Atypical GH Insensitivity Syndrome and Severe Insulin-Like Growth Factor-I Deficiency Resulting from Compound Heterozygous Mutations of the GH Receptor, Including a Novel Frameshift Mutation Affecting the Intracellular Domain

Publisher： Karger

E-ISSN： 1663-2826|74|6|406-411

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.74, Iss.6, 2010-07, pp. : 406-411

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Defining Insulin-Like Growth Factor-I Deficiency

By  

Hormone Research in Paediatrics, Vol. 65, Iss. 1, 2006-03 ,pp. : 9-14

Karger

Access to resources Recommend Favorite

Insulin-Like Growth Factor-I and Insulin-Like Growth Factor Binding Protein-3 Cotreatment versus Insulin-Like Growth Factor-I Alone in Two Brothers with Growth Hormone Insensitivity Syndrome: Effects on Insulin Sensitivity, Body Composition and Linear Growth

By  

Hormone Research in Paediatrics, Vol. 76, Iss. 5, 2011-09 ,pp. : 355-366

Karger

Access to resources Recommend Favorite

Adult and Near-Adult Height in Patients with Severe Insulin-Like Growth Factor-I Deficiency after Long-Term Therapy with Recombinant Human Insulin-Like Growth Factor-I

By  

Hormone Research in Paediatrics, Vol. 80, Iss. 1, 2013-07 ,pp. : 47-56

Karger

Access to resources Recommend Favorite

Insulin-Like Growth Factor -I Deficiency

By  

Hormone Research in Paediatrics, Vol. 55, Iss. 1, 2004-11 ,pp. : 17-20

Karger

Access to resources Recommend Favorite

Guidelines for Growth Hormone and Insulin-Like Growth Factor-I Treatment in Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-Like Growth Factor-I Deficiency

By  

Hormone Research in Paediatrics, Vol. 86, Iss. 6, 2016-11 ,pp. : 361-397

Karger

Access to resources Recommend Favorite