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See Latest ArticlesExpanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency
Journal of Clinical Endocrinology and Metabolism, 07/02/09
Dattani M et al. - IGHD patients with severe growth failure and a positive family history should be screened for genetic mutations; the evolving endocrinopathy observed in some of these patients suggests the need for long-term follow-up.
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A Molecular Basis for Variation in Clinical Severity of Isolated Growth Hormone Deficiency Type II
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Today in Basic Science/Genetics...keeping you current
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Prevalence of Pancreatic Diabetes in Patients Carrying Mutations or Polymorphisms of the PRSS1 Gene in the Han Population
Diabetes Technology & Therapeutics, 12/17/09
New Mutations in the RET Protooncogene-L881V - Associated with Medullary Thyroid Carcinoma and -R770Q - in a Patient with Mixed Medullar/Follicular Thyroid Tumour
Experimental and Clinical Endocrinology & Diabetes, 12/17/09
Intragenic GNAS Deletion Involving Exon A/B in Pseudohypoparathyroidism Type 1A Resulting in an Apparent Loss of Exon A/B Methylation: Potential for Misdiagnosis of Pseudohypoparathyroidism Type 1B
Journal of Clinical Endocrinology and Metabolism, 12/17/09
Today in Metabolism and Growth...keeping you current
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Predicting the Response to Growth Hormone Treatment in Short Children with Chronic Kidney Disease
Journal of Clinical Endocrinology and Metabolism, 12/17/09
Autoimmune polyglandular syndrome Type 3 and growth hormone deficiency
Pediatric Diabetes, 12/15/09
High-Calorie Glucose-Rich Food Attenuates Neuroglycopenic Symptoms in Patients with Addison's Disease
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