Management of the mitochondrial encephalopathies;Manejo de las encefalopatias mitocondriales

Revista de Neurologia

Volumn 27, Issue 156, 1998, Pages 289-296

  Garcia, L ^a  

^a Servicio de Neurologia Pediátrica   (United States)

Author keywords

Encephalomyopathies; Mitochondrial diseases; Neurometabolic disorders management

Indexed keywords

ALPHA TOCOPHEROL; ASCORBIC ACID; BIOTIN; CARNITINE; UBIQUINONE; VITAMIN; VITAMIN B COMPLEX; ZINC;

ARTICLE; BRAIN MITOCHONDRION; CLINICAL FEATURE; COENZYME; DISEASE CLASSIFICATION; ENCEPHALOMYOPATHY; GENETIC ASSOCIATION; HUMAN; MITOCHONDRIAL RESPIRATION; NEUROCHEMISTRY; PATHOPHYSIOLOGY; RISK FACTOR; SYMPTOM; VITAMIN SUPPLEMENTATION; ELECTROCARDIOGRAPHY; ELECTROENCEPHALOGRAPHY; INFANT; MITOCHONDRIAL ENCEPHALOMYOPATHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; REVIEW;

CHILD, PRESCHOOL; ELECTROCARDIOGRAPHY; ELECTROENCEPHALOGRAPHY; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MITOCHONDRIAL ENCEPHALOMYOPATHIES; VITAMINS;

EID: 0032467798     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: 10.33588/rn.27156.98088     Document Type: Article

References (3)

1. Clarke JTR. A clinical guide to inherited metabolic diseases. Cambridge: University Press; 1996.
2. Lyon G, Adams RD, Kolodny EH. Neurology of hereditary metabolic diseases of children. 2 ed. New York: McGraw-Hill; 1996.
3. Shanske S, DiMauro S. Diagnosis of the mitochondrial encephalomyopathies. Curr Opin Rheumatol 1997; 9: 496-503.