Detalhe da pesquisa
1.
The many faces of peroxisomal disorders: Lessons from a large Arab cohort.
Clin Genet
; 95(2): 310-319, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30561787
2.
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group.
BMC Neurol
; 15: 205, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26471939
3.
6-Pyruvoyltetrahydropterin Synthase Deficiency: Review and Report of 28 Arab Subjects.
Pediatr Neurol
; 96: 40-47, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30926181
4.
Infantile Serine Biosynthesis Defect Due to Phosphoglycerate Dehydrogenase Deficiency: Variability in Phenotype and Treatment Response, Novel Mutations, and Diagnostic Challenges.
J Child Neurol
; 32(6): 543-549, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28135894