Asfotase alfa therapy for children with hypophosphatasia.Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan.The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes.Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada.Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile HypophosphatasiaThe health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.Hypophosphatasia.Identifying Non-Duchenne Muscular Dystrophy-Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs: A Review.
P50
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P50
description
onderzoeker
@nl
name
Cheryl Rockman-Greenberg
@ast
Cheryl Rockman-Greenberg
@en
Cheryl Rockman-Greenberg
@es
Cheryl Rockman-Greenberg
@sl
type
label
Cheryl Rockman-Greenberg
@ast
Cheryl Rockman-Greenberg
@en
Cheryl Rockman-Greenberg
@es
Cheryl Rockman-Greenberg
@sl
prefLabel
Cheryl Rockman-Greenberg
@ast
Cheryl Rockman-Greenberg
@en
Cheryl Rockman-Greenberg
@es
Cheryl Rockman-Greenberg
@sl
P106
P21
P31
P569
1950-09-26T00:00:00Z