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List of works by Cheryl Rockman-Greenberg

ALPL mutations in adults with rheumatologic disorders and low serum alkaline phosphatase activity

scientific article published on 04 February 2019

Asfotase Alfa Treatment Improves Survival for Perinatal and Infantile Hypophosphatasia

scientific article

Asfotase alfa therapy for children with hypophosphatasia

scientific article

Caffeine is a risk factor for osteopenia of prematurity in preterm infants: a cohort study.

scientific article

Diagnosis and high incidence of hyperornithinemia-hyperammonemia-homocitrullinemia (HHH) syndrome in northern Saskatchewan

scientific article

Diagnostic delay is common among patients with hypophosphatasia: initial findings from a longitudinal, prospective, global registry

scientific article published on 14 February 2019

Efficacy and Safety of Asfotase Alfa in Infants and Young Children With Hypophosphatasia: A Phase 2 Open-Label Study

scientific article published on 01 July 2019

Enzyme replacement therapy in perinatal hypophosphatasia: Case report of a negative outcome and lessons for clinical practice.

scientific article published on 7 November 2017

Five-year efficacy and safety of asfotase alfa therapy for adults and adolescents with hypophosphatasia

scientific article published on 18 December 2018

Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians

scientific article published on 01 November 2019

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada

article

Hypophosphatasia

scientific article published on June 2013

Identifying Non-Duchenne Muscular Dystrophy-Positive and False Negative Results in Prior Duchenne Muscular Dystrophy Newborn Screening Programs: A Review

scientific article

Letter to the Editor: "Efficacy and Safety of Asfotase Alfa in Infants and Young Children With Hypophosphatasia: A Phase 2 Open-Label Study"

scientific article published on 01 August 2019

Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada

scientific article published on 26 February 2015

Newborn Screening for IKBKB Deficiency in Manitoba, Using Genetic Mutation Analysis

scientific article published on 04 October 2018

Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease.

scientific article published on 29 December 2015

The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

scientific article published on 3 February 2016

The prevalence of the HNF-1alpha G319S mutation in Canadian aboriginal youth with type 2 diabetes

scientific article

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