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You searched for: Author/Creator Waters, Paula J.

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1. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Issue 1 (11th February 2019)

3. HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec. Issue 12 (26th October 2019)

4. Molecular diagnosis of muscular diseases in outpatient clinics: A Canadian perspective. (April 2020)

5. Vitamin B12 deficiency in inflammatory bowel disease: a prospective observational pilot study. Issue 12 (December 2017)