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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
advances in neurology
adverse drug reaction
afebrile
amyloidosis
anesthesia, general
aneurysm
anterior horn cell disease
anti MAG antibodies
anticonvulsants
areflexia
arrhythmia, cardiac
asymptomatic
autism
autoimmune disease
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
central nervous system, infection of
cerebral cortical encephaliis
chewing, impaired
children
chromosome 17
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contractures, joint
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cotton-wool spots
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cushing's syndrome
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
delay in diagnosis
denervation of muscle
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
dysferlinopathy
dysplasia of C.N.S.
dyspnea
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
empty sella
entrapment neuropathy
enzyme, defect
epidermal nevus syndrome
Epstein-Barr virus
exercise
exophthalmus
eye, pain in
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
falling
false positive
familial
fatigue
fever
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globe, flattened posteriorly
Gowers maneuver
headache
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
heterotopia
hirsutism
histochemistry
hoarseness
hypercalcemia
hypertension
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hypothyroidism
inability to sit up
infantile spasm
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
Isaacs syndrome
Kobberling-Dunnigan syndrome
Kugelberg-Welander syndrome
learning disability
learning disability, in children
leg swelling
leukocytosis
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lymphadenopathy
lymphopenia
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
malignant optic glioma of adulthood
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, orbit
MRI, venography
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelitis
myelitis, transverse
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
nerve conduction studies
nerve injury
neurocutaneous disease
neuroendocrinology
neuroinfectious diseases
neurologic disease, diagnoses of
neurologic examination
neuromyotonia
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night sweats
obesity
optic chiasm, lesion of
optic disc
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, neoplasm of
optic nerve, tortuosity
optic neuritis
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optical coherence tomography
orthopnea
pain
pain, leg
palpitations
percussion induced muscle contraction
perineuritis
phakomatoses
plasma cell dyscrasia
polyneuropathy
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
radiculopathy
Red flags
respiratory failure
review article
rhabdomyolysis
rippling muscle disease
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
scoliosis
scotoma, central
seizure
shoulder, elevation
skin, lesions in neurologic disorders
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
splenomegaly
steppage gait
steroid
steroid therapy, CNS treatment and complications with
strokelike episodes
subarachnoid hemorrhage
subcutaneous nodules
survival motor neuron gene
syringomyelia
systemic illness
telangiectases, retinal
third nerve palsy
thirst
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
trauma
treatment of neurologic disorder
tripping
urinary frequency
urine, dark
visual acuity, decreased, monocular
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual symptoms
vital capacity
weakness
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
winging of scapula
workup
Showing articles 1400 to 1450 of 1609 << Previous Next >>

Inflammatory Myopathies
Ann Neurol 17:215-227, 317-3231985., Mastaglia,F.L.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Positron Emission Tomography & its Application to the Study of Cerebrovascular Disease in Man
Stroke 16:361-376, Powers,W.J.,et al, 1985

Decreased Morbidity from Acute Bacterial Spinal Epidural Abscesses Using Computed Tomography & Nonsurgical Treatment
Ann Neurol 17:350-355, Leys,D.,et al, 1985

Neurologic Complications of Systemic Cancer
In Neurologic Clinics 3:729-750, Patchell,R.A.&Posner,J.B., 1985

Heatstroke in a Chronic Schizophrenic Patient Treated with High-Potency Neuroleptics
General Hospital Psychiatry 7:361-363, Lazarus,A., 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Esophageal Lewy Bodies Associated With Ganglion Cell Loss in Achalasia. Similarity to Parkinsons Disease.
Gastroenterology 87:848-856, Qualman,S.J.,et al, 1984

Ophthalmologic Findings in Acquired Immune Deficiency Syndrome (AIDS)
Arch Ophthmol 102:201-206, Khadem,M.,et al, 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Clin. Path. Conference
Eastern Equine Encephalitis, Case Record 50-1984, NEJM 311:1559-1566984., , 1984

Clin. Path. Conference
Lyme Disease, with Meningo-polyneuritis (Bannwarth's Syndrome) , Case Record 29-1984, NEJM 311:172-1, 1, 198, 1984

Parkinson's Disease, 1984
Lancet 1:829-830, Williams,D.,et al, 1984

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

Pure Hemidystonia with Basal Ganglion Abnormalities on Positron Emission Tomography
Ann Neurol 15:228-233, Perlmutter,J.S.,et al, 1984

A Prospective Study of the Ophthalmologic Findings in the Acquired Immune Deficiency Syndrome
Am J Ophthalmol 97:133-142, Freeman,W.R.,et al, 1984

Clin. Path. Conference
Spinal Subdural Abscess, Case Record 47-1984, NEJM 311:1365-1370984., , 1984

Fractures of the Proximal End of the Humerus Caused by Convulsive Seizures
Injury 16:108-109, Kristiansen,B.&Christensen,S., 1984

Sphenoid Sinusitis
NEJM 309:1149-1154, Lew,D.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Nervous System Complications of Relapsing Polychondritis
Neurol 33:513-515, Sundaram,M.B.M.,et al, 1983

Adult Polyglucosan Body Disease:Clinical & Nerve Biopsy Findings in Two Cases
Ann Neurol 13:440-444, Vos,A.L.M.,et al, 1983

Sinusitis:Induced Subdural Empyema
Neurol 33:123-132, Kaufman,D.M.,et al, 1983

Carpal Tunnel Syndrome, Complication of Toxic Shock Syndrome
Arch Neurol 40:414-415, Sahs,A.L.,et al, 1983

Hypothalamic Astrocytoma
Arch Neurol 40:560-563, Haugh,R.M.,et al, 1983

Carotid Body Tumor Associated with Partial Horner's Syndrome & Facial Pain ("Raeder's Syndrome")
Arch Neurol 40:564-566, Harrington,H.J.,et al, 1983

Cyanotic Congenital Heart Disease with Suspected Stroke, Should All Patients Receive Antibiotics
Arch Neurol 40:209-212, Kurlan,R.,et al, 1983

Infantile Osteopetrosis & Neuronal Storage Disease
Neurol 33:437-441, Ambler,M.W.,et al, 1983

Positron Computed Tomography for Studies of Myocardial & Cerebral Function
Ann Int Med 98:339-359, Phelps,M.E.,et al, 1983

Alzheimer's Disease:Focal Cortical Changes Shown by Positron Emission Tomography
Neurol 33:961-965, Foster,N.L.,et al, 1983

Regional Cerebral Metab. Alter. in Dementia of the Alzheimer Type:Positron Emission Tomogr
J Comput Assist Tomogr 4:590-598, Friedland,R.P.,et al, 1983

Hypertrophic Neuropathy & Multiple Sclerosis
Neurol 33:1361-1364, Rosenberg,N.L.,et al, 1983

The Fluorodeoxyglucose 18F Scan in Alzheimer's Disease & Multi-infarct Dementia
Arch Neurol 40:711-714, Benson,D.F.,et al, 1983

Weightlifters Headache
Headache 23:193-194, Paulson,G.W., 1983

Remission From Polymyositis After Total Body Irradiation
BMJ 284:1915-1916, Hubbard,W.N.,et al, 1982

Spinal Metastases, A Retrospective Survey From A General Hospital
Brain 105:189-213, Stark,R.J.,et al, 1982

Intravascular Malignant Histiocytosis Mimicking CNS Vasculitis:An Immunopath. Diag. Approach
Ann Neurol 12:489-492, Krieger,C.,et al, 1982

Phenytoin-induced Arthritis
Neurol 32:1317-1318, Stalnikowicz,R.,et al, 1982

Acute Cervical Cord Injuries in Patients with Epilepsy
JNNP 45:884-892, Allen,J.W.,et al, 1982

Ocular Disorders Associated with a New Severe Acquired Cellular Immunodeficiency Syndrome
Am J Ophthalmol 93:393-402, Holland,G.N.,et al, 1982

Retinal Cotton-Wool Spots in a Patient with Pneumocystis Carinii Infection
NEJM 314:184-185, Kwok,S.,et al, 1982

The Neurologic Manifestations of Sinus Histiocytosis with Massive Lymphadenopathy
Neurol 32:365-371, Foucar,E.,et al, 1982

Life-Threatening Migraine
Arch Neurol 39:374-376, Ferguson,K.S.,et al, 1982

Spinal Cord Compression by Coccidioides Immitis Abscess
Arch Neurol 39:255-256, Delaney,P.,et al, 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Anterior Decompression of the Spine for Metastatic Epidural Cord Compression:A Promising Avenue of Therapy
Ann Neurol 11:28-34, Siegal,T.,et al, 1982

Inclusion Body Myositis Associated With Sjogren's Syndrome
Arch Neurol 39:186-188, Chad,D.,et al, 1982

Periodic Meningitis & Familial Mediterranean Fever
Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982

Herpes Simplex Encephalitis
JAMA 247:317-320, Whitley,R.J.,et al, 1982

Clin. Path. Conference
Acute Lymphoblastic Leukemia & Candidiasis, Case Record 45-1981, NEJM 305:1135-11461., , 1981



Showing articles 1400 to 1450 of 1609 << Previous Next >>