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Neurology
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June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism
C Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology
|
May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystonias
A Albanese, F Asmus, K P Bhatia, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
April 21, 2007
Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity
K J Schweitzer, S Behnke, I Liepelt, et al.
European Journal of Neurology
|
November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?
A Pilotto, C Schulte, A K Hauser, et al.
Annals of Neurology
|
February 24, 2001
Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families
F Asmus, A Zimprich, M Naumann, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
Membrane vesicles can contribute to cellulose degradation by <i>Teredinibacter turnerae</i>, a cultivable intracellular endosymbiont of shipworms
Mark T Gasser, Annie Liu, Marvin Altamia, et al.
European Journal of Neurology
|
May 26, 2006
A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force
A Albanese, M P Barnes, K P Bhatia, et al.
American Journal of Human Genetics
|
September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews
P L Kramer, G A Heiman, T Gasser, et al.
Science (New York, N.Y.)
|
July 18, 1997
Genetic complexity and Parkinson's disease
T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Parkinsonism & Related Disorders
|
July 2, 2008
German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations
Z K Wszolek, P Vieregge, R J Uitti, et al.
Page
of 32
Search research articles
Search
Showing results (251-260 of 316) with videos related to
Sort By:
Page
of 32
Neurology
|
June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphism
C Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology
|
May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystonias
A Albanese, F Asmus, K P Bhatia, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
April 21, 2007
Cross-sectional study discloses a positive family history for Parkinson's disease and male gender as epidemiological risk factors for substantia nigra hyperechogenicity
K J Schweitzer, S Behnke, I Liepelt, et al.
European Journal of Neurology
|
November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?
A Pilotto, C Schulte, A K Hauser, et al.
Annals of Neurology
|
February 24, 2001
Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families
F Asmus, A Zimprich, M Naumann, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
Membrane vesicles can contribute to cellulose degradation by <i>Teredinibacter turnerae</i>, a cultivable intracellular endosymbiont of shipworms
Mark T Gasser, Annie Liu, Marvin Altamia, et al.
European Journal of Neurology
|
May 26, 2006
A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS-ES Task Force
A Albanese, M P Barnes, K P Bhatia, et al.
American Journal of Human Genetics
|
September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-Jews
P L Kramer, G A Heiman, T Gasser, et al.
Science (New York, N.Y.)
|
July 18, 1997
Genetic complexity and Parkinson's disease
T Gasser, B Müller-Myhsok, Z K Wszolek, et al.
Parkinsonism & Related Disorders
|
July 2, 2008
German-Canadian family (family A) with parkinsonism, amyotrophy, and dementia - Longitudinal observations
Z K Wszolek, P Vieregge, R J Uitti, et al.
Page
of 32