Work

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

Year: 1991

Type: article

Study design: Observational Study

Source: Annals of Neurology

DOI: 10.1002/ana.410300512

Authors: Charles A. Stanley, Susan DeLeeuw, Paul M. Coates, Christine Vianey‐Liaud, Priscille Divry, Jean‐Paul Bonnefont, Jean‐Marie Saudubray, Morey Haymond, Friedrich K. Trefz, Galen N. Breningstall, Rebecca S. Wappner, Dennis J. Byrd, Claude Sansaricq, Ingrid Tein, Warren Grover, David Valle, S. Lane Rutledge, William R. Treem

Institutions: Children's Hospital of Philadelphia, Hôpital Debrousse, Hôpital Necker-Enfants Malades, Mayo Clinic, Heidelberg University, Park Nicollet Health Services, Riley Hospital for Children, Medizinische Hochschule Hannover, NYU Langone Health, New York University, Hospital for Sick Children, St. Christopher's Hospital for Children, Johns Hopkins University, University of Alabama at Birmingham, Hartford Hospital

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 Institute of Neurological Disorders and Stroke, National Center for Research Resources

Awards: General Clinical Research Center, PATHOGENESIS OF REYE SYNDROME

OpenAlex ID: W1978945178

FWCI: 5.259

Cites: 20

Cited by: 212

Related to: 10