Search filters

List of works by Bettina Balint

"Atypical" atypical parkinsonism: Critical appraisal of a cohort.

scientific article published on 14 December 2016

: The Great Imitator of MSA-C Within the ILOCAs

ADCY5 mutations are another cause of benign hereditary chorea

scientific article

Animals in the Brain

Ataxia with Oculomotor Apraxia Type 1-New Mutation, Characteristic Phenotype

Author Correction: Dystonia

scientific article published on 19 October 2018

B cells undergo unique compartmentalized redistribution in multiple sclerosis

scientific article published on September 15, 2011

B-cell populations discriminate between pediatric- and adult-onset multiple sclerosis

scientific article published on 15 December 2016

Brachial Neuritis After Botulinum Toxin Injections for Cervical Dystonia: A Need for a Reappraisal?

Cortical pencil lining in neuroferritinopathy: a diagnostic clue

scientific article published on April 2015

De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions

scientific article published on April 2016

Deconstructing Fahr's disease/syndrome of brain calcification in the era of new genes

scientific article

Dystonia

scientific article published on 20 September 2018

Dystonia in handcuffs: a picture typical of Lesch‐Nyhan syndrome

Dystonia: an update on phenomenology, classification, pathogenesis and treatment

scientific article

Early Ataxia and Subsequent Parkinsonism: PLA2G6 Mutations Cause a Continuum Rather Than Three Discrete Phenotypes.

scientific article published on 31 March 2016

Facial tremor in dystonia

scientific article published on 21 May 2014

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

Friend or foe? IgLON5 antibodies in a novel tauopathy with prominent sleep movement disorder, ataxia, and chorea

scientific article

Functional neurological disorders in Parkinson disease

scientific article published on 16 March 2018

Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options

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

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

scientific article

Hot topic: PNKP mutations cause ataxia with oculomotor apraxia type 4.

scientific article

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

scientific article published on 11 August 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

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

Intermittent head drops: the differential spectrum

scientific article published on 17 June 2015

KCNN2 mutation in autosomal-dominant tremulous myoclonus-dystonia

scientific article published on 25 March 2020

KMT2B: A new twist in dystonia genetics.

scientific article published on 20 February 2017

Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy

scientific article published on 20 April 2019

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

scientific article

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

scientific article

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

scientific article published on 10 April 2018

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

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

article published in 2018

Pragmatic Treatment of Stiff Person Spectrum Disorders

Progressive encephalomyelitis with rigidity and myoclonus: a new variant with DPPX antibodies

scientific article

Quick Flicks: Association of Paroxysmal Kinesigenic Dyskinesia and Tics.

scientific article

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

scientific article published on 16 March 2017

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

Reply to: Young- onset multiple system atrophy

scientific article published on 01 December 2018

Revisiting the Syndrome of "Obsessional Slowness"

Stiff person syndrome and other immune-mediated movement disorders - new insights

scientific article published on 3 June 2016

Stimulus Sensitive Foot Myoclonus: A Clue to Coeliac Disease

article by Silvia Jesús et al published April 2019 in Movement disorders clinical practice

T-cell homeostasis in pediatric multiple sclerosis: old cells in young patients

scientific article

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

The clinical syndrome of dystonia with anarthria/aphonia

scientific article

The interleukin‐7 receptor α chain contributes to altered homeostasis of regulatory T cells in multiple sclerosis ⬇️

scientific article published on February 1, 2011

Why is there motor deterioration in Parkinson's disease during systemic infections-a hypothetical view

scientific article published on 27 August 2015

Young-onset multiple system atrophy: Clinical and pathological features

scientific article published on 01 July 2018

Paulina is supported by:

About Paulina

Help