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The Prevention of Neurogenetic Disease
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Reversible Blindness Secondary to Acute Sphenoid Sinusitis
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Gliomas of the Anterior Visual Pathway
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Cerebrovascular Accident Associated with Anabolic Steroid Use in a Young Man
Neurol 44:2405-2406, Akhter,J.,et al, 1994
A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Chronic headache:Appropriate Use of Opiate Analgesics
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Neurofibromatosis Type 1:The Cognitive Phenotype
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Transesophageal Echocardiography & Contrast-TCD in the Detection of a Patent Foramen Ovale:Experiences with 111 Pts
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Paradoxical Embolism as a Cause of Ischemic Stroke of Uncertain Etiology:A Transcranial Doppler Sonographic Study
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Clinical Genetics in Neurological Disease
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Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
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Venous Sinus Thrombosis Associated with Androgens in a Healthy Young Man
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Neuro-Ophthalmological Presentation of Non-Invasive Aspergillus Sinus Disease in the Non-Immunocompromised Host
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Aspergillosis of the Brain and Paranasal Sinuses in Immunocompromised Patients:CT and MR Imaging Findings
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Myotonic Dystrophy
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Diagnosis of Carotid Artery Disease:Preliminary Experience with Maximum-Intensity-Projection Spiral CT Angiography
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Atrial Septal Aneurysm & Patent Foramen Ovale as Risk for Cryptogenic Stroke in Pts<55 Yrs of Age Using TEE
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Coital Cerebral Hemorrhage
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Lissencephaly:A Human Brain Malformation Associated with Deletion of the LIS1 Gene Located at Chromosome 17p13
JAMA 270:2838-2842, Dobyns,W.B.,et al, 1993
Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993
Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993
Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report
Neurol 43:617-618, Finkelman,R.,et al, 1993
Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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The DNA Laboratory and Neurolgoical Practice
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An Analysis of Ischemic Stroke in an Urban Southern California Population
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The Psychological Consequences of Predictive Testing for Huntington's Disease
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Patent Foramen Ovale as a Risk Factor for Cryptogenic Stroke
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Cavernous Sinus Syndrome and Systemic Lupus Erythematosus
Neurol 42:1842-1843, Melen,O.,et al, 1992
Causal Heterogeneity in Isolated Lissencephaly
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Population Screening for Fragile X
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Coronary Vasospasm Induced by Subcutaneous Sumatriptan
BMJ 304:1415, Willett,F.,et al, 1992
Dystrophinopathy in Isolated Cases of Myopathy in Females
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Unstable DNA Sequence in Myotonic Dystrophy
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Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
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De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
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Genetic Diagnosis of Gaucher's Disease
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Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992
The First Decade of Molecular Genetics in Neurology:Changing Clinical Thought and Practice
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GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
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Suprascapular Nerve Entrapment:Evaluation with MR Imaging
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Evolution of Oculomotor Nerve palsies
J Clin Neuro-Ophthalmol 12:21-25, Capo,H.,et al, 1992
Bacterial Meningitis in Elderly Patients:Clinical Picture and Course
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Aphasia
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A Clinical Study of Noonan Syndrome
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The Origin of Pain in Optic Neuritis, Determinants of Pain in 101 Eyes with Optic Neuritis
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Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
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Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
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Lisch Nodules in Neurofibromatosis Type I
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