» Articles » PMID: 5786203

Intermittent Cerebellar Ataxia Associated with Hyperpyruvic Acidemia, Hyperalaninemia, and Hyperalaninuria

Overview
Journal Pediatrics
Specialty Pediatrics
Date 1969 Jun 1
PMID 5786203
Citations 14
Authors
Affiliations
Soon will be listed here.
Citing Articles

Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities.

Whittle E, Chilian M, Karimiani E, Progri H, Buhas D, Kose M Genet Med. 2022; 25(2):100332.

PMID: 36520152 PMC: 9905285. DOI: 10.1016/j.gim.2022.11.001.


Dysautonomia in autism spectrum disorder: case reports of a family with review of the literature.

Lonsdale D, Shamberger R, Obrenovich M Autism Res Treat. 2012; 2011:129795.

PMID: 22937241 PMC: 3420600. DOI: 10.1155/2011/129795.


Dysautonomia, a heuristic approach to a revised model for etiology of disease.

Lonsdale D Evid Based Complement Alternat Med. 2008; 6(1):3-10.

PMID: 18955227 PMC: 2644268. DOI: 10.1093/ecam/nem064.


A review of the biochemistry, metabolism and clinical benefits of thiamin(e) and its derivatives.

Lonsdale D Evid Based Complement Alternat Med. 2006; 3(1):49-59.

PMID: 16550223 PMC: 1375232. DOI: 10.1093/ecam/nek009.


Megavitamin therapy in inherited metabolic disorders.

Kalhan S Indian J Pediatr. 1981; 48(394):635-46.

PMID: 7327660 DOI: 10.1007/BF02821592.