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Volumn 157, Issue 2, 1998, Pages
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Strategies for the treatment of cystathionine β-synthase deficiency: The experience of the Willink Biochemical Genetics Unit over the past 30 years
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Author keywords
Betaine; Cystathionine synthase deficiency; Homocystinuria; Treatment
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Indexed keywords
BETAINE;
CYSTATHIONINE BETA SYNTHASE;
FOLIC ACID;
METHIONINE;
PYRIDOXINE DERIVATIVE;
ADOLESCENT;
ADULT;
ARTICLE;
CELL DAMAGE;
CHILD;
CLINICAL ARTICLE;
DIET SUPPLEMENTATION;
DIET THERAPY;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
FEMALE;
FOLLOW UP;
GENETICS;
HUMAN;
MALE;
NEWBORN;
NEWBORN SCREENING;
PRIORITY JOURNAL;
ADOLESCENT;
ADULT;
BETAINE;
CHILD;
CHILD, PRESCHOOL;
CYSTATHIONINE BETA-SYNTHASE;
DOSE-RESPONSE RELATIONSHIP, DRUG;
FEMALE;
FOLIC ACID;
GASTROINTESTINAL AGENTS;
GENETIC SCREENING;
HOMOCYSTEINE;
HOMOCYSTINURIA;
HUMANS;
INFANT;
INFANT, NEWBORN;
MALE;
PREGNANCY;
PREGNANCY COMPLICATIONS;
PYRIDOXINE;
TREATMENT FAILURE;
TREATMENT OUTCOME;
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EID: 0031798844
PISSN: 09439676
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (74)
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References (6)
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