Results 111 to 120 of about 6,501 (209)

A Locus for Cerebral Cavernous Malformations Maps to Chromosome 7q in Two Families

open access: yesGenomics, 1995
Cavernous malformations (angiomas) affecting the central nervous system and retina can be inherited in autosomal dominant pattern (OMIM 116860). These vascular lesions may remain clinically silent or lead to a number of neurological symptoms including seizure, intracranial hemorrhage, focal neurological deficit, and migraine.
D A, Marchuk   +9 more
openaire   +2 more sources

Patient-reported outcome measures in patients with familial cerebral cavernous malformations: results from the Treat_CCM trial

open access: yesFrontiers in Neurology
BackgroundThe Phase 1/2 Treat_CCM randomized controlled trial for people with familial cerebral cavernous malformations (FCCMs) confirmed the safety of propranolol and suggested beneficial effects on intracerebral hemorrhage or new focal neurological ...
Jennifer M. T. A. Meessen   +14 more
doaj   +1 more source

Clinical and radiologic distinctions between familial cavernous malformation syndrome and cerebral amyloid angiopathy

open access: yesActa Neurochirurgica
Familial cerebral cavernous malformation syndrome (FCCM) is characterized by multiple hemorrhagic lesions and is sometimes mistaken for cerebral amyloid angiopathy (CAA).
KD Flemming   +6 more
semanticscholar   +1 more source

Cerebral cavernous malformation presenting as seizures [PDF]

open access: yes, 2020
Cerebral cavernous malformations (CCMs) is one of the rare vascular malformation. It is diagnosed by characteristic lesions on magnetic resonance imaging (MRI).
Brohi, Hazim   +3 more
core   +1 more source

Review of various intraoperative neurophysiologic monitoring techniques [PDF]

open access: yes, 2016
IONM is use to monitoring nervous tissues (including brain, spinal cord, cranial nerves and peripheral nerves) in real-time during surgeries, alert neurological injuries and corrective measures and prevent disability.
Ali, Liaquat   +2 more
core   +1 more source

Familial cerebral cavernous malformation: clinical case [PDF]

open access: yesNeurologie pro praxi, 2020
Júlia Travkina   +2 more
openaire   +1 more source

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23 [PDF]

open access: yes, 2015
19openopenAli G. Gharavi; Yan Yan; Francesco Scolari; F. Paolo Schena; Giovanni M. Frasca; Gian Marco Ghiggeri; Kerry Cooper; Antonio Amoroso; Battista Fabio Viola; Graziana Battini10; Gianluca Caridi8; Cristina Canova; Anita Farhi; Vairavan ...

core  

A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition [PDF]

open access: yes, 2017
We have studied a family with severe mental retardation characterized by the virtual absence of speech, autism spectrum disorder, epilepsy, late-onset ataxia, weakness and dystonia.
Feldman, Gerald   +9 more
core  

Plasma biomarkers in patients with familial cavernous malformation and their first-degree relatives: a cross-sectional study

open access: yesScientific Reports
Familial cerebral cavernous malformation (FCCM), especially severe cases, impose a heavy physical and psychological burden on patients and their families.
Chunwang Li   +16 more
doaj   +1 more source

Hernesniemi's 1001 and More Microneurosurgical Videos : Videobook of Neurosurgery [PDF]

open access: yes, 2017
Peer ...
Choque-Velasquez, Joham   +3 more
core  

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