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- 2023
-
Mark
Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy
(
- Contribution to journal › Article
-
Mark
Gut Microbiome Composition in Dystonia Patients
(
- Contribution to journal › Article
-
Mark
Comparison of dyskinesia profiles after L-DOPA dose challenges with or without dopamine agonist coadministration
(
- Contribution to journal › Article
- 2022
-
Mark
A relatively common hypomorphic variant in WARS2 causes monogenic disease
(
- Contribution to journal › Debate/Note/Editorial
- 2021
-
Mark
Striatal pathways in dyskinesia and dystonia
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Cross-disease analysis of depression, ataxia and dystonia highlights a role for synaptic plasticity and the cerebellum in the pathophysiology of these comorbid diseases
(
- Contribution to journal › Article
- 2020
-
Mark
Dystonia Non-Motor Symptoms Questionnaire (DNMSQuest) zur Erhebung nichtmotorischer Symptome bei Dystonie : Interkulturelle Adaptation in deutscher Sprache
(
- Contribution to journal › Article
-
Mark
New generation genetic testing entering the clinic
(
- Contribution to journal › Article
- 2019
-
Mark
Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemia
(
- Contribution to journal › Article
-
Mark
Variable Interpretation of the Dystonia Consensus Classification Items Compromises Its Solidity
(
- Contribution to journal › Article
-
Mark
Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia
(
- Contribution to journal › Article
- 2018
-
Mark
Animal models of l-dopa-induced dyskinesia in Parkinson's disease
(
- Contribution to journal › Scientific review
- 2017
-
Mark
A post hoc study on gene panel analysis for the diagnosis of dystonia
(
- Contribution to journal › Article
-
Mark
Using the shared genetics of dystonia and ataxia to unravel their pathogenesis
(
- Contribution to journal › Scientific review
-
Mark
Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation
(
- Contribution to journal › Debate/Note/Editorial
- 2016
-
Mark
Validation of an improved scale for rating L-DOPA-induced dyskinesia in the mouse and effects of specific dopamine receptor antagonists
(
- Contribution to journal › Article
-
Mark
Neurometabolic disorders are treatable causes of dystonia
(
- Contribution to journal › Article
-
Mark
Serotonergic perturbations in dystonia disorders-a systematic review
(
- Contribution to journal › Scientific review
- 2015
-
Mark
Practical guidance for CD management involving treatment of botulinum toxin: a consensus statement
(
- Contribution to journal › Scientific review
-
Mark
Non-motor symptoms in genetically defined dystonia : Homogenous groups require systematic assessment
(
- Contribution to journal › Scientific review
- 2013
-
Mark
Role of Gα(olf) in Familial and Sporadic Adult-Onset Primary Dystonia.
(
- Contribution to journal › Article
-
Mark
GNAL mutations cause adult-onset primary dystonia
(
- Contribution to journal › Published meeting abstract
- 2012
-
Mark
Genotype–phenotype correlations in THAP1 dystonia: Molecular foundations and description of new cases
(
- Contribution to journal › Article
- 2011
-
Mark
Diagnosis and Treatment of Common Forms of Tremor
(
- Contribution to journal › Article
- 2010
-
Mark
Familial late-onset focal dystonia in an African American family
(
- Contribution to journal › Published meeting abstract
- 2005
-
Mark
On the Causal Mechanisms of Stuttering
2005)(
- Thesis › Doctoral thesis (compilation)
- 2004
-
Mark
Stuttering and the basal ganglia circuits: a critical review of possible relations.
(
- Contribution to journal › Scientific review
- 2001
-
Mark
Pallidal and thalamic neurostimulation in severe tardive dystonia
(
- Contribution to journal › Article
- 1999
-
Mark
Clinical rating of dyskinesias in Parkinson's disease: use and reliability of a new rating scale
(
- Contribution to journal › Article