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acid maltase deficiency
advances in neurology
adverse drug reaction
alpha-fetoprotein
Alzheimer's disease
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, treatment of
anterior horn cell disease
anterior tibial muscle weakness
apraxia of eye movements
areflexia
arthrogryposis multiplex
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
atlanto axial dislocation, congenital
benign congenital hypotonia
Brugada syndrome
bulbar palsy, progressive
calf hypertrophy
carcinoembryonic antigen
carcinoma
cavernous sinus, syndrome
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 5
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
coma
complications
congenital heart disease
congenital myopathy
congestive heart failure
constipation
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
denervation of muscle
denervation potentials
dermatomyositis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
drooling
dysarthria
dystonia
dystrophin
efficacy
electrocardiogram, abnormal
electromyogram
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, muscle disease
epidemiology of neurology
eye movement, disorders of
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
Friedreich's ataxia
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
growth retardation
Guillain Barre syndrome
gynecomastia
heavy metal intoxication
hemangioma
history of neurology
Huntington's chorea
hypercapnia
hypertension
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infant, evaluation of
infantile tremor syndrome
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Isaacs syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
leukemia
lid closure, weakness of
life expectancy
liver disease
lordosis
lymphoma
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
mental retardation
misdiagnosis
molecular genetics
mononeuropathy
mortality
motor neuron disease
motor neuron disease, juvenile form
motor system
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, treatment of
myasthenic crisis
myocardial injury
myocytolysis
myokymia
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, mitochondrial
myopathy, thyroid disease causing
myositis
myotonia congenita
myotonia dystrophica
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic evaluation
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral, treatment
newborn, evaluation of
nusinersen
ocular motility, disorders of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
Oppenheim muscular dystrophy
paraparesis, familial spastic
Parkinson disease
pathology
patient information and support
periodic paralysis
periodic paralysis, thyrotoxic
phrenic nerve
placebo
poison, mercury
poison, neurologic problems with
poliomyelitis
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
post polio syndrome
preclinical
pregnancy, neurologic complications in
primary lateral sclerosis
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
radiation hypersensitivity
radiculopathy
respiratory failure
review article
RFLPs
risk-benefit assessment
safety
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
skin, lesions in neurologic disorders
SMN1 gene
spina bifida
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
stiff man syndrome
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
sudden death
survival motor neuron gene
telangiectases
term infant
Tolosa Hunt syndrome
tongue, fasciculations of
torticollis
treatment of neurologic disorder
tremor
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
vitamin E
vitamin E deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
weaning from respirator, failure to
weight loss
Werdnig-Hoffman disease
West disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1200 to 1250 of 8383 << Previous Next >>

Movement Disorders & AIDS
Neurol 37:37-41, Nath,A.,et al, 1987

Optico-Cerebral Syndrome:Simultaneous Hemodynamic Infarction of Optic Nerve & Brain
Neurol 37:263-268, Bogousslavsky,J.,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

Disseminated Cholesterol Embolism Presenting as Neuromyelitis Optica
BMJ 295:697, Goldman,M.,et al, 1987

Tuberculous Meningitis:Role of CT in Management and Prognosis
JNNP 50:30-36, Kingsley,D.P.E.,et al, 1987

Alternating Hemiplegia of Childhood
Int Pediatr 2:115-119, Aicardi,J., 1987

Critical Illness Polyneuropathy:A Complication of Sepsis and Multiple Organ Failure
Brain 110:819-842, Zochodne,D.W.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Spinal Myoclonus Associated with HTLV-III/LAV Infection
Arch Neurol 43:1203-1204, Berger,J.R.,et al, 1986

Delayed Postirradiation Lower Motor Neuron Syndrome
Ann Neurol 19:308-309, Gallego,J.,et al, 1986

CT Myelography in Spinal Cysticercosis
J Comput Assist Tomogr 10:195-198, Zee,C.,et al, 1986

Hydrocephalic Dementia & Spinal Cord Tumor, Report of a Case & Review of the Literature
Arch Neurol 43:714-718, Feldmann,E.,et al, 1986

Spastic Pure Motor Monoparesis
Ann Neurol 20:638-641, Ashizawa,T.,et al, 1986

Dolichoectatic Basilar Artery:A Review of 23 Cases
Stroke 17:1277-1281, Nishizaki,T.,et al, 1986

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Neonatal Paralytic Poliomyelitis
Arch Neurol 43:192-194, Bergeisen,G.H.,et al, 1986

Neurologic Complications of Carcinoid
Neurol 36:745-749, Parchell,R.A.&Posner,J.B., 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Causalgia as a Complication of Meningococcal Meningitis
BMJ 292:1710, McLelland,J.&Ellis,S.J., 1986

The AIDS Dementia Complex:I. Clinical Features
Ann Neurol 19:517-524, Navia,B.A.,et al, 1986

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

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Focal Epilepsy with Mesial Temporal Sclerosis after Acute Meningitis
Arch Neurol 42:1058-1060, Ounsted,C.,et al, 1985

Blepharospasm with Bilateral Basal Ganglia Infarction
Arch Neurol 42:1206-1208, Keane,J.R.&Young,J.A., 1985

Neurosyphilis
Arch Neurol 42:606-613, Simon,R.P., 1985

Continuous Intrathecal Baclofen for Severe Spasticity
Lancet 2:125-127, Penn,R.D.&Kroin,J.S., 1985

Lumbar Spinal Stenosis, Clinical Features, Diagnostic Procedures & Results of Surgical Treatment in 68 Patients
Ann Int Med 103:271-275, Hall,S.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Differential Diagnosis Between Radiation & Tumor Plexopathy of the Pelvis
Neurol 35:1-7, Thomas,J.E.,et al, 1985

Progressive Dementia, Visual Deficits, Amyotrophy, & Microinfarcts
Neurol 35:789-796, Kaplan,J.G.,et al, 1985

Neurocysticercosis:A New Classification Based on Active & Inactive Forms, A Study of 753 Cases
Arch Int Med 145:442-445, Sotelo,J.,et al, 1985

Alexander's Disease, A Disease of Astrocytes
Brain 108:367-385, Borrett,D.&Becker,L.E., 1985

Correlation of Electromyography with Computed Tomography in Evaluation of Lower Back Pain
Arch Neurol 41:594-597, Khatri,B.O.,et al, 1984

Iatrogenic Causalgia
Arch Neurol 41:821-824, Horowitz,S.H., 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Muscular Hypertrophy after Chronic Radiculopathy
Arch Neurol 41:397-398, Montagna,P.,et al, 1984

Intracranial Hemorrhage in the Term Newborn
Arch Neurol 41:30-34, Fenichel,G.M.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Brachial Plexopathy:Recurrent Cancer or Radiation
Neurol 34:1331-1335, Lederman,R.J.,et al, 1984

Diagnosis & Treatment of Lumbosacral Plexopathies in Patients with Cancer
Arch Neurol 41:1282-1285, Pettigrew,L.C.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

The Noncerebrovascular Complications of Chiropractic Manipulation
Neurol 34:684-685, Schmidley,J.W.,et al, 1984

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Neurological Complications of Acquired Immune Deficiency Syndrome:Analysis of 50 Patients
Ann Neurol 14:403-418, Snider,W.D.,et al, 1983

Presentation, Treatment, & Prognosis of Idiopathic Inflammatory Muscle Disease in a Rural Hospital
Am J Med 75:433-438, Hoffman,G.S.,et al, 1983

Early Diagnosis of Cervical Spinal Cord Meningioma
JAMA 249:1475-1476, Rosenbaum,L.H.,et al, 1983



Showing articles 1200 to 1250 of 8383 << Previous Next >>