Siegel AM - Search Results

1

CCM1 gene mutations in families segregating cerebral cavernous malformations.

Davenport WJ, Siegel AM, Dichgans J, Drigo P, Mammi I, Pereda P, Wood NW, Rouleau GA. Davenport WJ, et al. Among authors: siegel am. Neurology. 2001 Feb 27;56(4):540-3. doi: 10.1212/wnl.56.4.540. Neurology. 2001. PMID: 11222804

2

Krit1 missense mutations lead to splicing errors in cerebral cavernous malformation.

Verlaan DJ, Siegel AM, Rouleau GA. Verlaan DJ, et al. Among authors: siegel am. Am J Hum Genet. 2002 Jun;70(6):1564-7. doi: 10.1086/340604. Epub 2002 Apr 8. Am J Hum Genet. 2002. PMID: 11941540 Free PMC article.

3

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation.

Dupré N, Verlaan DJ, Hand CK, Laurent SB, Turecki G, Davenport WJ, Acciarri N, Dichgans J, Ohkuma A, Siegel AM, Rouleau GA. Dupré N, et al. Among authors: siegel am. Can J Neurol Sci. 2003 May;30(2):122-8. doi: 10.1017/s0317167100053385. Can J Neurol Sci. 2003. PMID: 12774951

4

CCM1 mutation screen of sporadic cases with cerebral cavernous malformations.

Verlaan DJ, Laurent SB, Sure U, Bertalanffy H, Andermann E, Andermann F, Rouleau GA, Siegel AM. Verlaan DJ, et al. Among authors: siegel am. Neurology. 2004 Apr 13;62(7):1213-5. doi: 10.1212/01.wnl.0000118299.55857.bb. Neurology. 2004. PMID: 15079030

5

No CCM2 mutations in a cohort of 31 sporadic cases.

Verlaan DJ, Laurent SB, Rouleau GA, Siegel AM. Verlaan DJ, et al. Among authors: siegel am. Neurology. 2004 Nov 23;63(10):1979. doi: 10.1212/01.wnl.0000144195.55540.9d. Neurology. 2004. PMID: 15557534 No abstract available.

6

CCM3 mutations are uncommon in cerebral cavernous malformations.

Verlaan DJ, Roussel J, Laurent SB, Elger CE, Siegel AM, Rouleau GA. Verlaan DJ, et al. Among authors: siegel am. Neurology. 2005 Dec 27;65(12):1982-3. doi: 10.1212/01.wnl.0000188903.75144.49. Neurology. 2005. PMID: 16380626

7

Cerebral cavernous malformations: mutations in Krit1.

Verlaan DJ, Davenport WJ, Stefan H, Sure U, Siegel AM, Rouleau GA. Verlaan DJ, et al. Among authors: siegel am. Neurology. 2002 Mar 26;58(6):853-7. doi: 10.1212/wnl.58.6.853. Neurology. 2002. PMID: 11914398 Review.

8

Mutational analysis of 206 families with cavernous malformations.

Laurans MS, DiLuna ML, Shin D, Niazi F, Voorhees JR, Nelson-Williams C, Johnson EW, Siegel AM, Steinberg GK, Berg MJ, Scott RM, Tedeschi G, Enevoldson TP, Anson J, Rouleau GA, Ogilvy C, Awad IA, Lifton RP, Gunel M. Laurans MS, et al. Among authors: siegel am. J Neurosurg. 2003 Jul;99(1):38-43. doi: 10.3171/jns.2003.99.1.0038. J Neurosurg. 2003. PMID: 12854741

9

[Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families].

Siegel AM, Bertalanffy H, Dichgans JJ, Elger CE, Hopf H, Hopf N, Keidel M, Kleider A, Nowak G, Pfeiffer RA, Schramm J, Spuck S, Stefan H, Sure U, Baumann CR, Rouleau GA, Verlaan DJ, Andermann E, Andermann F. Siegel AM, et al. Nervenarzt. 2005 Feb;76(2):175-80. doi: 10.1007/s00115-004-1779-3. Nervenarzt. 2005. PMID: 15702360 German.

10

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families.

Graeni C, Stepper F, Sturzenegger M, Merlo A, Verlaan DJ, Andermann F, Baumann CR, Bonassin F, Georgiadis D, Baumgartner RW, Rouleau GA, Siegel AM. Graeni C, et al. Among authors: siegel am. Neurosurg Rev. 2010 Jan;33(1):47-51. doi: 10.1007/s10143-009-0225-1. Epub 2009 Sep 17. Neurosurg Rev. 2010. PMID: 19760287 Free article.

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