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Movement Disorders Clinical Practice
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April 11, 2022
Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders
Diana A Olszewska, Sapna Rawal, Conor Fearon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 16, 2026
The Assessment of RAB32 p.Ser71Arg Variant Prevalence in Parkinson's Disease Across Selected African, European, and South American Cohorts
Diana A Olszewska, Alexandra I Soto-Beasley, Allan McCarthy, et al.
Neurobiology of Aging
|
September 24, 2024
Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Neurobiology of Aging
|
July 18, 2021
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
The Lancet. Neurology
|
November 17, 2023
The wisdom of our mentors: clinical pearls in movement disorders
Rui Araújo, Conor Fearon, Bettina Balint, et al.
Plos One
|
December 11, 2024
Accuracy of the diagnosis of pneumonia in Canadian pediatric emergency departments: A prospective cohort study
Joan L Robinson, James D Kellner, Jennifer Crotts, et al.
Brain : a Journal of Neurology
|
August 23, 2015
Closing the tau loop: the missing tau mutation
Allan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 27, 2023
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
BMJ Quality & Safety
|
July 19, 2022
How safe are paediatric emergency departments? A national prospective cohort study
Amy C Plint, Amanda S Newton, Antonia Stang, et al.
American Journal of Human Genetics
|
July 19, 2011
VPS35 mutations in Parkinson disease
Carles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
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of 12
Search research articles
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Showing results (101-110 of 112) with videos related to
Sort By:
Page
of 12
Movement Disorders Clinical Practice
|
April 11, 2022
Neuroimaging Pearls from the MDS Congress Video Challenge. Part 1: Genetic Disorders
Diana A Olszewska, Sapna Rawal, Conor Fearon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 16, 2026
The Assessment of RAB32 p.Ser71Arg Variant Prevalence in Parkinson's Disease Across Selected African, European, and South American Cohorts
Diana A Olszewska, Alexandra I Soto-Beasley, Allan McCarthy, et al.
Neurobiology of Aging
|
September 24, 2024
Corrigendum to: A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10 G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
Neurobiology of Aging
|
July 18, 2021
A clinical, molecular genetics and pathological study of a FTDP-17 family with a heterozygous splicing variant c.823-10G>T at the intron 9/exon 10 of the MAPT gene
Diana A Olszewska, Conor Fearon, Christopher McGuigan, et al.
The Lancet. Neurology
|
November 17, 2023
The wisdom of our mentors: clinical pearls in movement disorders
Rui Araújo, Conor Fearon, Bettina Balint, et al.
Plos One
|
December 11, 2024
Accuracy of the diagnosis of pneumonia in Canadian pediatric emergency departments: A prospective cohort study
Joan L Robinson, James D Kellner, Jennifer Crotts, et al.
Brain : a Journal of Neurology
|
August 23, 2015
Closing the tau loop: the missing tau mutation
Allan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 27, 2023
Genetic Testing in Parkinson's Disease
Gian Pal, Lola Cook, Jeanine Schulze, et al.
BMJ Quality & Safety
|
July 19, 2022
How safe are paediatric emergency departments? A national prospective cohort study
Amy C Plint, Amanda S Newton, Antonia Stang, et al.
American Journal of Human Genetics
|
July 19, 2011
VPS35 mutations in Parkinson disease
Carles Vilariño-Güell, Christian Wider, Owen A Ross, et al.
Page
of 12