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T Gasser

Showing results (251-260 of 316) with videos related to

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Neurology|June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphismC Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology|May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystoniasA 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 hyperechogenicityK 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 familiesF 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 shipwormsMark 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 ForceA 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-JewsP L Kramer, G A Heiman, T Gasser, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's diseaseT 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 observationsZ K Wszolek, P Vieregge, R J Uitti, et al.
Pageof 32

Showing results (251-260 of 316) with videos related to

Sort By:
Pageof 32
Neurology|June 4, 2008
Susceptibility to DYT1 dystonia in European patients is modified by the D216H polymorphismC Kamm, H Fischer, B Garavaglia, et al.
European Journal of Neurology|May 21, 2010
EFNS guidelines on diagnosis and treatment of primary dystoniasA 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 hyperechogenicityK 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 familiesF 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 shipwormsMark 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 ForceA 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-JewsP L Kramer, G A Heiman, T Gasser, et al.
Science (New York, N.Y.)|July 18, 1997
Genetic complexity and Parkinson's diseaseT 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 observationsZ K Wszolek, P Vieregge, R J Uitti, et al.
Pageof 32