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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 1850 to 1900 of 2141 << Previous Next >>

Family Studies in Tuberous Sclerosis
JAMA 249:1302-1304, Cassidy,S.B.,et al, 1983

Effect of a Single Oral Dose of Propranolol on Essential Tremor:A Double-Blind Controlled Study
Ann Neurol 13:165-177, Calzetti,S.,et al, 1983

Nadolol in Essential Tremor
Neurol 33:1076-1077, Koller,W.C., 1983

Phenobarbital & Propranolol in Essential Tremor:A Double-Blind Controlled Clinical Trial
Neurol 33:296-300, Baruzzi,A.,et al, 1983

Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983

Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983

A Family with Histologially Confirmed Alzheimer's Disease
Arch Neurol 40:203-208, Nee,L.E.,et al, 1983

Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
Neurol 33:81-86, Bird,T.D.,et al, 1983

Hyperekplexia
Arch Neurol 40:246-248, Kurczysnki,T.W., 1983

Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983

The Malignant Hyperthermia Syndrome
NEJM 309:416-418, Nelson,T.E.,et al, 1983

Periodic Meningitis & Familial Mediterranean Fever
Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

The Neuropathology of Glycine Encephalopathy:Five Cases with Immunohistochemical & Ultrastructural Observations
Neurol 32:975-985, Agamanolis,D.P.,et al, 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Narcolepsy-Cataplexy
Arch Neurol 39:164-168, Kales,A.,et al, 1982

Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

A Surgical Approach To The Treatment Of Fetal Hydrocephalus
NEJM 306:1320-1325, Clewell,W.H.,et al, 1982

Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
Lancet 2:852-853, Moloney,J.B.,et al, 1982

Where am I
BMJ 285:85-86, Godwin-Austen,R.B., 1982

Controlled Study of Metoprolol & Propranolol During Prolonged Administration in Patients with Essential Tremor
JNNP 45:893-897, Calzetti,S.,et al, 1982

Double-blind Controlled Study of Primidone in Essential Tremor:Preliminary Results
BMJ 285:608, Findley,L.J., 1982

Prevalence of Essential Tremor
Arch Neurol 39:750-751, Haerer,A.F.,et al, 1982

Genetics of Alzheimer's Disease
BMJ 284:1065-1066, Harris,R., 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Familial X-linked Addison Dise. as an Expression of Adrenoleukodystr. :C26 Fatty Acid in Cult. Skin Fibroblasts
Neurol 32:543-547, O'Neill,B.P.,et al, 1982

The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982

Essential Myoclonus
In Movement Disorder, CD Marsden & S Fahn (Ed) , Butterworth, London, 1982, p 207., , 1982

Benign Paroxysmal Torticollis in Infancy
Arch Dis Child 56:956-959, Deonna,T.,et al, 1981

Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981

Familial Hemiplegic Migraine:EEG & CT Scan Study of Two Cases
Ann Neurol 10:392-295, Gastaut,J.L.,et al, 1981

Placement Of Ventriculo-Amniotic Shunt For Hydrocephalus In A Fetus
NEJM 305:955, Clewell,W.H.,et al, 1981

Neurologic Complications of Hyperthyroidism
Arch Neurol 38:669-670, Bulens,C., 1981

A Family Affected with Intestinal Polyposis & Gliomas
Ann Neurol 10:390-392, Todd,D.W.,et al, 1981

Intensive Evaluation of Referred Unclassified Neuropathies Yields Improved Diagnosis
Ann Neurol 10:222-226, Dyck,P.J.,et al, 1981

Bilateral Vocal Cord Paralysis in a Patient With Familial Hypertrophic Neuropathy
Arch Neurol 38:532, Johnson,J.A.,et al, 1981

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Von Recklinghausen Neurofibromatosis
NEJM 305:1617-1627, Riccardi,V.M., 1981

Dominant Inheritance of Intracranial Berry Aneurysm
BMJ 283:824-825, Evans,T.W.,et al, 1981

Computed Tomography in Cerebrotendinous Xanthomatosis
Neurol 31:1463-1465, Berginer,V.M.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

The Familial Nature of MS:Empiric Recurrence Risks for First, Second-, & Third-degree Relatives of Pts
Neurol 31:1039-1041, Sadovnick,A.D.,et al, 1981



Showing articles 1850 to 1900 of 2141 << Previous Next >>