The adult and adolescent clinic for inborn errors of metabolism

Journal of Inherited Metabolic Disease

Volumn 23, Issue 3, 2000, Pages 215-228

  Brenton, D P ^a  

^a MIDDLESEX HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CAREER; CLINICAL ARTICLE; CONFERENCE PAPER; DIET THERAPY; EDUCATION; FAMILY LIFE; FEMALE; FOLLOW UP; HUMAN; LABORATORY; MALE; METABOLIC DISORDER; OUTCOMES RESEARCH; OUTPATIENT; OUTPATIENT DEPARTMENT; PEDIATRICIAN; PHYSICIAN;

ADOLESCENT; ADOLESCENT HEALTH SERVICES; ADULT; FORECASTING; HEALTH SERVICES; HUMANS; MARRIAGE; METABOLISM, INBORN ERRORS; TREATMENT OUTCOME;

EID: 0034079195     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005627911682     Document Type: Conference Paper

References (7)

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2. Kaiser-Kupfer M, Caruso R, Valle D (1991) Gyrate atrophy of the choroid and retina: chronic reduction of ornithine slows retinal degeneration. Arch Ophthalmol 109: 1539-1548.
3. Lee P, Smith I, Piesowicz A, Brenton D (1999) Spastic paraparesis after anaesthesia. Lancet 353: 554.
4. Macnab AJ (1976) A portable infusion system for the ambulant child. J Pediatr 88: 654-658.
5. Oberholzer VC, Levin B, Burgess EA, Young WF (1967) Methylmalonic aciduria: an inborn error of metabolism leading to chronic metabolic acidosis. Arch Dis Child 42: 492-504.
6. Ogasahara S, Engel AG, Frens D, Mark D (1989) Muscle co-enzyme Q deficiency in familial mitochondrial encephalomyopathy. Proc Natl Acad Sci USA 86: 2379-2382.
7. Westall RG (1963) Dietary treatment of a child with maple syrup urine disease (branched-chain keto-aciduria). Arch Dis Child 38: 485-491.