Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm

Paroxysmal exercise-induced dystonia due to GLUT1 mutation can be responsive to levodopa: a case report

(2014) Francesca Baschieri et al.   JOURNAL OF NEUROLOGY

The impact and prognosis for dystonia in childhood including dystonic cerebral palsy: a clinical and demographic tertiary cohort study

(2014) J.-P. Lin et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Phenotypic Spectrum of Glucose Transporter Type 1 Deficiency Syndrome (Glut1 DS)

(2013) Toni S. Pearson et al.   Current Neurology and Neuroscience Reports

Homovanillic acid in cerebrospinal fluid of 1388 children with neurological disorders

(2013) Marta Molero-Luis et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Miglustat: A Review of Its Use in Niemann-Pick Disease Type C

(2013) Katherine A. Lyseng-Williamson   DRUGS

A Post-Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases

(2013) Kornelia Neveling et al.   HUMAN MUTATION

Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study

(2013) Maarten J Titulaer et al.   LANCET NEUROLOGY

Phenomenology and classification of dystonia: A consensus update

(2013) Alberto Albanese et al.   MOVEMENT DISORDERS

Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

(2013) Michael Zech et al.   MOVEMENT DISORDERS

Special concerns in defining, studying, and treating dystonia in children

(2013) Jonathan W. Mink   MOVEMENT DISORDERS

Development and validation of a clinical guideline for diagnosing blepharospasm

(2013) G. Defazio et al.   NEUROLOGY

Treatment of Dystonia

(2013) Mary Ann Thenganatt et al.   Neurotherapeutics

Disease and patient characteristics in NP-C patients: findings from an international disease registry

(2013) Marc C Patterson et al.   Orphanet Journal of Rare Diseases

Dopa-Responsive Dystonia Revisited

(2012) Vera Tadic et al.   ARCHIVES OF NEUROLOGY

Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study

(2012) RUSSELL C DALE et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Treatment for dystonia in childhood

(2012) A. Roubertie et al.   EUROPEAN JOURNAL OF NEUROLOGY

Next-generation sequencing demands next-generation phenotyping

(2012) Raoul C.M. Hennekam et al.   HUMAN MUTATION

Autoimmune Basal Ganglia Disorders

(2012) Russell C. Dale et al.   JOURNAL OF CHILD NEUROLOGY

Genetic insights into the causes and classification of the cerebral palsies

(2012) Andres Moreno-De-Luca et al.   LANCET NEUROLOGY

Treatable inborn errors of metabolism causing intellectual disability: A systematic literature review

(2012) Clara D.M. van Karnebeek et al.   MOLECULAR GENETICS AND METABOLISM

Dystonia with brain manganese accumulation resulting fromSLC30A10mutations: A new treatable disorder

(2012) Maria Stamelou et al.   MOVEMENT DISORDERS

Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites

(2012) R. Saunders-Pullman et al.   NEUROLOGY

Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

(2012) Joep de Ligt et al.   NEW ENGLAND JOURNAL OF MEDICINE

Sepiapterin reductase deficiency: A Treatable Mimic of Cerebral Palsy

(2011) Jennifer Friedman et al.   ANNALS OF NEUROLOGY

Spectrum of movement disorders in encephalitis

(2010) U. K. Misra et al.   JOURNAL OF NEUROLOGY

Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis

(2010) Josep Dalmau et al.   LANCET NEUROLOGY

Definition and classification of hyperkinetic movements in childhood

(2010) Terence D. Sanger et al.   MOVEMENT DISORDERS

Dyskinetic cerebral palsy in Europe: trends in prevalence and severity

(2009) K Himmelmann et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Movement disorders in neuro-metabolic diseases

(2009) Neziha Gouider-Khouja et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Inborn errors of metabolism and motor disturbances in children

(2009) A. García-Cazorla et al.   JOURNAL OF INHERITED METABOLIC DISEASE