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Neurobiology of Aging
|
May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Perry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
June 26, 2020
Associations of non-pedunculated T1 colorectal adenocarcinoma outcome with consensus molecular subtypes, immunoscore, and microsatellite status: a multicenter case-cohort study
Krijn J C Haasnoot, Yara Backes, Leon M G Moons, et al.
The American Journal of Gastroenterology
|
January 14, 2022
Full-Thickness Scar Resection After R1/Rx Excised T1 Colorectal Cancers as an Alternative to Completion Surgery
Kim M Gijsbers, Miangela M Laclé, Sjoerd G Elias, et al.
Human Molecular Genetics
|
August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosis
Hylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.
United European Gastroenterology Journal
|
February 10, 2021
Tumour-stroma ratio has poor prognostic value in nonpedunculated T1 colorectal cancer: A multicentre case-cohort study
Hao Dang, Gabi W van Pelt, Krijn J C Haasnoot, et al.
Annals of Neurology
|
December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Michael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Michael A van Es, Jan H Veldink, Christiaan G J Saris, et al.
Nature Genetics
|
March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis
Paul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Nature Genetics
|
December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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of 10
Search research articles
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Showing results (91-100 of 99) with videos related to
Sort By:
Page
of 10
You have reached the last page of results.
This site can display upto 99 results.
Neurobiology of Aging
|
May 20, 2014
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
Perry T C van Doormaal, Nicola Ticozzi, Cinzia Gellera, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
June 26, 2020
Associations of non-pedunculated T1 colorectal adenocarcinoma outcome with consensus molecular subtypes, immunoscore, and microsatellite status: a multicenter case-cohort study
Krijn J C Haasnoot, Yara Backes, Leon M G Moons, et al.
The American Journal of Gastroenterology
|
January 14, 2022
Full-Thickness Scar Resection After R1/Rx Excised T1 Colorectal Cancers as an Alternative to Completion Surgery
Kim M Gijsbers, Miangela M Laclé, Sjoerd G Elias, et al.
Human Molecular Genetics
|
August 6, 2010
A large genome scan for rare CNVs in amyotrophic lateral sclerosis
Hylke M Blauw, Ammar Al-Chalabi, Peter M Andersen, et al.
United European Gastroenterology Journal
|
February 10, 2021
Tumour-stroma ratio has poor prognostic value in nonpedunculated T1 colorectal cancer: A multicentre case-cohort study
Hao Dang, Gabi W van Pelt, Krijn J C Haasnoot, et al.
Annals of Neurology
|
December 23, 2011
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
Michael A van Es, Helenius J Schelhaas, Paul W J van Vught, et al.
Nature Genetics
|
September 8, 2009
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
Michael A van Es, Jan H Veldink, Christiaan G J Saris, et al.
Nature Genetics
|
March 31, 2026
Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis
Paul J Hop, Maarten Kooyman, Brendan J Kenna, et al.
Nature Genetics
|
December 7, 2021
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
Wouter van Rheenen, Rick A A van der Spek, Mark K Bakker, et al.
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of 10