Results 111 to 120 of about 827,976 (177)
Spinal Cord Cavernous Malformation in a Patient with Familial Intracranial Cavernous Malformations
The case of a 30-year-old woman with a hemorrhage caused by a rare intramedullary cavernous malformation is presented. The patient underwent laminectomy with total removal of the lesion.
Stuart K. Lee, Robert F. Spetzler
core +1 more source
Familial cerebral cavernous malformation: clinical case [PDF]
Júlia Travkina +2 more
openaire +1 more source
Congenital multiple cavernous angiomas associated with thrombosed arteriovenous malformation of the brain - Case report [PDF]
A 16-year-old girl presented with multiple cerebral cavernous angiomas with calcifications due to repeated hemorrhages and a thrombosed cerebral arteriovenous malformation (AVM).
12082 +13 more
core
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
A Japanese Pedigree of Familial Cerebral Cavernous Malformations : A Case Report [PDF]
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.
Imada, Yasutaka +6 more
core
Supplementary data in support of manuscript: "Stereotactic radiosurgery for cerebral cavernous malformations: a systematic review"
Poorthuis, Michiel, Rinkel, Leon
core +1 more source
Walsh & Hoyt: Cavernous Malformations (Cavernous Angiomas)
A cavernous malformation is a vascular lesion composed of large vascular channels lined by flat endothelium and separated by a fibroconnective tissue stroma.
Andrew Lee, MD
core
Cerebral Cavernous Malformations (CCMs) are vascular lesions involving brain capillaries. They may occur sporadically or be inherited as autosomal dominant character.
Sara Guido
core +1 more source
Familial cerebral cavernous malformation presenting with epilepsy caused by mutation in the CCM2 gene: A case report. [PDF]
Ishii K +4 more
europepmc +1 more source

