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1. Clinicopathologic and molecular spectrum of RNASEH1-related mitochondrial disease. (June 2017)

2. Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations. Issue 1 (29th August 2012)

3. Identifying opportunities to advance health equity in interventional cardiology: Structural heart disease. Issue 4 (27th November 2021)

5. Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease. Issue 12 (13th January 2022)

6. Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features. (28th February 2013)

7. Surgical versus percutaneous multivessel coronary revascularization in patients with chronic kidney disease. (6th December 2019)