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J Stoessl

Showing results (91-100 of 102) with videos related to

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Neurology|March 13, 2002
Bilateral human fetal striatal transplantation in Huntington's diseaseR A Hauser, S Furtado, C R Cimino, et al.
Neurology|May 11, 2011
A family with Parkinsonism, essential tremor, restless legs syndrome, and depressionA Puschmann, R F Pfeiffer, A J Stoessl, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 20, 1998
Reproducibility of the distribution of carbon-11-SCH 23390, a dopamine D1 receptor tracer, in normal subjectsG L Chan, J E Holden, A J Stoessl, et al.
Neurology|May 12, 2004
Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ K Wszolek, R F Pfeiffer, Y Tsuboi, et al.
Brain : a Journal of Neurology|August 20, 2009
Longitudinal progression of sporadic Parkinson's disease: a multi-tracer positron emission tomography studyR Nandhagopal, L Kuramoto, M Schulzer, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|April 14, 2004
Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutationsK Hedrich, E-M Meyer, B Schüle, et al.
Neurology|February 21, 2012
Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian MennonitesR Saunders-Pullman, D Raymond, A J Stoessl, et al.
Neurology|August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcificationsZ K Wszolek, Y Baba, I R Mackenzie, et al.
Neurology|December 16, 2011
Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriersJ O Aasly, M Shi, V Sossi, et al.
Pageof 11

Showing results (91-100 of 102) with videos related to

Sort By:
Pageof 11
Neurology|March 13, 2002
Bilateral human fetal striatal transplantation in Huntington's diseaseR A Hauser, S Furtado, C R Cimino, et al.
Neurology|May 11, 2011
A family with Parkinsonism, essential tremor, restless legs syndrome, and depressionA Puschmann, R F Pfeiffer, A J Stoessl, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|May 20, 1998
Reproducibility of the distribution of carbon-11-SCH 23390, a dopamine D1 receptor tracer, in normal subjectsG L Chan, J E Holden, A J Stoessl, et al.
Neurology|May 12, 2004
Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ K Wszolek, R F Pfeiffer, Y Tsuboi, et al.
Brain : a Journal of Neurology|August 20, 2009
Longitudinal progression of sporadic Parkinson's disease: a multi-tracer positron emission tomography studyR Nandhagopal, L Kuramoto, M Schulzer, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|April 14, 2004
Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutationsK Hedrich, E-M Meyer, B Schüle, et al.
Neurology|February 21, 2012
Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian MennonitesR Saunders-Pullman, D Raymond, A J Stoessl, et al.
Neurology|August 23, 2006
Autosomal dominant dystonia-plus with cerebral calcificationsZ K Wszolek, Y Baba, I R Mackenzie, et al.
Neurology|December 16, 2011
Cerebrospinal fluid amyloid β and tau in LRRK2 mutation carriersJ O Aasly, M Shi, V Sossi, et al.
Pageof 11