Clinicopath Conf., Prolactinoma
NEJM 347:1604-1611, Case 35-2002, 2002
A 22-Year-Old Man with Progressive Bilateral Visual Loss
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A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
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Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
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Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
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A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
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Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005
A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Optic Neuropathy in Children With Lyme Disease
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Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
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Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998
Mucolipidosis Type IV; Characteristic MRI Findings
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Neuro-Ophthalmic Manifestations of Lyme Disease
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Optic Atrophy and Cerebral Infarcts Caused by Methanol Intoxication:MRI
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Long-term Prognosis in Cerebral Venous Thrombosis:Follow-up of 77 Patients
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Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
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Gliomas of the Anterior Visual Pathway
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Visual Failure and Optic Atrophy Associated with Chlorambucil Therapy
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Leber's Hereditary Optic Neuropathy, New Genetic Considerations
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Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
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Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Sarcoidosis of the Nervous System, A Clinical Approach
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Reversal of a Neurologic Paraneoplastic Syndrome with Octreotide (Sandostatin) in a Pt with Glucagonoma
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Craniopharyngyoma in Children
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
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The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
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MR Imaging of a Group I Case of Hallervorden-Spatz Disease
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Paraneoplastic Syndromes Involving the Eyes
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985
Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
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Sphenoid Sinus Mucocele
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Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
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Juvenile Metachromatic Leukodystrophy
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Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980
Pseudotumor Cerebri, Clinical Profile & Visual Outcome in 63 Patients
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Ocular Defects in Children with Cerebral Palsy
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Trichlorethylene
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Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
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Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978
Prolactin-Secreting Tumors & Hypogonadism in 22 Men
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Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
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Wyburn-Mason Syndrome, Report of Two Cases Without Retinal Involvement
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Medical Approach to Ophthalmopathy of Graves'Disease
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Dominant Juvenile Optic Atrophy
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Progressive Facial Hemiatrophy (Parry-Romberg Syndrome)
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