Rational Approach to the Diagnosis of Severe Growth Hormone Deficiency in the Newborn

Author:

Binder G.1,Weidenkeller M.1,Blumenstock G.2,Langkamp M.3,Weber K.1,Franz A. R.4

Affiliation:

1. Departments of Pediatric Endocrinology (G.Bi., M.W., K.W.), University Children’s Hospital, D-72076 Tuebingen, Germany

2. Department of Medical Biometry (G.Bl.), University of Tuebingen, D-72074 Tuebingen, Germany

3. Mediagnost (M.L.), Gesellschaft für Forschung und Herstellung von Diagnostika GmbH, D-72770 Reutlingen, Germany

4. Neonatology (A.R.F.), University Children’s Hospital, D-72076 Tuebingen, Germany

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference18 articles.

1. The course of neonatal cholestasis in congenital combined pituitary hormone deficiency;Binder;J Pediatr Endocrinol Metab,2007

2. Isolated GH deficiency with dominant inheritance: new mutations, new insights;Binder;J Clin Endocrinol Metab,2001

3. The role of growth hormone in determining birth size and early postnatal growth, using congenital growth hormone deficiency (GHD) as a model;Mehta;Clin Endocrinol (Oxf),2005

4. Diagnosis and management of growth hormone deficiency in childhood and adolescence. Part 1: diagnosis of growth hormone deficiency;Sizonenko;Growth Horm IGF Res,2001

5. Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: summary statement of the GH Research Society;Growth Hormone Research Society;J Clin Endocrinol Metab,2000

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