Results 111 to 120 of about 1,834 (180)

Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 gene. [PDF]

open access: yesNeurogenetics
Pilz RA   +7 more
europepmc   +1 more source

Disseminated cavernous malformations due to KRIT1 gene mutation causing seizure and spastic paraparesis

open access: yesAnnals of Indian Academy of Neurology
Saranya B Gomathy   +3 more
doaj   +1 more source

Cerebral cavernous malformation with secondary bacterial infection: illustrative case. [PDF]

open access: yesJ Neurosurg Case Lessons
Gujjari KS   +6 more
europepmc   +1 more source

Flow-Sensitive HEG1 Controls eNOS Activity to Prevent Endothelial Dysfunction, Hypertension, and Atherosclerosis. [PDF]

open access: yesArterioscler Thromb Vasc Biol
Clark MD   +14 more
europepmc   +1 more source

22207 - VARIABILIDAD FENOTÍPICA EN LA CAVERNOMATOSIS MÚLTIPLE CEREBRAL FAMILIAR Y UNA MUTACIÓN KRIT1 NO DESCRITA

open access: yesNeurology Perspectives
I. Esnaola Barriola   +5 more
doaj   +1 more source

Corrigendum: Cerebral Cavernous Malformations: Review of the Genetic and Protein–Protein Interactions Resulting in Disease Pathogenesis

open access: yesFrontiers in Surgery, 2017
Jacob F. Baranoski   +3 more
doaj   +1 more source

Clinical and molecular landscape of paediatric cerebral and spinal cavernous malformations. [PDF]

open access: yesBrain Commun
Benichi S   +25 more
europepmc   +1 more source

Molecular Pathways and Circulating Biomarkers in Cerebral Cavernous Malformations-A Systematic Review. [PDF]

open access: yesInt J Mol Sci
Karadachi HH   +15 more
europepmc   +1 more source

21229. NUEVA MUTACIÓN EN KRIT1 COMO CAUSANTE DE CAVERNOMATOSIS FAMILIAR

open access: yesNeurology Perspectives
L. Delgado Bárcena   +8 more
doaj   +1 more source

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