Results 141 to 150 of about 827,976 (177)

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

The effect of pregnancy and puerperium on haemorrhage risk in women with cerebral cavernous malformations: a case-crossover study. [PDF]

Eur Stroke J
Palermo M, Viglione V, Tosto F, Signorelli F, Albanese A, Olivi A, Doglietto F, Romozzi M, Sturiale CL.   +8 more
europepmc   +1 more source

Intervention or Conservative Management for Symptomatic Cerebral Cavernous Malformations: A Prospective, Population-Based Cohort Study. [PDF]

Neurology
Sandmann ACA, Verbaan D, Coutinho JM, Vandertop WP, White PM, Al-Shahi Salman R.   +5 more
europepmc   +1 more source

Aspirin Use and the Risk of Symptomatic Hemorrhage in Patients With Cerebral Cavernous Malformations and Ischemic Cerebrovascular Disease. [PDF]

Stroke Vasc Interv Neurol
Wang J, Tang J, Bai X, Jiao Y, Huo R, Zhang W, Wang Y, Yang Y, Cao Y.   +8 more
europepmc   +1 more source

Aeromedical decision-making for asymptomatic cerebral cavernous malformations in military pilots. [PDF]

Front Public Health
Zhang H, Ma L, Zhang CY, Zhou J, Zhou Y, Ma YD.   +5 more
europepmc   +1 more source

Sudden Bilateral Hearing Loss Is a Neurovascular Emergency. [PDF]

Case Rep Neurol Med
Aemaz Ur Rehman M, Aladawi M, Ubogu EE, Guerra-Castanon F.   +3 more
europepmc   +1 more source

Successful MRgFUS VIM Thalamotomy for Essential Tremor Nearby Cavernous Malformation: Image Case Report.

Stereotact Funct Neurosurg
Favi Bocca L, Davidson B, Lam B, Endre R, Huang Y, Hamani C, Lipsman N.   +6 more
europepmc   +1 more source

Familial Cerebral Cavernous Malformations [PDF]

Stroke, 2019
Blaine Hart, Marc C Mabray, Syed A Quadri   +2 more
exaly   +3 more sources

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Mutations in KRIT1 in Familial Cerebral Cavernous Malformations

Neurosurgery, 2000
The recognition of six unrelated Hispanic-American families in which cerebral cavernous malformations (CCM) segregated as an autosomal dominant trait established a genetic basis for this disease. Linkage analysis subsequently identified locus heterogeneity with disease genes for CCM at chromosomal regions 7q, 7p, and 3q. Recently, mutations in KRIT1, a
J, Zhang, R E, Clatterbuck, D, Rigamonti, H C, Dietz   +3 more
openaire   +2 more sources

A Japanese pedigree of familial cerebral cavernous malformations--a case report. [PDF]

Hiroshima journal of medical sciences, 2015
Familial cerebral cavernous malformations (FCCM) are autosomal-dominant vascular malformations. At present, 3 cerebral cavernous malformation genes (KRIT1/CCM1, MGC4607/CCM2, and PDCD10/CCM3) have been identified. Few genetic analyses of Japanese FCCM have been reported.
Imada, Yasutaka, Yuki, Kiyoshi, Migita, Keisuke, Sadatomo, Takashi, Kuwabara, Masashi, Yamada, Toru, Kurisu, Kaoru   +6 more
openaire   +2 more sources