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Orphanet Journal of Rare Diseases|May 2, 2023
The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continuedSimone Schröder, Gökhan Yigit, Yun Li, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2018
Polygenic load: Earlier disease onset but similar longitudinal progression in Parkinson's diseaseStefanie Lerche, Inga Liepelt-Scarfone, Isabel Wurster, et al.
Journal of Neurology|June 25, 2018
Validation of a novel Montreal Cognitive Assessment scoring algorithm in non-demented Parkinson's disease patientsPatricia Sulzer, Sara Becker, Walter Maetzler, et al.
Neurobiology of Aging|July 27, 2018
Deterioration of executive dysfunction in elderly with REM sleep behavior disorder (RBD)Stefanie Lerche, Gerrit Machetanz, Benjamin Roeben, et al.
Journal of Women'S Health (2002)|January 12, 2024
Declining Prevalence of <i>Trichomonas vaginalis</i> Diagnosed by Wet Mount in a Cohort of U.S. Women With and Without HIVElizabeth M Daubert, Jodie Dionne, Jessica Atrio, et al.
Frontiers in Neurology|December 4, 2023
Psychometric evaluation and reference values for the German Postconcussion Symptom Inventory (PCSI-SR8) in children aged 8-12 yearsMarina Zeldovich, Leonie Krol, Dagmar Timmermann, et al.
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