(Q29041708)

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

0 references

Howard L Geyer

1

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

Susan B Bressman

series ordinal

2

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

publication date

September 2006

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

volume

5

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

issue

9

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https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

27 March 2017

page(s)

780-790

1 reference

https://doi.org/10.1016%2FS1474-4422%2806%2970547-6

Primary writing tremor. A form of focal dystonia?

27 March 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Primary writing tremor.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Neurophysiological investigations in patients with primary writing tremor

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Changes in cortical inhibition during task-specific contractions in primary writing tremor patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia musculorum deformans. Analysis with electromyography.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Idiopathic cervical dystonia: clinical characteristics

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

The natural history and treatment of acquired hemidystonia: report of 33 cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Remission in spasmodic torticollis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Spontaneous remissions in spasmodic torticollis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in 61-year-old identical twins: observations over 45 years

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Spread of symptoms in idiopathic torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Age at onset as a factor in determining the phenotype of primary torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Epidemiology of focal and generalized dystonia in Rochester, Minnesota

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Genetic contribution to idiopathic adult-onset blepharospasm and cranial-cervical dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

A genetic study of idiopathic focal dystonias

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

The DYT1 phenotype and guidelines for diagnostic testing

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Autosomal recessive, DYT2-like primary torsion dystonia: a new family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Hereditary whispering dysphonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Idiopathic torsion dystonia: assignment of a gene to chromosome 18p in a German family with adult onset, autosomal dominant inheritance and purely focal distribution

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Paroxysmal kinesigenic choreoathetosis locus maps to chromosome 16p11.2-q12.1.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Phenotypic characterization of DYT13 primary torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial-cervical or upper limb onset

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Neuropathology of a case of dopa-responsive dystonia associated with a new genetic locus, DYT14.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

A novel locus for inherited myoclonus-dystonia on 18p11.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

The AAA+ protein torsinA interacts with a conserved domain present in LAP1 and a novel ER protein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspects.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Autosomal dominant guanosine triphosphate cyclohydrolase I deficiency (Segawa disease).

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dopa-responsive dystonia simulating cerebral palsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dopa-responsive childhood dystonia: a forme fruste with writer's cramp, triggered by exercise

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

GCH1 mutation in a patient with adult-onset oromandibular dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Long-term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa-responsive dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Lessons from a remarkable family with dopa-responsive dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

GTP cyclohydrolase I mutations in patients with dystonia responsive to anticholinergic drugs

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Recessively inherited L-DOPA-responsive dystonia caused by a point mutation (Q381K) in the tyrosine hydroxylase gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

A common point mutation in the tyrosine hydroxylase gene in autosomal recessive L-DOPA-responsive dystonia in the Dutch population

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: a clinical and molecular study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Alcohol-responsive myoclonic dystonia in a large family: dominant inheritance and phenotypic variation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

PROGRESSIVE LENTICULAR DEGENERATION: A FAMILIAL NERVOUS DISEASE ASSOCIATED WITH CIRRHOSIS OF THE LIVER

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

1 reference

7 January 2021

Cardiac Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Parkin disease: a phenotypic study of a large case series

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Camptocormia as a form of dystonia in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Camptocormia: pathogenesis, classification, and response to therapy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in corticobasal degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Limb dystonia in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dystonia in multiple system atrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Multiple system atrophy: a review of 203 pathologically proven cases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Clinical variants of idiopathic torsion dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Mid-brain pathology of Wilson's disease: MRI analysis of three cases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

The "double panda sign" in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Hallervorden and history

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Hallervorden-Spatz syndrome: clinical and magnetic resonance imaging correlations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Regional metabolism in primary torsion dystonia: effects of penetrance and genotype

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Decreased striatal D2 receptor binding in non-manifesting carriers of the DYT1 dystonia mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Cervical dystonia due to spinal cord ependymoma: involvement of cervical cord segments in the pathogenesis of dystonia.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Secondary cervical dystonia associated with structural lesions of the central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Hand dystonia secondary to cervical demyelinating lesion

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Successful treatment of childhood onset symptomatic dystonia with levodopa

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Oral phenylalanine loading in dopa-responsive dystonia: a possible diagnostic test

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Reduced lymphoblast neopterin detects GTP cyclohydrolase dysfunction in dopa-responsive dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dopa-responsive dystonia: A clinical and molecular genetic study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Dopa-responsive dystonia: mutation analysis of GCH1 and analysis of therapeutic doses of L-dopa. German Dystonia Study Group

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Treatment of Wilson Disease With Ammonium Tetrathiomolybdate

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Wilson's disease in patients presenting with liver disease: a diagnostic challenge.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Diagnostic significance of reduced serum caeruloplasmin concentration in neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Late-onset Wilson's disease with neurological involvement in the absence of Kayser-Fleischer rings

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Neurologic presentation of Wilson disease without Kayser-Fleischer rings

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Type C Niemann-Pick disease: spectrum of phenotypic variation in disruption of intracellular LDL-derived cholesterol processing

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021

Progressive dementia and epilepsy in a young adult: unusual intraneuronal inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2806%2970547-6

7 January 2021