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E M Valente

Showing results (31-40 of 61) with videos related to

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Annals of Neurology|October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic studyO Bandmann, E M Valente, P Holmans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4AF Brancati, E M Valente, N P Davies, et al.
Kidney International|August 11, 2006
Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the associationG Caridi, M Dagnino, A Rossi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
A family study on primary blepharospasmG Defazio, D Martino, M S Aniello, et al.
Journal of Medical Genetics|February 4, 2005
NPHP1 gene deletion is a rare cause of Joubert syndrome related disordersM Castori, E M Valente, M A Donati, et al.
Brain : a Journal of Neurology|January 5, 1999
The role of DYT1 in primary torsion dystonia in EuropeE M Valente, T T Warner, P R Jarman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2004
DJ-1 mutations in Parkinson's diseaseD G Healy, P M Abou-Sleiman, E M Valente, et al.
European Journal of Neurology|August 29, 2014
Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohortM Romani, I Kraoua, A Micalizzi, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2008
Impaired body movement representation in DYT1 mutation carriersM Fiorio, M Gambarin, G Defazio, et al.
European Journal of Neurology|May 29, 2009
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystoniaD Martino, M Muglia, G Abbruzzese, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
Annals of Neurology|October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic studyO Bandmann, E M Valente, P Holmans, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 23, 2003
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4AF Brancati, E M Valente, N P Davies, et al.
Kidney International|August 11, 2006
Nephronophthisis type 1 deletion syndrome with neurological symptoms: prevalence and significance of the associationG Caridi, M Dagnino, A Rossi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2006
A family study on primary blepharospasmG Defazio, D Martino, M S Aniello, et al.
Journal of Medical Genetics|February 4, 2005
NPHP1 gene deletion is a rare cause of Joubert syndrome related disordersM Castori, E M Valente, M A Donati, et al.
Brain : a Journal of Neurology|January 5, 1999
The role of DYT1 in primary torsion dystonia in EuropeE M Valente, T T Warner, P R Jarman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 7, 2004
DJ-1 mutations in Parkinson's diseaseD G Healy, P M Abou-Sleiman, E M Valente, et al.
European Journal of Neurology|August 29, 2014
Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohortM Romani, I Kraoua, A Micalizzi, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 24, 2008
Impaired body movement representation in DYT1 mutation carriersM Fiorio, M Gambarin, G Defazio, et al.
European Journal of Neurology|May 29, 2009
Brain-derived neurotrophic factor and risk for primary adult-onset cranial-cervical dystoniaD Martino, M Muglia, G Abbruzzese, et al.
Pageof 7