familial cerebral cavernous malformations Recently Published Documents

Cavernous Malformations ◽

Description of Two Families with New Mutations in Familial Cerebral Cavernous Malformations Genes

Journal of Stroke and Cerebrovascular Diseases ◽

10.1016/j.jstrokecerebrovasdis.2021.106130 ◽

2021 ◽

Vol 30 (12) ◽

pp. 106130

Author(s):

Pablo Iruzubieta ◽

David Campo-Caballero ◽

Jon Equiza ◽

Inés Albajar ◽

Naroa Sulibarría ◽

...

Keyword(s):

Cavernous Malformations ◽

Familial Cerebral Cavernous Malformations ◽

New Mutations

Lingual Seizures from Familial Cerebral Cavernous Malformations in a 4-year-old Child

Pediatric Neurology ◽

10.1016/j.pediatrneurol.2021.01.010 ◽

2021 ◽

Author(s):

Chethan K. Rao ◽

Raj D. Sheth

Keyword(s):

Cavernous Malformations ◽

Familial cerebral cavernous malformations

10.1148/cases.20213394 ◽

2021 ◽

Author(s):

Ali Salehpoor ◽

Kwasi Addae-Mensah, BSC, MD ◽

Blaine L. Hart, MD ◽

Marc C. Mabray, MD

Keyword(s):

Cavernous Malformations ◽

High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations Type 1 Cohort

American Journal of Neuroradiology ◽

10.3174/ajnr.a6584 ◽

2020 ◽

Vol 41 (6) ◽

pp. 1126-1130

Author(s):

M.C. Mabray ◽

J. Starcevich ◽

J. Hallstrom ◽

M. Robinson ◽

M. Bartlett ◽

...

Keyword(s):

Spinal Cord ◽

Cavernous Malformations ◽

High Prevalence ◽

Notch Signaling in Familial Cerebral Cavernous Malformations and Immunohistochemical Detection of Cleaved Notch1 Intracellular Domain

Methods in Molecular Biology - Cerebral Cavernous Malformations (CCM) ◽

10.1007/978-1-0716-0640-7_31 ◽

2020 ◽

pp. 427-435

Author(s):

Sana S. Hasan ◽

Andreas Fischer

Keyword(s):

Notch Signaling ◽

Immunohistochemical Detection ◽

Intracellular Domain ◽

Cavernous Malformations ◽

Orphan designation: 4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl, Treatment of familial cerebral cavernous malformations

Case Medical Research ◽

10.31525/cmr-23717fa ◽

2019 ◽

Author(s):

Keyword(s):

Cavernous Malformations ◽

Orphan Designation ◽

Orphan designation: 4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxyl, Treatment of familial cerebral cavernous malformations

Case Medical Research ◽

10.31525/cmr-2370f81 ◽

2019 ◽

Author(s):

Keyword(s):

Cavernous Malformations ◽

Orphan Designation ◽

Molecular diagnostic workflow, clinical interpretation of sequence variants, and data repository procedures in 140 individuals with familial cerebral cavernous malformations

Human Mutation ◽

10.1002/humu.23851 ◽

2019 ◽

Vol 40 (11) ◽

Cited By ~ 1

Author(s):

Carmela Fusco ◽

Massimiliano Copetti ◽

Tommaso Mazza ◽

Luigi Amoruso ◽

Sandra Mastroianno ◽

...

Keyword(s):

Molecular Diagnostic ◽

Data Repository ◽

Sequence Variants ◽

Cavernous Malformations ◽

Clinical Interpretation ◽

Combined Cerebral Microbleeds With Lacunar Infarctions in Familial Cerebral Cavernous Malformations

JAMA Neurology ◽

10.1001/jamaneurol.2019.1980 ◽

2019 ◽

Vol 76 (9) ◽

pp. 1117

Author(s):

Qi Wang ◽

Lingchao Meng ◽

Zhaoxia Wang

Keyword(s):

Cerebral Microbleeds ◽

Cavernous Malformations ◽