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N Rizzuto

Showing results (131-140 of 190) with videos related to

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Neurology|September 17, 1999
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22G M Fabrizi, T Cavallaro, F Taioli, et al.
Rivista Di Patologia Nervosa E Mentale|November 1, 1978
[Four cases of Creutzfeldt-Jakob's disease (author's transl)]R Scuccato, A M Iannucci, M Vio, et al.
Molecular and Cellular Probes|April 9, 2001
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff diseaseM Gomez-Lira, M Mottes, C Perusi, et al.
Cell and Tissue Research|November 1, 1996
Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitroG Moretto, D G Walker, P Lanteri, et al.
Human Genetics|May 26, 1998
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutationM Gomez-Lira, C Perusi, M Mottes, et al.
American Journal of Medical Genetics|February 25, 1998
Splicing mutation causes infantile Sandhoff diseaseM Gomez-Lira, C Perusi, M Mottes, et al.
Journal of Neuroimmunology|March 1, 1997
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathyB Bonetti, F Invernizzi, N Rizzuto, et al.
Journal of Neurology|May 1, 1996
Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological studyA Polo, F Teatini, S D'Anna, et al.
Italian Journal of Neurological Sciences|December 1, 1983
Histopathological and ultrastructural study of a case of infantile metachromatic leukodystrophyF Fenzi, G Moretto, A Maleci, et al.
Acta Neuropathologica|August 12, 2003
MELAS: clinical phenotype and morphological brain abnormalitiesM Sparaco, A Simonati, T Cavallaro, et al.
Pageof 19

Showing results (131-140 of 190) with videos related to

Sort By:
Pageof 19
Neurology|September 17, 1999
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22G M Fabrizi, T Cavallaro, F Taioli, et al.
Rivista Di Patologia Nervosa E Mentale|November 1, 1978
[Four cases of Creutzfeldt-Jakob's disease (author's transl)]R Scuccato, A M Iannucci, M Vio, et al.
Molecular and Cellular Probes|April 9, 2001
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff diseaseM Gomez-Lira, M Mottes, C Perusi, et al.
Cell and Tissue Research|November 1, 1996
Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitroG Moretto, D G Walker, P Lanteri, et al.
Human Genetics|May 26, 1998
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation and show different phenotypes; description of a novel null-type mutationM Gomez-Lira, C Perusi, M Mottes, et al.
American Journal of Medical Genetics|February 25, 1998
Splicing mutation causes infantile Sandhoff diseaseM Gomez-Lira, C Perusi, M Mottes, et al.
Journal of Neuroimmunology|March 1, 1997
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathyB Bonetti, F Invernizzi, N Rizzuto, et al.
Journal of Neurology|May 1, 1996
Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological studyA Polo, F Teatini, S D'Anna, et al.
Italian Journal of Neurological Sciences|December 1, 1983
Histopathological and ultrastructural study of a case of infantile metachromatic leukodystrophyF Fenzi, G Moretto, A Maleci, et al.
Acta Neuropathologica|August 12, 2003
MELAS: clinical phenotype and morphological brain abnormalitiesM Sparaco, A Simonati, T Cavallaro, et al.
Pageof 19