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A van Es

Showing results (421-430 of 480) with videos related to

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Neurology|May 26, 2010
Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouseI Taes, A Goris, R Lemmens, et al.
Seminars in Interventional Cardiology : SIIC|March 30, 2000
The ARTS study (Arterial Revascularization Therapies Study)P W Serruys, F Unger, B A van Hout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 12, 2020
TDP-43 proteinopathies: a new wave of neurodegenerative diseasesEva Maria Johanna de Boer, Viyanti K Orie, Timothy Williams, et al.
The Pharmacogenomics Journal|October 19, 2019
Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?Ruben P A van Eijk, Marinus J C Eijkemans, Stavros Nikolakopoulos, et al.
Neurology|January 11, 2008
Progranulin genetic variability contributes to amyotrophic lateral sclerosisK Sleegers, N Brouwers, S Maurer-Stroh, et al.
Archives of Neurology|February 10, 2010
FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsEwout J N Groen, Michael A van Es, Paul W J van Vught, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
Neurobiology of Aging|March 12, 2014
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathyMeinie Seelen, Anne E Visser, Daniel J Overste, et al.
Brain Communications|December 22, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosisJoke J F A van Vugt, Ramona A J Zwamborn, Egor Dolzhenko, et al.
Pageof 48

Showing results (421-430 of 480) with videos related to

Sort By:
Pageof 48
Neurology|May 26, 2010
Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouseI Taes, A Goris, R Lemmens, et al.
Seminars in Interventional Cardiology : SIIC|March 30, 2000
The ARTS study (Arterial Revascularization Therapies Study)P W Serruys, F Unger, B A van Hout, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 12, 2020
TDP-43 proteinopathies: a new wave of neurodegenerative diseasesEva Maria Johanna de Boer, Viyanti K Orie, Timothy Williams, et al.
The Pharmacogenomics Journal|October 19, 2019
Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?Ruben P A van Eijk, Marinus J C Eijkemans, Stavros Nikolakopoulos, et al.
Neurology|January 11, 2008
Progranulin genetic variability contributes to amyotrophic lateral sclerosisK Sleegers, N Brouwers, S Maurer-Stroh, et al.
Archives of Neurology|February 10, 2010
FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsEwout J N Groen, Michael A van Es, Paul W J van Vught, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 20, 2009
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosisMichael A Van Es, Paul W J Van Vught, Jan H Veldink, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2009
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorderBert van der Zwaag, Wouter G Staal, Ron Hochstenbach, et al.
Neurobiology of Aging|March 12, 2014
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathyMeinie Seelen, Anne E Visser, Daniel J Overste, et al.
Brain Communications|December 22, 2025
The role of disease-associated short tandem repeats in amyotrophic lateral sclerosisJoke J F A van Vugt, Ramona A J Zwamborn, Egor Dolzhenko, et al.
Pageof 48