The challenges of managing coexistent disorders with phenylketonuria: 30 cases-Reference-Cited by-同舟云学术

The challenges of managing coexistent disorders with phenylketonuria: 30 cases

Published:2015-12 Issue:4 Volume:116 Page:242-251
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

MacDonald A.,Ahring K.,Almeida M.F.,Belanger-Quintana A.,Blau N.,Burlina A.,Cleary M.,Coskum T.,Dokoupil K.,Evans S.,Feillet F.,Giżewska M.,Gokmen Ozel H.,Lotz-Havla A.S.,Kamieńska E.,Maillot F.,Lammardo A.M.,Muntau A.C.,Puchwein-Schwepcke A.,Robert M.,Rocha J.C.,Santra S.,Skeath R.,Strączek K.,Trefz F.K.,van Dam E.,van Rijn M.,van Spronsen F.,Vijay S.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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4. Co-existence of phenylketonuria and Fabry disease on a 3year-old boy: case report;Concolino;BMC Pediatr.,2010

5. Down's syndrome with phenylketonuria;Fisch;Clin. Pediatr. (Phila),1968

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