Triple A syndrome mimicking ALS
Author:
Publisher
Informa UK Limited
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/17482960802259016
Reference13 articles.
1. FAMILIAL GLUCOCORTICOID DEFICIENCY WITH ACHALASIA OF THE CARDIA AND DEFICIENT TEAR PRODUCTION
2. Neurological and adrenal dysfunction in the adrenal insufficiency/alacrima/achalasia (3A) syndrome.
3. Clinical and genetic characterization of families with triple A (Allgrove) syndrome
4. Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene
5. Mutant WD-repeat protein in triple-A syndrome
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1. Nuclear pore dysfunction and disease: a complex opportunity;Nucleus;2024-02-21
2. Neurophysiological Characteristics of Allgrove (Triple A) Syndrome: Case Report and Literature Review;Child Neurology Open;2021-01
3. Triple-A Syndrome (TAS): An In-Depth Overview on Genetic and Phenotype Heterogeneity;Protein & Peptide Letters;2020-12-02
4. 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
5. Triple A syndrome presenting as complicated hereditary spastic paraplegia;Molecular Genetics & Genomic Medicine;2018-10-31
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