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G A Nicholson

Showing results (51-60 of 115) with videos related to

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Journal of the Neurological Sciences|December 1, 1985
The creatine kinase reference interval. An assessment of intra- and inter-individual variationG A Nicholson, G Morgan, M Meerkin, et al.
Neurology|October 1, 1979
LDH-5 levels and electrophoresis support mediaA D Roses, M J Roses, G A Nicholson, et al.
Neurology|May 1, 1977
Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophyA D Roses, M J Roses, G A Nicholson, et al.
American Journal of Medical Genetics|December 18, 1998
Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetusS Rudnik-Schöneborn, G A Nicholson, G Morgan, et al.
Human Genetics|August 15, 2000
Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysisD J Hulme, I P Blair, J L Dawkins, et al.
Neurology|February 26, 2003
CMT with pyramidal features. Charcot-Marie-ToothS Vucic, M Kennerson, D Zhu, et al.
Annals of Neurology|March 23, 2001
Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutationP J Spira, D M Sharpe, G Halliday, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2000
Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsiesS Sander, R A Ouvrier, J G McLeod, et al.
Neurology|December 13, 2006
Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth diseaseI G Huttner, M L Kennerson, S W Reddel, et al.
Muscle & Nerve|November 1, 1986
The effect of aerobic exercise on serum creatine kinase activitiesG A Nicholson, G J Morgan, M Meerkin, et al.
Pageof 12

Showing results (51-60 of 115) with videos related to

Sort By:
Pageof 12
Journal of the Neurological Sciences|December 1, 1985
The creatine kinase reference interval. An assessment of intra- and inter-individual variationG A Nicholson, G Morgan, M Meerkin, et al.
Neurology|October 1, 1979
LDH-5 levels and electrophoresis support mediaA D Roses, M J Roses, G A Nicholson, et al.
Neurology|May 1, 1977
Lactate dehydrogenase isoenzyme in detecting carriers of Duchenne muscular dystrophyA D Roses, M J Roses, G A Nicholson, et al.
American Journal of Medical Genetics|December 18, 1998
Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetusS Rudnik-Schöneborn, G A Nicholson, G Morgan, et al.
Human Genetics|August 15, 2000
Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysisD J Hulme, I P Blair, J L Dawkins, et al.
Neurology|February 26, 2003
CMT with pyramidal features. Charcot-Marie-ToothS Vucic, M Kennerson, D Zhu, et al.
Annals of Neurology|March 23, 2001
Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutationP J Spira, D M Sharpe, G Halliday, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 23, 2000
Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsiesS Sander, R A Ouvrier, J G McLeod, et al.
Neurology|December 13, 2006
Proof of genetic heterogeneity in X-linked Charcot-Marie-Tooth diseaseI G Huttner, M L Kennerson, S W Reddel, et al.
Muscle & Nerve|November 1, 1986
The effect of aerobic exercise on serum creatine kinase activitiesG A Nicholson, G J Morgan, M Meerkin, et al.
Pageof 12