Jonathan W. Mink
Affiliations: | University of Rochester, Rochester, NY |
Area:
Motor System, Movement Disorders, Child Neurology, Batten DiseaseGoogle:
"Jonathan Mink"Mean distance: 13.53 (cluster 17) | S | N | B | C | P |
Parents
Sign in to add mentorDavid Adams | research assistant | 1978-1981 | Wesleyan | |
Harry M. Sinnamon | research assistant | 1978-1981 | Wesleyan | |
William Thomas Thach | grad student | 1981-1989 | Washington University | |
Joel S. Perlmutter | post-doc | Washington University | ||
(movement disorders fellowship) |
BETA: Related publications
See more...
Publications
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
Brima T, Freedman EG, Prinsloo KD, et al. (2024) Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): an auditory evoked potential study of the duration-evoked mismatch negativity (MMN). Journal of Neurodevelopmental Disorders. 16: 3 |
Brima T, Freedman EG, Prinsloo KD, et al. (2023) Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): An auditory evoked potential study of the duration-evoked mismatch negativity (MMN). Research Square |
Lewin AB, Murphy TK, Mink JW, et al. (2023) Brief youth self-report screener for tics: Can a subscale of the Motor tic, Obsession and compulsion, and Vocal tic Evaluation Survey (MOVES) identify tic disorders in youth? Evidence-Based Practice in Child and Adolescent Mental Health. 8: 1-11 |
Sapozhnikov Y, Mink JW, Augustine EF, et al. (2023) Teacher Knowledge of Tourette Syndrome and Associated Factors. Pediatric Neurology. 145: 80-87 |
Vermilion J, Augustine EF, Adams HR, et al. (2021) Risk Behaviors in Youth With and Without Tourette Syndrome. Pediatric Neurology. 126: 20-25 |
Masten MC, Augustine EF, Mink JW. (2021) Challenges of Phenotype-Genotype Correlations in Rare Diseases. Jama Ophthalmology. 139: 1323 |
Masten MC, Corre C, Paciorkowski AR, et al. (2021) A Diagnostic Confidence Scheme for CLN3 Disease. Journal of Inherited Metabolic Disease |
Augustine EF, Adams HR, de Los Reyes E, et al. (2021) Management of CLN1 Disease: International Clinical Consensus. Pediatric Neurology. 120: 38-51 |
Tang C, Han J, Dalvi S, et al. (2021) A human model of Batten disease shows role of CLN3 in phagocytosis at the photoreceptor-RPE interface. Communications Biology. 4: 161 |
Masten MC, Mink JW, Augustine EF. (2020) Batten disease: an expert update on agents in preclinical and clinical trials. Expert Opinion On Investigational Drugs. 1-6 |