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Expanding 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.
Today in Basic Science/Genetics...keeping you current
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Body Composition and Bone Mineral Density in Children with Premature Adrenarche and the Association of LRP5 Gene Polymorphisms with Bone Mineral Density
Journal of Clinical Endocrinology and Metabolism, 10/14/09
Ethanol extract of Fructus Ligustri Lucidi promotes osteogenesis of mesenchymal stem cells
Phytotherapy Research, 10/13/09
Clock genes, intestinal transport and plasma lipid homeostasis
Trends in Endocrinology and Metabolism, 10/16/09
Today in Metabolism and Growth...keeping you current
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Acanthosis Nigricans Identifies Youth at High Risk for Metabolic Abnormalities
The Journal of Pediatrics, 10/09/09
Depressive tendency in children with growth hormone deficiency
Journal of Paediatrics and Child Health, 10/23/09
The Glucagon Test in the Diagnosis of Growth Hormone Deficiency in Children With Short Stature Younger than 6 Years
Journal of Clinical Endocrinology and Metabolism, 10/29/09
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