OUTCOME OF MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY AFTER DIAGNOSIS
Saved in:
WILSON, C.J., ET AL., OUTCOME OF MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY AFTER DIAGNOSIS. ARCHIVES OF DISEASE IN CHILDHOOD, Vol. 80, no. 5 (1999), p. 459-462.
Ref.
77744
Sted:
SIIS R.186 Archivo
Palabras clave:
Alto riesgo, Detección, Diagnóstico, Discapacidad, Enfermedades del metabolismo, Factor de protección, Hermanos, Metabolopatías, Muerte, Recién nacido
Alto riesgo, Detección, Diagnóstico, Discapacidad, Enfermedades del metabolismo, Factor de protección, Hermanos, Metabolopatías, Muerte, Recién nacido
Lignende værker: OUTCOME OF MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY AFTER DIAGNOSIS
- SCREENING FOR MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY USING ELECTROSPRAY IONISATION TANDEM MASS SPECTROMETRY
- MOLYBDENUM COFACTOR DEFICIENCY:AN EASILY MISSED INBORN ERROR OF METABOLISM
- CLINICAL AND BIOCHEMICAL APPROACH TO THE NEONATE WITH A SUSPECTED INBORN ERROR OF AMINO ACID AND ORGANIC ACID METABOLISM
- LE NOUVEAU-NE DE MERE DIABETIQUE
- AN INBORN ERROR OF BILE ACID SYNTHESIS (3B-HYDROXY-A5-C27-STEROID DEHYDROGENASE DEFICIENCY) PRESENTING MALABSORPTION LEADING TO RICKETS
- ROLE OF MICROSOMAL ETHANOL-OXIDIZING SYSTEM IN REGULATION OF LINEOLEOYL-CoA DESATURASE ACTIVITY AFTER LONG-TERM ETHANOL ADMINISTRATION