Results 121 to 130 of about 64,001 (226)

Physiological cerebrospinal fluid interactions between brain and eye structures are altered after long‐duration spaceflight

Experimental Physiology, Volume 111, Issue 9, Page 4209-4222, 1 September 2026.
Abstract Long‐duration spaceflight represents an extreme challenge, triggering adaptive responses including spaceflight‐associated neuro‐ocular syndrome, characterized by diminished visual acuity and ocular changes, which is a significant health risk for Mars missions.
Ge Tang, Steven Jillings, Ben Jeurissen, Elena Tomilovskaya, Inna Nosikova, Alexandra Ryabova, Ekaterina Pechenkova, Viktor Petrovichev, Ilya Rukavishnikov, Stefan Sunaert, Paul M. Parizel, Lyudmila Makovskaya, Valentin Sinitsyn, Jan Sijbers, Jitka Annen, Steven Laureys, Angelique Van Ombergen, Seyed‐Ahmad Ahmadi, Floris L. Wuyts, Peter zu Eulenburg   +19 more
wiley   +1 more source

Cerebral Cavernous Malformations [PDF]

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2000
I, Fleetwood, W, Hu, M, Hudon
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

Cavernoma in a young adult: a case report

Egyptian Journal of Neurosurgery
Cavernomas or cavernous malformations of the central nervous system are acquired or hereditary vascular anomalies. Although they are present in 0.1–0.5% in the general population, they are usually asymptomatic and undetected until symptoms occur.
Hina Ali, Samar Zaki, Ehsan Bari, Sara Khowaja   +3 more
doaj   +1 more source

Transcondylar approach for resection of lateral medullary cavernous malformation.

, 2018
BACKGROUND: Resection of a medullary cavernous malformation requires aggressive exposure, but there is controversy on how much occipital condyle can be safely removed during the transcondylar approach.
Jean, Walter C, MD, Sweiss, Fadi
core  

Familial cerebral cavernous malformation.

, 2012
Cavernous malformations (CMs) occur in approximately 0.5% of the general population and represent 5-10% of the central nervous system vascular malformations. The majority of CMs appear sporadically but genetically determined familial forms account for 10%
Ziora Jakutowicz K, Matyja E, Kunert P, Dziedzic T, Marchel A., SIDOTI, Antonina   +5 more
core  

Spontaneous resolution of a Chiari malformation Type I and syrinx after supratentorial craniotomy for excision of a cavernous malformation

, 2012
The pathogenesis of Chiari malformation Type I (CM-I) and associated syringomyelia is incompletely understood. Patients often present in middle age with incidental or minimally symptomatic CM-I, whose management is controversial.
Schirmer, Clemens, MD
core   +1 more source

Comment on "Thoracic Intradural Extramedullary Cavernous Malformation Mimicking Meningioma". [PDF]

NMC Case Rep J
Shibaike Y.
europepmc   +1 more source

Reply to the Editor: "Thoracic Intradural Extramedullary Cavernous Malformation Mimicking Meningioma". [PDF]

NMC Case Rep J
Fukunaga T, Toyota S, Murakami T, Okuhara S, Nagano T, Okochi K, Nakashima K, Nakamura M, Yamada S, Achiha T, Kobayashi M, Kishima H.   +11 more
europepmc   +1 more source

Spontaneous hemorrhage of cavernous malformation in the region of the cochlear nucleus: A case report. [PDF]

Radiol Case Rep
Almaazmi R, Ahmad A, Schlemmer K, Dogar MA.   +3 more
europepmc   +1 more source