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Differential
(Click to cross reference)
abdominal distention
acromegaly
amaurosis fugax
amyloid
amyloidosis
areflexia
arrhythmia, cardiac
arteritis, temporal
arthralgia
ataxia
atypical
autoimmune disease
bacterial infection
blindness, monocular
brainstem, lesion of
cachexia
calcification, liver
calcification, lymph node
carcinoma
carcinoma of breast
carcinoma of stomach
cardiomyopathy
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, orbits
cavernous sinus
cavernous sinus, lesion of
cavernous sinus, syndrome
cerebellar atrophy, secondary
cerebellar degeneration
cerebrovascular accident
chemosis
chronic progressive external ophthalmoplegia
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
congestive heart failure
conjunctival injection
consanguinity
cough
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
cyst, benign intracranial
cysticercosis
deafness
diagnostic criteria
diarrhea
diplopia
diplopia, vertical
donut sign
dysthyroid ocularmyopathy
dysthyroidism
edema, periorbital
eosinophilic granulomatosis with polyangiitis
episcleritis
exophthalmus
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
extraocular muscle, metastasis to
eye movement, disorders of
eye, pain in
facial pain
familial
fatigue
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
forced duction test
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene mutation
genetic neurologic disorders
giant cell arteritis
granulomatosis with polyangiitis
Graves ophthalmopathy
head injury
headache
headache, bitemporal
heart block
heart block, complete
heralding manifestation
histochemistry of muscle
hyperphosphatasia
hyperthyroidism
idiopathic inflammatory orbital disease
IgG4, serum
IgG4-related disease
immunotherapy
infraorbital nerve
intestinal pseudoobstruction
jaw claudication
Kearns-Sayre syndrome
lacrimal gland enlargement
lateral rectus palsy
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
lid
liver function enzymes
lymph node biopsy
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
malformation, vascular
malformation, vascular, cerebral
maxillary nerves
medial rectus palsy
melanoma, malignant
meningeal enhancement
meningioma
meningitis, leukemic
methotrexate
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, extraocular muscle enhancement
MRI, optic nerve
MRI, orbit
mucormycosis
muscle biopsy
muscle biopsy, extraocular
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, ocular
mycosis fungoides
myocarditis
myopathy, mitochondrial
myopathy, necrotizing
myopathy, steroid responsive
myositis
myositis, ocular
nasal stuffiness
necrotizing vasculitis
neoplasm, metastatic to CNS
neoplasm, metastatic to muscle
neoplasm, metastatic to orbit
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuroophthalmology
neuropathy
ocular motility, disorders of
ocular myopathy
oculopharyngeal muscular dystrophy
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, recurrent
ophthalmoplegia, total
optic disc edema
optic nerve
optic nerve sheath enhancement
optic nerve, compression of
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
optic neuropathy, bilateral
orbit
orbit, biopsy
orbit, cellulitis of
orbit, inflammation in
orbit, lesions of
orbit, mass
orbit, meningioma of
orbit, neoplasms of
orbit, pseudotumor of
orbital apex
orbital apex syndrome
pain
pain, abdominal
pain, periorbital
parasellar syndrome
pathology
perineuritis
perineuritis, optic
photophobia
prognosis
progressive neurologic disorder
proptosis
proptosis, bilateral
proptosis, unilateral
ptosis
ptosis, bilateral
ptosis, unilateral
purpura
radiation therapy, CNS treatment and complications with
ragged-red fibers
rash
recurrent
respiratory tract infection
restrictive ophthalmopathy
retina, abnormal
retinal lesion
review article
rhabdomyosarcoma
rhabdomyosarcoma of orbit
risk factors
rituximab
salivary gland enlargement
sarcoidosis
scotoma
sedimentation rate, elevated
sensorineural hearing loss
serum alanine aminotransferase
sialadenitis
sinuses, diseases of
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
Stephens syndrome
steroid
steroid therapy, CNS treatment and complications with
superior ophthalmic vein
syncope
systemic illness
temporal artery, biopsy
thyroid stimulating immunoglobulins
thyrotoxicosis
thyrotropin-releasing hormone, stimulation test
Tolosa Hunt syndrome
tongue, enlarged
tram-track sign
transient neurologic deficit
trauma
treatment of neurologic disorder
trigeminal nerve
trigeminal nerve, abnormality of
trigeminal nerve, hypertrophy
trigeminal nerve, lesion of
trinucleotide repeats
ultrasonography
ultrasonography, orbit
vasculitides
vision, blurred
vision, blurred, monocular
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual loss
visual loss, alternating
visual loss, slow-unilateral
visual loss, sudden-unilateral
visual loss, transient
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
white matter disease
Showing articles 1800 to 1850 of 2760 << Previous Next >>

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Electrodiagnostic Abnormalities in 113 Consecutive Patients with Guillain-Barre Syndrome
Arch Neurol 47:881-887, Ropper,A.H.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Poliomyelitis Outbreak in Isreal in 1988:A Report with two Commentaries
Lancet 335:1192-1198, Slater,P.E.,et al, 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Relapse of Infant Botulism
Ann Neurol 28:187-189, Glauser,T.A.,et al, 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Lyme Polyradiculoneuropathy Presenting as Increasing Abdominal Girth
Neurol 40:373-375, Daffner,K.R.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Muscle Cramps
Arch Int Med 150:511-518, McGee,S.R., 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Bismuth Absorption and Myoclonic Encephalopathy During Bismuth Subsalicylate Therapy
Ann Int Med 112:140-141, Mendelowitz,P.C.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Unusual Cause of'Piriformis Muscle Syndrome'
Arch Neurol 47:1144-1146, Papadopoulos,S.M.,et al, 1990

Mandibular Nerve:MR vs. CT about 10 Proved Unusual Tumors
Neuroradiology 32:492-496, Marsot-Dupuch,K.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Aggravation of Myasthenia Gravis by Erythromycin
Ann Neurol 28:577-579, May,E.F.&Calvert,P.C., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Treatment of Spasticity with Botulinum Toxin:A Double-Blind Study
Ann Neurol 28:512-515, Snow,B.J.,et al, 1990



Showing articles 1800 to 1850 of 2760 << Previous Next >>