Disease: Paroxysmal nonkinesigenic dyskinesia
- <em>KCNMA1</em>-linked channelopathy
- <em>PRRT2</em> mutation in a Japanese woman: Adult-onset focal epilepsy coexisting with movement disorders and cerebellar atrophy
- A case of familial paroxysmal nonkinesigenic dyskinesia due to mutation of the PNKD gene in Chinese Mainland
- A Challenging Diagnosis of Atypical Glut1-DS: A Case Report and Literature Review
- A family with paroxysmal nonkinesigenic dyskinesia: genetic and treatment issues
- A family with paroxysmal nonkinesigenic dyskinesias (PNKD): evidence of mitochondrial dysfunction
- A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia
- A New Alternative Drug With Fewer Adverse Effects in the Treatment of Sydenham Chorea: Levetiracetam Efficacy in a Child
- A PDGFB mutation causes paroxysmal nonkinesigenic dyskinesia with brain calcification
- A rare paroxysmal movement disorder: mixed type of paroxysmal dyskinesia
- Accumulation of plasmacytoid dendritic cell is associated with a treatment response to DNA-damaging treatment and favorable prognosis in lung adenocarcinoma
- An emerging spectrum of variants and clinical features in <em>KCNMA1</em>-linked channelopathy
- Atypical Manifestations in Glut1 Deficiency Syndrome
- Bilateral deep brain stimulation for treatment of medically refractory paroxysmal nonkinesigenic dyskinesia
- BK channel properties correlate with neurobehavioral severity in three <em>KCNMA1</em>-linked channelopathy mouse models
- BK Channelopathies and <em>KCNMA1</em>-Linked Disease Models
- Classification of involuntary movements in dogs: Paroxysmal dyskinesias
- Clinical Features and Treatment in the Spectrum of Paroxysmal Dyskinesias: An Observational Study in South-West Castilla y Leon, Spain
- Clinical Features in Border Terrier Dogs with Paroxysmal Involuntary Movements
- Clonal lineage tracing reveals shared origin of conventional and plasmacytoid dendritic cells
- Damaging novel mutations in PIGN cause developmental epileptic-dyskinetic encephalopathy: a case report
- Dopamine dysregulation in a mouse model of paroxysmal nonkinesigenic dyskinesia
- EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency
- Effective Treatment of Paroxysmal Nonkinesigenic Dyskinesia With Oxcarbazepine
- Epileptic chorea: Another window into neural networks?
- Expanding the Phenotype of Homozygous <em>KCNMA1</em> Mutations; Dyskinesia, Epilepsy, Intellectual Disability, Cerebellar and Corticospinal Tract Atrophy
- Familial choreoathetosis due to novel heterozygous mutation in PDE10A
- Familial nonkinesigenic paroxysmal dyskinesia and intracranial calcifications: a new syndrome?
- Familial paroxysmal kinesigenic dyskinesia. A case description
- Familial paroxysmal nonkinesigenic dyskinesia: clinical and genetic analysis of a Taiwanese family
- Fatal paroxysmal non-kinesigenic dyskinesia
- Generalized Dystonia and Paroxysmal Dystonic Attacks due to a Novel <em>ATP1A3</em> Variant
- Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis
- Genetic Links to Episodic Movement Disorders: Current Insights
- Genetic updates on paroxysmal dyskinesias
- Genetics of dystonia
- Genetics of paroxysmal dyskinesias
- Genome-wide screening identifies Trim33 as an essential regulator of dendritic cell differentiation
- Hemiplegic Migraine in Glut1 Deficiency Syndrome and Paroxysmal Dyskinesia at Ketogenic Diet Induction: Case Report and Literature Review
- Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences
- Human CD34<sup>+</sup>-derived complete plasmacytoid and conventional dendritic cell vaccine effectively induces antigen-specific CD8<sup>+</sup> T cell and NK cell responses in vitro and in vivo
- Hyperglycemic unilateral choreoathetosis: hyperdensity of the contralateral basal ganglia on CT
- Innovative prognostic modeling in ESCC: leveraging scRNA-seq and bulk-RNA for dendritic cell heterogeneity analysis
- Interspecies comparison of the early transcriptomic changes associated with hepatitis B virus exposure in human and macaque immune cell populations
- Isolated Paroxysmal Non-kinesigenic Dystonia Associated with Homozygous PDHB Variant in an Indian Family
- Late onset of atypical paroxysmal non-kinesigenic dyskinesia with remote history of Graves' disease
- Lisdexamfetamine Therapy in Paroxysmal Non-kinesigenic Dyskinesia Associated with the <em>KCNMA1</em>-N999S Variant
- Mitochondrial HIGD1A inhibits hepatitis B virus transcription and replication through the cellular PNKD-NF-κB-NR2F1 nexus
- Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review
- Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients
- Myofibrillogenesis regulator 1 (MR-1): a potential therapeutic target for cancer and PNKD
- Nonketotic hyperglycemia presenting as choreoathetosis in a female schizophrenia patient
- Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation
- Paroxismal non-kinesigenic dyskinesia and hemidystonia associated with silent celiac disease
- Paroxysmal choreodystonic disorders
- Paroxysmal dyskinesia as an unusual and only presentation of subcortical white matter ischaemia: a report of two cases
- Paroxysmal Dyskinesia in Children: from Genes to the Clinic
- Paroxysmal dyskinesias
- Paroxysmal dyskinesias
- Paroxysmal Dyskinesias
- Paroxysmal dyskinesias - disorder categories, their causes and treatment
- Paroxysmal dyskinesias revisited: a review of 500 genetically proven cases and a new classification
- Paroxysmal Genetic Movement Disorders and Epilepsy
- Paroxysmal movement disorders
- Paroxysmal movement disorders
- Paroxysmal movement disorders - practical update on diagnosis and management
- Paroxysmal movement disorders and episodic ataxias
- Paroxysmal movement disorders: An update
- Paroxysmal movement disorders: Paroxysmal dyskinesia and episodic ataxia
- Paroxysmal Non-Kinesigenic Choreoathetosis Case Report and a Review of the Pathogenesis
- Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European families
- Paroxysmal non-kinesigenic dyskinesia, post-streptococcal syndromes and psychogenic movement disorders: a diagnostic challenge
- Paroxysmal Non-Kinesigenic Dyskinesia: Utility of the Quantification of GLUT1 in Red Blood Cells
- Paroxysmal nonkinesigenic dyskinesia with depression treated by bilateral electroconvulsive therapy
- Paroxysmal nonkinesigenic dyskinesia with tremor
- Paroxysmal Nonkinesigenic Dyskinesias Responsive to Carbamazepine in Fahr Syndrome: A Case Report
- Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis
- Phenotypes, genotypes, and the management of paroxysmal movement disorders
- Protein mutated in paroxysmal dyskinesia interacts with the active zone protein RIM and suppresses synaptic vesicle exocytosis
- PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation?
- PRRT2 gene-related paroxysmal disorders
- PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
- PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures
- Re-evaluation of PRRT2 mutations in paroxysmal disorders
- Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy
- RSM22, mtYsxC and PNKD-like proteins are required for mitochondrial translation in Trypanosoma brucei
- Screening of the <em>TMEM151A</em> Gene in Patients With Paroxysmal Kinesigenic Dyskinesia and Other Movement Disorders
- Striatal Indirect Pathway Dysfunction Underlies Motor Deficits in a Mouse Model of Paroxysmal Dyskinesia
- Striatal infarct with paroxysmal nonkinesigenic dyskinesia
- Successful treatment of disabling paroxysmal nonkinesigenic dyskinesia with deep brain stimulation of the globus pallidus internus
- Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis
- The Choreoathetotic Movement of Paroxysmal Nonkinesigenic Dyskinesia
- The clinical and genetic heterogeneity of paroxysmal dyskinesias
- The Clinical and Serological Effect of a Gluten-Free Diet in Border Terriers with Epileptoid Cramping Syndrome
- The Potential Immunomodulatory Effect of <em>Bifidobacterium longum</em> subsp. <em>longum</em> BB536 on Healthy Adults through Plasmacytoid Dendritic Cell Activation in the Peripheral Blood
- Transient Ischemic Attack after Eating Spicy Foods in Children: Think of Moya Moya Disease
- Treatment of Paroxysmal Dyskinesia
- Treatment of paroxysmal dyskinesias in children
- Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease
- Varied phenotypic spectrum presenting of paroxysmal exercise-induced dyskinesia: a Turkish family with SLC2A1 mutation