Results 161 to 170 of about 6,027 (196)

Transcriptomic signatures of individual cell types in cerebral cavernous malformation. [PDF]

Cell Commun Signal
Li Y, Girard R, Srinath A, Cruz DV, Ciszewski C, Chen C, Lightle R, Romanos S, Sone JY, Moore T, DeBiasse D, Stadnik A, Lee JJ, Shenkar R, Koskimäki J, Lopez-Ramirez MA, Marchuk DA, Ginsberg MH, Kahn ML, Shi C, Awad IA.   +20 more
europepmc   +1 more source

Cerebral Cavernous Malformation Bleeding Following Cerebrospinal Fluid Diversion Surgery: A Case Report and Literature Review. [PDF]

Cureus
Salem R, Almutairi OT, Albrahim M, Alomar N.   +3 more
europepmc   +1 more source

Hemorrhage of cerebral cavernous malformation in third trimester of pregnancy. [PDF]

Obstet Med
Merlino L, Del Prete F, Titi L, Piccioni MG.   +3 more
europepmc   +1 more source

Familial cerebral cavernous malformation presenting with cerebellopontine angle syndrome in a patient with autosomal dominant polycystic kidney disease. [PDF]

Neurol Perspect
Ghosh R, León-Ruiz M, Roy D, Benito-León J.   +3 more
europepmc   +1 more source

Large language models assisted multi-effect variants mining on cerebral cavernous malformation familial whole genome sequencing. [PDF]

Comput Struct Biotechnol J
Wang Y, Zuo J, Duan C, Peng H, Huang J, Zhao L, Zhang L, Dong Z.   +7 more
europepmc   +1 more source

Intracranial Hemorrhage Rate and Lesion Burden in Patients With Familial Cerebral Cavernous Malformation [PDF]

Journal of the American Heart Association, 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 seizures ...
Jeffrey Nelson, Cynthia Tsang, Obiora Okoye   +2 more
exaly   +2 more sources

Cerebral Cavernous Malformation Proteins in Barrier Maintenance and Regulation

International Journal of Molecular Sciences, 2020
Cerebral cavernous malformation (CCM) is a disease characterized by mulberry shaped clusters of dilated microvessels, primarily in the central nervous system. Such lesions can cause seizures, headaches, and stroke from brain bleeding.
Ye Li, Sean P Polster, Christopher R Weber   +2 more
exaly   +2 more sources

Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations [PDF]

Genetics in Medicine, 2015
PurposeThe phenotypic manifestations of cerebral cavernous malformation disease caused by rare PDCD10 mutations have not been systematically examined, and a mechanistic link to Rho kinase-mediated hyperpermeability, a potential therapeutic target, has ...
Robert Shenkar, Changbin Shi, Rebecca A Stockton   +2 more
exaly   +2 more sources

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Pediatric Cerebral Cavernous Malformations

Pediatric Neurology, 2021
Cerebral cavernous malformations are the second most common vascular malformations in the central nervous system, and over one-third are found in children. Lesions may be solitary or multiple, be discovered incidentally, be sporadic, or be secondary to familial cavernomatosis or radiation therapy.
Michael Paddock, Sarah Lanham, Kanwar Gill, Saurabh Sinha, Daniel J.A. Connolly   +4 more
openaire   +2 more sources

Cerebral Cavernous Malformations

New England Journal of Medicine, 2017
A 59-year-old man presented with a 1-year history of progressively worsening headaches. Imaging revealed multiple lesions, and genetic analysis confirmed a diagnosis of the familial cerebral cavernous malformation syndrome.
Ithamar, Ganmore, Anat, Achiron
openaire   +3 more sources