An update on the clinical and molecular characteristics of pseudohypoparathyroidism
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine
Reference45 articles.
1. Vitamin D deficiency rickets mimicking pseudohypoparathyroidism.;Akin;J Clin Res Pediatr Endocrinol,2010
2. Functional characterization of GNAS mutations found in patients with pseudohypoparathyroidism type Ic defines a new subgroup of pseudohypoparathyroidism affecting selectively Gsalpha-receptor interaction.;Thiele;Hum Mutat,2011
3. Transgenic overexpression of the extra-large Gsalpha variant XLalphas enhances Gsalpha-mediated responses in the mouse renal proximal tubule in vivo.;Liu;Endocrinology,2011
4. A novel aspect of GNAS imprinting: higher maternal expression of Galphas in human lymphoblasts, peripheral blood mononuclear cells, mammary adipose tissue, and heart.;Klenke;Mol Cell Endocrinol,2011
5. Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsalpha.;Mouallem;Clin Endocrinol (Oxf),2008
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