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A M Schaefer

Showing results (11-20 of 24) with videos related to

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Biochemical Pharmacology|December 11, 2012
Stimulation of the chemosensory TRPA1 cation channel by volatile toxic substances promotes cell survival of small cell lung cancer cellsEva A M Schaefer, Stefanie Stohr, Michael Meister, et al.
Veterinary Parasitology|January 4, 2017
Occurrence of blood parasites in seabirds admitted for rehabilitation in the Western Cape, South Africa, 2001-2013N J Parsons, N M Voogt, A M Schaefer, et al.
Neurology|April 9, 2008
Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutationJ Betts, M J Barron, S J Needham, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Neuromuscular Disorders : NMD|November 25, 2006
A scale to monitor progression and treatment of mitochondrial disease in childrenC Phoenix, A M Schaefer, J L Elson, et al.
Neuropathology and Applied Neurobiology|July 27, 2006
Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvementJ Betts, E Jaros, R H Perry, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletionsJ Betts-Henderson, E Jaros, K J Krishnan, et al.
Neurology|April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)A Agostino, L Valletta, P F Chinnery, et al.
Neurology|May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsG Hudson, M Deschauer, R W Taylor, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Biochemical Pharmacology|December 11, 2012
Stimulation of the chemosensory TRPA1 cation channel by volatile toxic substances promotes cell survival of small cell lung cancer cellsEva A M Schaefer, Stefanie Stohr, Michael Meister, et al.
Veterinary Parasitology|January 4, 2017
Occurrence of blood parasites in seabirds admitted for rehabilitation in the Western Cape, South Africa, 2001-2013N J Parsons, N M Voogt, A M Schaefer, et al.
Neurology|April 9, 2008
Gastrointestinal tract involvement associated with the 3243A>G mitochondrial DNA mutationJ Betts, M J Barron, S J Needham, et al.
Journal of Medical Genetics|February 6, 2004
Mitochondrial DNA deletion in "identical" twin brothersE L Blakely, L He, R W Taylor, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Cytochrome c oxidase deficient muscle fibres: substantial variation in their proportions within skeletal muscles from patients with mitochondrial myopathyM J Barron, P F Chinnery, D Howel, et al.
Neuromuscular Disorders : NMD|November 25, 2006
A scale to monitor progression and treatment of mitochondrial disease in childrenC Phoenix, A M Schaefer, J L Elson, et al.
Neuropathology and Applied Neurobiology|July 27, 2006
Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvementJ Betts, E Jaros, R H Perry, et al.
Neuropathology and Applied Neurobiology|February 4, 2009
Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletionsJ Betts-Henderson, E Jaros, K J Krishnan, et al.
Neurology|April 23, 2003
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)A Agostino, L Valletta, P F Chinnery, et al.
Neurology|May 10, 2006
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletionsG Hudson, M Deschauer, R W Taylor, et al.
Pageof 3