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A Simonati

Showing results (41-50 of 48) with videos related to

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Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
European Journal of Neurology|August 28, 2007
Dementia, delusions and seizures: storage disease or genetic AD?A Alberici, C Bonato, B Borroni, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
EFSA Journal. European Food Safety Authority|March 12, 2025
Modification of the existing maximum residue level for metalaxyl-M in honey, G Bellisai, G Bernasconi, et al.
Neurology|October 20, 2010
Pontocerebellar hypoplasia: clinical, pathologic, and genetic studiesD Cassandrini, R Biancheri, A Tessa, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Neuromuscular Disorders : NMD|July 10, 1999
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22A Simonati, G M Fabrizi, A Pasquinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
European Journal of Neurology|August 28, 2007
Dementia, delusions and seizures: storage disease or genetic AD?A Alberici, C Bonato, B Borroni, et al.
Neuropediatrics|July 4, 2007
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosisN Cannelli, N Nardocci, D Cassandrini, et al.
EFSA Journal. European Food Safety Authority|March 12, 2025
Modification of the existing maximum residue level for metalaxyl-M in honey, G Bellisai, G Bernasconi, et al.
Neurology|October 20, 2010
Pontocerebellar hypoplasia: clinical, pathologic, and genetic studiesD Cassandrini, R Biancheri, A Tessa, et al.
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
American Journal of Medical Genetics. Part A|September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathiesLorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Pageof 5