Most Viewed Abstracts
1. Report Shows Shift in Starting Salaries for Physicians 2. AHA Guidelines on Cardiac CT for Assessing Coronary Artery Disease 3. Rapid correction of low vitamin D status in nursing home residents 4. 2008 Exclusive Survey—Earnings: Good news for primary care income 5. Medicare pay-for-reporting effort draws fire from frustrated doctors
Your Article Summary
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.
Related Articles
Depressive tendency in children with growth hormone deficiency
Journal of Paediatrics and Child Health, 10/23/09
Relevance Score: 83%
Comparison of glucose and lipid metabolism and bone mineralization in patients with growth hormone deficiency with and without long-term growth hormone replacement
Metabolism-Clinical and Experimental, 10/26/09
Relevance Score: 82%
A Molecular Basis for Variation in Clinical Severity of Isolated Growth Hormone Deficiency Type II
Journal of Clinical Endocrinology and Metabolism, 10/29/09
Relevance Score: 81%
Hypopituitarism due to sports related head trauma and the effects of growth hormone replacement in retired amateur boxers
Pituitary, 10/29/09
Relevance Score: 81%
Growth without Growth Hormone and Similar Dysmorphic Features in Three Patients with Sporadic Combined Pituitary Hormone Deficiencies
Hormone Research, 10/27/09
Relevance Score: 81%
Today in Basic Science/Genetics...keeping you current
Receive free subspecialty "5-minute updates" via email
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
Receive free subspecialty "5-minute updates" via email
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
Journal of Clinical Endocrinology and Metabolism, 12/11/09
Sponsor
Article Search
Sponsor
Sponsor


See Latest Articles


