Search research articles
Contact Us
Filters
Showing results (31-40 of 36) with videos related to
Page
of 4
Sort By:
You have reached the last page of results.
This site can display upto 36 results.
Acta Neuropathologica Communications
|
September 21, 2022
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia
Sterre C M de Boer, Lauren Woolley, Merel O Mol, et al.
Alzheimer'S Research & Therapy
|
October 15, 2025
Genetic testing of common and rare variants in dementia patients from a memory clinic : Dementia-related genetic testing in memory clinic
Itziar de Rojas, Marc Hulsman, Niccoló Tesi, et al.
Brain : a Journal of Neurology
|
October 19, 2010
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia
Yasmin Namavar, Peter G Barth, Paul R Kasher, et al.
Orphanet Journal of Rare Diseases
|
February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
Veerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Nature Genetics
|
August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
Birgit S Budde, Yasmin Namavar, Peter G Barth, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 36) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 36 results.
Acta Neuropathologica Communications
|
September 21, 2022
Letter to the editor on a paper by Kaivola et al. (2020): carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is not associated with amyotrophic lateral sclerosis or frontotemporal dementia
Sterre C M de Boer, Lauren Woolley, Merel O Mol, et al.
Alzheimer'S Research & Therapy
|
October 15, 2025
Genetic testing of common and rare variants in dementia patients from a memory clinic : Dementia-related genetic testing in memory clinic
Itziar de Rojas, Marc Hulsman, Niccoló Tesi, et al.
Brain : a Journal of Neurology
|
October 19, 2010
Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia
Yasmin Namavar, Peter G Barth, Paul R Kasher, et al.
Orphanet Journal of Rare Diseases
|
February 15, 2014
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations
Veerle Rc Eggens, Peter G Barth, Jikke-Mien F Niermeijer, et al.
Translational Psychiatry
|
September 3, 2021
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Lianne M Reus, Iris E Jansen, Merel O Mol, et al.
Nature Genetics
|
August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
Birgit S Budde, Yasmin Namavar, Peter G Barth, et al.
Page
of 4