Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
abducens nerve paralysis, bilateral
acetylcholine receptor antibody
acne fulminans
Addison's disease
Adies pupil
adrenal crisis, acute
adverse drug reaction
amaurosis fugax
amaurosis fugax, unilateral vs.bilateral
amphiphysin antibodies
amyloid
amyotrophic lateral sclerosis, misdiagnosis
ANA
anemia
aneurysm
angiotensin-converting enzyme
anorexia
anti HMGCR antibody
anti Hu antibody
anti Jo1 antibody
anti Ku antibody
anti MAG antibodies
anti Mi2 antibody
anti NT5C1A
anti p155
anti Ri antibody
anti signal recognition particle antibody
anti Yo antibody
antibodies to voltage-gated calcium channels
anticholinesterase
anticonvulsants, untoward effects of
antistriational muscle antibody
antisynthetase syndrome
arachnoiditis
arbovirus
areflexia
arm weakness
arrhythmia, cardiac
arteritides
arteritis, temporal
arthralgia
arthritis
aspartate aminotransferase
aspiration
asthma
ataxia
ataxia, paroxysmal
ataxic gait
atlanto-axial subluxation
atrial fibrillation
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
Balint's syndrome
Barkhof MR criteria for MS
basal ganglia
basal ganglia, lesion of
basilar impression
biologic markers
blindness, sudden
blink reflex
brachial neuritis
brain biopsy
brain natriuretic peptide
brainstem
brainstem, infarction of
brainstem, lesion of
brainstem, tuberculoma of
bruising
bruit
burning skin
calcium channel dysfunction
cancer associated myopathy
carcinoma
carcinoma of breast
carcinoma of lung
carcinoma of ovary
cardiomyopathy
cardiovascular disease
carpal tunnel syndrome
CAT scan, chest
CAT scan, emission, abnormal
cauda equina, enhancement
celiac disease, childhood
central core disease
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebral infarction
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, young adult
cerebrovascular disease
chemical weapons
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
children
chills
chloride channel dysfunction
choking
chorea
chronic fatigue syndrome
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
collapsin response mediator protein 5 IgG
coma
complications
compression neuropathy
concentration, impaired
confusion
congenital birth defects
congenital myasthenic syndromes
congestive heart failure
constipation
contactin associated protein like 2 antibodies
contractures, joint
controversies in neurology
cost effectiveness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cyclophosphamide
cytokines
deafness
deafness, unilateral
DEET
degenerative diseases of CNS
delay in diagnosis
delirium
demyelinating disease
depression
dermatomyositis
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dural rheumatoid nodules
duvalumab
dysphagia
dysphonia
dyspnea
dystonia
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electromyogram, fasciculation potentials
electromyogram, incremental response
electron microscopy
ELISA
emergencies, neurologic
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, focal
encephalitis, paraneoplastic
encephalitis, recurrent
encephalomyelitis
encephalopathy
enzyme, muscle disease
enzyme, serum
eosinophilia
epidemiology of neurology
epistaxis
evidence-based research
exercise
exercise-related muscle strength increase
face, numbness of
facial nerve palsy
facial weakness
falling
false positive VDRL
familial
familial hemiplegic migraine
fatigue
fever
fibrillations
finger flexor weakness
finger weakness
flaccid paralysis
flu-like illness
fluorescent treponema antibody absorption/false positive
fundus, abnormality of
gag reflex, depressed
gait disorder
gait, waddling
gamma amino butyric acid
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy, horizontal
gender
gene
genetic counselling
genetic neurologic disorders
genetic testing
glutamic acid decarboxylase, antibody
granulomatosis, allergic
Guillain Barre syndrome
Gulf War syndrome
gynecomastia
hallucination
hallucination, visual
hand weakness
headache
hearing loss
heart block
heart murmur
heat intolerance
hemianopia, homonymous
hemiparesis
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus
herpes virus infection
hip pain
HLA
HMGcoA reductase inhibitors
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
Horner's syndrome
hot bath test
H-reflex testing
human herpesvirus 6
Huntington's chorea
hypercapnia
hypereosinophilic syndrome(HES)
hypergammaglobulinemia
hyperkalemia
hyperpigmentation of skin
hypersomnia
hypertension
hypertensive encephalopathy
hyperthyroidism
hypocalcemia
hypoglycorrhachia
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hyporeflexia
hypotension, systemic
iatrogenic neurologic disorders
idiopathic inflammatory myopathy
imbalance
immune checkpoint inhibitors
immune-related adverse events
immunologic disease
immunology and the nervous system
immunomodulation
immunosuppression
immunosuppressive agents
immunotherapy
impotence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
insect repellent
insecticides
intellectual deterioration
interstitial pulmonary fibrosis
intracerebral hemorrhage
intracranial hypertension, benign
intrinsic hand muscles, wasting of
ipilimumab
irritability
joint hypermobility
juvenile idiopathic inflammatory myopathy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
leucine rich glioma inactivated 1 antibodies
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
lid closure, weakness of
life expectancy
limb-girdle weakness
limbic encephalitis
livedo reticularis
liver function enzymes
lymphadenopathy
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malignancy screen
malignancy, occult
malignant hyperpyrexia
mastoiditis
mediastinum, mass of
mediastinum, widening
medulla oblongata, lesion of
melanoma, malignant
meningitis
meningitis, aseptic
meningitis, neutrophilic
meningitis, noninfectious
meningoencephalitis
mental status, abnormal
mestinon
methotrexate
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mixed connective tissue disease
molecular genetics
monomelic myositis
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
mosquito
movement disorder
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, muscle
MRI, spinal cord
MRI, sulcal hyperintensity
multiple myeloma
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple sclerosis, treatment of
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle stiffness
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, insidious onset of
muscle weakness, pattern
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, late-onset
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neuromuscular junction in
myasthenia gravis, paraneoplastic
myasthenia gravis, receptor site in
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic syndrome
myasthenic syndrome, treatment of
myelitis
myelopathy
myelopathy, chronic progressive
myocarditis
myocytolysis
myopathy
myopathy inflammatory, classification
myopathy, autoimmune
myopathy, carcinomatous
myopathy, drug-induced
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, inflammatory
myopathy, inflammatory, classification
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, necrotizing, immune-mediated
myopathy, quadriceps
myopathy, steroid induced
myopathy, steroid responsive
myopathy, toxic
myopathy, vacuolar
myositis
myositis specific autoantibody
myositis, bacterial
myositis, eosinophilic
myositis, focal
myositis, fungal
myositis, granulomatous
myositis, juvenile
myositis, ocular
myositis, overlap
myositis, parasitic
myotonia congenita
myotonia dystrophica
nasal septum, perforation of
nausea and vomiting
neck weakness
neoplasm, primary of CNS
nerve agents
nerve conduction studies
nerve root enhancement
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuronal cell surface antigen
neuronopathy, sensory
neuropathology, brain
neuropathy
neuropathy, iatrogenic
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, paraneoplastic
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, toxic
neuropathy, vasculitic, systemic
neurotoxic
neurotoxin
next-generation sequencing
night sweats
nivolumab
NMDA antagonists
ocular motility, disorders of
ocular myopathy
old age, neurology of
onconeural antibodies
ophthalmoplegia
ophthalmoplegia, plus syndrome
opsoclonus-myoclonus syndrome
optic neuritis
optic neuropathy
otitis, neurologic complications with
overlap syndrome
pain
pain, abdominal
pain, leg
pain, testicular
papilledema
paralysis, acute
paralysis, acute areflexic
paramyotonia congenita
paraneoplastic cerebellar degeneration
paresthesias
paroxysmal neurologic deficits
pathognomonic
pathology
pembrolizumab
periarteritis nodosa
pericarditis
periodic paralysis
periodic paralysis, thyrotoxic
peripheral nerve, lesion of
photosensitivity, skin
plasmapheresis
pleocytosis of cerebrospinal fluid
pleurisy
pneumonia
POEMS syndrome
poison, organophosphate
polycythemia, primary
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyalgia rheumatica
polymyositis
polymyositis, eosinophilic
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
pons, lesion of
positive sharp waves
posterior inferior cerebellar artery syndrome
postviral fatigue syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
practice guidelines
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proximal muscle atrophy
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
ptosis, unilateral
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, tonic
Purkinje cell
purkinje cell cytoplastic autoantibody
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia, transient
quality of life
rapidly progressing neurologic illness
rash
Raynaud's phenomenon
recurrent
Red flags
remote effect of cancer on the nervous system
renal biopsy
renal failure
renal failure, acute
repetitive nerve stimulation
research
respiratory failure
respiratory tract infection
reticulum cell sarcoma
retinal artery occlusion
retinopathy
reversible neurologic disorder
review article
rhabdomyolysis
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rheumatoid pachymeningitis
rhinorrhea
rigidity
risk factors
safety
sarcoidosis
sclerodactyly
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate
sedimentation rate, elevated
seizure
sensorineural hearing loss
serologic testing
seronegative
serum alanine aminotransferase
sex reassignment surgery
sicca syndrome
single-fiber electromyography
sinusitis
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, tight
skin, translucent
sodium channel dysfunction
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 6
splenomegaly
splinter hemorrhages
statin therapy
statin therapy, discontinuation
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
Still's disease
strokelike episodes
subarachnoid hemorrhage
subcutaneous edema
subcutaneous nodules
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
telangiectases
telangiectases, periungual
temporal lobe, lesion
temporal lobe, lesion, bilateral
tensilon test, false positive
testicular biopsy
thalamus, infarction, bilateral
thalamus, lesion of
third nerve palsy
thrombocytopenia
thymectomy
thymoma
thyroiditis
thyrotoxicosis
tinnitus
tongue, fasciculations of
toxic encephalopathy
transgender
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
unconsciousness
uremia
urine, dark
vaccination, neurologic complications with
vasculitides
vasospasm, cerebral
Venereal Disease Research Laboratory test
vertigo
viral infection
viral infection, CNS
viral myopathy
vision, blurred
visual field defect
visual loss
walking frame
walking, difficulty with
war
weakness
weakness, acute
weakness, episodic
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
West Nile fever
wheelchair
white matter disease
wide based gait
workup
wound healing, poor
xerophthalmia
xerostomia
Showing articles 1350 to 1400 of 1798 << Previous Next >>

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

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

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,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

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

Evolution of Brain MRI Abnormalities in Limbic Encephalitis
Neurol 40:1304-1306, Dirr,L.Y.,et al, 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

Autoantibody Synthesis in the Central Nervous System of Patients with Paraneoplastic Syndromes
Neurol 40:1085-1091, Furneaux,H.F.,et al, 1990

Trigeminal Sensory Neuropathy Associated with Connective Tissue Diseases
Neurol 40:891-896, Hagen,N.A.,et al, 1990

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

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Specificity of Calcium Channel Autoantibodies in Lambert-Eaton Myasthenic Syndrome
Lancet 2:640-643, Sher,E.,et al, 1989

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Pyomyositis in a Child with Acquired Immunodeficiency Syndrome
Am J Dis Child 143:779-781, Raphael,S.A.,et al, 1989

Nicotinic Acid-Associated Myopathy:A Report of Three Cases
Am J Med 86:481-483, Litin,S.C.&Snderson,C.G., 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Lymphocytic Hypophysitis, Report of 3 New Cases and Review of the Literature
Medicine 66:240-256, Cosman,F.,et al, 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Polymyositis and HTLV-I Antibodies
Ann Neurol 25:311, Francis,D.A.&Hughes,R.A.C., 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

HTLV-I Polymyositis in a Patient Also Infected with the Human Immunodeficiency Virus
NEJM 320:992-995, Wiley,C.A.,et al, 1989

Implantation of Tissue Into the Brain, An Immunologic Perspective
JAMA 261:2674-2676, Gill,T.J.&Lund,R.D., 1989

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Chronic Fatigue Syndrome-One Entity or Many?
NEJM 319:1726-1728, Swartz,M.N., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Severely Threatening Events and Marked Life Difficulties Preceding Onset or Exacerbation of MS
JNNP 52:8-13, Grant,I.,et al, 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Antineural Autoantibodies in Patients with Paraneoplastic Cerebellar Degeneration
Arch Neurol 46:1225-1229, Tsukamoto,T.,et al, 1989



Showing articles 1350 to 1400 of 1798 << Previous Next >>