Growth hormone secretion among adult patients with Prader-Willi syndrome due to different genetic subtypes.

Grugni, G; Giardino, D; Crinò, A; Malvestiti, F; Ballarati, L; Di Giorgio, G; Marzullo, P

Grugni, G; Giardino, D; Crinò, A; Malvestiti, F; Ballarati, L; Di Giorgio, G; Marzullo, P.

Affiliation

Grugni G; Division of Auxology, S. Giuseppe Hospital, Research Institute, Istituto Auxologico Italiano, Verbania, Italy. g.grugni@auxologico.it

J Endocrinol Invest ; 34(7): 493-7, 2011.

Article in En | MEDLINE | ID: mdl-20651469

Subject(s)

Human Growth Hormone/metabolism; Prader-Willi Syndrome/genetics; Prader-Willi Syndrome/metabolism; Adolescent; Adult; Arginine/administration & dosage; Chromosomes, Human, Pair 15; Female; Growth Hormone-Releasing Hormone/administration & dosage; Human Growth Hormone/blood; Humans; Male; Uniparental Disomy; Young Adult

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Human Growth Hormone Type of study: Prognostic_studies Limits: Adolescent / Adult / Female / Humans / Male Language: En Journal: J Endocrinol Invest Year: 2011 Type: Article Affiliation country: Italy

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