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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 correlates
P J Lamont, M B Davis, N W Wood
Archives of Disease in Childhood
|
July 1, 1997
Pearson's syndrome without marrow involvement
A A Morris, P J Lamont, P T Clayton
Neurology
|
December 1, 1991
Plasmapheresis in children with Guillain-Barré syndrome
P 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 mutation
P 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 involvement
L 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 progression
P 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 analysis
P 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 MYH2
M 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 syndrome
R 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.
Page
of 2
Search research articles
Search
Showing results (1-10 of 16) with videos related to
Sort By:
Page
of 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 correlates
P J Lamont, M B Davis, N W Wood
Archives of Disease in Childhood
|
July 1, 1997
Pearson's syndrome without marrow involvement
A A Morris, P J Lamont, P T Clayton
Neurology
|
December 1, 1991
Plasmapheresis in children with Guillain-Barré syndrome
P 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 mutation
P 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 involvement
L 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 progression
P 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 analysis
P 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 MYH2
M 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 syndrome
R 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.
Page
of 2