GH secretion in a cohort of children with pseudohypoparathyroidism type Ia-Reference-Cited by-同舟云学术

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GH secretion in a cohort of children with pseudohypoparathyroidism type Ia

Published:2007-02 Issue:2 Volume:30 Page:97-103
ISSN:0391-4097
Container-title:Journal of Endocrinological Investigation
language:en
Short-container-title:J Endocrinol Invest

Author:

de Sanctis L.,Bellone J.,Salerno M.,Faleschini E.,Caruso-Nicoletti M.,Cicchetti M.,Concolino D.,Balsamo A.,Buzi F.,Ghizzoni L.,de Sanctis C.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://link.springer.com/content/pdf/10.1007/BF03347406.pdf

Reference40 articles.

1. Albright F, Burnett CH, Smith PH, Parson W. Pseudohypoparathyroidism — an example of “Seabright Banatam syndrome”. Endocrinology 1942, 30: 922–32.

2. Weinstein LS. Albright hereditary osteodystrophy, pseudohypoparathyroidism, and Gs deficiency. In: Spiegel AM ed. G proteins, receptors, and disease. Totowa, NJ: Humana Press Totowa. 1998, 23–56.

3. Levine MA. Pseudohypoparathyroidism. In: Bilezikian JP, Raisz LG, Rodan GA eds. Principles of bone biology. San Diego: Academic Press. 2002, 1137–63.

4. Shima M, Nose O, Shimizu K, Seino Y, Yabuuchi H, Saito T. Multiple associated endocrine abnormalities in a patient with pseudohypoparathyroidism type 1a. Eur J Pediatr 1988, 147: 536–8.

5. Levine MA, Ahn TG, Klupt SF, Kaufman KD, et al. Genetic deficiency of the alpha subunit of the guanine nucleotide-binding protein G(s) as the molecular basis for Albright hereditary osteodystrophy. Proc Nat Acad Sci USA 1988, 85: 617–21.

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