Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
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Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988
Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
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Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
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The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988
The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
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Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987
Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987
Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987
Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987
Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
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Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987
Cervical Epidural Abscess
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Familial Spastic Paraparesis & Deafness, A New X-Linked Neurodegenerative Disorder
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Phosphorylase Deficiency
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Association of High Cyanide & Low Sulphur Intake in Cassava-Induced Spastic Paraparesis
Lancet 2:1211-1213, Cliff,J.,et al, 1985
McArdle's Disease in the 1980s
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Vacuolar Myelopathy Pathologically Resembling Subacute Combined Degeneration in Patients with AIDS
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Portal-Systemic Myelopathy after Portacaval Shunt Surgery
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Adrenoleukodystrophy:Clinical & Biochemical Manifestations in Carriers
Neurol 34:798-801, O'Neill,B.P.,et al, 1984
Clinical Epidemology of Toxic-Oil Syndrome
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Neurological Aspect of Hyponatraemia
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Familial Spastic Paraplg, Peroneal Neuropathy, & Crural Hypopig, A New Neurocut Synd
Neurol 31:754-757, Stewart,R.M.,et al, 1981
Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980
Transient Spastic Paraparesis Following Abdominal Aortography:Management with Cerebrospinal Fluid Lavage
Ann Neurol 3:185, Morariu,M.A., 1978
Jamaica Ginger Paralysis
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A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978
The Cervical Myelopathy Associated with Rheumatoid Arthritis:Analysis of 32 Patients, with Two Post-mortem Cases
Ann Neurol 3:144, Nakano,K.K.,et al, 1978
Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
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Rigid Spine Syndrome:A Type I Fiber Myopathy
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Spinal Cord Compression in Thalassaemia
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Neurologic Disorders in Renal Failure (1st of Two Parts)
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The Thyroid Gland:Its Relationship to Neurology
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Important Advances in Clinical Medicine
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Spinal Epidural Abscess
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Spinal Cord Compression by Extramedullary Hemopoietic Tissue in Sickle Cell Anemia
J Neurosurg 43:483, Ammoumi,A.A.,et al, 1975
Neurotoxicity of Commonly Used Antineoplastic Agents
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Lymphomatoid Granulomatosis
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Neurocutaneous Disease
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Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025
Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025
Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025
A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025
A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025
Postprocedural Brachial Neuritis:Clinical, Electrodiagnostic, and Neuroimaging Features
AJNR 46:1050-1055, Ambati,V.S.,et al, 2025
A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,et al, 2025
Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
NEJM 392:268-276, Case 2-2025, 2025
A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025
Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025