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M Pandolfo

Showing results (61-70 of 116) with videos related to

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European Journal of Human Genetics : EJHG|January 1, 1995
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 17, 2019
Electrophysiological evidence for limited progression of the proprioceptive impairment in Friedreich ataxiaG Naeije, M Bourguignon, V Wens, et al.
International Journal of Pharmaceutics|September 10, 2008
Pharmacoscintigraphic and pharmacokinetic evaluation on healthy human volunteers of sustained-release floating minitablets containing levodopa and carbidopaJ Goole, B Van Gansbeke, G Pilcer, et al.
Journal of Neurology|April 15, 2004
Is the Addenbrooke's cognitive examination effective to detect frontotemporal dementia?J C Bier, M Ventura, V Donckels, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 9, 2006
Novel mutations in the arylsulfatase A gene in eight Italian families with metachromatic leukodystrophyM Bertelli, S Gallo, A Buda, et al.
Journal of the American Association for Laboratory Animal Science : JAALAS|March 3, 2021
Comparison of Juvenile Feed Protocols on Growth and Spawning in ZebrafishStephen C Frederickson, Mark D Steinmiller, Tiffany Rae Blaylock, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in Italian Lesch-Nyhan patients: identification of nine novel mutationsM Bertelli, D Randi, V Micheli, et al.
American Journal of Human Genetics|January 1, 1995
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsiesD Lorenzetti, D Pareyson, A Sghirlanzoni, et al.
American Journal of Human Genetics|August 1, 1990
Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15M Pandolfo, G Sirugo, A Antonelli, et al.
Pageof 12

Showing results (61-70 of 116) with videos related to

Sort By:
Pageof 12
European Journal of Human Genetics : EJHG|January 1, 1995
Evidence of linkage between susceptibility to multiple sclerosis and HLA-class II loci in Italian multiplex familiesM Eoli, M Pandolfo, A Amoroso, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|December 17, 2019
Electrophysiological evidence for limited progression of the proprioceptive impairment in Friedreich ataxiaG Naeije, M Bourguignon, V Wens, et al.
International Journal of Pharmaceutics|September 10, 2008
Pharmacoscintigraphic and pharmacokinetic evaluation on healthy human volunteers of sustained-release floating minitablets containing levodopa and carbidopaJ Goole, B Van Gansbeke, G Pilcer, et al.
Journal of Neurology|April 15, 2004
Is the Addenbrooke's cognitive examination effective to detect frontotemporal dementia?J C Bier, M Ventura, V Donckels, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|May 9, 2006
Novel mutations in the arylsulfatase A gene in eight Italian families with metachromatic leukodystrophyM Bertelli, S Gallo, A Buda, et al.
Journal of the American Association for Laboratory Animal Science : JAALAS|March 3, 2021
Comparison of Juvenile Feed Protocols on Growth and Spawning in ZebrafishStephen C Frederickson, Mark D Steinmiller, Tiffany Rae Blaylock, et al.
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
Journal of Inherited Metabolic Disease|October 27, 2004
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in Italian Lesch-Nyhan patients: identification of nine novel mutationsM Bertelli, D Randi, V Micheli, et al.
American Journal of Human Genetics|January 1, 1995
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsiesD Lorenzetti, D Pareyson, A Sghirlanzoni, et al.
American Journal of Human Genetics|August 1, 1990
Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15M Pandolfo, G Sirugo, A Antonelli, et al.
Pageof 12