First diagnosis of Martin-Albright syndrome in a 58-year-old patient-Reference-Cited by-同舟云学术

First diagnosis of Martin-Albright syndrome in a 58-year-old patient

Published:2009-01 Issue:1 Volume:7 Page:43-45
ISSN:1610-0379
Container-title:Journal der Deutschen Dermatologischen Gesellschaft
language:en
Short-container-title:

Author:

Quist Sven R.,Franke Ingolf,Hiort Olaf,Gollnick Harald P.,Leverkus Martin

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1610-0387.2008.06862.x/fullpdf

Reference7 articles.

1. Un cas de tétanie idiopathique chronique. Échec thérapeutique de la graffe d'un adénome parathyroïdien. Revue médicale de la Suisse Romande;Martin;Lausanne,1940

2. Pseudo-hypoparathyroidism - example of ‘Seabright-Bantam syndrome’; report of three cases. Endocrinology;Albright;Baltimore,1942

3. Calcinosis cutis in Albright hereditary osteodystrophy: pseudohypoparathyroidism type Ia;Folster-Holst;Hautarzt,2006

4. Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy;De Nanclares;J Clin Endocrinol Metab,2007

5. Analysis of the GNAS1-gene in Albright's hereditary osteodystrophy;Ahrens;J Clin Endocrinol Metab,2001

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1. Dermale Osteome als erstes Symptom einer hereditären Albright‐Osteodystrophie bei einem zehn Monate alten Mädchen;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-07

2. Dermal osteomata as first symptom of Albright’s hereditary osteodystrophy in a 10‐month‐old girl;JDDG: Journal der Deutschen Dermatologischen Gesellschaft;2020-03-25