• A 66-Year-Old Woman with a Progressive, Longitudinally Extensive, Tract Specific, Myelopathy
• A case of cystinuria presenting with cerebellar ataxia and dementia
• A case of Sjögren syndrome with subacute combined degeneration-like posterior column lesion on cervical MRI
• A case with posterior column ataxia associated with cerebellar ataxia and sensory neuropathy
• A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
• A Novel FLVCR1 Variant Implicated in Retinitis Pigmentosa
• A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1
• A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling
• A splice-site variant in FLVCR1 produces retinitis pigmentosa without posterior column ataxia
• Allografts for Skin Closure during In Utero Spina Bifida Repair in a Sheep Model
• An Atypical Clinical Presentation of Post-traumatic Syringomyelia: A Case Report and Brief Review of the Literature
• An autopsy case of an aged patient with spinocerebellar ataxia type 2
• An autosomal recessive disorder with posterior column ataxia and retinitis pigmentosa
• An unusual case of familial ALS and cerebellar ataxia
• Ataxic gait following total gastrectomy for gastric cancer
• Autosomal recessive cerebellar ataxias
• Autosomal recessive posterior column ataxia and retinitis pigmentosa
• Autosomal recessive posterior column ataxia with retinitis pigmentosa caused by novel mutations in the FLVCR1 gene
• Biallelic RFC1-expansion in a French multicentric sporadic ataxia cohort
• Can vitamin B12 deficiency manifest with acute posterolateral or posterior cord syndrome?
• Case of sensory ataxic ganglionopathy-myelopathy in copper deficiency
• Changes in Cancer Functional Assessment Set and Functional Independence Measure After Intradural Extramedullary Tumor Resection: A Case Report
• Chronic acquired sensory neuron diseases
• Clinical and imaging characteristics of posterior column ataxia with retinitis pigmentosa with a specific FLVCR1 mutation
• Clinical core symptoms of posterior spinal artery ischemia
• Clinical management of Friedreich's Ataxia: a report of two cases
• Clinical, hematological, and imaging observations in a 25-year-old woman with abetalipoproteinemia
• Clinical, pathological and functional characterization of riboflavin-responsive neuropathy
• Clinicopathological features of acute autonomic and sensory neuropathy
• Copper deficiency myelopathy: A report of two cases
• Copper deficiency-associated myelopathy in cryptogenic hyperzincemia: a case report
• Cryopreserved human umbilical cord as a meningeal patch during in utero spina bifida repair in a modified ovine model
• Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease
• Endovascular repair and open repair surgery of thoraco-abdominal aortic aneurysms cause drastically different types of spinal cord injury
• Evaluating the child with unsteady gait
• Expanded genetic insight and clinical experience of DNMT1-complex disorder
• Expression and purification of the heme exporter FLVCR1a
• Extending the phenotype of posterior column ataxia with retinitis pigmentosa caused by variants in FLVCR1
• Familial segmental spinal myoclonus: a rare clinical feature of Friedreich's ataxia
• FLVCR1-related disease as a rare cause of retinitis pigmentosa and hereditary sensory autonomic neuropathy
• Friedreich ataxia
• Friedreich ataxia: the clinical picture
• Heme and FLVCR-related transporter families SLC48 and SLC49
• Hereditary Ataxia: A Focus on Heme Metabolism and Fe-S Cluster Biogenesis
• Imaging appearance of myelopathy secondary to nitrous oxide abuse: a case report and review of the literature
• Intravenous Immunoglobulin and Mycophenolate Mofetil for Long-Standing Sensory Neuronopathy in Sjögren's Syndrome
• Isolated degeneration of the posterior column as a distinct entity--a clinical and electrophysiologic follow-up study
• Isolated juvenile macular dystrophy without posterior column ataxia associated with FLVCR1 mutation
• Isolation of a novel iris-specific and leucine-rich repeat protein (oculoglycan) using differential selection
• Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL): assessment of the involved white matter tracts by MRI
• Lhermitte Sign
• Longitudinally extensive dorsal column spinal cord lesion with sensory ganglionopathy
• Mfsd7b facilitates choline transport and missense mutations affect choline transport function
• Mitochondrial pathophysiology in Friedreich's ataxia
• Motor neuron involvement expands the neuropathological phenotype of late-onset ataxia in RFC1 mutation (CANVAS)
• Motor neuron pathology in CANVAS due to RFC1 expansions
• Mutations in FLVCR1 cause posterior column ataxia and retinitis pigmentosa
• Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception
• Mutations of FLVCR1 in posterior column ataxia and retinitis pigmentosa result in the loss of heme export activity
• Neuroimaging Applications in Chronic Ataxias
• Neuroimaging in Sensory Neuronopathy
• Neuropathological Findings in Cerebellar Ataxia With Neuropathy and Vestibular Areflexia Syndrome
• Neuropathology in classical and variant ataxia-telangiectasia
• Neuropsychiatric manifestations ushering pernicious anemia
• Next-generation analysis on hereditary neurodegenerative disorders using next-generation sequencers
• Non-cerebellar ataxias: posterior column-like ataxia and cerebellar-like ataxia
• Non-type I cystinuria associated with mental retardation and ataxia in a Korean boy with a new missence mutation(G173R) in the SLC7A9 gene
• Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders
• Phenotypic spectrum of autosomal recessive retinitis pigmentosa without posterior column ataxia caused by mutations in the FLVCR1 gene
• Phosphodiesterase Inhibitors Revert Axonal Dystrophy in Friedreich's Ataxia Mouse Model
• Post-Vaccination/Post-COVID Immune-Mediated Demyelination of the Brain and Spinal Cord: A Novel Neuroimaging Finding
• Posterior column ataxia and retinitis pigmentosa: a distinct clinical and genetic disorder
• Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome 1q31-q32
• Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the <em>FLVCR1</em> gene
• Posterior column ataxia with retinitis pigmentosa (PCARP) in an Iranian patient associated with the FLVCR1 gene
• Posterior column ataxia with retinitis pigmentosa coexisting with sensory-autonomic neuropathy and leukemia due to the homozygous p.Pro221Ser FLVCR1 mutation
• Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1
• Posterior cord syndrome associated with postoperative seroma: The case to perform a complete neurologic exam
• Posterior paresis due to a malignant lymphoma in a goat
• Potential Treatment of Retinal Diseases with Iron Chelators
• Present efforts in the medical genome center at the University of Tokyo Hospital
• Proprioceptive pathways to posterior parietal areas MIP and LIPv from the dorsal column nuclei and the postcentral somatosensory cortex
• Rare autosomal dominant POLG1 mutation in a family with metabolic strokes, posterior column spinal degeneration, and multi-endocrine disease
• Romberg Test
• Sensory ganglionopathy due to gluten sensitivity
• Severe ataxia with neuropathy in hereditary gelsolin amyloidosis
• Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia
• Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathology
• Structural basis of lipid head group entry to the Kennedy pathway by FLVCR1
• Study of micronutrients (copper, zinc and vitamin B12) in posterolateral myelopathies
• Subacute combined degeneration caused by nitrous oxide intoxication: case reports
• Subacute combined degeneration of the spinal cord caused by nitrous oxide anaesthesia
• Subacute combined degeneration without nutritional anemia
• Subacute copper-deficiency myelopathy in a patient with occult celiac disease
• Suspected hereditary cervicothoracic vertebral subluxation with cervical myopathy in Poll Merino sheep
• Tabes Dorsalis in a Patient Presenting With Right Lower Extremity Paresthesia and Cervical Spine Pain
• Transient Dorsal Column Dysfunction After Extreme Cervical Deformity Correction: Report of 3 Cases
• Tropical ataxic neuropathy - A century old enigma
• Two different pathogenic mechanisms, dying-back axonal neuropathy and pancreatic senescence, are present in the YG8R mouse model of Friedreich's ataxia
• Unraveling the genetic and molecular basis of posterior column ataxia and retinitis pigmentosa