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N H Thomas

Showing results (11-20 of 23) with videos related to

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Archives of Disease in Childhood|November 1, 1993
Mycoplasma pneumoniae infection and neurological diseaseN H Thomas, J E Collins, S A Robb, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two casesN H Thomas, J Z Heckmatt, E Rodillo, et al.
Journal of the Royal Society of Medicine|May 29, 1998
Hereditary sensory and autonomic neuropathy with anhidrosis (type IV)A E Haworth, N H Thomas, L J Cook, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 7, 2001
Lower limb and back pain in Guillain-Barré syndrome and associated contrast enhancement in MRI of the cauda equinaJ M Wilmshurst, N H Thomas, R O Robinson, et al.
Journal of Medical Genetics|November 10, 2000
Identification of three novel frameshift mutations in patients with Friedreich's ataxiaM A Pook, S A Al-Mahdawi, N H Thomas, 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 Human Genetics : EJHG|November 5, 1998
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophyJ E Taylor, N H Thomas, C M Lewis, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Journal of Geophysical Research. Planets|October 1, 2020
Hydrogen Variability in the Murray Formation, Gale Crater, MarsN H Thomas, B L Ehlmann, W Rapin, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Archives of Disease in Childhood|November 1, 1993
Mycoplasma pneumoniae infection and neurological diseaseN H Thomas, J E Collins, S A Robb, et al.
Neuromuscular Disorders : NMD|March 1, 1994
Continuous muscle fibre activity (Isaacs' syndrome) in infancy: a report of two casesN H Thomas, J Z Heckmatt, E Rodillo, et al.
Journal of the Royal Society of Medicine|May 29, 1998
Hereditary sensory and autonomic neuropathy with anhidrosis (type IV)A E Haworth, N H Thomas, L J Cook, et al.
Acta Paediatrica (Oslo, Norway : 1992)|July 7, 2001
Lower limb and back pain in Guillain-Barré syndrome and associated contrast enhancement in MRI of the cauda equinaJ M Wilmshurst, N H Thomas, R O Robinson, et al.
Journal of Medical Genetics|November 10, 2000
Identification of three novel frameshift mutations in patients with Friedreich's ataxiaM A Pook, S A Al-Mahdawi, N H Thomas, 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 Human Genetics : EJHG|November 5, 1998
Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophyJ E Taylor, N H Thomas, C M Lewis, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Journal of Geophysical Research. Planets|October 1, 2020
Hydrogen Variability in the Murray Formation, Gale Crater, MarsN H Thomas, B L Ehlmann, W Rapin, et al.
Journal of Medical Genetics|March 1, 1992
Prenatal prediction of spinal muscular atrophyR J Daniels, G K Suthers, K E Morrison, et al.
Pageof 3