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Showing results (631-640 of 667) with videos related to

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The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Nature|July 18, 2012
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisChi-Hong Wu, Claudia Fallini, Nicola Ticozzi, et al.
Biorxiv : the Preprint Server for Biology|December 9, 2024
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosisOlivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Mis-spliced transcripts generate <i>de novo</i> proteins in TDP-43-related ALS/FTDSahba Seddighi, Yue A Qi, Anna-Leigh Brown, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
JAMA Neurology|June 1, 2016
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral SclerosisIsabella Fogh, Kuang Lin, Cinzia Tiloca, et al.
Pageof 67

Showing results (631-640 of 667) with videos related to

Sort By:
Pageof 67
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Neurobiology of Aging|October 22, 2018
Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohortGijs H P Tazelaar, Annelot M Dekker, Joke J F A van Vugt, et al.
Nature|July 18, 2012
Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosisChi-Hong Wu, Claudia Fallini, Nicola Ticozzi, et al.
Biorxiv : the Preprint Server for Biology|December 9, 2024
Sex-specific DNA methylation differences in Amyotrophic lateral sclerosisOlivia A Grant, Alfredo Iacoangeli, Ramona A J Zwamborn, et al.
Biorxiv : the Preprint Server for Biology|February 7, 2023
Mis-spliced transcripts generate <i>de novo</i> proteins in TDP-43-related ALS/FTDSahba Seddighi, Yue A Qi, Anna-Leigh Brown, et al.
Nature Communications|July 2, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Neuron|November 26, 2020
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral SclerosisRamita Dewan, Ruth Chia, Jinhui Ding, et al.
Nature Communications|November 13, 2022
The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease durationSarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp, et al.
Frontiers in Cellular Neuroscience|January 2, 2023
Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence dataAhmad Al Khleifat, Alfredo Iacoangeli, Ashley R Jones, et al.
JAMA Neurology|June 1, 2016
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral SclerosisIsabella Fogh, Kuang Lin, Cinzia Tiloca, et al.
Pageof 67