• "Neuroacanthocytosis" - Overdue for a Taxonomic Update
• A Case of Chorea-Acanthocytosis with FDG PET/CT Imaging
• A Case of McLeod's Syndrome Presenting with Severe Decompensated Heart Failure
• A case report of O'Sullivan-McLeod syndrome
• A chorea-acanthocytosis patient with novel mutations in the VPS13A gene without acanthocyte
• A Man With Progressive Chorea and Abnormal Trunk Movements
• A Novel <em>XK</em> Gene Mutation Causative of McLeod Syndrome
• A novel c.82insC (p.Tyr28Leufs85X) mutation in the XK gene associated with the McLeod phenotype
• A Novel XK Gene Mutation Causative of McLeod Syndrome
• A partnership between the lipid scramblase XK and the lipid transfer protein VPS13A at the plasma membrane
• A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs
• Acanthocyte Sedimentation Rate as a Diagnostic Biomarker for Neuroacanthocytosis Syndromes: Experimental Evidence and Physical Justification
• Acanthocytes Identified in Huntington's Disease
• Acanthocytosis
• Acanthocytosis
• Acupuncture for treating symptoms associated with chorea-acanthocytosis: A CARE-compliant case report
• An Autopsy Series of Seven Cases of VPS13A Disease (Chorea-Acanthocytosis)
• Analysis of Brain, Blood, and Testis Phenotypes Lacking the <em>Vps13a</em> Gene in C57BL/6N Mice
• Basal Ganglia Syndrome in a Male With an XK Gene Variant but Without XK Disease (McLeod Syndrome)
• Brain F-18 FDG and F-18 FP-CIT PET/CT Findings of c.856_860delCTCTA Mutation McLeod Syndrome
• Cardiac manifestation is evident in chorea-acanthocytosis but different from McLeod syndrome
• Case-report of neuroacanthocytosis associated with a compound mutation in the VPS13A gene
• Chorea
• Chorea-acanthocytosis
• Chorea-acanthocytosis associated with two novel heterozygous mutations in the VPS13A gene
• Chorea-acanthocytosis with a novel mutation in the vacuolar protein sorting 13 homolog a gene: A case report
• Chorea-acanthocytosis: Time-dependent changes of symptoms and imaging findings
• Chronic granulomatous disease and McLeod syndrome: Stem cell transplant and transfusion support in a 2-year-old patient-a case report
• Chronic Granulomatous Disease with the McLeod Phenotype: a French National Retrospective Case Series
• Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population
• Clinical Spectrum of Movement Disorders in Neurology Inpatients in a Tertiary Care Centre
• Combined Dendritic and Axonal Deterioration Are Responsible for Motoneuronopathy in Patient-Derived Neuronal Cell Models of Chorea-Acanthocytosis
• Commentary: Acanthocytes identified in Huntington's disease
• Compound Heterozygous VPS13A Variants in a Patient with Neuroacanthocytosis: A Case Report and Review of the Literature
• COVID-19 and patient engagement in health research: What have we learned?
• COVID-19 et participation des patients à la recherche médicale: qu’avons-nous appris?
• Decreased Na⁺/K⁺ ATPase Expression and Depolarized Cell Membrane in Neurons Differentiated from Chorea-Acanthocytosis Patients
• Deep brain stimulation for chorea-acanthocytosis: a systematic review
• Dilative cardiomyopathy displaying double trouble etiology: Myocarditis and Mcleod syndrome?
• Discriminating chorea-acanthocytosis from Huntington's disease with single-case voxel-based morphometry analysis
• Effect of rapamycin on lysosomal accumulation in a CRISPR/Cas9-based cellular model of VPS13A deficiency
• Efficacy of Electroconvulsive Therapy for the Treatment of Movement Disorders: A Literature Review
• Endosomal recycling defects link Huntington's disease with McLeod syndrome
• Enlarging the clinical spectrum of chorea-acanthocytosis
• Erysense, a Lab-on-a-Chip-Based Point-of-Care Device to Evaluate Red Blood Cell Flow Properties With Multiple Clinical Applications
• Exome sequencing of choreoacanthocytosis reveals novel mutations in VPS13A and co-mutation in modifier gene(s)
• Heterozygous VPS13A and PARK2 Mutations in a Patient with Parkinsonism and Seizures
• How we approach transfusions in a patient with high risk of alloimmunization from McLeod phenotype
• Hyperpigmentation Probably Related to Haloperidol in a Patient with Neuroacanthocytosis
• Identification of four novel mutations in VSP13A in Iranian patients with Chorea-acanthocytosis (ChAc)
• Identification of two compound heterozygous VPS13A large deletions in chorea-acanthocytosis only by protein and quantitative DNA analysis
• Interaction between VPS13A and the XK scramblase is important for VPS13A function in humans
• McLeod Syndrome in a Commercial Airline Pilot
• McLeod syndrome with a novel XK frameshift mutation: A case report
• Morvan Fibrillary Chorea Associated with Monoclonal B Cell Lymphocytosis
• Movement disorders and neuropathies: overlaps and mimics in clinical practice
• Multisystem pathology in McLeod syndrome
• Nemaline Rods in a Patient of Chorea-Acanthocytosis with a Novel Pathogenic Mutation of VPS13A Gene
• Neuroacanthocytosis
• Neuroacanthocytosis
• Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement
• Neuroacanthocytosis Syndromes: The Clinical Perspective
• Neuroacanthocytosis: a case report of chorea-acanthocytosis
• Neurodegeneration with Brain Iron Accumulation: Two Additional Cases with Dystonic Opisthotonus
• Neurofilament light chain in serum is significantly increased in chorea-acanthocytosis
• Neuropathology of McLeod Syndrome
• Novel <em>VPS13A</em> Gene Mutations in a South Asian, Indian Patient with Chorea‑acanthocytosis
• Novel c.435delC mutation in XK gene found in a Taiwanese patient with McLeod syndrome
• Novel heterozygous VPS13A pathogenic variants in chorea-neuroacanthocytosis: a case report
• Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report
• Orofacial Dyskinesia in a Young Man
• Orofacial manifestations of chorea-acanthocytosis: case presentation and literature review
• Osmotic gradient ektacytometry - a novel diagnostic approach for neuroacanthocytosis syndromes
• Pharmacological interventions for lipid transport disorders
• Physiological and Pathogenesis Significance of Chorein in Health and Disease
• Polysomnographic findings in the ultra-rare McLeod syndrome: further documentation of sleep apnea as a possible feature
• Proceedings of the Eleventh International Meeting on Neuroacanthocytosis Syndromes
• Proceedings of the Tenth International Meeting on Neuroacanthocytosis Syndromes
• Seizures in Alzheimer's disease are highly recurrent and associated with a poor disease course
• Sleep disorders in McLeod syndrome: A case series
• Sleep Disorders in Patients with Choreic Syndromes
• Sphingolipid and Phospholipid Levels Are Altered in Human Brain in Chorea-Acanthocytosis
• Subthalamic nucleus deep brain stimulation in two siblings with chorea-acanthocytosis
• Targeting Lyn Kinase in Chorea-Acanthocytosis: A Translational Treatment Approach in a Rare Disease
• The binding of the APT1 domains to phosphoinositides is regulated by metal ions in vitro
• The Erythrocyte Sedimentation Rate and Its Relation to Cell Shape and Rigidity of Red Blood Cells from Chorea-Acanthocytosis Patients in an Off-Label Treatment with Dasatinib
• The first case report of McLeod syndrome in an infant with a novel mutation (c.89C&gt;A, p. Ser30X) in XK
• The first case report of McLeod syndrome in an infant with a novel mutation (c.89C>A, p. Ser30X) in XK
• The Spectrum of Movement Disorders in Neuroacanthocytosis Syndromes: A Video Series
• The XK plasma membrane scramblase and the VPS13A cytosolic lipid transporter for ATP-induced cell death
• Therapeutic targeting of Lyn kinase to treat chorea-acanthocytosis
• Three new XK alleles; two associated with a McLeod RBC phenotype
• Tongue Protrusion Dystonia in Pantothenate Kinase-Associated Neurodegeneration
• Tongue-biting ataxia that appeared to be a psychiatric disorder: a case of neuroacanthocytosis
• Two case reports of chorea-acanthocytosis and review of literature
• Very Long Time Persistent HyperCKemia as the First Manifestation of McLeod Syndrome: A Case Report
• VPS13 Forum Proceedings: XK, XK-Related and VPS13 Proteins in Membrane Lipid Dynamics
• XK is a partner for VPS13A: a molecular link between Chorea-Acanthocytosis and McLeod Syndrome
• XK-Associated McLeod Syndrome: Nonhematological Manifestations and Relation to VPS13A Disease
• Yeast as a Model to Find New Drugs and Drug Targets for <em>VPS13</em>-Dependent Neurodegenerative Diseases