Expanding Knowledge of the Causes of Childhood Chorea

GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments

(2023) Maria Novelli et al.   PARKINSONISM & RELATED DISORDERS

Cachexia, chorea, and pain in chronic nonbacterial osteitis and inflammatory bowel disease: a case report

(2023) Ladan Agharokh et al.   Journal of Medical Case Reports

Chorea following SARS-CoV-2 infection and vaccination: a systematic review of reported cases

(2023) Elena Cecilia Rosca et al.   INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES

Efficacy of Caffeine in ADCY5 ‐Related Dyskinesia: A Retrospective Study

(2022) Aurélie Méneret et al.   MOVEMENT DISORDERS

Autoimmune and Paraneoplastic Chorea: A Review of the Literature

(2022) Kevin Kyle et al.   Frontiers in Neurology

The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders

(2022) Belén Pérez‐Dueñas et al.   MOVEMENT DISORDERS

RHOBTB2 mutations expand the phenotypic spectrum of alternating hemiplegia of childhood

(2021) Sara Zagaglia et al.   NEUROLOGY

Neurological manifestations of SARS-CoV-2 infection in hospitalised children and adolescents in the UK: a prospective national cohort study

(2021) Stephen T J Ray et al.   Lancet Child & Adolescent Health

A Novel Homozygous ADCY5 Variant is Associated with a Neurodevelopmental Disorder and Movement Abnormalities

(2021) Rauan Kaiyrzhanov et al.   Movement Disorders Clinical Practice

New-Onset Movement Disorders Associated with COVID-19

(2021) Pedro Renato P. Brandão et al.   Tremor and Other Hyperkinetic Movements

Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia

(2020) Diane Doummar et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Protein changes in synaptosomes of Huntington's disease knock-in mice are dependent on age and brain region

(2020) Ellen Sapp et al.   NEUROBIOLOGY OF DISEASE

Paroxysmal movement disorder with response to carbamazepine in a patient with RHOBTB2 developmental and epileptic encephalopathy

(2020) Carlotta Spagnoli et al.   PARKINSONISM & RELATED DISORDERS

Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect

(2019) Elodie Hainque et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

Phosphodiesterase 10A IgG

(2019) Anastasia Zekeridou et al.   NEUROLOGY

Chorea-related mutations in PDE10A result in aberrant compartmentalization and functionality of the enzyme

(2019) Gonzalo S. Tejeda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila

(2018) Jonas Straub et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea

(2018) Vincenzo Salpietro et al.   MOVEMENT DISORDERS

Takayasu arteritis in childhood: misdiagnoses at disease onset and associated diseases

(2018) Gleice Clemente et al.   RHEUMATOLOGY INTERNATIONAL

Inherited and Acquired Choreas

(2018) Claudio M. de Gusmao et al.   Seminars in Pediatric Neurology

Phosphodiesterase-10A Inverse Changes in Striatopallidal and Striatoentopeduncular Pathways of a Transgenic Mouse Model of DYT1 Dystonia

(2017) Vincenza D'Angelo et al.   JOURNAL OF NEUROSCIENCE

The distribution of phosphodiesterase 2A in the rat brain

(2012) D.T. Stephenson et al.   NEUROSCIENCE

A prospective study of acute movement disorders in children

(2010) RUSSELL C DALE et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Peripheral neuropathy and neurological disorders in an unselected Brazilian population-based cohort of IBD patients

(2007) G. R. Oliveira et al.   INFLAMMATORY BOWEL DISEASES