Results 131 to 140 of about 3,789 (186)

Genetic mutation and blue rubber bleb nevus syndrome: case reports and literature review. [PDF]

Front Genet
Xing Y, Liu H, Liu H, Ding X, Jing X.
europepmc   +1 more source

Single-nucleus DNA sequencing reveals hidden somatic loss-of-heterozygosity in Cerebral Cavernous Malformations. [PDF]

Nat Commun, 2023
Ressler AK, Snellings DA, Girard R, Gallione CJ, Lightle R, Allen AS, Awad IA, Marchuk DA.   +7 more
europepmc   +1 more source

Association of Quality of Life Domains and Clinical Symptoms in Patients With Familial Cerebral Cavernous Malformation. [PDF]

J Am Heart Assoc
Tsang C, Nelson J, Vassar R, Ko NU, McCulloch C, Smith ER, Vadivelu S, Akers A, Lee C, Zabramski J, Torbey MT, Awad IA, Kim H, Brain Vascular Malformation Consortium CCM Investigators.   +13 more
europepmc   +1 more source

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

Frontiers in Surgery, 2017
Jacob F. Baranoski, M. Yashar S. Kalani, Colin J. Przybylowski, Joseph M. Zabramski   +3 more
doaj   +1 more source

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

Prevalence, genetic and clinical characteristics in first-degree relatives of patients with familial cerebral cavernous malformations in China. [PDF]

Stroke Vasc Neurol
Li C, Zhuo L, Kang Y, Liu P, Huang W, Li Q, Ma K, Huang S, Lin X, Zhuang W, Wang H, Chen D, Wang H, He Q, Gao Z, Niu X, Jing Y, Yan L, Gao B, Wang D, Lin S, Wu S, Lin Y, Kang D, Lin F.   +24 more
europepmc   +1 more source

Driving Rho GTPase activity in endothelial cells regulates barrier integrity [PDF]

, 2010
Beckers, C.M.L., Hinsbergh, V.W.M. van, Nieuw Amerongen, G.P. van   +2 more
core   +1 more source

Cerebral cavernous malformation 2 (CCM2); neurotrophic tyrosine kinase receptor 1 (NTRK1; TrkA) [PDF]

Science-Business eXchange, 2009
openaire   +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

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