• A - 154 Neuropsychological Profile of a Patient Post Anoxic Brain Injury with Balint Syndrome: a Case Study Five Years Post-Injury
• A case of an African American man with ataxia and oculomotor apraxia 2
• A Hyalinized Trichilemmoma of the Eyelid in a Teenager
• A new MRI marker of ataxia with oculomotor apraxia
• A rare case of atypical Cogan's syndrome presenting as encephalitis
• Acute Limb Ischemia in Cogan Syndrome
• An elusive ciliopathy: Joubert syndrome
• Asymmetric Balint's syndrome with multimodal agnosia, bilateral agraphesthesia, and ineffective kinesthetic reading due to subcortical hemorrhage in the left parieto-occipito-temporal area
• Asymmetric oculomotor apraxia, optic ataxia, and simultanagnosia with right hemispatial neglect from a predominantly left-sided lesion of the parieto-occipital area
• Ataxia with oculomotor apraxia type 2 (AOA2): an eye movement study of two siblings
• Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage
• Ataxia with oculomotor apraxia type 2: not always an easy diagnosis
• Atypical Cogan syndrome as a differential diagnosis of sudden sensorineural hearing loss
• Atypical Cogan's Syndrome Mimicking Giant Cell Arteritis Successfully Treated with Early Administration of Tocilizumab
• Atypical Cogan's Syndrome with Large-vessel Vasculitis Successfully Treated with Tocilizumab
• Atypical Cogan's syndrome: A case report
• Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker
• Behcet's and Cogan's syndromes - The Variable Vessel Vasculitides
• Bilateral injury of the superior longitudinal fasciculus in a patient with Balint syndrome
• Brothers with ocular motor apraxia, juvenile nephronophthisis, and mild cerebellar defects
• CD3(-)CD4(+) Lymphocytic Variant Hypereosinophilic Syndrome: Diagnostic Tools Revisited
• CD3^-CD4⁺ Lymphocytic Variant Hypereosinophilic Syndrome: Diagnostic Tools Revisited
• Characteristics and Outcomes of Idiopathic and Non-idiopathic Ocular Motor Apraxia in Children
• Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia
• Clinical description of a Cogan-Reese type iridocorneal endothelial syndrome using anterior segment optical coherence tomography and specular microscopy
• Clinical Presentation of Ataxia-Telangiectasia
• Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1
• Cogan syndrome following SARS-COV-2 infection
• Cogan Syndrome with Aortic Regurgitation and Multiple Vasculopathy
• Cogan syndrome: a case report and review of the literature
• Cogan Syndrome: A Case Study and Review of the Literature
• Cogan syndrome: A challenging diagnosis
• Cogan's syndrome is more than just keratitis: a case-based literature review
• Cogan's syndrome: State of the art of systemic immunosuppressive treatment in adult and pediatric patients
• Combination of olfactory aplasia and congenital ocular motor apraxia: a previously unreported association
• Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
• Congenital ocular motor apraxia with wheel-rolling ocular torsion-a neurodiagnostic phenotype of Joubert syndrome
• Corneal dystrophies
• Delayed Diagnosis of Childhood-Onset Huntington Disease in an 8-Year-Old Boy With Ocular Motor Apraxia
• Dominant negative variants in <em>IKZF2</em> cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay
• Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay
• Dual corneal involvement by endothelial and epithelial corneal dystrophies in Steinert's disease: A case of triple dystrophy
• Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome
• Evolocumab and lipoprotein apheresis combination therapy may have synergic effects to reduce low-density lipoprotein cholesterol levels in heterozygous familial hypercholesterolemia: A case report
• Exploring the Pathogenicity of SETX I1942T Variant in Ataxia with Oculomotor Apraxia Type 2 Through Segregation Analysis
• Eyelid Mass in Boston Keratoprosthesis Type 2
• Germ cell arrest associated with aSETX mutation in ataxia oculomotor apraxia type 2
• Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report
• Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia
• High myopia and vitreal veils in a patient with Poretti- Boltshauser syndrome due to a novel homozygous <em>LAMA1</em> mutation
• High myopia and vitreal veils in a patient with Poretti- Boltshauser syndrome due to a novel homozygous LAMA1 mutation
• How to assess blepharoptosis via telemedicine: method and its reliability
• Infantile-onset saccade initiation delay (congenital ocular motor apraxia)
• Integrating visual search, eye movement training and reversing prism exposure in the treatment of Balint-Holmes syndrome: a single case report
• Interstitial keratitis diagnosis and treatment
• Intrathecal injection of methotrexate combined with dexamethasone for Cogan's syndrome with neurological involvement: A case report and literature review
• Modalities of reading acquisition in three siblings with infantile-onset saccade initiation delay (Cogan congenital ocular motor apraxia): A longitudinal study
• Mucopolysaccharidosis Type I-Associated Corneal Disease: A Clinicopathologic Study
• Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2
• Mutational analysis of SYNJ1 gene (PARK20) in Parkinson's disease in a Taiwanese population
• Mutations in PNKP cause recessive ataxia with oculomotor apraxia type 4
• Myeloid Sarcoma with Megakaryoblastic Differentiation Arising in the Conjunctiva
• Nail Lichen Planus in a Patient with Cogan Syndrome: Report of a Case and Discussion
• Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study
• NPTX1-related oculomotor apraxia: an intra-hemispheric disconnection disorder
• Ocular Dysfunctions Presenting in Tacrolimus-Induced Posterior Reversible Encephalopathy Syndrome: A Case Presentation
• OCULAR MANIFESTATIONS OF PORETTI-BOLTSHAUSER SYNDROME: FINDINGS FROM MULTIMODAL IMAGING AND ELECTROPHYSIOLOGY
• Oculomotor apraxia and dilated cardiomyopathy with ataxia syndrome: A case report
• Oculomotor apraxia and disrupted sleep with nocturnal ballistic bouts in ADCY5-related disease
• Oculomotor apraxia in Gaucher disease
• Our experience with micropulse cyclophotocoagulation in the therapy of glaucoma
• Paediatric Cogan´s syndrome - review of literature, case report and practical approach to diagnosis and management
• Paediatric Cogans syndrome - review of literature, case report and practical approach to diagnosis and management
• Partial Balint's syndrome and left homonymous hemianopsia presenting after resection of a right occipito-parietal glioblastoma
• Pearls & Oy-sters: Ocular motor apraxia as essential differential diagnosis to supranuclear gaze palsy: Eyes up
• Pearls &amp; Oy-sters: Ocular motor apraxia as essential differential diagnosis to supranuclear gaze palsy: Eyes up
• Persistence of Infantile-Onset Saccade Initiation Delay (Congenital Ocular Motor Apraxia): An Update on a Young Adult
• Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
• Phenotypic spectrum of patients with Poretti-Boltshauser syndrome: Patient report of antenatal ventriculomegaly and esophageal atresia
• Pitfalls in ataxia with ocular motor apraxia type 1: pseudodominant inheritance and very late onset
• PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema
• Posterior Scleritis: A Unique Sequela of Cogan Syndrome
• Ptosis Correction
• Ptosis Correction
• Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia-oculomotor apraxia 4 and pilocytic astrocytoma
• Report of 2 pediatric cases with atypical Cogan's syndrome and a systematic review
• Retinal Avascularity and Neovascularization Associated With LAMA1 (laminin1) Mutation in Poretti-Boltshauser Syndrome
• RETINAL CHANGES IN PORETTI-BOLTSHAUSER SYNDROME: RETINA AS A WINDOW TO THE BRAIN
• Snakebite envenomation-induced posterior reversible encephalopathy syndrome presenting with Balint syndrome
• Speech reception after cochlear implantation for Cogan's syndrome: Case series following CARE guidelines
• Sudden hearing loss and Crohn disease: when Cogan syndrome must be suspected
• Target temperature in post-arrest comatous patients. Is something changed in the postpandemic era?
• Teaching Video NeuroImage: Oculomotor Apraxia as the Only Presentation of Diffuse Intrinsic Pontine Glioma
• Teaching Video NeuroImages: Characteristic head jerks in congenital oculomotor apraxia due to Joubert syndrome
• Teaching Video NeuroImages: Posterior Cortical Atrophy Presenting With Balint Syndrome
• The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued
• Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia
• Vertigo and ocular inflammation: Cogan syndrome
• Visual and cross-modal cues increase the identification of overlapping visual stimuli in Balint's syndrome
• XRCC1 mutation is associated with PARP1 hyperactivation and cerebellar ataxia