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Leslie Morrison

Showing results (61-70 of 82) with videos related to

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Cerebrovascular Diseases (Basel, Switzerland)|January 10, 2014
Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutationHélène Choquet, Jeffrey Nelson, Ludmila Pawlikowska, et al.
Cerebrovascular Diseases (Basel, Switzerland)|December 5, 2014
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severityHélène Choquet, Ludmila Pawlikowska, Jeffrey Nelson, et al.
Neurology. Genetics|January 5, 2024
Role of Rho-Associated Kinase in the Pathophysiology of Cerebral Cavernous MalformationsCenk Ayata, Helen Kim, Leslie Morrison, et al.
Neurology|January 16, 2016
Author responsePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Neurology|August 14, 2021
Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous MalformationsChristine K Fox, Jeffrey Nelson, Charles E McCulloch, et al.
Developmental Medicine and Child Neurology|August 29, 2012
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxiaAllison Brashear, Jonathan W Mink, Deborah F Hill, et al.
Molecular Genetics & Genomic Medicine|September 7, 2021
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformationForam Choksi, Shantel Weinsheimer, Jeffrey Nelson, et al.
Journal of the American Heart Association|January 25, 2023
Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous MalformationShantel Weinsheimer, Jeffrey Nelson, Adib A Abla, et al.
Stroke|March 27, 2019
Familial Cerebral Cavernous MalformationsAtif Zafar, Syed A Quadri, Mudassir Farooqui, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Cerebrovascular Diseases (Basel, Switzerland)|January 10, 2014
Association of cardiovascular risk factors with disease severity in cerebral cavernous malformation type 1 subjects with the common Hispanic mutationHélène Choquet, Jeffrey Nelson, Ludmila Pawlikowska, et al.
Cerebrovascular Diseases (Basel, Switzerland)|December 5, 2014
Polymorphisms in inflammatory and immune response genes associated with cerebral cavernous malformation type 1 severityHélène Choquet, Ludmila Pawlikowska, Jeffrey Nelson, et al.
Neurology. Genetics|January 5, 2024
Role of Rho-Associated Kinase in the Pathophysiology of Cerebral Cavernous MalformationsCenk Ayata, Helen Kim, Leslie Morrison, et al.
Neurology|January 16, 2016
Author responsePeter B Kang, Leslie Morrison, Susan T Iannaccone, et al.
Journal of Child Neurology|September 1, 2007
Consensus statement for standard of care in spinal muscular atrophyChing H Wang, Richard S Finkel, Enrico S Bertini, et al.
Neurology|August 14, 2021
Seizure Incidence Rates in Children and Adults With Familial Cerebral Cavernous MalformationsChristine K Fox, Jeffrey Nelson, Charles E McCulloch, et al.
Developmental Medicine and Child Neurology|August 29, 2012
ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxiaAllison Brashear, Jonathan W Mink, Deborah F Hill, et al.
Molecular Genetics & Genomic Medicine|September 7, 2021
Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformationForam Choksi, Shantel Weinsheimer, Jeffrey Nelson, et al.
Journal of the American Heart Association|January 25, 2023
Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous MalformationShantel Weinsheimer, Jeffrey Nelson, Adib A Abla, et al.
Stroke|March 27, 2019
Familial Cerebral Cavernous MalformationsAtif Zafar, Syed A Quadri, Mudassir Farooqui, et al.
Pageof 9