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P J Lamont

Showing results (1-10 of 16) with videos related to

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Brain : a Journal of Neurology|April 1, 1997
Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlatesP J Lamont, M B Davis, N W Wood
Archives of Disease in Childhood|July 1, 1997
Pearson's syndrome without marrow involvementA A Morris, P J Lamont, P T Clayton
Neurology|December 1, 1991
Plasmapheresis in children with Guillain-Barré syndromeP J Lamont, H M Johnston, V A Berdoukas
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutationP J Lamont, R L Jacob, F L Mastaglia, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 1995
Recurrent lymphomatoid granulomatosis and isolated CNS involvementL H Sekhon, M K Morgan, E L Salisbury, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progressionP J Lamont, V Dubowitz, D N Landon, et al.
Archives of Disease in Childhood|October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysisP J Lamont, R Surtees, C E Woodward, et al.
Clinical Genetics|December 23, 2014
Adult onset distal and proximal myopathy with complete ophthalmoplegia associated with a novel de novo p.(Leu1877Pro) mutation in MYH2M Cabrera-Serrano, V A Fabian, J Boutilier, et al.
Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.
European Journal of Neurology|August 28, 2007
Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important?C L Wilson, M C Fahey, L A Corben, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Brain : a Journal of Neurology|April 1, 1997
Identification and sizing of the GAA trinucleotide repeat expansion of Friedreich's ataxia in 56 patients. Clinical and genetic correlatesP J Lamont, M B Davis, N W Wood
Archives of Disease in Childhood|July 1, 1997
Pearson's syndrome without marrow involvementA A Morris, P J Lamont, P T Clayton
Neurology|December 1, 1991
Plasmapheresis in children with Guillain-Barré syndromeP J Lamont, H M Johnston, V A Berdoukas
Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutationP J Lamont, R L Jacob, F L Mastaglia, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 1, 1995
Recurrent lymphomatoid granulomatosis and isolated CNS involvementL H Sekhon, M K Morgan, E L Salisbury, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Fifty year follow-up of a patient with central core disease shows slow but definite progressionP J Lamont, V Dubowitz, D N Landon, et al.
Archives of Disease in Childhood|October 15, 1998
Clinical and laboratory findings in referrals for mitochondrial DNA analysisP J Lamont, R Surtees, C E Woodward, et al.
Clinical Genetics|December 23, 2014
Adult onset distal and proximal myopathy with complete ophthalmoplegia associated with a novel de novo p.(Leu1877Pro) mutation in MYH2M Cabrera-Serrano, V A Fabian, J Boutilier, et al.
Neurology|August 1, 1997
A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndromeR M Chalmers, P J Lamont, I Nelson, et al.
European Journal of Neurology|August 28, 2007
Quality of life in Friedreich ataxia: what clinical, social and demographic factors are important?C L Wilson, M C Fahey, L A Corben, et al.
Pageof 2