Results 101 to 110 of about 827,976 (177)

Giant posterior fossa cavernous malformations in 2 infants with familial cerebral cavernomatosis: the case for early screening

, 2010
The author reports the details in 2 cases of infants with familial cerebral cavernomatosis who presented in dire condition from hemorrhagic posterior fossa cavernous malformations. In Case 1, a 4-month-old boy presented with opisthotonos, gaze palsy, and
Sean M. Lew
core   +1 more source

Familial Cerebral Cavernous Malformations: A Case Report

Asian Journal of Medicine and Health
Aims: Describe the main imaging findings of familial cerebral cavernous malformations. Presentation of Case: This is the clinical case of a 68-year-old woman with a history of type 2 diabetes mellitus and long-standing systemic arterial hypertension. She presents to the neurology outpatient clinic reporting dizziness, temporal-spatial disorientation ...
Hernández, Jesús Octavio Tafoya, Vázquez, Rodolfo Alberto del Corral, Sotto, Leidi Johana Rodríguez, Buesaco, Julián Andrés Bucheli, Gomez, Joaquín Núñez, Macias, Agustín Parra   +5 more
openaire   +2 more sources

Oral Clues to Osler Disease

Journal of General and Family Medicine, Volume 27, Issue 5, September 2026.
Mika Watanabe, Yuki Otsuka, Yuya Yokota, Fumio Otsuka   +3 more
wiley   +1 more source

First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencing.

, 2018
Familial cerebral cavernous malformations (CCMs) predispose to seizures and hemorrhagic stroke. Molecular genetic analyses of CCM1, CCM2, and CCM3 result in a mutation detection rate of up to 98%.
Strom, T.M., Sure, U., Rath, M., Pagenstecher, A., Hoffjan, S., Dammann, P., Spiegler, S., Felbor, U.   +7 more
core   +1 more source

Cerebral cavernous malformations as a disease of vascular permeability: from bench to bedside with caution

, 2010
Tremendous insight into the molecular and genetic pathogenesis of cerebral cavernous malformations (CCMs) has been gained over the past 2 decades. This includes the identification of 3 distinct genes involved in familial CCMs.
Robert Shenkar, Sanjay Yadla, Peter G. Campbell, Pascal M. Jabbour, Issam A. Awad, Changbin Shi   +5 more
core   +1 more source

Disease models in cerebral cavernous malformations

, 2020
Cerebral cavernous malformation (CCM) is a rare disease of genetic origin characterized by dilated and leaky capillaries occurring mainly in the central nervous system.
Trabalzini L., Glading A. J., Finetti F.
core   +1 more source

Abstract Supplement HIV Glasgow 8–11 November 2026, Glasgow, UK/Virtual

Journal of the International AIDS Society, Volume 29, Issue S6, November 2026.
wiley   +1 more source

Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study. [PDF]

Neuroradiology, 2023
Geraldo AF, Alves CAPF, Luis A, Tortora D, Guimarães J, Abreu D, Reimão S, Pavanello M, de Marco P, Scala M, Capra V, Vaz R, Rossi A, Schwartz ES, Mankad K, Severino M.   +15 more
europepmc   +1 more source

The Emerging Role of the Gut Microbiome in Cerebral Cavernous Malformation: A New Novel Therapeutic Strategy? [PDF]

Cerebral cavernous malformation (CCM) is a cluster of abnormal blood vessels in the brain that leads to severe neurological deficits, seizures, and fatal hemorrhagic stroke. Currently, there is no available drug treatment for CCM.
Jaesung P. Choi, Hamidreza Sadegh, Sadegh, H, Choi, JP, Choi, Jaesung P, Sadegh, Hamidreza   +5 more
core   +1 more source

Circulating Plasma miRNA Homologs in Mice and Humans Reflect Familial Cerebral Cavernous Malformation Disease. [PDF]

Transl Stroke Res, 2023
Romanos SG, Srinath A, Li Y, Xie B, Chen C, Li Y, Moore T, Bi D, Sone JY, Lightle R, Hobson N, Zhang D, Koskimäki J, Shen L, McCurdy S, Lai CC, Stadnik A, Piedad K, Carrión-Penagos J, Shkoukani A, Snellings D, Shenkar R, Sulakhe D, Ji Y, Lopez-Ramirez MA, Kahn ML, Marchuk DA, Ginsberg MH, Girard R, Awad IA.   +29 more
europepmc   +1 more source