Elisa Schleider
Overview
Explore the profile of Elisa Schleider including associated specialties, affiliations and a list of published articles.
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Articles
4
Citations
206
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Recent Articles
1.
Schleider E, Stahl S, Wustehube J, Walter U, Fischer A, Felbor U
Neurogenetics
. 2010 Sep;
12(1):83-6.
PMID: 20862502
Mutations in CCM1, CCM2, or CCM3 lead to cerebral cavernous malformations, one of the most common hereditary vascular diseases of the brain. Endothelial cells within these lesions are the main...
2.
Voss K, Stahl S, Hogan B, Reinders J, Schleider E, Schulte-Merker S, et al.
Hum Mutat
. 2009 Apr;
30(6):1003-11.
PMID: 19370760
Cerebral cavernous malformations (CCMs) may cause recurrent headaches, seizures, and hemorrhagic stroke and have been associated with loss-of-function mutations in CCM1/KRIT1, CCM2, and CCM3/programmed cell death 10 (PDCD10). The CCM3/PDCD10...
3.
Stahl S, Gaetzner S, Voss K, Brackertz B, Schleider E, Surucu O, et al.
Hum Mutat
. 2008 Feb;
29(5):709-17.
PMID: 18300272
Cerebral cavernous malformations (CCM) are prevalent cerebrovascular lesions predisposing to chronic headaches, epilepsy, and hemorrhagic stroke. Using a combination of direct sequencing and MLPA analyses, we identified 15 novel and...
4.
Voss K, Stahl S, Schleider E, Ullrich S, Nickel J, Mueller T, et al.
Neurogenetics
. 2007 Jul;
8(4):249-56.
PMID: 17657516
Individuals carrying a mutation in one of the three cerebral cavernous malformation genes (CCM1/KRIT1, CCM2, CCM3) cannot be clinically distinguished, raising the possibility that they act within common molecular pathways....