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acanthocytosis
acetylcholine
advances in neurology
algorithm
Alzheimer's disease
amantadine
amyotrophic lateral sclerosis
anticholinesterase
antioxidant
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
Babinski sign
Bassen-Kornzweig syndrome
biologic markers
blindness
blood dyscrasias, neurologic findings with
brainstem, atrophy
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar vermis
cerebral glucose metabolism
cerebrovascular accident
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
congestive heart failure
consanguinity
controversies in neurology
cornea, abnormal
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dentatorubral-pallidoluysian atrophy
dexterity, impaired
diabetes mellitus
disability, neurological
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
endocardial fibrosis
ethics in neurology
eye movement, disorders of
falling
familial
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gargoylism
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
Guillain Barre syndrome
Hallgren's syndrome
hammertoes
head injury
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypotonia
imbalance
incoordination
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Laurence-Moon-Bardet-Biedl syndrome
lecithin
leg weakness, bilateral
Leigh's disease
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
malformation, CNS, congenital
malondialdehyde
Marinesco-Sjogren syndrome
mental retardation
metabolic disorder, primary
misdiagnosis
mitochondrial disease
molecular genetics
MRI
MRI, abnormal
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myelomalacia
myopathy
myopia
myotonia dystrophica
nerve conduction studies
neuritis
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, amyloid
nystagmus
obesity
ocular motility, disorders of
ocular myopathy
optic atrophy
paraparesis, familial spastic
Parkinson disease
pathologic reflex
pes cavus
physostigmine
polydactyly
polyneuropathy
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudoretinitis pigmentosa
psychiatric disorder
remote effect of cancer on the nervous system
retinitis pigmentosa
retinopathy
review article
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
sensory loss
spastic ataxia
spasticity
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
staggering
tandem gait, ataxic
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
Usher's syndrome
vibratory sensation
vibratory sensation, abnormal
visual evoked response
visual field defect
visual fields, constricted
vitamin deficiency
vitamin E
vitamin E deficiency
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
Showing articles 1150 to 1200 of 1254 << Previous Next >>

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Eye Movements in Ataxia-telangiectasia
Neurol 28:1099-1104, Baloh,R.W.,et al, 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978

Varicella & Acute Cerebellar Ataxia
Arch Neurol 35:769-771, Peters,A.C.B.,et al, 1978

Acute & Chronic Progressive Encephalopathy Due to Gasoline Sniffing
Neurol 28:507-510, Valpey,R.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

Ataxic Hemiparesis
Arch Neurol 35:126, Fisher,C.M., 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

Persistent Cerebellar Ataxia after Exposure to Toluene
Ann Neurol 2:440, Boor,J.W.,et al, 1977

More about Poisoning by Phencyclidine ("PCP, ""Angel Dust")
NEJM 297:1405, 1977. (Letter), Herskowitz,J.,et al, 1977

Lower Motor Neuron Disease with Spinocerebellar Degeneration
Ann Neurol 2:524, Page,R.W.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Tonic Pupils with Acute Ophthalmoplegic Polyneuritis
Ann Neurol 2:393, Keane,J.R., 1977

The Central Nervous System in a Case of Neurolathyrism
Neurol 27:1176, Striefler,M.,et al, 1977

Reversible Corticospinal Tract Disease Due to Hyperthyrodisim
Arch Neurol 34:647, Garcia,C.A.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Case Record of the M. G. H.
Glioblastoma Multiforme of Pons, NEJM 296:8651977., , 1977

Supratentorial Arachnoid Cysts in Adults:A Discussion of Two Cases from a Pathophysiologic & Surgical Perspective
Arch Neurol 34:276, Dyck,P.,et al, 1977

The Serological Diagnosis of St. Louis Encephalitis in Patient with Syndr. of Opsoclonia, Body Tremulousness, & Benign Encephalitis
Ann Neurol 1:596, Estrin,W., 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

DiGeorge Syndrome Associated with Glioma & Two Kinds of Viral Infection
NEJM 296"1235, Asamoto,H., 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Subacute meningitis heralding a diffuse granulomatous angiitis: (Wegener's granulomatosis? )
Neurol, 27:2621977., Atcheson,S.G.,et al, 1977

Fisher's Syndrome:A Pharmacological Study of the Pupils
Ann Neurol 2:63, Okajima,T.,et al, 1977

Cerebrovascular diseases
In Harrison's Principles of Internal Medicine, 1977. McGraw-Hill Book Co. , p1., , 1977

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Downbeating Nystagmus & Hereditary Cerebellar Degeneration, Levin DB, et al, In Neuro-ophthalmology Update
Masson Publishing USA, INC. 1977 P 337-338., Smith,J.L., 1977

Ocular Motor Abnormalities in Hereditary Cerebellar Ataxia
Brain 99:207-234, Zee,D.S.,et al, 1976

Hypophosphatemia Mimicking Acute Guillain-Barre-Strohl Syndrome
JAMA 235:1040-1041, Weintraub,M.I., 1976

Nerve-Growth Factor in Familial Dysautonomia
NEJM 295:671, Montalcini,R.L., 1976

Case Records of the MGH
Giant cell Angiitis, intracranial NEJM 295:9441976., , 1976

Progressive Rubella Panencephalitis
Arch Neurol 33:722, Wolinsky,J.S.,et al, 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Chronic Meningitis
Medicine 55:341, Ellner,J.J.,et al, 1976

Normocalcemic Tetany
Neurol 26:825, Isgreen,W.P., 1976

Progressive Spastic Paraparesis & Adrenal Insufficiency
Arch Neurol 33:678, Gumbinas,M.,et al, 1976

The Thyroid Gland:Its Relationship to Neurology
In Handbook of Clin Neurol, Vinken & Bruyn (Ed) , North Holland Publ Co, Amsterdam 27:255, Greene,R., 1976

MGH-CPC-Gliomatosis Cerebri of Cerebellum & Brainstem
NEJM 292:852, , 1975

MGH-CPC-Ataxic Telangiectasia & Left Frontal Lobe Glioma
NEJM 292:1231, , 1975

Platelet-Inhibiting Drugs in the Prevention of Clinical Thrombotic Disease
NEJM 293:174, Genton,E.,et al, 1975

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975



Showing articles 1150 to 1200 of 1254 << Previous Next >>