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Journal of Alzheimer'S Disease : JAD
|
July 19, 2011
Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathway
Walter Maetzler, Anne Kathrin Stapf, Claudia Schulte, et al.
Journal of Alzheimer'S Disease : JAD
|
February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body disease
Walter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 29, 2008
Autonomic dysfunction in different subtypes of multiple system atrophy
Claudia Schmidt, Birgit Herting, Silke Prieur, et al.
Acta Neurochirurgica
|
June 24, 2010
Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 10, 2010
Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Neuroepidemiology
|
September 21, 2013
Evaluation of progression markers in the premotor phase of Parkinson's disease: the progression markers in the premotor phase study
Inga Liepelt-Scarfone, Katharina Gauss, Walter Maetzler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 26, 2010
Analysis of ACTA2 in European Moyamoya disease patients
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Frontiers in Neurology
|
August 24, 2019
Mobility Deficits Assessed With Mobile Technology: What Can We Learn From Brain Iron-Altered Animal Models?
Franziska Hopfner, Markus A Hobert, Corina Maetzler, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain
Julia Fuchs, Ales Tichopad, Yulia Golub, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 7, 2017
Progression markers of motor deficits in Parkinson's disease: A biannual 4-year prospective study
Sebastian Heinzel, Felix P Bernhard, Benjamin Roeben, et al.
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of 55
Search research articles
Search
Showing results (231-240 of 547) with videos related to
Sort By:
Page
of 55
Journal of Alzheimer'S Disease : JAD
|
July 19, 2011
Serum and cerebrospinal fluid uric acid levels in lewy body disorders: associations with disease occurrence and amyloid-β pathway
Walter Maetzler, Anne Kathrin Stapf, Claudia Schulte, et al.
Journal of Alzheimer'S Disease : JAD
|
February 17, 2010
The CST3 BB genotype and low cystatin C cerebrospinal fluid levels are associated with dementia in Lewy body disease
Walter Maetzler, Benjamin Schmid, Matthis Synofzik, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 29, 2008
Autonomic dysfunction in different subtypes of multiple system atrophy
Claudia Schmidt, Birgit Herting, Silke Prieur, et al.
Acta Neurochirurgica
|
June 24, 2010
Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
August 10, 2010
Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Neuroepidemiology
|
September 21, 2013
Evaluation of progression markers in the premotor phase of Parkinson's disease: the progression markers in the premotor phase study
Inga Liepelt-Scarfone, Katharina Gauss, Walter Maetzler, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 26, 2010
Analysis of ACTA2 in European Moyamoya disease patients
Constantin Roder, Vera Peters, Hidetoshi Kasuya, et al.
Frontiers in Neurology
|
August 24, 2019
Mobility Deficits Assessed With Mobile Technology: What Can We Learn From Brain Iron-Altered Animal Models?
Franziska Hopfner, Markus A Hobert, Corina Maetzler, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
December 29, 2007
Genetic variability in the SNCA gene influences alpha-synuclein levels in the blood and brain
Julia Fuchs, Ales Tichopad, Yulia Golub, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 7, 2017
Progression markers of motor deficits in Parkinson's disease: A biannual 4-year prospective study
Sebastian Heinzel, Felix P Bernhard, Benjamin Roeben, et al.
Page
of 55