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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.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
December 31, 2004
Spinocerebellar ataxia and hypergonadotropic hypogonadism associated with familial sensorineural hearing loss
N A Georgopoulos, S Papapetropoulos, E Chroni, et al.
Brain : a Journal of Neurology
|
August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy
M M Reilly, D Adams, D R Booth, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2004
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India
K K Sinha, P F Worth, D K Jha, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 1, 1994
Cortical myoclonus in Huntington's disease
P D Thompson, K P Bhatia, P Brown, et al.
Neurology
|
January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
E Matthews, R Labrum, M G Sweeney, et al.
Brain : a Journal of Neurology
|
March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplication
P K Thomas, W Marques, M B Davis, et al.
Cancer Research
|
March 15, 1992
A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer
B Carritt, K Kok, A van den Berg, et al.
Brain : a Journal of Neurology
|
October 13, 2007
Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions
D Fialho, S Schorge, U Pucovska, et al.
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of 11
Search research articles
Search
Showing results (81-90 of 106) with videos related to
Sort By:
Page
of 11
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.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology
|
December 31, 2004
Spinocerebellar ataxia and hypergonadotropic hypogonadism associated with familial sensorineural hearing loss
N A Georgopoulos, S Papapetropoulos, E Chroni, et al.
Brain : a Journal of Neurology
|
August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy
M M Reilly, D Adams, D R Booth, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2004
Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India
K K Sinha, P F Worth, D K Jha, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 1, 1994
Cortical myoclonus in Huntington's disease
P D Thompson, K P Bhatia, P Brown, et al.
Neurology
|
January 2, 2009
Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
E Matthews, R Labrum, M G Sweeney, et al.
Brain : a Journal of Neurology
|
March 1, 1997
The phenotypic manifestations of chromosome 17p11.2 duplication
P K Thomas, W Marques, M B Davis, et al.
Cancer Research
|
March 15, 1992
A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer
B Carritt, K Kok, A van den Berg, et al.
Brain : a Journal of Neurology
|
October 13, 2007
Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions
D Fialho, S Schorge, U Pucovska, et al.
Page
of 11