Zobrazeno 1 - 10
of 1 248
pro vyhledávání: '"cerebral cavernous malformations"'
Publikováno v:
Biomarker Research, Vol 12, Iss 1, Pp 1-26 (2024)
Abstract Background Cerebral cavernous malformations (CCMs) are vascular abnormalities associated with deregulated angiogenesis. Their pathogenesis and optimal treatment remain unclear. This study aims to investigate the molecular signatures of cupro
Externí odkaz:
https://doaj.org/article/5afcd3aafc65486ab5331abc99ca247f
Akademický článek
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Autor:
Karthik Ashok, Tyra Martinez, Julie Sesen, Sana Nasim, Shih-Shan Lang, Gregory Heuer, Alexander Tucker, Miguel Alejandro Lopez-Ramirez, Edward R. Smith, Aram Ghalali
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
IntroductionCerebral cavernous malformations (CCMs) are pathologic lesions comprised of clusters of thin-walled capillaries characterized by abnormal proliferation, angiogenesis, and bleeding secondary to somatic or germline mutations in endothelial
Externí odkaz:
https://doaj.org/article/ee79889bef1142a6b7720f85d260a626
Autor:
Jacob Croft, Brian Grajeda, Liyuan Gao, Johnathan Abou-Fadel, Ahmed Badr, Victor Sheng, Jun Zhang
Publikováno v:
Diagnostics, Vol 14, Iss 17, p 1895 (2024)
Cerebral cavernous malformations (CCMs) are abnormal expansions of brain capillaries that increase the risk of hemorrhagic strokes, with CCM1 mutations responsible for about 50% of familial cases. The disorder can cause irreversible brain damage by c
Externí odkaz:
https://doaj.org/article/d28ca9dc856340f2a304e2daff6286f8
Publikováno v:
Romanian Journal of Neurology, Vol 22, Iss 2, Pp 147-150 (2023)
Cerebral malformations, known as cavernomas, are low flow vascular malformations that have a multilobulated appearance. A large percent of cavernous malformations have seizures as initial symptoms. We report a case of a 48 years old patient presented
Externí odkaz:
https://doaj.org/article/4a9ad59fccec4f17b15b4cd5ab26d09f
Autor:
Jacob Croft, Brian Grajeda, Luis A. Aguirre, Johnathan S. Abou-Fadel, Cameron C. Ellis, Igor Estevao, Igor C. Almeida, Jun Zhang
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 9, p 4740 (2024)
Cerebral cavernous malformations (CCMs) are a neurological disorder characterized by enlarged intracranial capillaries in the brain, increasing the susceptibility to hemorrhagic strokes, a major cause of death and disability worldwide. The limited tr
Externí odkaz:
https://doaj.org/article/90b0ca8b52ac4538bbe9194bbd5a8b57
Publikováno v:
Journal of the Formosan Medical Association, Vol 121, Iss 11, Pp 2331-2337 (2022)
Hereditary cerebral cavernous malformations (CCMs) are characterized by clustered dilated capillary-like vessels in the brain. Autosomal dominant polycystic kidney disease (PKD) is characterized by renal cysts and extra-renal abnormalities. We report
Externí odkaz:
https://doaj.org/article/b91ed3e08a014a029aa359db7635c6c7
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 29, Iss 2, p 75 (2024)
Background: Cerebral Cavernous Malformations (CCMs) are brain vascular abnormalities associated with an increased risk of hemorrhagic strokes. Familial CCMs result from autosomal dominant inheritance involving three genes: KRIT1 (CCM1), MGC4607 (CCM2
Externí odkaz:
https://doaj.org/article/f83722fadd054426ad971563903f164a
Akademický článek
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Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Duchenne muscular dystrophy (DMD) is an X-linked recessive inherited disorder caused by the absence of the Dystrophin protein. Cerebral cavernous malformations (CCMs) are the most common vascular abnormalities in the central nervo
Externí odkaz:
https://doaj.org/article/ce31f180a8d74b6187cfc6e3248d1eac