Work

Short‐chain L ‐3‐hydroxyacyl‐CoA dehydrogenase deficiency in muscle: A new cause for recurrent myoglobinuria and encephalopathy

Year: 1991

Type: article

Study design: Case Report

Source: Annals of Neurology

DOI: 10.1002/ana.410300315

Authors: I. Tein, D. C. De Vivo, D. E. Hale, J. T. R. Clarke, H. Zinman, R. Laxer, A. Shore, S. Dimauro

Institutions: NewYork–Presbyterian Hospital, Columbia University Irving Medical Center, Columbia University, Children's Hospital of Philadelphia, University of Pennsylvania, University of Toronto, Hospital for Sick Children

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of Neurological Disorders and Stroke

Awards: G137493147, G536614631, PATHOGENESIS OF REYE SYNDROME

OpenAlex ID: W2066982585

FWCI: 3.105

Cites: 17

Cited by: 84

Related to: 10