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Neurology
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September 7, 2007
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
W C Nichols, V E Elsaesser, N Pankratz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2009
Alpha-synuclein and familial Parkinson's disease
Nathan Pankratz, William C Nichols, Veronika E Elsaesser, et al.
Neuroscience Letters
|
September 26, 2006
Mutations in DJ-1 are rare in familial Parkinson disease
Nathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Neurology
|
November 7, 2008
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
W C Nichols, N Pankratz, D K Marek, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 18, 1997
Test/retest reproducibility of iodine-123-betaCIT SPECT brain measurement of dopamine transporters in Parkinson's patients
J P Seibyl, K Marek, K Sheff, et al.
The Journal of Prevention of Alzheimer'S Disease
|
December 7, 2017
Vanutide Cridificar (ACC-001) and QS-21 Adjuvant in Individuals with Early Alzheimer's Disease: Amyloid Imaging Positron Emission Tomography and Safety Results from a Phase 2 Study
C H van Dyck, C Sadowsky, G Le Prince Leterme, et al.
Neurology
|
May 29, 2003
Evidence for more widespread cerebral pathology in early HD: an MRI-based morphometric analysis
H D Rosas, W J Koroshetz, Y I Chen, et al.
NPJ Parkinson'S Disease
|
February 1, 2019
Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
L M Chahine, A Iranzo, A Fernández-Arcos, et al.
Translational Psychiatry
|
September 17, 2014
Tauopathy PET and amyloid PET in the diagnosis of chronic traumatic encephalopathies: studies of a retired NFL player and of a man with FTD and a severe head injury
E M Mitsis, S Riggio, L Kostakoglu, et al.
Neurology
|
January 26, 2005
The role of radiotracer imaging in Parkinson disease
B Ravina, D Eidelberg, J E Ahlskog, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 112) with videos related to
Sort By:
Page
of 12
Neurology
|
September 7, 2007
LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8
W C Nichols, V E Elsaesser, N Pankratz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 5, 2009
Alpha-synuclein and familial Parkinson's disease
Nathan Pankratz, William C Nichols, Veronika E Elsaesser, et al.
Neuroscience Letters
|
September 26, 2006
Mutations in DJ-1 are rare in familial Parkinson disease
Nathan Pankratz, Michael W Pauciulo, Veronika E Elsaesser, et al.
Neurology
|
November 7, 2008
Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
W C Nichols, N Pankratz, D K Marek, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
September 18, 1997
Test/retest reproducibility of iodine-123-betaCIT SPECT brain measurement of dopamine transporters in Parkinson's patients
J P Seibyl, K Marek, K Sheff, et al.
The Journal of Prevention of Alzheimer'S Disease
|
December 7, 2017
Vanutide Cridificar (ACC-001) and QS-21 Adjuvant in Individuals with Early Alzheimer's Disease: Amyloid Imaging Positron Emission Tomography and Safety Results from a Phase 2 Study
C H van Dyck, C Sadowsky, G Le Prince Leterme, et al.
Neurology
|
May 29, 2003
Evidence for more widespread cerebral pathology in early HD: an MRI-based morphometric analysis
H D Rosas, W J Koroshetz, Y I Chen, et al.
NPJ Parkinson'S Disease
|
February 1, 2019
Basic clinical features do not predict dopamine transporter binding in idiopathic REM behavior disorder
L M Chahine, A Iranzo, A Fernández-Arcos, et al.
Translational Psychiatry
|
September 17, 2014
Tauopathy PET and amyloid PET in the diagnosis of chronic traumatic encephalopathies: studies of a retired NFL player and of a man with FTD and a severe head injury
E M Mitsis, S Riggio, L Kostakoglu, et al.
Neurology
|
January 26, 2005
The role of radiotracer imaging in Parkinson disease
B Ravina, D Eidelberg, J E Ahlskog, et al.
Page
of 12