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A Quattrone

Showing results (131-140 of 273) with videos related to

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Clinical Genetics|February 21, 2007
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseasesG Annesi, U Aguglia, P Tarantino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2009
A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASILC Ungaro, P Servillo, Rosalucia Mazzei, et al.
Neuroimage|September 20, 2014
Increased functional connectivity within mesocortical networks in open peopleL Passamonti, A Terracciano, R Riccelli, et al.
Cephalalgia : an International Journal of Headache|October 27, 2010
Abnormal pressure waves in headache sufferers with bilateral transverse sinus stenosisF Bono, D Salvino, T Tallarico, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 25, 1998
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthoodU Aguglia, A Gambardella, E Le Piane, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 11, 2008
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosisP Valentino, A Labate, R Nisticò, et al.
Neurology|August 9, 2006
Bilateral transverse sinus stenosis predicts IIH without papilledema in patients with migraineF Bono, D Messina, C Giliberto, et al.
Cerebellum (London, England)|December 6, 2024
Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 GenesE Fratto, Maurizio Morelli, J Buonocore, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 8, 2000
A conserved AU-rich element in the 3' untranslated region of bcl-2 mRNA is endowed with a destabilizing function that is involved in bcl-2 down-regulation during apoptosisN Schiavone, P Rosini, A Quattrone, et al.
Pageof 28

Showing results (131-140 of 273) with videos related to

Sort By:
Pageof 28
Clinical Genetics|February 21, 2007
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseasesG Annesi, U Aguglia, P Tarantino, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 5, 2009
A pathogenic rare mutation on exon 22 of the NOTCH3 gene disclosed in an Italian patient affected by CADASILC Ungaro, P Servillo, Rosalucia Mazzei, et al.
Neuroimage|September 20, 2014
Increased functional connectivity within mesocortical networks in open peopleL Passamonti, A Terracciano, R Riccelli, et al.
Cephalalgia : an International Journal of Headache|October 27, 2010
Abnormal pressure waves in headache sufferers with bilateral transverse sinus stenosisF Bono, D Salvino, T Tallarico, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 25, 1998
Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthoodU Aguglia, A Gambardella, E Le Piane, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|October 11, 2008
Anti-GM1 antibodies are not associated with cerebral atrophy in patients with multiple sclerosisP Valentino, A Labate, R Nisticò, et al.
Neurology|August 9, 2006
Bilateral transverse sinus stenosis predicts IIH without papilledema in patients with migraineF Bono, D Messina, C Giliberto, et al.
Cerebellum (London, England)|December 6, 2024
Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 GenesE Fratto, Maurizio Morelli, J Buonocore, et al.
Neuromuscular Disorders : NMD|February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective studyL Padua, D Pareyson, I Aprile, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 8, 2000
A conserved AU-rich element in the 3' untranslated region of bcl-2 mRNA is endowed with a destabilizing function that is involved in bcl-2 down-regulation during apoptosisN Schiavone, P Rosini, A Quattrone, et al.
Pageof 28