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Movement Disorders : Official Journal of the Movement Disorder Society|July 27, 2019
Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controlsIlir Agalliu, Roberto A Ortega, Marta San Luciano, et al.
Brain Injury|March 21, 2025
Quality of life after brain injury in children and adolescents questionnaire - validation of the proxy version (QOLIBRI-KID/ADO-Proxy)Nicole von Steinbuechel, Marina Zeldovich, Ivana Holloway, et al.
Nature|April 30, 2015
Th17 cells transdifferentiate into regulatory T cells during resolution of inflammationNicola Gagliani, Maria Carolina Amezcua Vesely, Andrea Iseppon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 20, 2016
Arm swing as a potential new prodromal marker of Parkinson's diseaseAnat Mirelman, Hagar Bernad-Elazari, Avner Thaler, et al.
European Journal of Human Genetics : EJHG|March 3, 2016
Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome)Alessia Micalizzi, Andrea Poretti, Marta Romani, et al.
Brain : a Journal of Neurology|October 21, 2017
Metformin reverses TRAP1 mutation-associated alterations in mitochondrial function in Parkinson's diseaseJulia C Fitzgerald, Alexander Zimprich, Daniel A Carvajal Berrio, et al.
Oncotarget|January 27, 2018
Personalized therapy: CNS HGNET-BCOR responsiveness to arsenic trioxide combined with radiotherapyClaudia Paret, Alexandra Russo, Henrike Otto, et al.
Neurology|January 4, 2013
Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutationsSabine Rudnik-Schöneborn, Jan Senderek, Joanna C Jen, et al.
Cell Stem Cell|March 12, 2013
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expressionPeter Reinhardt, Benjamin Schmid, Lena F Burbulla, et al.
Translational Psychiatry|January 22, 2019
Cognitive impairment and autistic-like behaviour in SAPAP4-deficient miceClaudia Schob, Fabio Morellini, Ora Ohana, et al.
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