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Items: 1 to 20 of 138

1.

Familial cerebral cavernous malformation.

Dziedzic T, Kunert P, Matyja E, Ziora-Jakutowicz K, Sidoti A, Marchel A.

Folia Neuropathol. 2012;50(2):152-8.

2.

Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 gene.

Garaci F, Marsili L, Riant F, Marziali S, Cécillon M, Pasquarelli R, Sangiuolo F, Floris R, Novelli G, Tournier-Lasserve E, Brancati F.

Neuroradiol J. 2015 Jun;28(3):289-93. doi: 10.1177/1971400915591688.

3.

Features of a Chinese family with cerebral cavernous malformation induced by a novel CCM1 gene mutation.

Wang X, Liu XW, Lee N, Liu QJ, Li WN, Han T, Wei KK, Qiao S, Chi ZF.

Chin Med J (Engl). 2013;126(18):3427-32.

PMID:
24034083
4.

Genomic causes of multiple cerebral cavernous malformations in a Japanese population.

Tsutsumi S, Ogino I, Miyajima M, Ikeda T, Shindo N, Yasumoto Y, Ito M, Arai H.

J Clin Neurosci. 2013 May;20(5):667-9. doi: 10.1016/j.jocn.2012.05.041. Epub 2013 Feb 26.

PMID:
23485406
5.

A Novel MGC4607/CCM2 Gene Mutation Associated with Cerebral Spinal and Cutaneous Cavernous Angiomas.

Cigoli MS, De Benedetti S, Marocchi A, Bacigaluppi S, Primignani P, Gesu G, Citterio A, Tassi L, Mecarelli O, Pulitano P, Penco S.

J Mol Neurosci. 2015 Jul;56(3):602-7. doi: 10.1007/s12031-015-0555-0. Epub 2015 Apr 14.

PMID:
25869611
6.

Value of gradient-echo magnetic resonance imaging in the diagnosis of familial cerebral cavernous malformation.

Lehnhardt FG, von Smekal U, Rückriem B, Stenzel W, Neveling M, Heiss WD, Jacobs AH.

Arch Neurol. 2005 Apr;62(4):653-8.

PMID:
15824268
7.

Differential angiogenesis function of CCM2 and CCM3 in cerebral cavernous malformations.

Zhu Y, Wu Q, Xu JF, Miller D, Sandalcioglu IE, Zhang JM, Sure U.

Neurosurg Focus. 2010 Sep;29(3):E1. doi: 10.3171/2010.5.FOCUS1090.

PMID:
20809750
8.

[Cerebral cavernous malformation--its genetic and biological background].

Fujimura M, Tominaga T.

Brain Nerve. 2008 Nov;60(11):1271-4. Review. Japanese.

PMID:
19069160
9.

Highly variable penetrance in subjects affected with cavernous cerebral angiomas (CCM) carrying novel CCM1 and CCM2 mutations.

Gianfrancesco F, Cannella M, Martino T, Maglione V, Esposito T, Innocenzi G, Vitale E, Liquori CL, Marchuk DA, Squitieri F.

Am J Med Genet B Neuropsychiatr Genet. 2007 Jul 5;144B(5):691-5.

PMID:
17440989
10.

Lesions from patients with sporadic cerebral cavernous malformations harbor somatic mutations in the CCM genes: evidence for a common biochemical pathway for CCM pathogenesis.

McDonald DA, Shi C, Shenkar R, Gallione CJ, Akers AL, Li S, De Castro N, Berg MJ, Corcoran DL, Awad IA, Marchuk DA.

Hum Mol Genet. 2014 Aug 15;23(16):4357-70. doi: 10.1093/hmg/ddu153. Epub 2014 Apr 3.

11.

Familial cerebral cavernous malformation: report of a further Italian family.

Nannucci S, Pescini F, Poggesi A, Ciolli L, Patrosso MC, Marocchi A, Inzitari D, Penco S, Pantoni L.

Neurol Sci. 2009 Apr;30(2):143-7. doi: 10.1007/s10072-009-0020-3. Epub 2009 Jan 30.

PMID:
19184323
12.

[Gene mutations in patients with hereditary cavernous malformations].

Belousova OB, Bulygina ES, Okishev DN, Prohorchuk EB, Tsygankova SV, Pronin IN, Shishkina LV, Ryzhova MV, Skryabin KG, Konovalov AN.

Zh Nevrol Psikhiatr Im S S Korsakova. 2017;117(6):66-72. doi: 10.17116/jnevro20171176166-72. Russian.

PMID:
28745674
13.

Cerebral Cavernous Malformation, Familial.

Morrison L, Akers A.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2018.
2003 Feb 24 [updated 2016 Aug 4].

14.

Clinical, magnetic resonance imaging, and genetic study of 5 Italian families with cerebral cavernous malformation.

Battistini S, Rocchi R, Cerase A, Citterio A, Tassi L, Lando G, Patrosso MC, Galli R, Brunori P, Sgrò DL, Pitillo G, Lo Russo G, Marocchi A, Penco S.

Arch Neurol. 2007 Jun;64(6):843-8.

PMID:
17562932
15.

Genetics of cerebral cavernous malformations: current status and future prospects.

Choquet H, Pawlikowska L, Lawton MT, Kim H.

J Neurosurg Sci. 2015 Sep;59(3):211-20. Epub 2015 Apr 22. Review.

16.

Familial versus sporadic cavernous malformations: differences in developmental venous anomaly association and lesion phenotype.

Petersen TA, Morrison LA, Schrader RM, Hart BL.

AJNR Am J Neuroradiol. 2010 Feb;31(2):377-82. doi: 10.3174/ajnr.A1822. Epub 2009 Oct 15.

17.

A Japanese pedigree of familial cerebral cavernous malformations--a case report.

Imada Y, Yuki K, Migita K, Sadatomo T, Kuwabara M, Yamada T, Kurisu K.

Hiroshima J Med Sci. 2014 Dec;63(4):43-8.

PMID:
25707093
18.

Cerebral cavernous malformations with diffuse manifestation: A benign entity?

Tsutsumi S, Ogino I, Miyajima M, Arai H, Ito M, Yasumoto Y.

J Neurol Sci. 2016 Aug 15;367:335-41. doi: 10.1016/j.jns.2016.06.012. Epub 2016 Jun 15.

PMID:
27423615
19.

Identification of a c.601C>G mutation in the CCM1 gene in a kindred with multiple skin, spinal and cerebral cavernous malformations.

Haghighi A, Fathi D, Shahbazi M, Motahari MM, Friedman B.

J Neurol Sci. 2013 Nov 15;334(1-2):97-101. doi: 10.1016/j.jns.2013.07.2518. Epub 2013 Aug 7.

PMID:
24007869
20.

CCM2 gene polymorphisms in Italian sporadic patients with cerebral cavernous malformation: a case-control study.

D'Angelo R, Scimone C, Rinaldi C, Trimarchi G, Italiano D, Bramanti P, Amato A, Sidoti A.

Int J Mol Med. 2012 Jun;29(6):1113-20. doi: 10.3892/ijmm.2012.927. Epub 2012 Feb 28.

PMID:
22378217

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