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Movement Disorders : Official Journal of the Movement Disorder Society
|
November 1, 1994
Cortical myoclonus in Huntington's disease
P D Thompson, K P Bhatia, P Brown, et al.
Brain : a Journal of Neurology
|
June 10, 1998
Abnormal motor unit synchronization of antagonist muscles underlies pathological co-contraction in upper limb dystonia
S F Farmer, G L Sheean, M J Mayston, et al.
Neurology
|
October 11, 1992
Parkinson's disease in twins studied with 18F-dopa and positron emission tomography
D J Burn, M H Mark, E D Playford, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene
|
May 1, 1990
Long-term follow-up of patients with Leishmania (Viannia) braziliensis infection and treated with Glucantime
E M Netto, P D Marsden, E A Llanos-Cuentas, et al.
Neurology
|
February 1, 1997
Cabergoline in the treatment of early Parkinson's disease: results of the first year of treatment in a double-blind comparison of cabergoline and levodopa. The PKDS009 Collaborative Study Group
U K Rinne, F Bracco, C Chouza, et al.
Annals of Neurology
|
February 1, 1992
Striatal D2 receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy, measured with 11C-raclopride and positron emission tomography
D J Brooks, V Ibanez, G V Sawle, et al.
Nature
|
July 10, 1980
The role of D-1 and D-2 receptors
M Schachter, P Bédard, A G Debono, et al.
American Journal of Human Genetics
|
November 8, 2018
Understanding the Hidden Complexity of Latin American Population Isolates
Jazlyn A Mooney, Christian D Huber, Susan Service, et al.
Nature Communications
|
April 25, 2017
A multi-crystal method for extracting obscured crystallographic states from conventionally uninterpretable electron density
Nicholas M Pearce, Tobias Krojer, Anthony R Bradley, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype
I A Anselm, I M Anselm, F S Alkuraya, et al.
Page
of 102
Search research articles
Search
Showing results (921-930 of 1,014) with videos related to
Sort By:
Page
of 102
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 1, 1994
Cortical myoclonus in Huntington's disease
P D Thompson, K P Bhatia, P Brown, et al.
Brain : a Journal of Neurology
|
June 10, 1998
Abnormal motor unit synchronization of antagonist muscles underlies pathological co-contraction in upper limb dystonia
S F Farmer, G L Sheean, M J Mayston, et al.
Neurology
|
October 11, 1992
Parkinson's disease in twins studied with 18F-dopa and positron emission tomography
D J Burn, M H Mark, E D Playford, et al.
Transactions of the Royal Society of Tropical Medicine and Hygiene
|
May 1, 1990
Long-term follow-up of patients with Leishmania (Viannia) braziliensis infection and treated with Glucantime
E M Netto, P D Marsden, E A Llanos-Cuentas, et al.
Neurology
|
February 1, 1997
Cabergoline in the treatment of early Parkinson's disease: results of the first year of treatment in a double-blind comparison of cabergoline and levodopa. The PKDS009 Collaborative Study Group
U K Rinne, F Bracco, C Chouza, et al.
Annals of Neurology
|
February 1, 1992
Striatal D2 receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy, measured with 11C-raclopride and positron emission tomography
D J Brooks, V Ibanez, G V Sawle, et al.
Nature
|
July 10, 1980
The role of D-1 and D-2 receptors
M Schachter, P Bédard, A G Debono, et al.
American Journal of Human Genetics
|
November 8, 2018
Understanding the Hidden Complexity of Latin American Population Isolates
Jazlyn A Mooney, Christian D Huber, Susan Service, et al.
Nature Communications
|
April 25, 2017
A multi-crystal method for extracting obscured crystallographic states from conventionally uninterpretable electron density
Nicholas M Pearce, Tobias Krojer, Anthony R Bradley, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
X-linked creatine transporter defect: a report on two unrelated boys with a severe clinical phenotype
I A Anselm, I M Anselm, F S Alkuraya, et al.
Page
of 102