Bettina Balint (B Balint)

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Topics

Botulinum Toxin

Affordable Care Act

Cognitive Impairment

Top Venues

Movement disorders clinical practice

European journal of neurology

Movement disorders : official journal of the Movement Disorder Society

This page only lists publications with an associated author ORCID identifier.

Publications

Bettina Balint, Shermyn Xiumin Neo, Francesca Magrinelli, Eoin Mulroy, Anna Latorre, Maria Stamelou, Huw R Morris, Amit Batla, Kailash P Bhatia
Ethnic Differences in Atypical Parkinsonism-is South Asian PSP Different? Movement disorders clinical practice (2024)
Kailash P Bhatia, Bettina Balint
Autoimmunity Panels: Needs and Implementation in the Underdeveloped Regions and how to Approach the Disparities. Movement disorders clinical practice 11 (2) (2023)
Lisette H Koens, Marrit R Klamer, Deborah A Sival, Bettina Balint, Kailash P Bhatia, Maria Fiorella Contarino, Martje E van Egmond, Roberto Erro, Jennifer Friedman, Victor S C Fung, Christos Ganos, Manju A Kurian, Anthony E Lang, Eavan M McGovern, Emmanuel Roze, Tom J de Koning, Marina A J Tijssen
A Screening Tool to Quickly Identify Movement Disorders in Patients with Inborn Errors of Metabolism. Movement disorders : official journal of the Movement Disorder Society (2023)
Kailash P Bhatia, Bettina Balint
Autoimmunity Panels: Needs and Implementation in the Underdeveloped Regions and how to Approach the Disparities. Movement disorders clinical practice 11 (2) (2023)
Evdokia Efthymiou, Christian R Baumann, Bettina Balint
The Expanding Field of Autoimmune Sleep-Wake Disorders-Implications for the Movement Disorders Clinical Practice. Movement disorders clinical practice 10 (10) (2023)
Kailash P Bhatia, Bettina Balint
Autoimmunity Panels: Needs and Implementation in the Underdeveloped Regions and how to Approach the Disparities. Movement disorders clinical practice 11 (2) (2023)
Benjamin Vlad, Ilijas Jelcic, Bettina Balint
Parkinsonism due to Coxsackie B Virus Infection-Case Report and Literature Review. Movement disorders clinical practice 10 (Suppl 3) (2023)
Bettina Balint
Isolated Dystonia with NMDAR Antibodies: Expanding the Phenotype or Illustrating the Intricacies of Antibody Testing? Movement disorders clinical practice 10 (4) (2023)
Bettina Balint
Relevance of Antibody Testing in Movement Disorders. Movement disorders clinical practice 10 (Suppl 2) (2023)
Daniel Macías-García, Bettina Balint
Disentangling the Phenotypes of Anti-IgLON5 Disease: When Clinical Suspicion Matters. Movement disorders clinical practice 9 (4) (2022)
Eoin Mulroy, Bettina Balint, Kailash P Bhatia
Homer-3 Antibody Disease: A Potentially Treatable MSA-C Mimic. Movement disorders clinical practice 9 (2) (2022)
Emilia M Gatto, Ruth H Walker, Claudio Gonzalez, Martin Cesarini, Giovanni Cossu, Christopher D Stephen, Bettina Balint, Maria C Rodriguez Oroz, Joseph Jankovic, Francesca Morgante, Hyder A Jinnah, null null
Worldwide barriers to genetic testing for movement disorders. European journal of neurology 28 (6) (2021)
Bettina Balint, Kailash P Bhatia, Josep Dalmau
Reply to: Comparing VUS and AUS: Parallels and Differences in Neurogenetics and Neuroimmunology. Movement disorders : official journal of the Movement Disorder Society 36 (10) (2021)
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, Anna Latorre, Mark J Edwards, Bettina Balint, Purba Basu, Christopher Kobylecki, Sergiu Groppa, Anaita Hegde, Eoin Mulroy, Carlos Estevez-Fraga, Anshita Arora, Hrishikesh Kumar, Susanne A Schneider, Patrick A Lewis, Zane Jaunmuktane, Tamas Revesz, Sonia Gandhi, Nicholas W Wood, John A Hardy, Michele Tinazzi, Vivek Lal, Henry Houlden, Kailash P Bhatia
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism. Movement disorders : official journal of the Movement Disorder Society (2021)
Bettina Balint, R Guerreiro, S Carmona, N Dehghani, Anna Latorre, C Cordivari, K P Bhatia, J Bras
KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia. European journal of neurology 27 (8) (2020)
Bettina Balint, G Charlesworth, M Stamelou, L Carr, N E Mencacci, N W Wood, K P Bhatia
Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy. European journal of neurology 26 (9) (2019)