Clinical presentations of inherited mitochondrial fatty acid oxidation disorders: An update

International Pediatrics

Volumn 12, Issue 1, 1997, Pages 34-40

  Saudubray, J M ^a   Martin, D ^a   Poggi Travert, F ^a   Billette de Villemeur, T ^a   Spada, M ^a   Bartuli, A ^a   Jouvet, P ^a   Brivet, M ^a   Slama, A ^a   Vianey Liaud, C ^a   Demaugre, F ^a   Bonnefont, J P ^a   Rabier, D ^a   Charpentier, C ^a   Kamoun, P ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CARNITINE; GLUCOSE;

CARDIOMYOPATHY; CATABOLISM; CLINICAL FEATURE; COMA; CONGENITAL MALFORMATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENERGY METABOLISM; FATTY ACID METABOLISM; FATTY ACID OXIDATION; GENETIC DISORDER; HEART BEAT; HUMAN; HYPOGLYCEMIA; KIDNEY DISEASE; MAJOR CLINICAL STUDY; MYOGLOBINURIA; MYOPATHY; PERIPHERAL NEUROPATHY; RETINITIS PIGMENTOSA; REVIEW; SUDDEN INFANT DEATH SYNDROME;

EID: 0031395503     PISSN: 08856265     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (56)