Results 131 to 140 of about 1,951 (186)

Recurrent somatic copy number alterations in resected cerebral cavernous malformations. [PDF]

Hum Genomics
Ressler AK, Debose-Scarlett E, Fuenzalida A, Lightle R, Weinsheimer S, Faughnan ME, Spiekerkoetter E, Schimmel K, Lawton M, Kim H, Awad I, Marchuk DA.   +11 more
europepmc   +1 more source

Advancing the Performance of Anion Exchange Membrane Electrolysis by Employing a Powder-Based Ionomer during Anode Catalyst Layer Fabrication. [PDF]

ACS Appl Energy Mater
Chan AL, Clauser AL, Parimuha MR, Young JL, Sugar JD, Alia SM.   +5 more
europepmc   +1 more source

Posterior fossa cavernous malformation mimicking meningioma: A case report. [PDF]

Radiol Case Rep
Valdivia D, Cook B, Novakovic N, Egladyous A, Boukhar S, Movahed-Ezazi M, Baisre A, Sundararajan S, Sherman J, Sun H.   +9 more
europepmc   +1 more source

TLNRD1 is a CCM complex component and regulates endothelial barrier integrity. [PDF]

J Cell Biol
Ball NJ, Ghimire S, Follain G, Pajari AO, Wurzinger D, Vaitkevičiūtė M, Cowell AR, Berki B, Ivaska J, Paatero I, Goult BT, Jacquemet G.   +11 more
europepmc   +1 more source

In toto resection of a rare intradural extramedullary cavernous malformation on the S1 nerve root: illustrative case. [PDF]

J Neurosurg Case Lessons
van de Goor A, Schuermans VNE, Postma AA, Boselie TFM.   +3 more
europepmc   +1 more source

Developmental venous anomaly related to de novo cerebral cavernous malformation: Imaging findings from two cases. [PDF]

Radiol Case Rep
Tovar SG, Parra AF.
europepmc   +1 more source

Cerebral vascular malformations: pathogenesis and therapy. [PDF]

MedComm (2020)
He Q, Huo R, Sun Y, Zheng Z, Xu H, Zhao S, Ni Y, Yu Q, Jiao Y, Zhang W, Zhao J, Cao Y.   +11 more
europepmc   +1 more source

Natural history of familial cerebral cavernous malformations: the CCM_Italia cohort study. [PDF]

Front Neurol
Lanfranconi S, Scola E, Novelli D, Poggesi A, Pescini F, Pavanello M, Romano F, D'Alessandris QG, Marani W, Signorelli F, Iaconetta G, Torelli G, Fainardi E, Severino M, Remore LG, Bertani GA, Conte G, Capra V, Vasamì A, Nicolis E, Contino G, Ronchi D, Palmieri MC, Previtali A, Mattogno PP, Sturiale CL, Solarino ME, Caliulo R, Bozzi MT, Fratini F, Zanier ER, Latini R, Meessen JMTA, Locatelli M, and the CCM_Italia investigators.   +34 more
europepmc   +1 more source

Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. [PDF]

Eur J Hum Genet
Chaussenot A, Ayrignac X, Chatron N, Granchon-Riolzir T, Labauge P, Tournier-Lasserve E, Riant F.   +6 more
europepmc   +1 more source