology. 76:843-850
Summary Objective A recent study evidenced by metyrapone test a central adrenal insufficiency (CAI) in 60% of Prader–Willi syndrome (PWS) children. These results were not confirmed in investigations with low [Low-Dose Tetracosactrin Stimulation Tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48d158b47b546ace481bb03ee919ace
https://doi.org/10.1111/j.1365-2265.2011.04313.x
https://doi.org/10.1111/j.1365-2265.2011.04313.x
Autor:
Franco Meschi, Giuseppe Chiumello, Matteo Viscardi, Andrea Rigamonti, Alessandro Poscia, Riccardo Bonfanti, Roseila Battaglino, Frontino Giulio
Publikováno v:
Acta Diabetologica. 47:295-300
A study was conducted to evaluate the accuracy of GlucoDay (A. Menarini Diagnostics) during 48 h of continuous glucose monitoring (CGMS) in type 1 diabetic adolescents and use this novel approach to assess otherwise ignored nocturnal hypoglycaemias,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b8e20a169b9dc6dc65e171aa1a02d64
https://doi.org/10.1007/s00592-010-0181-9
https://doi.org/10.1007/s00592-010-0181-9
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 73:S49-S55
Objective Aim of the present review is to offer a concise but complete discussion about pathologies with pediatric otorhinolaryngological interest recognizing: (i) growth disorders, (ii) chromosomal disorders, and (iii) tumors. Methods Pathologies ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40ff8bb73b78980c6f5962960fdabeb9
https://doi.org/10.1016/s0165-5876(09)70010-2
https://doi.org/10.1016/s0165-5876(09)70010-2
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
https://doi.org/10.1007/bf03345738
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:4453-4458
Context: Patients with congenital adrenal hyperplasia (CAH) receive glucocorticoids as replacement therapy. Glucocorticoid therapy is the most frequent cause of drug-induced osteoporosis. Objective: The objective of the study was to evaluate bone min
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96b25ecc8fb33d4ce571414842efefd3
https://doi.org/10.1210/jc.2005-2823
https://doi.org/10.1210/jc.2005-2823
Autor:
Mohamad Maghnie, Sabrina Pilia, Giuseppe Chiumello, Sandro Loche, Gabriella Pozzobon, Maria Grazia Ubertini, Linda Ambrosini, Natascia Di Iorgi, Lucia Ghizzoni, Marco Cappa, Carmine Tinelli, Renata Lorini
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 91:2900-2905
Context: It has been reported that patients with multiple pituitary hormone deficiencies (MPHDs) achieve a greater final height, compared with patients with isolated GH deficiency (IGHD). However, the outcome of patients with permanent GH deficiency
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9837acff6bc8ab3e172694bbf5fcba68
https://doi.org/10.1210/jc.2006-0050
https://doi.org/10.1210/jc.2006-0050
Autor:
Marie-Françoise Roland-Cachera, Giulio Testolin, Paolo Brambilla, Giuseppe Chiumello, Corrado G. Testolin, André Briend, Alessandro Salvatoni
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59e435c816540566c87d64c21136def2
https://doi.org/10.1111/j.1749-6632.2000.tb06497.x
https://doi.org/10.1111/j.1749-6632.2000.tb06497.x