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M G Sweeney

Showing results (41-50 of 48) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 2009
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patientsI Trender-Gerhard, M G Sweeney, P Schwingenschuh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Oncogene|July 11, 2012
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutationsZ Yao, A W E Jones, E Fassone, et al.
Journal of Medical Genetics|July 10, 2009
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testingR W Labrum, S Rajakulendran, T D Graves, et al.
Neurology|August 12, 2011
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up studyH Jacobi, P Bauer, P Giunti, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 2009
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patientsI Trender-Gerhard, M G Sweeney, P Schwingenschuh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1995
Bilateral simultaneous optic neuropathy in adults: clinical, imaging, serological, and genetic studiesS P Morrissey, F X Borruat, D H Miller, et al.
Journal of the Neurological Sciences|January 1, 1994
Mitochondrial DNA mutation underlying Leigh's syndrome: clinical, pathological, biochemical, and genetic studies of a patient presenting with progressive myoclonic epilepsyM G Sweeney, S R Hammans, L W Duchen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2007
Multiple mitochondrial DNA deletions in monozygotic twins with OPMDM M K Muqit, A J Larner, M G Sweeney, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, et al.
Oncogene|July 11, 2012
PGC-1β mediates adaptive chemoresistance associated with mitochondrial DNA mutationsZ Yao, A W E Jones, E Fassone, et al.
Journal of Medical Genetics|July 10, 2009
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testingR W Labrum, S Rajakulendran, T D Graves, et al.
Neurology|August 12, 2011
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up studyH Jacobi, P Bauer, P Giunti, et al.
Pageof 5