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Frontiers in Neurology|April 5, 2021
Modeling and Bioinformatics Identify Responders to G-CSF in Patients With Amyotrophic Lateral SclerosisSiw Johannesen, J Russell Huie, Bettina Budeus, et al.
Annals of Neurology|March 15, 2016
GSK3ß-dependent dysregulation of neurodevelopment in SPG11-patient induced pluripotent stem cell modelHimanshu K Mishra, Iryna Prots, Steven Havlicek, et al.
Annals of Neurology|December 11, 2007
Long-term course and mutational spectrum of spatacsin-linked spastic paraplegiaUte Hehr, Peter Bauer, Beate Winner, et al.
Brain & Development|October 24, 2015
LIS1-associated classic lissencephaly: A retrospective, multicenter survey of the epileptogenic phenotype and response to antiepileptic drugsSaskia M Herbst, Christiane R Proepper, Tobias Geis, et al.
Oligonucleotides|July 20, 2007
Inhibition of TGF-beta2 with AP 12009 in recurrent malignant gliomas: from preclinical to phase I/II studiesPeter Hau, Piotr Jachimczak, Reimar Schlingensiepen, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
47 patients with FLNA associated periventricular nodular heterotopiaMax Lange, Burkhard Kasper, Axel Bohring, et al.
Neuropediatrics|August 30, 2024
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly PatientsChristiane R Proepper, Sofia M Schuetz, Lisa-Maria Schwarz, et al.
Orphanet Journal of Rare Diseases|May 23, 2026
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephalyChristiane R Proepper, Lisa-Maria Schwarz, Sofia M Schuetz, et al.
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