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Annals of Neurology|September 3, 2002
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizuresWenli Gu, Eylert Brodtkorb, Ortrud K SteinleinSeizure|August 11, 2012
The PRRT2 mutation c.649dupC is the so far most frequent cause of benign familial infantile convulsionsOrtrud K Steinlein, M Villain, C KorenkeEpilepsy Research|December 4, 2003
No evidence for a seriously increased malignancy risk in LGI1-caused epilepsyEylert Brodtkorb, Karl O Nakken, Ortrud K SteinleinSeminars in Pediatric Neurology|July 26, 2002
Congenital myasthenic syndromesJoern P Sieb, Simone Kraner, Ortrud K SteinleinPlos One|December 27, 2018
Kidney cancer characteristics and genotype-phenotype-correlations in Birt-Hogg-Dubé syndromeElke C Sattler, Marlene Reithmair, Ortrud K SteinleinNeurogenetics|September 25, 2003
Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsyWenli Gu, Thomas Sander, Tim Becker, et al.Epilepsy Research|May 14, 2003
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2Karin Dedek, Lucia Fusco, Nicole Teloy, et al.BMC Medical Genetics|November 24, 2011
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfectaOrtrud K Steinlein, Eric Aichinger, Holger Trucks, et al.Frontiers in Medicine|November 29, 2023
Risk of pneumothorax in Birt-Hogg-Dubé syndrome during pregnancy and birthOrtrud K Steinlein, Marlene Reithmair, Zulfiya Syunyaeva, et al.Epilepsia|June 11, 2005
Speech-induced aphasic seizures in epilepsy caused by LGI1 mutationEylert Brodtkorb, Ralf P Michler, Wenli Gu, et al.Pageof 19