Triple-A Syndrome - The First Chinese Patient with Novel Mutations in the AAAS Gene-Reference-Cited by-同舟云学术

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Triple-A Syndrome - The First Chinese Patient with Novel Mutations in the AAAS Gene

Published:2006-01 Issue:5 Volume:19 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Lam Y.Y.,Lo I.F.M.,Shek C.C.,Tong T.M.F.,Ng D.K.K.,Tong T.F.,Choi M.S.,Lam S.T.S.,Ho C.S.

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

https://www.degruyter.com/document/doi/10.1515/JPEM.2006.19.5.765/pdf

Reference22 articles.

1. FAMILIAL GLUCOCORTICOID DEFICIENCY WITH ACHALASIA OF THE CARDIA AND DEFICIENT TEAR PRODUCTION

2. Glucocorticoid and Partial Mineralocorticoid Deficiency Associated with Achalasia*

3. Allgrove syndrome: an autosomal recessive syndrome of ACTH insensitivity, achalasia and alacrima

4. Adrenal Insufficiency After Achalasia in the Triple-A Syndrome

5. Familial Achalasia with Absent Tear Production

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical decision making and application of an active rehabilitation program for a person with the neuromuscular symptoms of Allgrove syndrome: a case report;Physiotherapy Theory and Practice;2018-12-03

2. Molecular Genetics of Inherited Glucocorticoid Deficiency;eLS;2014-10-15

3. Long-term clinical follow-up and molecular genetic findings in eight patients with triple A syndrome;European Journal of Pediatrics;2012-04-28

4. An Alu-mediated rearrangement causing a 3.2kb deletion and a novel two base pair deletion in AAAS gene as the cause of triple A syndrome;Molecular Genetics and Metabolism;2007-12

5. Current World Literature;Current Opinion in Endocrinology, Diabetes & Obesity;2007-06

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