• A Case of Drug-resistant Epilepsy Associated with Ring Chromosome 20
• A case of epilepsy with ring chromosome 20 syndrome
• A de novo supernumerary genomic discontinuous ring chromosome 21 in a child with mild intellectual disability
• A further case of familial ring chromosome 20 mosaicism - molecular characterization of the ring and review of the literature
• A patient with ring chromosome 20 syndrome and AGTR2 polymorphisms
• A unique clone involving multiple structural chromosome rearrangements in a myelodysplastic syndrome case
• Assessing the role of ketogenic dietary therapy in ring chromosome 20 syndrome: A patient-led approach
• Autosomal ring chromosomes in human genetic disorders
• Candidate Genes Associated with Delayed Neuropsychomotor Development and Seizures in a Patient with Ring Chromosome 20
• Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
• Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male
• Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20
• Chromosome imbalances associated with epilepsy
• Co-occurrence of 16p13.11 microdeletion and ring chromosome 20 syndrome
• Cognitive impairment and abnormal behaviour related to ring chromosome 20 aberration
• Comorbidities of Rare Epilepsies: Results from the Rare Epilepsy Network
• Continuous midazolam infusion for refractory nonconvulsive status epilepticus in children
• Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20
• Early pattern of epilepsy in the ring chromosome 20 syndrome
• Electro-clinical phenotypes of chromosome disorders associated with epilepsy in the absence of dysmorphism
• Electroclinical characteristics of a patient with ring chromosome 20 syndrome
• Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 years
• Electroclinical Improvement in a Patient with Ring Chromosome 20 Syndrome Treated with Zonisamide: A Case Report
• Emerging neuroimaging contribution to the diagnosis and management of the ring chromosome 20 syndrome
• Epilepsy and ring chromosome 20: case report
• Epilepsy in ring chromosome 20 syndrome
• Epilepsy in Ring Chromosome 20 Syndrome Might Have Variable Clinical Features
• Epilepsy responds to vagus nerve stimulation in ring chromosome 20 syndrome
• Epilepsy-related brain networks in ring chromosome 20 syndrome: an EEG-fMRI study
• Exploring dopaminergic activity in ring chromosome 20 syndrome: a SPECT study
• Exploring dopaminergic activity in ring chromosome 20 syndrome: a SPECT study
• Frontal motor seizure following non-convulsive status epilepticus in ring chromosome 20 syndrome
• Gelastic seizures in ring chromosome 20 syndrome: a case report with video illustration
• Genetic investigations on 8 patients affected by ring 20 chromosome syndrome
• Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
• Genomic alterations in primary gastric cancers analyzed by comparative genomic hybridization and clinicopathological factors
• Ictal involvement of the nigrostriatal system in subtle seizures of ring chromosome 20 epilepsy
• Ictal magnetoencephalographic study in a patient with ring 20 syndrome
• Identification of a novel human zinc finger protein gene ZNF313
• Improvement of epilepsy with lacosamide in a patient with ring chromosome 20 syndrome
• Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20
• Intractable epilepsy with ring chromosome 20 syndrome treated with vagal nerve stimulation: case report and review of the literature
• Intravenous methylprednisolone is a potential add on therapy for Ring chromosome 20 syndrome
• Involvement of the basal ganglia in refractory epilepsy: an 18F-fluoro-L-DOPA PET study using 2 methods of analysis
• KIAP, a novel member of the inhibitor of apoptosis protein family
• Lenalidomide induced durable remission in a patient with MDS/MPN-with ring sideroblasts and thrombocytosis with associated 5q- syndrome
• Lennox-Gastaut syndrome and epilepsy with myoclonic-astatic seizures
• Life with r(20)-Ring chromosome 20 syndrome
• Lithium improved behavioral and epileptic symptoms in an adolescent with ring chromosome 20 and bipolar disorder not otherwise specified
• Long-term EEG in patients with the ring chromosome 20 epilepsy syndrome
• Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20
• Malignant brain tumor repeats: a three-leaved propeller architecture with ligand/peptide binding pockets
• Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis
• Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients
• More severe epilepsy and cognitive impairment in the offspring of a mother with mosaicism for the ring 20 chromosome
• Mosaic ring 20 with no detectable deletion by FISH analysis: Characteristic seizure disorder and literature review
• Mosaicism and phenotype in ring chromosome 20 syndrome
• New association between ring chromosome 20 syndrome and hypomelanosis of Ito
• Non-convulsive status in the ring chromosome 20 syndrome: a video illustration of 3 cases
• PET evidence for a role of the basal ganglia in patients with ring chromosome 20 epilepsy
• Phenotypical heterogeneity of morpheic seizures in ring chromosome 20 syndrome: a videopolysomnographic evidence
• Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome
• Praxis-induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome
• Prenatal diagnosis of a fetus with a ring chromosome 20 characterized by array-CGH
• Rare epileptic syndrome of ring chromosome 20 with epileptic encephalopathy: a case report
• RARS with fibrosis and del(20q) transformed into ALL
• Real-world experience with cannabidiol as add-on treatment in drug-resistant epilepsy
• Refractory and lethal status epilepticus in a patient with ring chromosome 20 syndrome
• Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome
• Regarding: 'Mosaicism and seizure onset in ring chromosome 20 syndrome'
• Ring (20) chromosome epileptic syndrome
• Ring 20 chromosome syndrome with epilepsy and dysmorphic features: a case report
• Ring 20 syndrome mosaicism and epilepsy: a case with duplication of two BAC clones in 20q11.21-q11.22 defined by genome array-CGH
• Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome
• Ring chromosome 20
• Ring chromosome 20 epilepsy syndrome in children: electroclinical features
• Ring chromosome 20 epilepsy syndrome in children: electroclinical features
• Ring chromosome 20 syndrome
• Ring chromosome 20 syndrome with intractable epilepsy
• Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci
• Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children
• Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature
• Ring Chromosome 20 Syndrome: Genetics, Clinical Characteristics, and Overlapping Phenotypes
• Ring chromosome 20 with nonconvulsive status epilepticus: electroclinical correlation of a rare epileptic syndrome
• Ring chromosome 20, hypersensitivity to valproate and hyperammonemic encephalopathy
• Ring chromosome 20: a distinctive syndrome identifiable by electroclinical diagnosis
• Ring chromosome 20: a pediatric potassium channelopathy responsive to treatment with ezogabine
• Ring chromosome 20: an epileptic channel disorder?
• Ring-20-syndrome and loss of telomeric regions
• Significant Improvements of EEG and Clinical Findings With Oral Lacosamide in a Patient With Ring Chromosome 20
• Sleep in ring chromosome 20 syndrome: a peculiar electroencephalographic pattern
• Specificity of electroclinical features in the diagnosis of ring chromosome 20
• Stimulation of the centromedian nucleus in refractory epilepsy associated to ring chromosome 20
• Supernumerary ring chromosome 20 in a mother and her child
• Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations
• The evolving electroclinical syndrome of "epilepsy with ring chromosome 20"
• The Multifaceted Syndromic Primary Immunodeficiencies in Children
• The role of vagus nerve stimulation in genetic etiologies of drug-resistant epilepsy: a meta-analysis
• Transcriptome analysis of a ring chromosome 20 patient cohort
• Two siblings with similar phenotypes: one of them had ring 20 chromosome