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Mark Heverin

Showing results (31-40 of 89) with videos related to

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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2019
Equivalency and practice effects of alternative versions of the Edinburgh Cognitive and Behavioral ALS Screen (ECAS)Emmet Costello, Katie Lonergan, Caoifa Madden, et al.
Journal of Neurology|February 4, 2018
Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyadsTom Burke, Orla Hardiman, Marta Pinto-Grau, et al.
Neurology. Clinical Practice|November 29, 2021
Patterns of Language Impairment in Early Amyotrophic Lateral SclerosisMarta Pinto-Grau, Bronagh Donohoe, Sarah O'Connor, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 18, 2019
Longitudinal analysis of sniff nasal inspiratory pressure assessed using occluded and un-occluded measurement techniques in amyotrophic lateral sclerosis and primary lateral sclerosisDeirdre Murray, James Rooney, Anna Campion, et al.
HRB Open Research|April 17, 2020
The C9orf72 expansion is associated with accelerated respiratory function decline in a large Amyotrophic Lateral Sclerosis cohortJames Rooney, Deirdre Murray, Anna Campion, et al.
Neurology. Genetics|May 31, 2018
Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016Marie Ryan, Mark Heverin, Mark A Doherty, et al.
Studies in Health Technology and Informatics|October 3, 2025
A Proposed Feasibility Process: Lessons Learned from the Precision MS ProjectSinead Impey, Sinead Jordan, Linda Douris, et al.
Annals of Neurology|July 10, 2013
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosisSusan Byrne, Mark Heverin, Marwa Elamin, et al.
Annals of Clinical and Translational Neurology|May 12, 2017
A Cross-sectional population-based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survivalTom Burke, Marta Pinto-Grau, Katie Lonergan, et al.
Genomics|January 27, 2015
Homozygosity mapping in an Irish ALS case-control cohort describes local demographic phenomena and points towards potential recessive risk lociRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|December 14, 2019
Equivalency and practice effects of alternative versions of the Edinburgh Cognitive and Behavioral ALS Screen (ECAS)Emmet Costello, Katie Lonergan, Caoifa Madden, et al.
Journal of Neurology|February 4, 2018
Longitudinal predictors of caregiver burden in amyotrophic lateral sclerosis: a population-based cohort of patient-caregiver dyadsTom Burke, Orla Hardiman, Marta Pinto-Grau, et al.
Neurology. Clinical Practice|November 29, 2021
Patterns of Language Impairment in Early Amyotrophic Lateral SclerosisMarta Pinto-Grau, Bronagh Donohoe, Sarah O'Connor, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 18, 2019
Longitudinal analysis of sniff nasal inspiratory pressure assessed using occluded and un-occluded measurement techniques in amyotrophic lateral sclerosis and primary lateral sclerosisDeirdre Murray, James Rooney, Anna Campion, et al.
HRB Open Research|April 17, 2020
The C9orf72 expansion is associated with accelerated respiratory function decline in a large Amyotrophic Lateral Sclerosis cohortJames Rooney, Deirdre Murray, Anna Campion, et al.
Neurology. Genetics|May 31, 2018
Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016Marie Ryan, Mark Heverin, Mark A Doherty, et al.
Studies in Health Technology and Informatics|October 3, 2025
A Proposed Feasibility Process: Lessons Learned from the Precision MS ProjectSinead Impey, Sinead Jordan, Linda Douris, et al.
Annals of Neurology|July 10, 2013
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosisSusan Byrne, Mark Heverin, Marwa Elamin, et al.
Annals of Clinical and Translational Neurology|May 12, 2017
A Cross-sectional population-based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survivalTom Burke, Marta Pinto-Grau, Katie Lonergan, et al.
Genomics|January 27, 2015
Homozygosity mapping in an Irish ALS case-control cohort describes local demographic phenomena and points towards potential recessive risk lociRussell L McLaughlin, Kevin P Kenna, Alice Vajda, et al.
Pageof 9