SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
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Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
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Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
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Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
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Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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A 28-Year-Old Woman with Vision Loss and an Unusual Gait
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A Middle-Aged Man with Progressive Gait Abnormalities
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Hypointensity of the Basal Ganglia in Adults with Glucose Transporter Protein Type 1 Deficiency Syndrome: A Novel Magnetic Resonance Imaging Finding
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Complex Ataxia
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Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
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Diseases of the Nervous System Caused by Nutritional Deficiency, Vitamin B12 (Cobalamin) Deficiency (Subacute Combined Degeneration)
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
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Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
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The Hot Cross Bun Sign in the Patients with Spinocerebellar Ataxia
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
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Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
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Neurologic Aspects of Cobalamin Deficiency
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Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
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Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
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Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
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Subacute Combined Degeneration of the Spinal Cord
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Atypical Alzheimer's Disease with Spastic Paresis & Ataxia
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Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
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Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979
The Central Nervous System in a Case of Neurolathyrism
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Brain Stem Tumors of Childhood & Adolescence
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A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
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A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024
A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
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A 48-Year-Old Man With Spasticity and Progressive Ataxia
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
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A Triad of Tremor, Ataxia, and Cognitive Impairment
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A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
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Neurosyphilis
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A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018
Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018
An Unusual Fundus Finding in a Teenage Girl
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