Martin Häusler

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in <i>KCNJ10</i>

Ute I. Scholl, Murim Choi, Tiewen Liu et al. · Proceedings of the National Academy of Sciences · 2009 · 484 citations · Full text

Clinical Disorders, Mendelian Disorder, Genetic Disorder +14

Clinical and neuroradiological differences of paediatric acute disseminating encephalomyelitis with and without antibodies to the myelin oligodendrocyte glycoprotein

Matthias Baumann, Kamil Şahin, Christian Lechner et al. · Journal of Neurology Neurosurgery & Psychiatry · 2014 · 310 citations

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10

Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood

Andreas van Baalen, Martin Häusler, Rainer Boor et al. · Epilepsia · 2010 · 229 citations · Full text

Rituximab Treatment and Long-term Outcome of Patients With Autoimmune Encephalitis

Franziska Thaler, Luise Zimmermann, Stefan Kammermeier et al. · Neurology Neuroimmunology & Neuroinflammation · 2021 · 158 citations · Full text