Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Blaine L. Hart"'
Autor:
Shantel Weinsheimer, Jeffrey Nelson, Adib A. Abla, Nerissa U. Ko, Cynthia Tsang, Obiora Okoye, Joseph M. Zabramski, Amy Akers, Atif Zafar, Marc C. Mabray, Blaine L. Hart, Leslie Morrison, Charles E. McCulloch, Helen Kim
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 3 (2023)
Background Familial cerebral cavernous alformation (CCM) is an autosomal dominant disease caused by mutations in KRIT1, CCM2, or PDCD10. Cases typically present with multiple lesions, strong family history, and neurological symptoms, including seizur
Externí odkaz:
https://doaj.org/article/8ab82691916d45ebbda5e8a5a7c586e9
Autor:
Foram Choksi, Shantel Weinsheimer, Jeffrey Nelson, Ludmila Pawlikowska, Christine K. Fox, Atif Zafar, Marc C. Mabray, Joseph Zabramski, Amy Akers, Blaine L. Hart, Leslie Morrison, Charles E. McCulloch, Helen Kim
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Background To investigate whether common variants in EPHB4 and RASA1 are associated with cerebral cavernous malformation (CCM) disease severity phenotypes, including intracranial hemorrhage (ICH), total and large lesion counts. Methods Famil
Externí odkaz:
https://doaj.org/article/9f363bcd55e644af80ceef59a0f22455
Autor:
Jeffrey Nelson, Ludmila Pawlikowska, Shantel Weinsheimer, Amy Akers, Marc C. Mabray, Christine K. Fox, Leslie Morrison, Helen Kim, Joseph M. Zabramski, Blaine L. Hart, Charles E. McCulloch, Atif Zafar
Publikováno v:
Neurology
Neurology, vol 97, iss 12
Neurology, vol 97, iss 12
Background and ObjectivesSeizure incidence rates related to familial cerebral cavernous malformation (FCCM) are not well described, especially for children. To measure the seizure incidence rate, examine seizure predictors, and characterize epilepsy
Publikováno v:
Clin Imaging
Cerebrovascular malformations occur in both sporadic and inherited patterns. This paper reviews imaging and clinical features of cerebrovascular malformations with a genetic basis. Genetic diseases such as familial cerebral cavernous malformations an
Autor:
Atif Zafar, Hosung Kim, J. Hallstrom, Myranda Robinson, Juliana Starcevich, Mary R. Bartlett, Blaine L. Hart, Jeffrey Nelson, Marc C. Mabray, Leslie Morrison
Publikováno v:
AJNR Am J Neuroradiol
AJNR. American journal of neuroradiology, vol 41, iss 6
AJNR. American journal of neuroradiology, vol 41, iss 6
BACKGROUND AND PURPOSE: Cavernous malformations occur most often in the brain but can occur in the spinal cord. Small studies of patients with familial cerebral cavernous malformations suggested a prevalence of spinal cord cavernous malformations of
Autor:
Savannah Cheek, Richard A. Campbell, Christine L. Petranovich, Blaine L. Hart, Leslie Morrison
Publikováno v:
Journal of behavioral and brain science
Purpose This study aimed to characterize mood and quality of life and to examine the associations of these areas with subjective cognitive concerns and attitudes toward genetic testing for the Common Hispanic Mutation, a gene that has been associated
Autor:
Christine K. Fox, Atif Zafar, Amy Akers, Blaine L. Hart, Marc C. Mabray, Foram Choksi, Jeffrey Nelson, Shantel Weinsheimer, Helen Kim, Joseph M. Zabramski, Charles E. McCulloch, Ludmila Pawlikowska, Leslie Morrison
Publikováno v:
Molecular Genetics and Genomic Medicine, vol 9, iss 10
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Background To investigate whether common variants in EPHB4 and RASA1 are associated with cerebral cavernous malformation (CCM) disease severity phenotypes, including intracranial hemorrhage (ICH), total and large lesion counts. Methods Familial CCM c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6e5936fb80df38f3540b4748cc3199
https://escholarship.org/uc/item/4w47f85x
https://escholarship.org/uc/item/4w47f85x
Autor:
Leslie Morrison, Michael T. Lawton, Mark L. Kahn, Syed A. Quadri, Myranda Robinson, Helen Kim, Catherine Vigil, Blaine L. Hart, Alan T. Tang, Atif Zafar, Marc C. Mabray, Asad Ikram, Mudassir Farooqui, Howard Yonas
Publikováno v:
Stroke. 50:1294-1301
Autor:
Blaine L. Hart, Barrett J. Zlotoff, Leslie Morrison, Vernon J. Forrester, Athanasios K. Manole
Publikováno v:
Am J Med Genet A
Familial cerebral cavernous malformations due to the common Hispanic mutation (FCCM1-CHM) is an endemic condition among the Hispanic population of the Southwestern United States associated with significant morbidity and mortality. Cutaneous vascular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087c02eff19aeb6a5216c6cf3d0767f2
https://europepmc.org/articles/PMC8208466/
https://europepmc.org/articles/PMC8208466/