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Brain : a Journal of Neurology|July 15, 2011
A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathiesTammaryn Lashley, Jonathan D Rohrer, Rina Bandopadhyay, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2006
Health-related quality of life in multiple system atrophyAnette Schrag, Felix Geser, Michaela Stampfer-Kountchev, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 6, 2010
Presentation, diagnosis, and management of multiple system atrophy in Europe: final analysis of the European multiple system atrophy registryMartin Köllensperger, Felix Geser, Jean-Pierre Ndayisaba, et al.
The Lancet. Neurology|February 9, 2013
The natural history of multiple system atrophy: a prospective European cohort studyGregor K Wenning, Felix Geser, Florian Krismer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2008
Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD studyChristopher F McNicoll, Jeanne C Latourelle, Marcy E MacDonald, et al.
Human Genetics|July 1, 2008
Replication of association between ELAVL4 and Parkinson disease: the GenePD studyAnita L DeStefano, Jeanne Latourelle, Mark F Lew, et al.
Movement Disorders Clinical Practice|September 29, 2023
Development and Validation of a Prognostic Model to Predict Overall Survival in Multiple System AtrophySabine Eschlboeck, Georg Goebel, Christine Eckhardt, et al.
BMC Medicine|November 7, 2008
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD studyJeanne C Latourelle, Mei Sun, Mark F Lew, et al.
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