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NPJ Parkinson'S Disease|May 5, 2025
Differences in age-related distribution of CSF alpha-synuclein seeding and Alzheimer profiles between PD with and without GBA1 variantsStefanie Lerche, Isabel Wurster, Benjamin Roeben, et al.
Klinische Monatsblatter Fur Augenheilkunde|September 1, 2025
Patient Safety and Risk Management in an Accumulation of Postoperative Endophthalmitis Cases after Vitrectomy in a University Eye ClinicCarsten Framme, Helmut G Sachs, Maria Cartes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 25, 2011
Cerebrospinal fluid fatty acids in glucocerebrosidase-associated Parkinson's diseaseStefan P Schmid, Erwin D Schleicher, Alexander Cegan, et al.
Microbiome|October 2, 2023
Analysis of strain, sex, and diet-dependent modulation of gut microbiota reveals candidate keystone organisms driving microbial diversity in response to American and ketogenic dietsAnna C Salvador, M Nazmul Huda, Danny Arends, et al.
Zootaxa|July 30, 2023
Lessons from the genomic analysis of Hesperiidae (Lepidoptera) holotypes in the MIZA collection (Maracay, Venezuela)Jing Zhang, Qian Cong, Jinhui Shen, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|February 11, 2012
Early conversion to a sirolimus-based, calcineurin-inhibitor-free immunosuppression in the SMART trial: observational results at 24 and 36months after transplantationMarkus Guba, Johann Pratschke, Christian Hugo, et al.
Neurology|October 14, 2022
Cognitive-Driven Activities of Daily Living Impairment as a Predictor for Dementia in Parkinson Disease: A Longitudinal Cohort StudySara Becker, Merle Bode, Kathrin Brockmann, et al.
Annals of Neurology|July 12, 2019
Gait analysis with wearables predicts conversion to parkinson diseaseSilvia Del Din, Morad Elshehabi, Brook Galna, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|November 23, 2021
[Epidemiology and treatment of retinopathy of prematurity. The Hannover data in the Retina.net ROP registry from 2001-2017]Stella H Akman, Johanna M Pfeil, Andreas Stahl, et al.
Neurology|December 21, 2007
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like diseaseM Henneke, P Combes, S Diekmann, et al.
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