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Journal of Neural Transmission. Parkinson'S Disease and Dementia Section
|
January 1, 1993
3H-spiperone binding to lymphocytes fails in the differential diagnosis of de novo Parkinson syndromes
G Arnold, B Bondy, O Bandmann, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 21, 1999
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases
H R Morris, J C Janssen, O Bandmann, et al.
Neurology
|
February 26, 2003
The phenylalanine loading test in the differential diagnosis of dystonia
O Bandmann, M Goertz, J Zschocke, et al.
Bone
|
December 27, 2022
Increased fracture risk in Parkinson's disease - An exploration of mechanisms and consequences for fracture prediction with FRAX
M Schini, P Bhatia, H Shreef, et al.
Annals of Neurology
|
October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic study
O Bandmann, E M Valente, P Holmans, et al.
Journal of Neural Transmission. Supplementum
|
January 1, 1995
Epidemiological, genetic, pharmacological, kinesiological, nuclear medical (IBZM-SPECT), standard and functional MRI studies on Parkinson's disease and related disorders and economic evaluation of Parkinson's disease therapy--clinical projects in the BMFT-research program Munich: "Parkinson's disease and other basal ganglia disorders"
W H Oertel, C Trenkwalder, T Gasser, et al.
AJNR. American Journal of Neuroradiology
|
March 20, 2010
Corpus callosum morphology and microstructure assessed using structural MR imaging and diffusion tensor imaging: initial findings in adults with neurofibromatosis type 1
E L Wignall, P D Griffiths, N G Papadakis, et al.
Neurology
|
December 28, 2006
CNS involvement in hereditary neuropathy with pressure palsies (HNPP)
B Tackenberg, J C Möller, H Rindock, et al.
Neurology
|
September 11, 2002
Copper genes are not implicated in the pathogenesis of focal dystonia
O Bandmann, F Asmus, D Sibbing, et al.
Page
of 5
Search research articles
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Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Journal of Neural Transmission. Parkinson'S Disease and Dementia Section
|
January 1, 1993
3H-spiperone binding to lymphocytes fails in the differential diagnosis of de novo Parkinson syndromes
G Arnold, B Bondy, O Bandmann, et al.
Neurology
|
December 31, 1997
Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration
O Bandmann, M G Sweeney, S E Daniel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 21, 1999
The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases
H R Morris, J C Janssen, O Bandmann, et al.
Neurology
|
February 26, 2003
The phenylalanine loading test in the differential diagnosis of dystonia
O Bandmann, M Goertz, J Zschocke, et al.
Bone
|
December 27, 2022
Increased fracture risk in Parkinson's disease - An exploration of mechanisms and consequences for fracture prediction with FRAX
M Schini, P Bhatia, H Shreef, et al.
Annals of Neurology
|
October 20, 1998
Dopa-responsive dystonia: a clinical and molecular genetic study
O Bandmann, E M Valente, P Holmans, et al.
Journal of Neural Transmission. Supplementum
|
January 1, 1995
Epidemiological, genetic, pharmacological, kinesiological, nuclear medical (IBZM-SPECT), standard and functional MRI studies on Parkinson's disease and related disorders and economic evaluation of Parkinson's disease therapy--clinical projects in the BMFT-research program Munich: "Parkinson's disease and other basal ganglia disorders"
W H Oertel, C Trenkwalder, T Gasser, et al.
AJNR. American Journal of Neuroradiology
|
March 20, 2010
Corpus callosum morphology and microstructure assessed using structural MR imaging and diffusion tensor imaging: initial findings in adults with neurofibromatosis type 1
E L Wignall, P D Griffiths, N G Papadakis, et al.
Neurology
|
December 28, 2006
CNS involvement in hereditary neuropathy with pressure palsies (HNPP)
B Tackenberg, J C Möller, H Rindock, et al.
Neurology
|
September 11, 2002
Copper genes are not implicated in the pathogenesis of focal dystonia
O Bandmann, F Asmus, D Sibbing, et al.
Page
of 5