Urinary organic acid screening in children with developmental language delay-Reference-Cited by-同舟云学术

Urinary organic acid screening in children with developmental language delay

Published:1999-10 Issue:7 Volume:22 Page:815-820
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Michelson M.¹,Harel S.²,Gutman A.³,Lerman-Sagie T.¹

Affiliation:

1. ; Pediatric Neurology Unit and Metabolism Clinic; Wolfson Medical Center; Holon Israel

2. Child Development Center and Pediatric Neurology Unit; Dana Children's Hospital, Tel-Aviv Medical Center, Tel-Aviv, Sackler School of Medicine, Tel-Aviv University; Tel-Aviv Israel

3. ; Department of Clinical Biochemistry; Hadassah University Hospital; Jerusalem Israel

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005558108125/fullpdf

Reference18 articles.

1. Communication disorders in preschool children, the physician's responsibility;Allen;J Dev Behav Pediatr,1989

2. 3-Methylglutaconic aciduria: A marker for as yet unspecified disorders and the relevance of prenatal diagnosis in a ‘new’ type (‘type 4’);Chitayat;J Inher Metab Dis,1992

3. A familial syndrome of infantile optic atrophy, movement disorder, and spastic paraplegia;Costeff;Neurology,1989

4. Inherited 3-methyl-glutaconic aciduria in two brothersanother defect of leucine metabolism;Duran;J Pediatr,1982

5. 3-Methyl-glutaconyl coenzyne A hydratase deficiency: a new case;Gibson;J Inher Metab Dis,1992

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