Felbor U - Search Results

1

Authors' response to the letter by Dr. Eisa-Beygi.

Reinhard M, Schuchardt F, Meckel S, Heinz J, Felbor U, Sure U, Geisen U. Reinhard M, et al. Among authors: felbor u. J Neurol Sci. 2016 Oct 15;369:392. doi: 10.1016/j.jns.2016.06.057. Epub 2016 Jun 28. J Neurol Sci. 2016. PMID: 27393041 No abstract available.

2

Propranolol stops progressive multiple cerebral cavernoma in an adult patient.

Reinhard M, Schuchardt F, Meckel S, Heinz J, Felbor U, Sure U, Geisen U. Reinhard M, et al. Among authors: felbor u. J Neurol Sci. 2016 Aug 15;367:15-7. doi: 10.1016/j.jns.2016.04.053. Epub 2016 May 6. J Neurol Sci. 2016. PMID: 27423555

3

First large genomic inversion in familial cerebral cavernous malformation identified by whole genome sequencing.

Spiegler S, Rath M, Hoffjan S, Dammann P, Sure U, Pagenstecher A, Strom T, Felbor U. Spiegler S, et al. Among authors: felbor u. Neurogenetics. 2018 Jan;19(1):55-59. doi: 10.1007/s10048-017-0531-7. Epub 2017 Dec 2. Neurogenetics. 2018. PMID: 29197946

4

Loss of CCM3 impairs DLL4-Notch signalling: implication in endothelial angiogenesis and in inherited cerebral cavernous malformations.

You C, Sandalcioglu IE, Dammann P, Felbor U, Sure U, Zhu Y. You C, et al. Among authors: felbor u. J Cell Mol Med. 2013 Mar;17(3):407-18. doi: 10.1111/jcmm.12022. Epub 2013 Feb 7. J Cell Mol Med. 2013. PMID: 23388056 Free PMC article.

5

Highly variable intrafamilial manifestations of a CCM3 mutation ranging from acute childhood cerebral haemorrhage to late-onset meningiomas.

Fauth C, Rostasy K, Rath M, Gizewski E, Lederer AG, Sure U, Zschocke J, Felbor U. Fauth C, et al. Among authors: felbor u. Clin Neurol Neurosurg. 2015 Jan;128:41-3. doi: 10.1016/j.clineuro.2014.10.023. Epub 2014 Nov 6. Clin Neurol Neurosurg. 2015. PMID: 25462093 No abstract available.

6

Correlation of the venous angioarchitecture of multiple cerebral cavernous malformations with familial or sporadic disease: a susceptibility-weighted imaging study with 7-Tesla MRI.

Dammann P, Wrede K, Zhu Y, Matsushige T, Maderwald S, Umutlu L, Quick HH, Hehr U, Rath M, Ladd ME, Felbor U, Sure U. Dammann P, et al. Among authors: felbor u. J Neurosurg. 2017 Feb;126(2):570-577. doi: 10.3171/2016.2.JNS152322. Epub 2016 May 6. J Neurosurg. 2017. PMID: 27153162

7

Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex.

Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Sürücü O, Kunze E, Netzer C, Korenke C, Finckh U, Habek M, Poljakovic Z, Elbracht M, Rudnik-Schöneborn S, Bertalanffy H, Sure U, Felbor U. Stahl S, et al. Among authors: felbor u. Hum Mutat. 2008 May;29(5):709-17. doi: 10.1002/humu.20712. Hum Mutat. 2008. PMID: 18300272

8

A two-hit mechanism causes cerebral cavernous malformations: complete inactivation of CCM1, CCM2 or CCM3 in affected endothelial cells.

Pagenstecher A, Stahl S, Sure U, Felbor U. Pagenstecher A, et al. Among authors: felbor u. Hum Mol Genet. 2009 Mar 1;18(5):911-8. doi: 10.1093/hmg/ddn420. Epub 2008 Dec 16. Hum Mol Genet. 2009. PMID: 19088124 Free PMC article.

9

CCM1 gene deletion identified by MLPA in cerebral cavernous malformation.

Gaetzner S, Stahl S, Sürücü O, Schaafhausen A, Halliger-Keller B, Bertalanffy H, Sure U, Felbor U. Gaetzner S, et al. Among authors: felbor u. Neurosurg Rev. 2007 Apr;30(2):155-9; discussion 159-60. doi: 10.1007/s10143-006-0057-1. Epub 2006 Dec 23. Neurosurg Rev. 2007. PMID: 17187287

10

Cerebral cavernous malformation protein CCM1 inhibits sprouting angiogenesis by activating DELTA-NOTCH signaling.

Wüstehube J, Bartol A, Liebler SS, Brütsch R, Zhu Y, Felbor U, Sure U, Augustin HG, Fischer A. Wüstehube J, et al. Among authors: felbor u. Proc Natl Acad Sci U S A. 2010 Jul 13;107(28):12640-5. doi: 10.1073/pnas.1000132107. Epub 2010 Jun 24. Proc Natl Acad Sci U S A. 2010. PMID: 20616044 Free PMC article.

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