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Movement Disorders : Official Journal of the Movement Disorder Society
|
December 30, 2014
Parkinson's disease correlates with promoter methylation in the α-synuclein gene
Lasse Pihlstrøm, Victoria Berge, Aina Rengmark, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 26, 2005
[Malignant hyperthermia--a hereditary and potentially life-threatening condition]
Tonje Haugen, Mathias Toft, Clemens R Müller, et al.
Journal of Parkinson'S Disease
|
April 8, 2026
Pupil-light reflex in early-stage Parkinson's disease
Solveig Ej Dalbro, Lasse Pihlstrøm, Emilia Kerty, et al.
BMC Neurology
|
February 23, 2018
Risk variants of the α-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study
Kari Anne Bjørnarå, Lasse Pihlstrøm, Espen Dietrichs, et al.
Annals of Human Genetics
|
March 26, 2014
Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease
Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå, et al.
Parkinsonism & Related Disorders
|
May 18, 2016
Low frequency of GCH1 and TH mutations in Parkinson's disease
Aina Rengmark, Lasse Pihlstrøm, Jan Linder, et al.
Plos One
|
August 15, 2014
Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period
Silje Bjerknes, Inger Marie Skogseid, Terje Sæhle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 9, 2016
A cumulative genetic risk score predicts progression in Parkinson's disease
Lasse Pihlstrøm, Kristina Rebekka Morset, Espen Grimstad, et al.
NPJ Parkinson'S Disease
|
October 21, 2020
Subthalamic deep brain stimulation improves sleep and excessive sweating in Parkinson's disease
Silje Bjerknes, Inger Marie Skogseid, Tuva Jin Hauge, et al.
Genes
|
September 23, 2022
A Novel Nonsense Variant in <i>GRM1</i> Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
Hammad Yousaf, Ambrin Fatima, Zafar Ali, et al.
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of 13
Search research articles
Search
Showing results (21-30 of 129) with videos related to
Sort By:
Page
of 13
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 30, 2014
Parkinson's disease correlates with promoter methylation in the α-synuclein gene
Lasse Pihlstrøm, Victoria Berge, Aina Rengmark, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke
|
October 26, 2005
[Malignant hyperthermia--a hereditary and potentially life-threatening condition]
Tonje Haugen, Mathias Toft, Clemens R Müller, et al.
Journal of Parkinson'S Disease
|
April 8, 2026
Pupil-light reflex in early-stage Parkinson's disease
Solveig Ej Dalbro, Lasse Pihlstrøm, Emilia Kerty, et al.
BMC Neurology
|
February 23, 2018
Risk variants of the α-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study
Kari Anne Bjørnarå, Lasse Pihlstrøm, Espen Dietrichs, et al.
Annals of Human Genetics
|
March 26, 2014
Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease
Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå, et al.
Parkinsonism & Related Disorders
|
May 18, 2016
Low frequency of GCH1 and TH mutations in Parkinson's disease
Aina Rengmark, Lasse Pihlstrøm, Jan Linder, et al.
Plos One
|
August 15, 2014
Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period
Silje Bjerknes, Inger Marie Skogseid, Terje Sæhle, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 9, 2016
A cumulative genetic risk score predicts progression in Parkinson's disease
Lasse Pihlstrøm, Kristina Rebekka Morset, Espen Grimstad, et al.
NPJ Parkinson'S Disease
|
October 21, 2020
Subthalamic deep brain stimulation improves sleep and excessive sweating in Parkinson's disease
Silje Bjerknes, Inger Marie Skogseid, Tuva Jin Hauge, et al.
Genes
|
September 23, 2022
A Novel Nonsense Variant in <i>GRM1</i> Causes Autosomal Recessive Spinocerebellar Ataxia 13 in a Consanguineous Pakistani Family
Hammad Yousaf, Ambrin Fatima, Zafar Ali, et al.
Page
of 13