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of 3
pro vyhledávání: '"Simon, Novak"'
Autor:
Harald Weng, Andreas Gerhardinger, Eva Rossier, Alina Henn, Günther Rettenberger, Simon Novak, Birgit Zirn
Publikováno v:
Clinical Dysmorphology. 27:27-30
Heterozygous microdeletions of chromosome 2p21 encompassing only the SIX2 gene have been described in two families to date. The clinical phenotype comprised autosomal-dominant inherited frontonasal dysplasia with ptosis in one family. In the second f
Autor:
Judith, Kröll-Seger, Ian William, Mothersill, Simon, Novak, Ritva Anneli, Sälke-Kellermann, Günter, Krämer
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 8(3)
We report on a 3-year-old boy with myoclonic-astatic epilepsy who developed myoclonic status epilepticus with continuous twitching of the face and unresponsiveness under monotherapy with levetiracetam. Recently, a nonconvulsive status epilepticus in
Autor:
Christian Herdeg, Karl K. Haase, Alexander Kranzhöfer, Armin Bohnet, Karl R. Karsch, Barbara Horch, Hartmut Hanke, Andreas Baumbach, Simon Novak, Martin Oberhoff
Publikováno v:
Cardiovascular research. 38(3)
Objective: Recent investigations revealed the importance of endothelial cell integrity and function in the pathogenesis of restenosis after angioplasty. Agents which stimulate reendothelialization may prevent restenosis after interventional procedure