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Differential
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athetosis
athetosis, causes of
benign essential tremor
CAT scan
chorea
chorea, causes of
chorea, familial benign
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
dystonia
dystonia musculorum deformens
equinovarus
familial
gene
genetic neurologic disorders
Gilles de la Tourette syndrome
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
movement disorder
Parkinson disease
tardive dyskinesia
torticollis
tremor
writers cramp
Showing articles 2100 to 2150 of 2934 << Previous Next >>

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Prolonged Intermittent Drooling & Oromotor Dyspraxia in Benign Childhood Epilepsy with Centrotemporal Spikes
Epilepsia 30:564-568, Roulet,E.,et al, 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Trochanteric Sciatic Neuropathy
Neurol 39:1539-1541, Crisci,C.,et al, 1989

Multifocal Fibrosclerosis with Hypertrophic Intracranial Pachymeningitis
Neurol 39:1345-1349, Berger,J.R.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

The Rational Management of Idiopathic Intracranial Hypertension
Arch Neurol 46:1049-1051, Corbett,J.J.&Thompson,H.S., 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Brain Abscess:Association with Pulmonary Arteriovenous Fistula and Hereditary Hemorrhagic Telangiectasia:3 Cases
Am J Med 85:718-720, Gelfand,M.S.,et al, 1988

Portosystemic Encephalopathy in Hereditary Hemorrhagic Telangiectasia
Am J Med 85:858-860, Fagel,W.J.,et al, 1988

MR Imaging of the Brain in Myelopathy Associated with Human T-Cell Lymphotropic Virus Type I
J Comput Assist Tomogr 12:750-754, Hara,Y.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Adoption and Genetic Prediction for Huntington's Disease
Lancet 2:1069-1070, Morris,M.,et al, 1988

Transient Tic Disorder and the Spectrum of Tourette's Syndrome
Arch Neurol 45:1200-1201, Kurlan,R.,et al, 1988

Massive Carbamazepine Overdose:Clinical & Pharmacologic Observations in Five Episodes
Neurol 38:755-759, Weaver,D.F.,et al, 1988

Risk of Brain Infarction in Familial Hypercholesterolemia
Stroke 19:1097-1100, Kaste,M.&Koivisto,P., 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988

Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
Wertelecki. W. , et al, NEJM 319:276-2838., , 1988

Carbamazepine:An Alternative Drug for the Treatment of Nonhereditary Chorea
Pediatrics 82:492-495, Roig,M.,et al, 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Familial Parkinsonism, Apathy, Weight Loss & Central Hypoventilation:Successful Long-Term Management
Neurol 38:637-639, Roy,E.P.,et al, 1988

Parkinson's Disease in a Nationwide Twin Cohort
Neurol 38:1217-1219, Marttila,R.J.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Dystrophin
Editorial, Lancet 2:429-4301988., , 1988

Respiratory Muscle Dysfunction in Hereditary Motor Sensory Neuropathy, Type I
Arch Int Med 148:1739-1740, Eichacker,P.Q.,et al, 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

The Incidence of Pseudotumor Cerebri, Population Studies in Iowa and Louisiana
Arch Neurol 45:875-877, Durcan,F.J.,et al, 1988

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Pseudotumor Cerebri in Men
Arch Neurol 45:866-872, Digre,K.B.&Corbett,J.J., 1988

Autonomic Nervous Function in Huntington's Disease
Arch Neurol 45:309-312, DenHeijer,J.C.,et al, 1988

Improvement of Cerebral CT Abnor Following Liver Transplant in a Patient with Wilson Disease
J Comput Assist Tomogr 12:138-149, Rothfus,W.E.,et al, 1988

Magnetic Resonance Imaging in Familial Paroxysmal Ataxia
Arch Neurol 45:547-549, Vighetto,A.,et al, 1988

Computed Tomography and Magnetic Resonance Imaging in Adult-Onset Leukodystrophy
Arch Neurol 45:1004-1008, Schwankhaus,J.D.,et al, 1988

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Risk of Dementia in Relatives of Patient with Alzheimer's Disease
Neurol 38:786-790, Huff,F.J.,et al, 1988

Normal Ageing, Impaired Cognitive Function, & Senile Dementia of the Alzheimer's Type:A Continuum
Lancet 1:1265-1267, Brayne,C.&Calloway,P., 1988

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Transient CNS Deficits:A Common, Benign Syndrome in Young Adults
Neurol 38:831-836, Levy,D.E., 1988

Tetrabenazine Therapy of Dystonia, Chorea, Tics, & Other Dyskinesias
Neurol 38:391-394, Jankovic,J.&Orman,J., 1988

Lyme Disease & Its Neurologic Complications
Arch Neurol 45:99-104, Finkel,M.F., 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Genetic Factors in Myasthenia Gravis:A Family Study
Neurol 38:38-42, Kerzin-Storrar,L.,et al, 1988



Showing articles 2100 to 2150 of 2934 << Previous Next >>