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P Tonali

Showing results (311-320 of 320) with videos related to

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Nature Neuroscience|April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gatingH L Wang, M Milone, K Ohno, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 29, 1997
Ischaemic myelopathy associated with cocaine: clinical, neurophysiological, and neuroradiological featuresV Di Lazzaro, D Restuccia, A Oliviero, et al.
European Journal of Neurology|February 24, 2006
Coeliac disease presenting with acute disseminated encephalomyelitisM Mirabella, A Cianfoni, M Bucci, et al.
Neuroscience|April 22, 2006
Modulation of laser-evoked potentials by experimental cutaneous tonic painM Valeriani, P Tonali, D Le Pera, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's diseaseM Sabatelli, L Quaranta, F Madia, et al.
Pain|September 23, 2003
Reduced habituation to experimental pain in migraine patients: a CO(2) laser evoked potential studyM Valeriani, M de Tommaso, D Restuccia, et al.
Neurology|September 17, 1999
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13S Servidei, F Capon, A Spinazzola, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Annals of Neurology|June 9, 1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotypeE Ricci, G Galluzzi, G Deidda, et al.
American Journal of Human Genetics|March 31, 2000
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophyM Raffaele Di Barletta, E Ricci, G Galluzzi, et al.
Pageof 32

Showing results (311-320 of 320) with videos related to

Sort By:
Pageof 32
You have reached the last page of results.This site can display upto 320 results.
Nature Neuroscience|April 9, 1999
Acetylcholine receptor M3 domain: stereochemical and volume contributions to channel gatingH L Wang, M Milone, K Ohno, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 29, 1997
Ischaemic myelopathy associated with cocaine: clinical, neurophysiological, and neuroradiological featuresV Di Lazzaro, D Restuccia, A Oliviero, et al.
European Journal of Neurology|February 24, 2006
Coeliac disease presenting with acute disseminated encephalomyelitisM Mirabella, A Cianfoni, M Bucci, et al.
Neuroscience|April 22, 2006
Modulation of laser-evoked potentials by experimental cutaneous tonic painM Valeriani, P Tonali, D Le Pera, et al.
Neuromuscular Disorders : NMD|June 14, 2002
Peripheral neuropathy with hypomyelinating features in adult-onset Krabbe's diseaseM Sabatelli, L Quaranta, F Madia, et al.
Pain|September 23, 2003
Reduced habituation to experimental pain in migraine patients: a CO(2) laser evoked potential studyM Valeriani, M de Tommaso, D Restuccia, et al.
Neurology|September 17, 1999
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13S Servidei, F Capon, A Spinazzola, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Annals of Neurology|June 9, 1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotypeE Ricci, G Galluzzi, G Deidda, et al.
American Journal of Human Genetics|March 31, 2000
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophyM Raffaele Di Barletta, E Ricci, G Galluzzi, et al.
Pageof 32