Sporadic Triple A (Allgrove) Syndrome with Novel Tandem Mutations-Reference-Cited by-同舟云学术

Sporadic Triple A (Allgrove) Syndrome with Novel Tandem Mutations

Published:2021-03-01 Issue:5 Volume:60 Page:799-802
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Miyazawa Haruna¹,Kimura Manami¹,Yonezawa Hisashi¹,Maeda Tetsuya¹

Affiliation:

1. Division of Neurology and Gerontology, Department of Internal Medicine, School of Medicine, Iwate Medical University, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/60/5/60_5201-20/_pdf

Reference19 articles.

1. 1. Allgrove J, Clayden GS, Grant DB, Macaulay JC. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet 1: 1284-1286, 1978.

2. 2. Clark AJL, Weber A. Adrenocorticotropin insensitivity syndromes. Endocr Rev 19: 828-843, 1998.

3. 3. Flokas ME, Tomani M, Agdere L, Brown B. Triple A syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach. Pediatr Health Med Ther 10: 99-106, 2019.

4. 4. deFreitas MRG, Orsini M, Araújo APQC, et al. Allgrove syndrome and motor neuron disease. Neurol Int 10: 7436, 2018.

5. 5. Vishnu VY, Modi M, Prabhakar S, Bhansali A, Goyal MK. 'A' motor neuron disease. J Neurol Sci 336: 251-253, 2014.

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1. A 16-year-old boy presented with triple-A syndrome associated with neuromuscular disorders: a case report;Annals of Medicine & Surgery;2024-02-05

2. Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review;Child Neurology Open;2021-01