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Marina Frontali

Showing results (11-20 of 32) with videos related to

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Journal of Human Genetics|January 10, 2014
A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutationLiana Veneziano, Elide Mantuano, Claudio Catalli, et al.
Clinical Rehabilitation|August 19, 2007
Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot studyPaola Zinzi, Dario Salmaso, Rosa De Grandis, et al.
Journal of the Neurological Sciences|November 4, 2008
Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic AtaxiaLiana Veneziano, Serena Guida, Elide Mantuano, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Plos One|June 27, 2013
Is the oxidant/antioxidant status altered in CADASIL patients?Jonica Campolo, Renata De Maria, Caterina Mariotti, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Plos One|May 24, 2018
Does arterial hypertension influence the onset of Huntington's disease?Leire Valcárcel-Ocete, Asier Fullaondo, Gorka Alkorta-Aranburu, et al.
The Lancet. Neurology|September 1, 2015
Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trialSilvia Romano, Giulia Coarelli, Christian Marcotulli, et al.
Journal of the Neurological Sciences|February 5, 2010
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2Elide Mantuano, Silvia Romano, Liana Veneziano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 11, 2011
Impaired vasoreactivity in mildly disabled CADASIL patientsJonica Campolo, Renata De Maria, Marina Frontali, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Human Genetics|January 10, 2014
A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutationLiana Veneziano, Elide Mantuano, Claudio Catalli, et al.
Clinical Rehabilitation|August 19, 2007
Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot studyPaola Zinzi, Dario Salmaso, Rosa De Grandis, et al.
Journal of the Neurological Sciences|November 4, 2008
Newly characterised 5' and 3' regions of CACNA1A gene harbour mutations associated with Familial Hemiplegic Migraine and Episodic AtaxiaLiana Veneziano, Serena Guida, Elide Mantuano, et al.
Clinical Neurology and Neurosurgery|March 11, 2018
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegiaGiulia Coarelli, Silvia Romano, Lorena Travaglini, et al.
Plos One|June 27, 2013
Is the oxidant/antioxidant status altered in CADASIL patients?Jonica Campolo, Renata De Maria, Caterina Mariotti, et al.
Neurogenetics|October 2, 2004
A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signsMaria Spadaro, Simona Ursu, Frank Lehmann-Horn, et al.
Plos One|May 24, 2018
Does arterial hypertension influence the onset of Huntington's disease?Leire Valcárcel-Ocete, Asier Fullaondo, Gorka Alkorta-Aranburu, et al.
The Lancet. Neurology|September 1, 2015
Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trialSilvia Romano, Giulia Coarelli, Christian Marcotulli, et al.
Journal of the Neurological Sciences|February 5, 2010
Identification of novel and recurrent CACNA1A gene mutations in fifteen patients with episodic ataxia type 2Elide Mantuano, Silvia Romano, Liana Veneziano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 11, 2011
Impaired vasoreactivity in mildly disabled CADASIL patientsJonica Campolo, Renata De Maria, Marina Frontali, et al.
Pageof 4