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Differential
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acromegaly
Addison's disease
Aldrich's syndrome
alkalosis
alkalosis, respiratory
ANA
anemia
antibiotics, neurologic complications with
areflexia
arthropathy
ataxia
ataxia, cerebellar
basal ganglia, calcification of
basal ganglia, lesion, bilateral
behavioral disorder
bitemporal visual field defect
blood dyscrasias, neurologic findings with
cafe au lait spots
calcification, intracranial
calcium, serum
carcinoma of pancreas
cardiomyopathy
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, isodense lesion with acute hemorrhage
cataracts
central nervous system, infection of
cerebral vasculature, calcification
cerebrospinal fluid, elevated protein of
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
coma
compression fracture
confusion
congestive heart failure
craniopharyngioma
creatine phosphokinase isoenzyme elevation
creatine phosphokinase(CPK)elevated
Cushing's syndrome
deafness
dementia
dementia, reversible
dementia, treatment of
dentate nuclei
depression
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diplopia
dural sinus thrombosis
dysarthria
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalitis
enzyme, muscle disease
epinephrine
erethism
exophthalmus
eye movement, disorders of
Fahr disease
familial
fasciculation
fatigue
fibrous dysplasia
fontanel, bulging
gait disorder
genetic neurologic disorders
genetic testing
hallucination, auditory
hand pain
Hand-Schuller-Christian disease
hearing loss
heart block
hepatolenticular degeneration(Wilson's disease)
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperphosphatasia
hyperthyroidism
hyperventilation
hypocalcemia
hypocalcemia, causes of
hypoglycemia
hypokalemic periodic paralysis
hypomagnesemia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypopituitarism
hypothalamus
hypothalamus, disturbance of
hypothyroidism
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, children
intracranial pressure, increased
intrinsic hand muscles, wasting of
islet cell tumor
Kearns-Sayre syndrome
lactic dehydrogenase(LDH)
laryngismus stridulus
macrocephaly
malabsorption
mastoiditis
McCune-Albright syndrome
menarche
mental retardation
metachromatic leukodystrophy
misdiagnosis
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI pattern
MRI, abnormal
multiple sclerosis
multiple sclerosis, cognitive presenttion
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
myasthenia gravis
myoedema
myopathy
myopathy, hypocalcemic
myopathy, mitochondrial
myopathy, proximal
myopathy, thyroid disease causing
myotonia
myxedema coma
myxedema, neurologic manifestations of
Nelson's syndrome
neoplasm, intracranial
neoplasm, pituitary
neuroendocrinology
neuroophthalmology
neuropsychiatry
obesity
octreotide
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
overlap syndrome
pain, abdominal
panic attacks
papilledema
paranoia
parathormone
parathyroid adenoma
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal neurologic deficits
pernicious anemia
personality change
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
poison, neurologic problems with
porphyria
precocious puberty
primary aldosteronism
primary familial brain calcification
pseudohypoparathyroidism
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, cause of
ptosis
ptosis, bilateral
ragged-red fibers
renal biopsy
renal dysplasia
renal failure
retinal degeneration
retinitis pigmentosa
rigidity
sedimentation rate, elevated
seizure
seizure, neonatal
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
somatostatin analogue
spasmophilia
spongy degeneration of brain
status tetanicus
steroid therapy, CNS treatment and complications with
stiff joints
striopallidodentate calcifications, familial idiopathic
syphilis, neurologic complications with
systemic lupus erythematosus
tetany
tetany, latent
tetany, normocalcemic
tetracycline
thalamus, lesion of-bilateral
thyrotoxicosis
tongue, enlarged
treatment of neurologic disorder
tremor
tremor, intention
Trousseau's sign
visual field defect
visual field defect, altitudinal
visual loss
vitamin A
von Bonsdorff's sign
weakness
white matter disease
Showing articles 1050 to 1100 of 2218 << Previous Next >>

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
Ann Neurol 39:818-823, Holloway,R.G., 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Prospective Evaluation of MRI Lumbosacral Nerve Root Enhancement in Acute Guillain-Barre Syndrome
Neurol 47:813-817, Gorson,K.C.,et al, 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Lyme Neuroborreliosis Disguised as Normal Pressure Hydrocephalus
Neurol 46:1743-1745, Danek,A.,et al, 1996

Lyme Radiculoneuritis Treated with Intravenous Immunoglobin
Neurol 46:1174-1175, Crisp,D.&Ashby,P., 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
Lancet 347:28-29, Heafield,M.T.E.,et al, 1996

Evaluation of Extracranial Vertebral Artery Dissection with Duplex Color-Flow Imaging
Stroke 27:290-295, Bartels,E.&Flugel,K.A., 1996

Middle Cerebral Artery Dissection:A Clinicopathologic Study
Neurol 45:1929-1931, Sharif,A.A.,et al, 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Serial Magnetic Resonance Imaging in Isolated Angiitis of the Central Nervous System
Neurol 45:1462-1465, Ehsan,T.,et al, 1995

Recurrent Stroke and Thrombo-Occlusive Events in the Antiphospholipid Syndrome
Ann Neurol 38:119-124, Levine,S.R.,et al, 1995

Cranial Nerve Enhancement in the Guillain-Barre Syndrome
AJNR 16:923-925, Fulbright,R.K.,et al, 1995

Vertebral Artery Injury after Acute Cervical Spine Trauma:MR Angiography & Assess of Clin Consequences
AJR 164:443-447, 4481995., Friedman,E.,et al, 1995

Acute Bacterial Myositis Due to Staphylococcus Aureus Septicemia
Neurol 45:390-391, Sato,K.,et al, 1995

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Invasive Aspergillosis:A Complication of Treatment of Temporal Arteritis
J Neuro-Ophthalmol 15:36-38, Wiggins,R.E., 1995

Lyme Neuroborreliosis
Ann Neurol 37:691-702, Garcia-Monco,J.C.&Benach,J.L., 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Common Variable Immunodeficiency and Inclusion Body Myositis:A Distinct Myopathy Mediated by Natural Killer Cells
Ann Neurol 37:806-810, Dalakas,M.C.&Illa,I., 1995

Levonorgestrel Implants and Intracranial Hypertension
NEJM 332:1720-1721, Alder,J.B.,et al, 1995

Benign Intracranial Hypertension in Children with Growth Hormone Deficiency Treated with Growth Hormone
J Pediatr 126:996-999, Malozowski,S.,et al, 1995

Gadopentetate Dimeglumine-Enhanced MR in the Diagnosis of the Tolosa-Hunt Syndrome
AJNR 16:942-944, Zournas,C.,et al, 1995

High Resolution MRI of Anterior Visual Pathway in Pts with Optic Neuropathies Using Fast Spin Echo & Phased Array Local Coils
JNNP 58:562-569, Gass,A.,et al, 1995

Magnetic Resonance Visualization of the Swollen Optic Disc in Papilledema
J Neuro-Ophthalmol 15:122-124, Brodsky,M.C.&Glasier,C.M., 1995

Neuro-Ophthalmic Features of Cerebral Venous Obstruction
Arch Neurol 52:880-885, Purvin,V.A.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Hereditary Sensory and Autonomic Neuropathy with Cataracts, Mental Retardation, and Skin Lesions:Five Cases
Neurol 45:1405-1408, Heckmann,J.M.,et al, 1995

The Predictive Value of CSF Dynamic Tests in Patients with the Idiopathic Adult Hydrocephalus Syndrome
Arch Neurol 52:783-789, Malm,J.,et al, 1995

Intracranial Arteries:Prospective Blinded Comparative Study of MR Angiography and DSA in 50 patients
Radiology 195:451-456, Klaus,W.S.,et al, 1995

Benign Focal Cerebral Vasculitis:Case Report
Neurol 45:1731-1734, Berger,J.R.,et al, 1995

Effects of Surgically Induced Weight Loss on Idiopathic Intracranial Hypertension in Morbid Obesity
Neurol 45:1655-1659, Sugerman,H.J.,et al, 1995

Stroke Patterns in Unilateral Atherothrombotic Occlusion of the Internal Carotid Artery
Stroke 26:422-425, Mounier-Vehier,F.,et al, 1995

Guidelines for Carotid Endarterectomy
Stroke 26:188-201, Moore,W.S.,et al, 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Progressive Cerebral Occlusive Disease after Radiation Therapy
Stroke 26:131-136, Bitzer,M.&Topka,H., 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Increased Incidence of Aortic Aneurysm and Dissection in Giant Cell (Temporal) Arteritis
Ann Int Med 122:502-507, Evans,J.M.,et al, 1995

Cranial MRI in Ataxia-Telangiectasia
Neuroradiology 37:77-82, Sardanelli,F.,et al, 1995



Showing articles 1050 to 1100 of 2218 << Previous Next >>