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Pediatric Neurology Briefs: Volume 19, Issue 08

Thiamine-Responsive Congenital Lactic Acidosis Without MC Open Access (recommended)

Descriptions

Resource type(s)
Article
Keyword
Cardiomyopathy
Mitochondrial Encephalomyopathy
Congenital Lactic Acidosis
Rights
Attribution 4.0 International

Creator
Millichap, J. Gordon
Abstract
Six infants with thiamine-responsive congenital lactic acidosis (CLA), normal pyruvate dehydrogenase complex activity, and no evidence of mitochondrial encephalomyopathy, are reported from Tottori University, Yonago; National Childrens Medical Center, Tokyo, and other centers in Japan.
Publisher
DigitalHub. Galter Health Sciences Library
Pediatric Neurology Briefs Publishers
Date Created
2005
Original Identifier
PNB-19-58-b
Language
English
Subject: MESH
Neurosurgery
Child
Nervous System Diseases
Brain Diseases
Pediatrics
Infant
Neurology
Child Development
DOI
10.15844/pedneurbriefs-19-8-3

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Mime type: application/pdf
File size: 2640.6 kB