Author/Creator: Pitceathly, Robert - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Pitceathly, Robert

1. 237 SLC25A46 mutations cause a spectrum of disorders including CMT2 with optic atrophy. Issue 12 (14th November 2019)

Authors:: Doherty, Carolynne; Pipis, Menelaos; Cortese, Andrea; Poh, Roy; Polke, James; Pitceathly, Robert; Rossor, Alexander; Reilly, Mary
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 90:Issue 12(2019)
Page Start:: e58
Record Type:: Journal Article
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2. THE MEDICAL RESEARCH COUNCIL NEUROMUSCULAR CENTRE FOR TRANSLATIONAL RESEARCH MITOCHONDRIAL DISEASE PATIENT COHORT STUDY UK: FROM CONCEPTUALISATION TO UTILISATION. Issue 11 (9th October 2013)

Authors:: Nesbitt, Victoria; Pitceathly, Robert; Cockell, Simon; Poulton, Joanna; Rahman, Shamima; Hanna, Michael; Taylor, Robert; Chinnery, Patrick; Turnbull, Douglass; McFarland, Robert
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 84:Issue 11(2013)
Page Start:: e2
Record Type:: Journal Article
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