Search research articles
Contact Us
Filters
Showing results (191-200 of 316) with videos related to
Page
of 32
Sort By:
Neurology
|
April 11, 2001
A polymorphism in the intronic region of the IL-1alpha gene and the risk for Parkinson's disease
R C Dodel, F Lohmüller, Y Du, et al.
Neurology
|
June 16, 2005
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa
F Asmus, V Horber, J Pohlenz, et al.
Clinical Chemistry
|
February 4, 1999
Rapid detection of a pentanucleotide deletion polymorphism in the human alpha2-macroglobulin gene
R C Dodel, K R Bales, M R Farlow, et al.
Microbiology Resource Announcements
|
December 10, 2024
Closing the genome of <i>Teredinibacter turnerae</i> T7902 by long-read nanopore sequencing
Mark T Gasser, Annie Liu, Ron Flatau, et al.
Neurology
|
July 26, 2006
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
K M Liebetanz, J Winkelmann, C Trenkwalder, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress
|
January 1, 1997
[Kidney transplantation from living donors]
P Vogelbach, A Schütz, I Binet, et al.
Gene Therapy
|
August 15, 2008
Prevention of interferon-stimulated gene expression using microRNA-designed hairpins
M Bauer, N Kinkl, A Meixner, et al.
European Journal of Pain (London, England)
|
March 31, 2012
Cerebral somatic pain modulation during autogenic training in fMRI
R P Naglatzki, M Schlamann, T Gasser, et al.
Human Gene Therapy
|
August 17, 2000
Nonviral glial cell-derived neurotrophic factor gene transfer enhances survival of cultured dopaminergic neurons and improves their function after transplantation in a rat model of Parkinson's disease
M Bauer, M Meyer, L Grimm, et al.
Stroke
|
March 10, 2001
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
G Iannucci, M Dichgans, M Rovaris, et al.
Page
of 32
Search research articles
Search
Showing results (191-200 of 316) with videos related to
Sort By:
Page
of 32
Neurology
|
April 11, 2001
A polymorphism in the intronic region of the IL-1alpha gene and the risk for Parkinson's disease
R C Dodel, F Lohmüller, Y Du, et al.
Neurology
|
June 16, 2005
A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa
F Asmus, V Horber, J Pohlenz, et al.
Clinical Chemistry
|
February 4, 1999
Rapid detection of a pentanucleotide deletion polymorphism in the human alpha2-macroglobulin gene
R C Dodel, K R Bales, M R Farlow, et al.
Microbiology Resource Announcements
|
December 10, 2024
Closing the genome of <i>Teredinibacter turnerae</i> T7902 by long-read nanopore sequencing
Mark T Gasser, Annie Liu, Ron Flatau, et al.
Neurology
|
July 26, 2006
RLS3: fine-mapping of an autosomal dominant locus in a family with intrafamilial heterogeneity
K M Liebetanz, J Winkelmann, C Trenkwalder, et al.
Langenbecks Archiv Fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft Fur Chirurgie. Kongress
|
January 1, 1997
[Kidney transplantation from living donors]
P Vogelbach, A Schütz, I Binet, et al.
Gene Therapy
|
August 15, 2008
Prevention of interferon-stimulated gene expression using microRNA-designed hairpins
M Bauer, N Kinkl, A Meixner, et al.
European Journal of Pain (London, England)
|
March 31, 2012
Cerebral somatic pain modulation during autogenic training in fMRI
R P Naglatzki, M Schlamann, T Gasser, et al.
Human Gene Therapy
|
August 17, 2000
Nonviral glial cell-derived neurotrophic factor gene transfer enhances survival of cultured dopaminergic neurons and improves their function after transplantation in a rat model of Parkinson's disease
M Bauer, M Meyer, L Grimm, et al.
Stroke
|
March 10, 2001
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
G Iannucci, M Dichgans, M Rovaris, et al.
Page
of 32