Maladies héréditaires du métabolisme : signes anténatals et diagnostic biologique-Reference-Cited by-同舟云学术

Maladies héréditaires du métabolisme : signes anténatals et diagnostic biologique

Published:2012-09 Issue:9 Volume:19 Page:959-969
ISSN:0929-693X
Container-title:Archives de Pédiatrie
language:fr
Short-container-title:Archives de Pédiatrie

Author:

Brassier A.,Ottolenghi C.,Boddaert N.,Sonigo P.,Attié-Bitach T.,Millischer-Bellaiche A.-E.,Baujat G.,Cormier-Daire V.,Valayannopoulos V.,Seta N.,Piraud M.,Chadefaux-Vekemans B.,Vianey-Saban C.,Froissart R.,de Lonlay P.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference51 articles.

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3. Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism;Prasad;Congenit Anom (Kyoto),2007

4. Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids;De Koning;J Inherit Metab Dis,2002

5. 3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis;Jaeken;Arch Dis Child,1996

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