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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
adverse drug reaction
alopecia
amenorrhea
anasarca
anemia
anorexia
arteriopathy
arteritides
arteritis, temporal
arthralgia
arthritis
ascites
aspirin
ataxia
ataxia telangiectasia
ataxic gait
autonomic dysfunction
B 12 deficiency
bacterial infection
basal ganglia, lesion of
Beau's lines
biologic markers
biotin deficiency
biotinidase deficiency
brain atrophy
brain scan, abnormal
brainstem, lesion of
breast feeding
cafe au lait spots
carcinoma
cardiomyopathy
Castleman's disease
CAT scan, emission, abnormal
cataracts
cerebral arteries
cerebral atherosclerosis
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, young adult
children
chorea
chromosome 8
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coma
comorbidities
confusion
confusional state, acute
congestive heart failure
conjunctival injection
conjunctivitis
Coombs test, positive
cortical vein thrombosis
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve palsies
cranial neuropathy, multiple
Cushing's syndrome
cytoid bodies
degenerative diseases of CNS
delirium
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diet
diplopia
dural sinus thrombosis
dyspnea
echocardiogram
echocardiogram, LVH
edema, pedal
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emergencies, neurologic
encephalopathy
enzyme, defect
erythema nodosum
evoked potentials
eye movement, disorders of
facial hair, excessive
facial pain
facial weakness
failure to thrive
false positive VDRL
familial
fatigue
fever
fingernails, abnormal
fingernails, white
foot drop
fornix, lesion of
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
glycosuria
gray hair
Griscelli syndrome
growth retardation
gynecomastia
hair analysis
hair, loss
hallucination
hand pain
headache
hearing loss
hemifacial atrophy
hepatomegaly
hepatosplenomegaly
herniated disc, thoracic
hirsutism
Horner's syndrome
HTRA1 gene
hypercoagulable state
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hypertension
hypertrichosis
hypocomplementemia
hypogonadism
hypokalemia
hyponatremia
hypothermia
hypotonia
immunodeficiency
immunoelectrophoresis, serum
immunosuppression
impotence
infant, evaluation of
infantile tremor syndrome
infection
internal capsule
intracranial pressure, increased
jaw pain
Kawasaki disease
leg swelling
leukemia
leuko-araiosis
leukocytosis
leukoencephalopathy
leukopenia
life expectancy
liver disease
liver function enzymes
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphohistiocytosis
lymphoma involving CNS
lymphopenia
meningitis
meningitis, aseptic
meningoencephalitis
mental status, abnormal
mesial temporal lobe
metabolic acidosis
metabolic alkalosis
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitoxantrone
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mortality
MRI
MRI, abnormal
MRI, diffusion weighted
multiple myeloma
multiple sclerosis
multiple sclerosis, treatment of
muscle pain
muscle weakness, proximal
myelination of nervous system
myelitis
myeloma, osteosclerotic
myelopathy
myocardial injury
myocarditis
myoclonus
myocytolysis
myositis
nausea and vomiting
neck trauma
neonatal screening, genetic neurologic disorders
neoplasm, hormone producing, ectopic
nephritis
nerve biopsy
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, motor, multifocal
neuropathy, peripheral
neutropenia
night sweats
nystagmus
nystagmus, rotary
nystagmus, spontaneous
oculocutaneous albinism
ophthalmoplegia
optic atrophy
optic neuritis
P300
pain, back
palpitations
papilledema
paranoia
pericarditis
photophobia
pink eye
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
POEMS syndrome
poliosis
polymyalgia rheumatica
polyneuropathy
pons, lesion of
postpartum
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
pulmonary embolism
purpura
quadriparesis
radiation therapy, CNS treatment and complications with
rash
Raynaud's phenomenon
retinal detachment
reversible neurologic disorder
review article
risk factors
scalp necrosis
schizophrenia
scleroderma
scleroderma, neurologic involvement with
scotoma
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, neonatal
short stature
skin cancer
skin, lesions in neurologic disorders
skin, pale
skin, thickened
slurred speech
small vessel disease
somatosensory evoked potentials
spinal cord, lesion of
splenomegaly
spondylolysis
spondylosis
steroid psychosis
steroid therapy, CNS treatment and complications with
subcortical U fibers
subcutaneous nodules
substantia nigra
symmetric brain lesions
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, skin changes in
temporal lobe, lesion
term infant
thirst
thrombocytopenia
thrombocytosis
thrombotic thrombocytopenia purpura
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberculosis
tuberculosis, miliary
urinary frequency
urinary tract infection
urticaria
uveitis
vasculitides
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vision, blurred
visual acuity, decreased
visual loss
vitamin deficiency
vitiligo
Vogt-Koyanagi-Harada syndrome
weakness, generalized
weight loss
Werner's syndrome
white hair
white matter disease
whites
Showing articles 1200 to 1250 of 1370 << Previous Next >>

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,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

MR Imaging in Adrenoleukomyeloneuropathy
J Comput Assist Tomogr 9:793-796, Bewermeyer,H.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

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

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

Hereditary Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
NEJM 311:948-953, Eldridge,R.,et al, 1984

Progressive Multifocal Leukoencephalopathy in a Patient with Acquired Immune Deficiency Syndrome
Arch Neurol 41:780-782, Bernick,C.,et al, 1984

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

Computed Tomography in Late-Onset Metachromatic Leucodystrophy
Neuroradiology 26:39-44, Schipper,H.I.,et al, 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

CT Abnormalities & Altered Methotrexate Clearance in Children with CNS Leukemia
Neurol 34:229-233, Duffner,P.K.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
Arch Neurol 41:1293-1296, Dave,P.,et al, 1984

Ultrasound Brain Scanning in The Newborn
BMJ 289:337-338, Chiswick,M.L., 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Ischaemia & Haemorrhage in the Premature Brain
Editorial, Lancet 2:847-8481984., , 1984

Progressive Multifocal Leukoencephalopathy in a Renal Transplant Recipient
Am J Med 77:333-337, Saxton,C.R.,et al, 1984

Temporal Lobe Epilepsy:An Extrahypothalamic Pathogenesis for Polycystic Ovarian Syndrome
Neurol 34:1389-1393, Herzog,A.G.,et al, 1984

Adrenoleukodystrophy:Early Frontal Lobe Involvement on Computed Tomography
J Comput Assist Tomogr 8:128-130, MacDonald,J.T.,et al, 1984

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

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

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

Metachromatic Leukodystrophy (MLD) , XV. Adult MLD with Focal Lesions by Computed Tomography
Arch Neurol 40:354-355, Skomer,C.,et al, 1983

Osteosclerotic Myeloma & Peripheral Neuropathy
Neurol 33:202-210, Kelly,J.J.,et al, 1983

Computed Tomography in Acute Disseminated Encephalomyelitis
Ann Neurol 13:567-572, Lukes,S.A.,et al, 1983

Computerized Tomography as a Diagnostic Aid in Acute Hemorrhagic Leukoencephalitis
Ann Neurol 13:331-333, Rothstein,T.L.,et al, 1983

Intensive Immunosuppression in Progressive Multiple Sclerosis
NEJM 308:173-180, Hauser,S.L.,et al, 1983

Progressive Multifocal Leukoencephalopathy in Acquired Immunodeficiency Syndrome
NEJM 309:492-493, Bedri,J.,et al, 1983

Multiple Malignant Astrocytomas in a Patient with Spontaneous Progressive Multifocal Leukoencephalopathy
Ann Neurol 14:183-188, Sima,A.A.F.,et al, 1983

Unilateral Straight Hair in Congenital Horner Syndrome Due to Stellate Ganglion Tumor
Ann Neurol 13:345-346, Shewmon,D.A., 1983

Protective Effect of Vitamin E (DL-Alpha-Tocopherol) Against Intraventricular Haemorrhage in Premature Babies
BMJ 287:81-84, Chiswick,M.L.,et al, 1983

Noninvasive CT Diagnosis of Infantile Alexander Disease:Pathologic Correlation
J Comput Assist Tomogr 7:509-516, Trommer,B.L.,et al, 1983

Phenobarbitone for Prevention of Periventricular Haemorrhage in Very Low Birth-Weight Infants
Lancet 2:1168-1170, Whjitelaw,A.,et al, 1983

Computed Tomography in Krabbe's Disease:Comparison with Neuropathology
Neuroradiology 25:323-327, Ieshima,A.,et al, 1983

Real-Time Ultrasonography of the Neonatal Head
JAMA 250:3212-3215, Rose,W.S.,et al, 1983

Leukoencephalopathy After Inhaling"Heroin"Pyrolysate
Lancet 2:1233-1237, Wolters,E.C.,et al, 1982

Clin. Path. Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 5-1982, NEJM 306:286-29382., , 1982

Primary Cerebellopontine Progressive Multifocal Leukoencephalopathy Diagnosed Premortem by Cerebellar Biopsy
Ann Neurol 11:199-202, Jones,H.R.,et al, 1982

Progressive Multifocal Leukoencephalopathy in Myasthenia Gravis
Ann Neurol 11:218-219, Dawson,D.M., 1982

Progressive Multifocal Leukoencephalopathy:Failure of Cytarabine Therapy
Neurol 32:200-203, Smith,C.R.,et al, 1982

Leukoencephalopathy Associated with Extensive Burns
JNNP 45:898-904, Gregorios,J.B., 1982

Progressive Multifocal Leukoencephalopathy In A Male Homosexual With T-Cell Immune Deficiency
NEJM 307:1436-1438, Miller,J.R.,et al, 1982

Computed Cranial Tomography in Congenital Rubella Syndrome
Arch Neurol 39:420-421, Ishikawa,A.,et al, 1982

Brain Biopsy in the Diagnosis of Cerebral Mycosis Fungoides
JNNP 45:175-178, Tremblay,G.F.,et al, 1982

Intraventricular Hemorrhage In The Premature Infant
NEJM 306:1464-1468, Molteni,R.A.,et al, 1982

Adrenoleukodystrophy, Unusual Computed Tomographic Appearance
Arch Neurol 39:782-783, Young,R.S.K.,et al, 1982

Carbamazepine & Hematological Monitoring
Ann Neurol 11:309-312, Hart,R.G.,et al, 1982

Tethered Cord Syndrome in Adults
J Neurosurg 57:32-47, Pang,D.&Wilberger,J.E.Jr., 1982



Showing articles 1200 to 1250 of 1370 << Previous Next >>