Dietary compliance in ornithine aminotransferase deficiency

Journal of Inherited Metabolic Disease

Volumn 29, Issue 1, 2006, Pages 240-

  Santos, Lucia ^a   Fiona, White J ^a   Walter, John H ^a  

^a ROYAL MANCHESTER CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ORNITHINE; ORNITHINE OXOACID AMINOTRANSFERASE; PYRIDOXINE;

AMINO ACID BLOOD LEVEL; ARTICLE; CLINICAL ARTICLE; DIET RESTRICTION; DIET SUPPLEMENTATION; DIETARY INTAKE; DISEASE ASSOCIATION; DISEASE COURSE; EARLY DIAGNOSIS; ENZYME DEFICIENCY; FEMALE; HUMAN; HYPERORNITHINEMIA; MALE; ORNITHINE OXOACID AMINOTRANSFERASE DEFICIENCY; PATIENT COMPLIANCE; RATING SCALE; TREATMENT OUTCOME;

AMINO ACID METABOLISM, INBORN ERRORS; ARGININE; FEMALE; HUMANS; LYSINE; MALE; ORNITHINE-OXO-ACID TRANSAMINASE; PATIENT COMPLIANCE; RETINAL DEGENERATION;

EID: 33645657345     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-006-0286-z     Document Type: Article

References (2)

1. Peltola K, Heinonen OJ, Nanto-Salonen K, Pulkki K, Simell O (2000) Oral lysine feeding in gyrate atrophy with hyperornithinaemia - a pilot study. J Inherit Metab Dis 23: 305-307.
2. Santinelli R, Costagliola C, Tolone C, et al (2004) Low-protein diet and progression of retinal degeneration in gyrate atrophy of the choroids and retina: A twenty-six-year follow-up. J Inherit Metab Dis 27: 187-196.