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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset
E M Valente, A R Bentivoglio, E Cassetta, et al.
Annals of Neurology
|
March 23, 2001
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset
E M Valente, A R Bentivoglio, E Cassetta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 15, 2000
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study
A Münchau, E M Valente, G A Shahidi, et al.
European Journal of Neurology
|
March 23, 2016
Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration
I Kraoua, M Romani, D Tonduti, et al.
Cerebellum (London, England)
|
June 5, 2021
PIGQ-Related Glycophosphatidylinositol Deficiency Associated with Nonprogressive Congenital Ataxia
G Zanni, F D'Abrusco, F Nicita, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 18, 2003
Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia
F Brancati, E M Valente, M Castori, et al.
Stem Cell Research
|
May 20, 2025
Production and characterisation of four Joubert syndrome patient-derived induced pluripotent stem cell (iPSC) lines with mutations in either RPGRIP1L or CPLANE1 genes
L Pollara, E de Gregorio, V Buonofiglio, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2009
Joubert syndrome with bilateral polymicrogyria: clinical and neuropathological findings in two brothers
L Giordano, A Vignoli, L Pinelli, et al.
Neurology
|
February 25, 2005
The epsilon-sarcoglycan gene in myoclonic syndromes
E M Valente, M J Edwards, P Mir, et al.
Neurobiology of Disease
|
February 27, 2016
Exposure to low-dose rotenone precipitates synaptic plasticity alterations in PINK1 heterozygous knockout mice
G Martella, G Madeo, M Maltese, et al.
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Showing results (41-50 of 61) with videos related to
Sort By:
Page
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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
August 7, 2001
Identification of a novel primary torsion dystonia locus (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset
E M Valente, A R Bentivoglio, E Cassetta, et al.
Annals of Neurology
|
March 23, 2001
DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset
E M Valente, A R Bentivoglio, E Cassetta, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 15, 2000
A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study
A Münchau, E M Valente, G A Shahidi, et al.
European Journal of Neurology
|
March 23, 2016
Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration
I Kraoua, M Romani, D Tonduti, et al.
Cerebellum (London, England)
|
June 5, 2021
PIGQ-Related Glycophosphatidylinositol Deficiency Associated with Nonprogressive Congenital Ataxia
G Zanni, F D'Abrusco, F Nicita, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 18, 2003
Role of the dopamine D5 receptor (DRD5) as a susceptibility gene for cervical dystonia
F Brancati, E M Valente, M Castori, et al.
Stem Cell Research
|
May 20, 2025
Production and characterisation of four Joubert syndrome patient-derived induced pluripotent stem cell (iPSC) lines with mutations in either RPGRIP1L or CPLANE1 genes
L Pollara, E de Gregorio, V Buonofiglio, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2009
Joubert syndrome with bilateral polymicrogyria: clinical and neuropathological findings in two brothers
L Giordano, A Vignoli, L Pinelli, et al.
Neurology
|
February 25, 2005
The epsilon-sarcoglycan gene in myoclonic syndromes
E M Valente, M J Edwards, P Mir, et al.
Neurobiology of Disease
|
February 27, 2016
Exposure to low-dose rotenone precipitates synaptic plasticity alterations in PINK1 heterozygous knockout mice
G Martella, G Madeo, M Maltese, et al.
Page
of 7