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Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids.
De Koning, T J; Duran, M; Van Maldergem, L; Pineda, M; Dorland, L; Gooskens, R; Jaeken, J; Poll-The, B T.
Affiliation
  • De Koning TJ; Department of Metabolic Diseases, University Medical Center Utrecht, The Netherlands. t.dekoning@wkz.azu.nl
J Inherit Metab Dis ; 25(2): 119-25, 2002 May.
Article in En | MEDLINE | ID: mdl-12118526
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Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Serine / Carbohydrate Dehydrogenases / Microcephaly Type of study: Screening_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Inherit Metab Dis Year: 2002 Document type: Article Affiliation country: Netherlands Country of publication: United States
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Seizures / Serine / Carbohydrate Dehydrogenases / Microcephaly Type of study: Screening_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: J Inherit Metab Dis Year: 2002 Document type: Article Affiliation country: Netherlands Country of publication: United States