Cite

Porter PJ, Willinsky RA, Harper W, Wallace MC. Cerebral cavernous malformations: natural history and prognosis after clinical deterioration with or without hemorrhage. J Neurosurg 1997; 87(2): 190-97.10.3171/jns.1997.87.2.01909254081PorterPJWillinskyRAHarperWWallaceMCCerebral cavernous malformations: natural history and prognosis after clinical deterioration with or without hemorrhageJ Neurosurg199787219097Open DOISearch in Google Scholar

Tournier-Lasserve E. Familial cerebral cavernous malformation. Orphanet encyclopedia. 2014Tournier-Lasserve E. Familial cerebral cavernous malformation. Orphanet encyclopedia2014Search in Google Scholar

Labauge P, Laberge S, Brunereau L, Levy C, Tournier-Lasserve E. Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Societe Francaise de Neurochirurgie. Lancet 1998; 352: 1892–97.LabaugePLabergeSBrunereauLLevyCTournier-LasserveEHereditary cerebral cavernous angiomas: clinical and genetic features in 57 French familiesSociete Francaise de Neurochirurgie. Lancet199835218929710.1016/S0140-6736(98)03011-6Search in Google Scholar

Petersen TA, Morrison LA, Schrader RM, Hart BL. Familial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotype. AJNR Am J Neuroradiol 2010; 31(2): 377–82.1983379610.3174/ajnr.A1822PetersenTAMorrisonLASchraderRMHartBLFamilial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotypeAJNR Am J Neuroradiol201031237782445594919833796Search in Google Scholar

Verlaan DJ, Laurent SB, Sure U, Bertalanffy H, Andermann E, Andermann F, Rouleau G.A, Siegel A.M. CCM1 mutation screen of sporadic cases with cerebral cavernous malformations. Neurology 2004; 62(7): 1213–15.1507903010.1212/01.WNL.0000118299.55857.BBVerlaanDJLaurentSBSureUBertalanffyHAndermannEAndermannFRouleauG.ASiegelA.MCCM1 mutation screen of sporadic cases with cerebral cavernous malformationsNeurology200462712131515079030Search in Google Scholar

Labauge P, Brunereau L, Coubes P, Clanet M, Tannier C, Laberge S, Levy C. Appearance of new lesions in two nonfamilial cerebral cavernoma patients. Eur Neurol 2001; 45(2): 83–88.10.1159/00005210011244270LabaugePBrunereauLCoubesPClanetMTannierCLabergeSLevyCAppearance of new lesions in two nonfamilial cerebral cavernoma patientsEur Neurol2001452838811244270Open DOISearch in Google Scholar

Rigamonti D, Hadley MN, Drayer BP, Johnson PC, Hoenig-Rigamonti K, Knight JT, Spetzler RF. Cerebral cavernous malformations. Incidence and familial occurrence. N Engl J Med 1988; 319(6): 343–47.339319610.1056/NEJM198808113190605RigamontiDHadleyMNDrayerBPJohnsonPCHoenig-RigamontiKKnightJTSpetzlerRFCerebral cavernous malformations. Incidence and familial occurrenceN Engl J Med19883196343473393196Search in Google Scholar

Morrison L, Akers A. Cerebral Cavernous Malformation, Familial. 2003 Feb 24. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® 1993-2018. Available from: https://www.ncbi.nlm.nih.gov/books/NBK1293/MorrisonLAkersACerebral Cavernous Malformation, Familial 2003 Feb 24AdamMPArdingerHHPagonRAet al., editorsGeneReviews®1993-2018Available fromhttps://www.ncbi.nlm.nih.gov/books/NBK1293/Search in Google Scholar

Choquet H, Pawlikowska L, Lawton MT, Kim H. Genetics of cerebral cavernous malformations: current status and future prospects. J Neurosurg Sci 2015; 59(3): 211-20.25900426ChoquetHPawlikowskaLLawtonMTKimHGenetics of cerebral cavernous malformations: current status and future prospectsJ Neurosurg Sci201559321120Search in Google Scholar

Gault J, Awad IA, Recksiek P, Shenkar R, Breeze R, Handler M, Kleinschmidt-DeMasters BK. Cerebral cavernous malformations: somatic mutations in vascular endothelial cells. Neurosurgery 2009; 65(1): 138-44.10.1227/01.NEU.0000348049.81121.C119574835GaultJAwadIARecksiekPShenkarRBreezeRHandlerMKleinschmidt-DeMastersBKCerebral cavernous malformations: somatic mutations in vascular endothelial cellsNeurosurgery200965113844272244119574835Open DOISearch in Google Scholar

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