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Differential
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acanthocytosis
amyloidosis
amyotrophic lateral sclerosis
arrhythmia, cardiac
arthrogryposis multiplex
ataxia, cerebellar
Bassen-Kornzweig syndrome
blindness
cardiomyopathy
cataracts
Charcot-Marie-Tooth
Cockayne's syndrome
congestive heart failure
consanguinity
cornea, abnormal
deafmute
deafness
dermatomyositis
dwarfism
electroencephalogram, abnormalities of
familial
Friedreich's ataxia
gargoylism
genetic neurologic disorders
glaucoma
Guillain Barre syndrome
Guillain Barre syndrome, familial
Hallgren's syndrome
heart block
Hurler's syndrome
idiopathic polyneuropathy
Kearns-Sayre syndrome
keratoconus
klippel feil syndrome
Laurence-Moon-Bardet-Biedl syndrome
malformation, CNS, congenital
mental retardation
mononeuropathy
motor neuron disease
mucopolysaccharidoses
muscle diseases, characteristics of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, thyroid disease causing
myopia
myositis
myotonia dystrophica
neuritis
neuritis, causes of
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, motor
obesity
ocular myopathy
poliomyelitis
polydactyly
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic relapsing
polyneuropathy, familial
porphyria
pseudoretinitis pigmentosa
psychiatric disorder
retinitis pigmentosa
retinopathy
review article
sarcoidosis
schizophrenia
seizure
sensory polyneuropathy
Spielmeyer Vogt syndrome
stiff man syndrome
torticollis
Usher's syndrome
visual field defect
visual fields, constricted
Werdnig-Hoffman disease
Showing articles 1650 to 1700 of 2113 << Previous Next >>

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987

Risk Factors for Generalized Tonic-Clonic Seizures:A Population-Based Case-Control Study in Rochester, Minnesota
Neurol 37:1315-1322, Rocca,W.A.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

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

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Dementia of the Alzheimer Type:Clinical & Family Study of 22 Twin Pairs
Neurol 37:359-363, Nee,L.E.,et al, 1987

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987

Von Hippel-Lindau Disease in an Adolescent
Pediatrics 79:632-637, Seitz,M.L.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Adult Polycystic Kidney Disease & Intracranial Aneurysms
BMJ 295:526, Saifuddin,A.&Dathan,J.R.E., 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Analysis of Risk Factors for Stroke in a Cohort of Men Born in 1913
NEJM 317:521-526, Welin,L.,et al, 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

Essential Tremor:A Review
Neurol 37:1194-1197, Findley,L.J.&Koller,W.C., 1987

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

Risk Factors for Alzheimer's Disease:A Case-Control Study
Neurol 37:1630-1633, Shalat,S.T.,et al, 1987

Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
Arch Int Med 147:1317-1320, Sloan,J.B.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Tourette Syndrome
Editorial, Lancet 1:3081987., , 1987

Hereditary Neuropathy with Liability to Pressure Palsies
In Handbk of Clin Neurol, Elsevier Sci Publ Co, NY 51:551-562987., Cherry,S.&Mayer,R.F., 1987

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

The Inheritance of Gilles De La Tourette's Syndrome & Associated Behaviors
NEJM 315:993-997, Pauls,D.L.&Leckman,J.F., 1986

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986

Familial Myoclonic Dementia Masquerading as Creutzfeldt-Jakob Disease
Ann Neurol 20:231-239, Little,B.W.,et al, 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

A Population-Based Study of Multiple Sclerosis in Twins
NEJM 315:1638-1642, Ebers,G.C.,et al, 1986

Familial Hyperlipidemia in Stroke in the Young
Stroke 17:1142-1145, Bansal,B.C.,et al, 1986

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 1986

Benign Versive or Circling Epilepsy with Bilateral 3-Cps Spike- & -Wave Discharges in Late Childhood
Ann Neurol 19:301-303, Gastaut,H.,et al, 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986



Showing articles 1650 to 1700 of 2113 << Previous Next >>