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You searched for: Author/Creator Martí, Ramon

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1. Deoxynucleoside Therapy for Thymidine Kinase 2–Deficient Myopathy. Issue 2 (17th June 2019)

4. Dysfunctional mitochondrial translation and combined oxidative phosphorylation deficiency in a mouse model of hepatoencephalopathy due to Gfm1 mutations. Issue 1 (16th December 2021)

5. Increased dNTP pools rescue mtDNA depletion in human POLG‐deficient fibroblasts. Issue 6 (8th March 2019)

6. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by the MNGIE International Network. Issue 2 (8th September 2020)

9. Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy. (2nd June 2015)

10. Severe TK2 enzyme activity deficiency in patients with mild forms of myopathy. (2nd June 2015)