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1. 3‐Hydroxyisobutyric acid dehydrogenase deficiency: Expanding the clinical spectrum and quantitation of D‐ and L‐3‐Hydroxyisobutyric acid by an LC–MS/MS method. Issue 3 (7th March 2022)

2. A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population. Issue 3 (27th September 2016)

3. Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups. Issue 1 (25th July 2015)

4. Expanding the Molecular and Clinical Phenotype of SSR4‐CDG. Issue 11 (27th August 2015)

5. Experiences of caregivers of children with inherited metabolic diseases: a qualitative study. Issue 1 (December 2016)

6. Families' healthcare experiences for children with inherited metabolic diseases: protocol for a mixed methods cohort study. Issue 2 (22nd February 2022)

7. Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians. (November 2019)

8. PHKA2 variants expand the phenotype of phosphorylase B kinase deficiency to include patients with ketotic hypoglycemia only. Issue 10 (12th June 2021)

9. Response to correspondence of NDUFS4‐related Leigh syndrome in Hutterites. Issue 5 (28th March 2017)

10. Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double‐blind, pilot study. (10th June 2015)