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List of works by Bettina Balint

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Glycine receptor antibodies in PERM and related syndromes: characteristics, clinical features and outcomes

scientific article published on June 20, 2014
Glatiramer acetate improves regulatory T-cell function by expansion of naive CD4(+)CD25(+)FOXP3(+)CD31(+) T-cells in patients with multiple sclerosis

scientific article published on 31 July 2009
Progressive encephalomyelitis with rigidity and myoclonus: a new variant with DPPX antibodies

scientific article
Interferon beta-induced restoration of regulatory T-cell function in multiple sclerosis is prompted by an increase in newly generated naive regulatory T cells

scientific article published in November 2008
ADCY5 mutations are another cause of benign hereditary chorea

scientific article
B cells undergo unique compartmentalized redistribution in multiple sclerosis

scientific article published on September 15, 2011
De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

scientific article published on April 2016
Dystonia: an update on phenomenology, classification, pathogenesis and treatment

scientific article
Fine-tuning of regulatory T cell function: the role of calcium signals and naive regulatory T cells for regulatory T cell deficiency in multiple sclerosis

scientific article published on 10 April 2013
The interleukin‐7 receptor α chain contributes to altered homeostasis of regulatory T cells in multiple sclerosis

scientific article published on February 1, 2011
T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients

scientific article
Movement disorders with neuronal antibodies: syndromic approach, genetic parallels and pathophysiology

scientific article
Dystonia

scientific article published on 20 September 2018
Cortical pencil lining in neuroferritinopathy: a diagnostic clue

scientific article published on April 2015
Importance of cerebrospinal fluid analysis in the era of McDonald 2010 criteria: a German-Austrian retrospective multicenter study in patients with a clinically isolated syndrome

scientific article published on 11 October 2016
B-cell populations discriminate between pediatric- and adult-onset multiple sclerosis

scientific article published on 15 December 2016
Stiff person syndrome and other immune-mediated movement disorders - new insights

scientific article published on 3 June 2016
Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes

scientific article
Redefining progressive encephalomyelitis with rigidity and myoclonus after the discovery of antibodies to glycine receptors

scientific article published on 16 March 2017
Functional neurological disorders in Parkinson disease

scientific article published on 16 March 2018
Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes

scientific article published on 31 March 2016
Young-onset multiple system atrophy: Clinical and pathological features

scientific article published on 01 July 2018
Why is there motor deterioration in Parkinson's disease during systemic infections-a hypothetical view

scientific article published on 27 August 2015
Friend or Foe? IgLON5 antibodies in a novel tauopathy with prominent sleep movement disorder, ataxia, and chorea

scientific article published on May 27, 2014
Facial tremor in dystonia

scientific article published on 21 May 2014
The clinical features, underlying immunology, and treatment of autoantibody-mediated movement disorders

scholarly article by Valentina Damato et al published 1 September 2018 in Movement Disorders
Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy

scientific article published on 20 April 2019
"Atypical" atypical parkinsonism: Critical appraisal of a cohort

scientific article published on 14 December 2016
Pragmatic Treatment of Stiff Person Spectrum Disorders

Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus

article published in 2018
Quick Flicks: Association of Paroxysmal Kinesigenic Dyskinesia and Tics

scientific article
Oculomotor apraxia and disrupted sleep with nocturnal ballistic bouts in ADCY5-related disease

scientific article published on 10 April 2018
Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options

KMT2B: A new twist in dystonia genetics

scientific article published on 20 February 2017
: The Great Imitator of MSA-C Within the ILOCAs

Hot topic: Recessive mutations in the a3(VI) collagen gene COL6A3 cause early‐onset isolated dystonia

scientific article published on August 11, 2015
Ataxia with Oculomotor Apraxia Type 1-New Mutation, Characteristic Phenotype

Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome

scientific article
Revisiting the Syndrome of "Obsessional Slowness"

Author Correction: Dystonia

scientific article published on 19 October 2018
Animals in the Brain

Reply to: Young- onset multiple system atrophy

scientific article published on 01 December 2018
Intermittent head drops: the differential spectrum

scientific article published on 17 June 2015
Stimulus Sensitive Foot Myoclonus: A Clue to Coeliac Disease

article by Silvia Jesús et al published April 2019 in Movement disorders clinical practice
The clinical syndrome of dystonia with anarthria/aphonia

scientific article
Reopening the case for anti-basal ganglia antibodies (ABGAs): identification of dopamine-2 receptor antibodies associated with movement disorders

scientific article published in June 2013
Paroxysmal Asymmetric Dystonic Arm Posturing-A Less Recognized but Characteristic Manifestation of ATP1A3-related disease

article by Bettina Balint et al published April 2019 in Movement disorders clinical practice
Hot topic: PNKP mutations cause ataxia with oculomotor apraxia type 4

scientific article published on March 11, 2016
Brachial Neuritis After Botulinum Toxin Injections for Cervical Dystonia: A Need for a Reappraisal?

KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia

scientific article published on 25 March 2020

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