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The Journal of Biological Chemistry|November 3, 2011
Identification of a new fatty acid synthesis-transport machinery at the peroxisomal membraneMerle Hillebrand, Søren W Gersting, Amelie S Lotz-Havla, et al.
EMBO Reports|November 10, 2016
Peroxisomal protein PEX13 functions in selective autophagyMing Y Lee, Rhea Sumpter, Zhongju Zou, et al.
Journal of Neuroimmunology|March 27, 2012
MicroRNA regulation in experimental autoimmune encephalomyelitis in mice and marmosets resembles regulation in human multiple sclerosis lesionsJuliane Lescher, Franziska Paap, Verena Schultz, et al.
The Lancet. Neurology|August 2, 2012
Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification studyHendrik Rosewich, Holger Thiele, Andreas Ohlenbusch, et al.
Neurology|February 14, 2014
The expanding clinical and genetic spectrum of ATP1A3-related disordersHendrik Rosewich, Andreas Ohlenbusch, Peter Huppke, et al.
AJNR. American Journal of Neuroradiology|March 10, 2026
Multiparametric MRI analysis of clinical outcome after hematopoietic stem cell transplantation in juvenile Metachromatic LeukodystrophyManuel Strölin, Samuel Gröschel, Christiane Kehrer, et al.
Clinical Neuroradiology|April 21, 2026
Automated Deep Learning-Based Demyelination Load Segmentation in Metachromatic LeukodystrophyPascal Martin, Joël Schaerer, Thomas Cajgfinger, et al.
Neurobiology of Disease|July 13, 2020
Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severityElinor Lazarov, Merle Hillebrand, Simone Schröder, et al.
Brain : a Journal of Neurology|November 13, 2024
ATP1A3 dysfunction causes motor hyperexcitability and afterhyperpolarization loss in a dystonia modelEvgeny E Akkuratov, Francesca Sorrell, Laurence D Picton, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|March 22, 2023
Retrospective Pediatric Cohort Study Validates NEOS Score and Demonstrates Applicability in Children With Anti-NMDAR EncephalitisMarc Nikolaus, Philipp Rausch, Kevin Rostásy, et al.
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