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Journal of General Internal Medicine|December 5, 2024
Automated Text Message-Based Program to Improve Uncontrolled Blood Pressure in Primary Care Patients: A Randomized Clinical TrialEric Bressman, Klea Profka, Laurie Norton, et al.Annals of Neurology|November 30, 1999
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31T G Nygaard, D Raymond, C Chen, et al.Neurobiology of Disease|August 20, 2019
Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competitionElena Arystarkhova, Ihtsham U Haq, Timothy Luebbert, et al.Journal of Aquatic Animal Health|April 4, 2025
Identical sequence types of Yersinia ruckeri associated with lethal disease in wild-caught invasive Blue Catfish and cultured hybrid catfish (Channel Catfish ♀ × Blue Catfish ♂) from disparate aquatic ecosystemsChristine L Densmore, Madeleine Hendrix, Stephen R Reichley, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterizationRachel Saunders-Pullman, Johann Hagenah, Vijay Dhawan, et al.Frontiers in Neurology|June 6, 2019
Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's DiseaseTal Kozlovski, Alexis Mitelpunkt, Avner Thaler, et al.Neurology|March 9, 2005
High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screeningJ Hagenah, R Saunders-Pullman, K Hedrich, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2022
Differences in Sex-Specific Frequency of Glucocerebrosidase Variant Carriers and Familial ParkinsonismRoberto A Ortega, Susan B Bressman, Deborah Raymond, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|January 30, 2013
Neural correlates of executive functions in healthy G2019S LRRK2 mutation carriersAvner Thaler, Anat Mirelman, Rick C Helmich, et al.Human Molecular Genetics|June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.Pageof 30