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G Chiumello

Showing results (201-210 of 214) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Final height in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the Italian experienceV L Brunelli, G Russo, S Bertelloni, et al.
American Journal of Medical Genetics|February 5, 1998
Comparison of clinical-radiological and molecular findings in hypochondroplasiaC Prinster, P Carrera, M Del Maschio, et al.
Hormone Research in Paediatrics|September 19, 2012
POI: a score to modulate GH treatment in children with Prader-Willi syndromeA Salvatoni, J Berini, G Chiumello, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, et al.
Mutation Research|September 29, 2004
Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancyG Saltini, M C Proverbio, G Malferrari, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 11, 2012
Metabolic syndrome in adult patients with Prader-Willi syndromeG Grugni, A Crinò, G Bedogni, et al.
Journal of Endocrinological Investigation|June 6, 2009
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescenceS Bertelloni, A Balsamo, L Giordani, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|January 22, 2010
Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesityP Brambilla, A Crinò, G Bedogni, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 7, 2016
Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort studyD Fintini, G Grugni, S Bocchini, et al.
American Journal of Human Genetics|October 1, 1996
Genetic homogeneity of autoimmune polyglandular disease type IP Björses, J Aaltonen, A Vikman, et al.
Pageof 22

Showing results (201-210 of 214) with videos related to

Sort By:
Pageof 22
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 6, 2003
Final height in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the Italian experienceV L Brunelli, G Russo, S Bertelloni, et al.
American Journal of Medical Genetics|February 5, 1998
Comparison of clinical-radiological and molecular findings in hypochondroplasiaC Prinster, P Carrera, M Del Maschio, et al.
Hormone Research in Paediatrics|September 19, 2012
POI: a score to modulate GH treatment in children with Prader-Willi syndromeA Salvatoni, J Berini, G Chiumello, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, et al.
Mutation Research|September 29, 2004
Identification of a novel polymorphism in the fibronectin type II domain of the SEL1L gene and possible relation to the persistent hyperinsulinemic hypoglycemia of infancyG Saltini, M C Proverbio, G Malferrari, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 11, 2012
Metabolic syndrome in adult patients with Prader-Willi syndromeG Grugni, A Crinò, G Bedogni, et al.
Journal of Endocrinological Investigation|June 6, 2009
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescenceS Bertelloni, A Balsamo, L Giordani, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|January 22, 2010
Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesityP Brambilla, A Crinò, G Bedogni, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 7, 2016
Disorders of glucose metabolism in Prader-Willi syndrome: Results of a multicenter Italian cohort studyD Fintini, G Grugni, S Bocchini, et al.
American Journal of Human Genetics|October 1, 1996
Genetic homogeneity of autoimmune polyglandular disease type IP Björses, J Aaltonen, A Vikman, et al.
Pageof 22