Diagnosis of dystonic syndromes—a new eight-question approach

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Nature Reviews Neurology

• Publication date

  2012-03-20

• Fields of study

  Medicine

• Identifiers
  DOI 10.1038/nrneurol.2012.39PMID 22430107
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Demonstration of striatopallidal iron deposition in chorea-acanthocytosis by susceptibility-weighted imaging

  2011cited by this paper
• Differential diagnosis of dystonia

  2010cited by this paper
• Inherited metabolic disorders and stroke part 2: homocystinuria, organic acidurias, and urea cycle disorders.

  2010cited by this paper
• THAP1 mutations (DYT6) are an additional cause of early-onset dystonia

  2010cited by this paper
• Dystonia‐plus syndromes

  2010cited by this paper
• Secondary dystonia – clinical clues and syndromic associations

  2010cited by this paper
• The diagnostic challenge of primary dystonia: Evidence from misdiagnosis

  2010cited by this paper
• The phenomenology of the geste antagoniste in primary blepharospasm and cervical dystonia

  2010cited by this paper
• Myoclonus‐dystonia: An update

  2009cited by this paper
• Complicated recessive dystonia parkinsonism syndromes

  2009cited by this paper
• Inborn errors of metabolism and motor disturbances in children

  2009cited by this paper
• The monogenic primary dystonias.

  2009cited by this paper
• Genetics and treatment of dystonia.

  2009cited by this paper
• Does neurophysiological testing provide the information we need to improve the clinical management of primary dystonia?

  2009cited by this paper
• Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.

  2009cited by this paper
• Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients

  2009cited by this paper
• The paroxysmal dyskinesias

  2009cited by this paper
• Psychogenic movement disorders

  2009cited by this paper
• Is this dystonia?

  2009cited by this paper
• Clinical and genetic delineation of neurodegeneration with brain iron accumulation

  2008cited by this paper
• T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation

  2008cited by this paper
• The Neurological Presentation of Ceruloplasmin Gene Mutations

  2008cited by this paper
• Hepatic cirrhosis, dystonia, polycythaemia and hypermanganesaemia—A new metabolic disorder

  2008cited by this paper
• Consensus Statement of the Movement Disorder Society on Tremor

  2008cited by this paper
• Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)

  2007cited by this paper
• Neurologic phenotypes associated with acanthocytosis

  2007cited by this paper
• Focal Hand Dystonia Secondary to Basal Ganglia Germinoma

  2007cited by this paper
• Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome

  2007cited by this paper
• Prevalence of cervical dystonia and spasmodic torticollis in the United States general population.

  2007cited by this paper
• Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.

  2006cited by this paper
• Brain MRI in neurodegeneration with brain iron accumulation with and without PANK2 mutations.

  2006cited by this paper
• PLA2G6, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron

  2006cited by this paper
• A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS‐ES Task Force

  2006cited by this paper
• Prevalence study of primary dystonia in Iceland

  2006cited by this paper
• The diagnosis of dystonia.

  2006cited by this paper
• Movement disorders associated with hyperthyroidism: Expanding the phenotype

  2006cited by this paper
• Secondary cervical dystonia in iatrogenic hypoparathyroidism associated with extensive brain calcifications.

  2006cited by this paper
• Severe tongue protrusion dystonia

  2006cited by this paper
• Wilson disease in septuagenarian siblings: Raising the bar for diagnosis

  2005cited by this paper
• Prevalence of movement disorders in men and women aged 50-89 years (Bruneck Study cohort): a population-based study.

  2005cited by this paper
• Neuroacanthocytosis: new developments in a neglected group of dementing disorders.

  2005cited by this paper
• Neuroacanthocytosis

  2005cited by this paper
• Myoclonus–dystonia: Detection of novel, recurrent, and de novo SGCE mutations

  2004cited by this paper
• Management of movement disorders in glutaryl-CoA dehydrogenase deficiency: Anticholinergic drugs and botulinum toxin as additional therapeutic options

  2004cited by this paper
• Neurological disorders in 166 patients with basal ganglia calcification: a statistical evaluation

  2004cited by this paper
• Long-term course of l-dopa-responsive dystonia caused by tyrosine hydroxylase deficiency

  2004cited by this paper
• Clinical features of adult GM1 gangliosidosis: Report of three Indian patients and review of 40 cases

  2004cited by this paper
• Epidemiology of primary dystonia.

  2004cited by this paper
• Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

  2004cited by this paper
• Age at onset as a factor in determining the phenotype of primary torsion dystonia

  2004cited by this paper
• Wilson’s disease: diagnostic errors and clinical implications

  2004cited by this paper
• Faces of the giant panda and her cub: MRI correlates of Wilson’s disease

  2003cited by this paper
• Impaired sequence learning in carriers of the DYT1 dystonia mutation

  2003cited by this paper
• Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.

  2003cited by this paper
• Dystonia: A disorder of motor programming or motor execution?

  2002cited by this paper
• Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia.

  2002cited by this paper
• A case of aceruloplasminaemia: abnormal serum ceruloplasmin protein without ferroxidase activity

  2002cited by this paper
• The genetics of primary dystonias and related disorders.

  2002cited by this paper
• Acanthocytosis and neurological disorders

  2001cited by this paper
• Sensory function of basal ganglia

  2001cited by this paper
• Somatosensory disinhibition in dystonia

  2001cited by this paper
• Clinical report of three patients with hereditary hemochromatosis and movement disorders

  2000cited by this paper
• A lesion of the anterior thalamus producing dystonic tremor of the hand.

  2000cited by this paper
• Dystonia update.

  2000cited by this paper
• A prevalence study of primary dystonia in eight European countries

  2000cited by this paper
• Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease).

  1999cited by this paper
• Striatal biopterin and tyrosine hydroxylase protein reduction in dopa-responsive dystonia

  1999cited by this paper
• Alterations of motor cortical inhibition in patients with dystonia

  1998cited by this paper
• The natural history of tardive dystonia. A long-term follow-up study of 107 cases.

  1998cited by this paper
• Exteroceptive and interoceptive stimuli in dystonia

  1998cited by this paper
• Dystonia after striatopallidal and thalamic stroke: clinicoradiological correlations and pathophysiological mechanisms

  1998cited by this paper
• The role of DYT1 in primary torsion dystonia in Europe.

  1998cited by this paper
• Idiopathic focal dystonia: a disorder of muscle spindle afferent processing?

  1997cited by this paper
• Symptomatic Dystonias Associated with Structural Brain Lesions: Report of 16 Cases

  1996cited by this paper
• Is dystonia a sensory disorder?

  1995cited by this paper
• Movement disorders following lesions of the thalamus or subthalamic region

  1994cited by this paper
• Wilson's disease: the problem of delayed diagnosis.

  1992cited by this paper
• Symptomatic Dystonia: Clinical Profile of 46 Brazilian Patients

  1992cited by this paper
• Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.

  1991cited by this paper
• Idiopathic cervical dystonia: Clinical characteristics

  1991cited by this paper
• The neurotoxicology and pathology of organomercury, organolead, and organotin.

  1990cited by this paper
• 2-1. THE NEUROTOXICOLOGY AND PATHOLOGY OF ORGANOMERCURY, ORGANOLEAD, AND ORGANOTIN ( 「Environmental toxicology」)

  1990cited by this paper
• Idiopathic dystonia among ashkenazi jews: Evidence for autosomal dominant inheritance

  1989cited by this paper
• Epidemiology of focal and generalized dystonia in Rochester, Minnesota

  1988cited by this paper
• Dystonia in homocystinuria.

  1988cited by this paper
• The anatomical basis of symptomatic hemidystonia.

  1985cited by this paper
• Hemidystonia: a report of 22 patients and a review of the literature.

  1985cited by this paper
• The varied clinical expressions of dystonia.

  1984cited by this paper
• Hemi-dystonia secondary to localised basal ganglia tumour.

  1984cited by this paper
• Pure hemidystonia with basal ganglion abnormalities on positron emission tomography

  1984cited by this paper

• Dystonia: Far more than just a pain in the neck

  2024influential citation
• Oromandibular dystonia and temporomandibular disorders.

  2021cites this paper
• Phase-locked transcranial electrical brain stimulation for tremor suppression in dystonic tremor syndromes

  2021cites this paper
• The Dystonias.

  2019cites this paper
• The Dystonias.

  2019cites this paper
• Moving forward in childhood-onset movement disorders

  2019cites this paper
• Crossing barriers: a multidisciplinary approach to children and adults with young-onset movement disorders

  2018cites this paper
• Animal Models of Movement Disorders

  2017cites this paper
• Invited Review Dystonia

  2017cites this paper
• A post hoc study on gene panel analysis for the diagnosis of dystonia

  2017cites this paper
• Association analysis of TOR1A polymorphisms rs2296793 and rs3842225 in a Chinese population with cervical dystonia.

  2016cites this paper
• Generalized Torsion Dystonia

  2016cites this paper
• Dystonia: a clinician‘s guide to diagnosis, pathophysiology and treatment

  2014cites this paper
• A Beautician's Dystonia: Long-Lasting Effect of Botulinum Toxin

  2014cites this paper
• Striatal dopamine D1‐like receptor binding is unchanged in primary focal dystonia

  2013cites this paper
• Engineering animal models of dystonia

  2013cites this paper