Association of a Nicotinic Receptor Mutation with Reduced Height and Blunted Physostigmine-Stimulated Growth Hormone Release

Author:

Fedi Marco12,Bach Leon A.3,Berkovic Samuel F.2,Willoughby John O.4,Scheffer Ingrid E.2,Reutens David C.12

Affiliation:

1. Southern Clinical School, Monash University (D.C.R., M.F.), Clayton, Victoria 3168, Australia

2. Department of Medicine, Austin Hospital (M.F., S.F.B., I.E.S., D.C.R.), The University of Melbourne, Heidelberg, Victoria 3084 Australia

3. Department of Medicine, Alfred Hospital (L.A.B.), Monash University, Prahran, Victoria 3181, Australia

4. Centre for Neuroscience (J.O.W.), Flinders University, Adelaide, South Australia 5001, Australia

Publisher

The Endocrine Society

Subject

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

Reference20 articles.

1. Genetic disorders in the growth hormone-insulin-like growth factor-I axis.;Walenkamp;Horm Res,2006

2. Autosomal dominant nocturnal frontal lobe epilepsy;Scheffer;A distinctive clinical disorder. Brain,1995

3. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.;Steinlein;Nat Genet,1995

4. Clinical pharmacokinetics of physostigmine in patients with Alzheimer’s disease.;Asthana;Clin Pharmacol Ther,1995

5. Neuroendocrine control of growth hormone secretion.;Muller;Physiol Rev,1999

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