• <em>VLDLR</em> Cerebellar Hypoplasia
• A case of chronic subdural hematoma in a hemodialyzed patient
• A case of Cronkhite-Canada syndrome with vestibular disturbances
• A case of superficial siderosis of the central nervous system with bilateral vestibular dysfunction
• A deletion in the VLDLR gene in Eurasier dogs with cerebellar hypoplasia resembling a Dandy-Walker-like malformation (DWLM)
• A developmental study of relative needs satisfactions of youth: equilibrium--disequilibrium
• A homozygous mutation of VWA3B causes cerebellar ataxia with intellectual disability
• A missense founder mutation in VLDLR is associated with Dysequilibrium Syndrome without quadrupedal locomotion
• A novel homozygous variant in an Iranian pedigree with cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4
• A simple mathematical model applied to selection of the sodium profile during profiled haemodialysis
• Acute interhemispheric subdural hematoma due to hemodialysis: case report
• Association between small ubiquitin-related modifier-1 gene polymorphism and non-syndromic oral clefting
• Autosomal recessive cerebellar hypoplasia in the Hutterite population
• Autosomal recessive spinocerebellar ataxias in Japan
• Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium test
• Broadening the Clinical Spectrum of Very Low Density Lipoprotein Receptor Associated Dysequilibrium Syndrome
• CANVAS an update: clinical presentation, investigation and management
• Cerebellar ataxia with normal intellect associated with a homozygous truncating variant in CA8
• Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation
• Cerebellar/spinocerebellar syndromes
• Challenges of diagnostic exome sequencing in an inbred founder population
• Changes in visual evoked potentials in children on chronic dialysis treatment
• Characterization of a novel zebrafish (Danio rerio) gene, wdr81, associated with cerebellar ataxia, mental retardation and dysequilibrium syndrome (CAMRQ)
• Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family
• Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia
• Clinical correlation of dysequilibrium syndrome and 4-hydroxybutyric aciduria
• Compound Heterozygosity in Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome Type 4
• Core hypothermia in multiple sclerosis: case report with magnetic resonance imaging localization of a thalamic lesion
• Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2
• Decrease of Horizontal Canal Vestibulo-Oculomotor Reflex Gain in the Elderly with Dysequilibrium without Lifetime Vertigo
• Degradation routes of trafficking-defective VLDLR mutants associated with Dysequilibrium syndrome
• Depressive phenomenology at the outset of neuropaediatric diseases
• Diagnosis and management of post-traumatic vertigo
• Dialysis dysequilibrium syndrome in neurosurgical patients
• Dialysis dysequilibrium syndrome(DDS)
• DISEQUILIBRIUM BETWEEN AGONIST AND ANTAGONIST MUSCLES IN MYOPATHIES DEMONSTRATED BY AN ELECTROMYOGRAPHIC METHOD
• Disequilibrium syndrome and prevention in nonhemodialysis patients
• Evidence for a disequilibrium pH in the proximal tubule of rat kidney
• Gastric function and phosphorus-calcium disequilibrium during chronic evolutive polyarthritis
• Genetic Insights into the causal relationship between cannabis use and diabetic phenotypes: A genetic correlation and Mendelian randomization study
• Hereditary congenital unilateral deafness: a new disorder?
• Human balance, the evolution of bipedalism and dysequilibrium syndrome
• Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome
• Impaired trafficking of the very low density lipoprotein receptor caused by missense mutations associated with dysequilibrium syndrome
• Inferior cerebellar hypoplasia resembling a Dandy-Walker-like malformation in purebred Eurasier dogs with familial non-progressive ataxia: a retrospective and prospective clinical cohort study
• Interventions for preventing haemodialysis dysequilibrium syndrome
• Ionic and metabolic disequilibrium in the confuso-oneiric episode of acute alcoholism: therapeutic results
• It is more "unbalanced" than you think
• Long-term EEG monitoring in uremic children on chronic dialysis treatment
• Long-term good results of surgical treatment for spontaneous epi- and subdural hematoma in a female patient on maintenance hemodialysis
• Low serum dopamine-beta-hydroxylase activity in the dysequilibrium syndrome
• Medulloblastoma presenting as dialysis disequilibrium syndrome
• Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
• Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome
• Mutations in VLDLR as a cause for autosomal recessive cerebellar ataxia with mental retardation (dysequilibrium syndrome)
• Neuro-ophthalmologic findings in humans with quadrupedal locomotion
• Neurological complications in renal failure: a review
• Neurological complications in uremia
• Neurology and the kidney
• Neurotropic T-cell lymphocytosis: a cutaneous expression of CLIPPERS
• Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites
• Novel homozygous variant of carbonic anhydrase 8 gene expanding the phenotype of cerebellar ataxia, mental retardation, and disequilibrium syndrome subtype 3
• Opsoclonus-myoclonus-dysequilibrium syndrome: cytological and immunological dynamics in the serial cerebrospinal fluid in two patients
• Osmotic demyelination syndrome in end-stage renal disease after recent hemodialysis: MRI of the brain
• Osmotic demyelination syndrome with a dysequilibrium syndrome: reversible MRI findings
• Ototoxicity-related dysequilibrium
• Pathogenetic and preventive aspects of non-progressive ataxic syndromes
• Pathologo-anatomical characteristics of hyperosmolar and other comatous conditions
• Pharmacologic treatment of fibromyalgia
• Phenotypical spectrum of cerebellar ataxia associated with a novel mutation in the CA8 gene, encoding carbonic anhydrase (CA) VIII
• PHYSIOPATHOLOGY OF GENERALIZED EDEMA. 1. CONCEPT; ETIOPATHOGENESIS; VASCULOTISSULAR AND RENAL FACTORS. HEMODYNAMIC DISEQUILIBRIUM. ALDOSTERONE
• Pituitary crisis and acute renal failure--a case report
• Re-evaluation of the dysequilibrium syndrome
• Recent onset disequilibrium mimicking acute vestibulopathy in early multiple sclerosis
• Relations between motor disequilibrium and sensory development in strabismus
• Role of blood urea and serum sodium concentrations in the pathogenesis of the dialysis dysequilibrium syndrome
• Simulation, mental disequilibrium or schizophrenia
• Structural Characterization of Carbonic Anhydrase VIII and Effects of Missense Single Nucleotide Variations to Protein Structure and Function
• Superior semi-circular canal dehiscence syndrome: quantifying the effectiveness of treatment from the patient's perspective
• Surfactant protein-C promoter variants associated with neonatal respiratory distress syndrome reduce transcription
• Telovelar surgical approach
• Temporal bone histopathology in dominantly inherited audiovestibular syndrome
• The dialysis dysequilibrium syndrome
• THE DILEMMA OF THE ARTIST: DISEQUILIBRIUM OR OVERSTEPPING HIS LIMITATIONS
• The dysequilibrium syndrome in cerebral palsy. Clinical aspects and treatment
• The dysequilibrium syndrome in experimental hemodialysis
• The dysequilibrium syndrome: a study of the etiology and pathogenesis
• The dysequilibrium syndrome. A genetic study
• The effects of response disequilibrium on social media use: A laboratory analogue
• The recovery of the fluid balance after hemodialysis and hemofiltration
• The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
• Transmastoid repair of superior semicircular canal dehiscence
• Treatment of diabetic coma with low-dose injections of insulin
• Two cases of medically and surgically intractable SUNCT: a reason for caution and an argument for a central mechanism
• Two Siblings with Cerebellar Ataxia, Mental Retardation, and Disequilibrium Syndrome 4 and a Novel Variant of ATP8A2
• Very mild features of dysequilibrium syndrome associated with a novel VLDLR missense mutation
• Vestibular dysfunction in Gulf War syndrome
• Wernicke's encephalopathy associated with hemodialysis: report of two cases and review of the literature
• Wernicke's encephalopathy in patients on peritoneal dialysis or hemodialysis
• Whole exome sequencing is necessary to clarify ID/DD cases with de novo copy number variants of uncertain significance: Two proof-of-concept examples