Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
agitation
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
anemia
angina pectoris
angiography, neurologic complications with
angioneurotic edema
ankle edema
anticholinergic drugs
anticholinergic drugs, side effects of
anticoagulant, complications of
aphasia
aphasia, global
areflexia
arrhythmia, cardiac
arsenic
arthralgia
ascending paralysis
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
atherosclerosis, generalized
autism
autonomic dysfunction
bacterial infection
bacterial infection, CNS
BAL
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
behavioral disorder
bone marrow suppression
brain biopsy
BUN, elevated
Canavan's disease
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
catatonia
catatonia, lethal
central nervous system, infection of
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cherry red spot
chest pain
chest x-ray, abnormal
children
chromosomal abnormality
chromosome 6
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cocaine
coma
confusion
conjunctivitis
coronary artery bypass
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
dementia
dementia, rapidly progressive
demyelinating disease
dermatitis
developmental milestones, loss of
developmental retardation
diarrhea
diet
disseminated intravascular coagulation(DIC)
distal muscle weakness
drug abuse
drug abuse, neurologic complications of
drug abuse, toxic screen In
drug induced neurologic disorders
drug withdrawal
dystonia
ecchymoses
edema, pedal
electrocardiogram, abnormal
electromyogram
embolism
embolism, atheromatous
embolism, cholesterol
embolism, retinal
emergencies, neurologic
encephalopathy
encephalopathy, acute
encephalopathy, neonatal
endocarditis
endocarditis, marantic
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
erythrocyte
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
failure to thrive
familial
fatigue
feeding disorder
femoral artery catheterization
fever
fibrin split products
filariasis
fingernails, abnormal
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangrene
gastroenteritis
gastrointestinal bleeding
gene
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
glycogen storage disease
gram negative rod
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hallucination
hand weakness
head lag
headache
headache, severe
heart murmur
heavy metal intoxication
helminthic infection of CNS
hematuria, gross
hematuria, microscopic
hemiplegia
hemoglobinuria
hepatitis
hepatosplenomegaly
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hyperglycinemia
hyperkeratosis
hypertension
hyperthermia
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
inborn errors of metabolism
infection
intraaortic balloon pump
ischemic exercise test
lactic dehydrogenase(LDH)
Legionella pneumophilia
Legionnaires'disease
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
leukopenia
levamisole
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
Loa loa
loiasis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
McArdle's disease
Mees lines
meningitis, aseptic
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
microangiopathic hemolytic anemia
misdiagnosis
mitochondrial disease
mitral valve vegetation
molecular genetics
mortality
MRI
MRI, abnormal
MRI, demyelinating disease
MRI, diffusion weighted
MRI, false negative
multinucleated giant cell
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
myoclonic jerks
myoglobinuria
myopathy
nausea and vomiting
nerve conduction studies
neuritis, heavy metals causing
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, peripheral
neuropathy, toxic
neurotransmitter
opisthotonus
optic atrophy
ornithine transcarbamylase deficiency
pain
pain, back
pain, flank
pancreatitis
pancytopenia
paraphasias
parasitic infection, CNS
paresthesias
paresthesias, feet
paresthesias, hands
PAS positive
pathology
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
personality change
petechiae
phenylketonuria
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
polyneuropathy
position sensation, abnormal
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
pruritus
psychomotor retardation
pulmonary infiltrates
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
renal failure
renal infarct
respiratory failure
review article
rhabdomyolysis
rigidity
risk factors
Sandhoff's disease
screaming
second wind phenomena
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
self-mutilation
semialdehyde dehydrogenase deficiency
serologic testing
serotonin syndrome
skin, biopsy
skin, lesions in neurologic disorders
spinal cord, infarction of
splenic infarcts
splinter hemorrhages
spongy degeneration of brain
stuporous
sweating
sweating, abnormality of
thrombocytopenia
treatment of neurologic disorder
tropical disease
urea-cycle enzymopathies
uremia
urinalysis, abnormal
urinary casts
urine test for metabolic disorders
urine test in toxic screen
urine, dark
urine, white blood cells in
vasculitides
weakness
weight loss
white matter disease
Showing articles 250 to 300 of 3460 << Previous Next >>

Cyclosporine-Assoc Seizures in Bone Marrow Transplant Given Busulfan & Cyclophosphamide Prep
Transplantation 52:310-315, Ghany,A.M.,et al, 1991

Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991

Staphylococcal Pyomyositis in Patients Infected by the Human Immunodeficiency Virus
Am J Med 90:595-600, Schwartzman,W.A.,et al, 1991

Carbamazepine-Induced Antinuclear Antibodies & Systemic Lupus Erythematosus-Like Syndrome
Epilepsia 32:128-129, DeGiorgio,C.M.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Leukoaraiosis, Intracerebral Hemorrhage, and Arterial Hypertension
Stroke 21:1419-1423, Inzitari,D.,et al, 1990

The Evaluation and Treatment of Seizures
NEJM 323:1468-1474, Scheuer,M.L.&Pedley,T.A., 1990

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 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

Progressive Multifocal Leukoencephalopathy-Remission with Cytarabine
J Infection 20:51-54, O'Riordan,T.,et al, 1990

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

Cerebrotendinous Xanthomatosis:Clinical and MRI Study (A Case Report)
JNNP 53:76-78, Fiorelli,M.,et al, 1990

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

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

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

Serial MR Studies in Menkes Disease
J Comput Assist Tomogr 13:113-115, Blaser,S.I.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Hypersensitivity to Carbamazepine Presenting with a Leukemoid Reaction, Eosinophilia, Erythroderma, and Renal Failure
Neurol 39:436-438, Ray-Chaudhuri,K.,et al, 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

Cranial Nerve Deficit:A Clue to the Diagnosis of Ethylene Glycol Poisoning
Am J Med 87:91-92, Palmer,B.F.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Leukoaraiosis and Intracerebral Hematoma
Stroke 20:1016-1020, Selekler,K.&Erzen,C., 1989

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Dementia Due to Vascular Disease-A Multifactorial Disorder
Stroke 19:1291-1299, Scheinberg,P., 1988

Positron Emission Tomography in a Patient with Progressive Multifocal Leukoencephalopathy
Neurol 38:1864-1867, Kiyosawa,M.,et al, 1988

An Adolescent with Intermittent Headache, Transient Hemiparesis, and Urinary Abnormalities
J Pediatr 113:769-776, Gruskin,A.B.&Chang,C., 1988

Nuclear Magnetic Resonance Image White Matter Lesions & Risk Factors for Stroke in Normal Individuals
Stroke 19:263-265, Lechner,H.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Pyomyositis in a Patient with the Acquired Immunodeficiency Syndrome
Arch Int Med 148:1608-1610, Gaut,P.,et al, 1988

Periventricular White Matter Changes & Dementia, Clinical, Neuropsych, Radiology & Pathological Correl
Arch Neurol 45:637-641, Gupta,S.R.,et al, 1988

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy, Chronic Lymphocytic Leukemia, Case Record 45-1988, NEJM, 19:8-1280,1988., 1988

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

Carbamazepine Side Effects in Children and Adults
Pellock. J. M. , Epilepsia 28:S64-S707., , 1987

Neuroleptic Malignant Syndrome:Review and Analysis of 115 Cases
Biol Psychiatry 22:1004-1020, Addonizio,G.,et al, 1987

Leukoencephalopathy in Patients with Ischemic Stroke
Stroke 18:896-899, Bugousslavsky,J.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Binswanger's Disease:A Review
Stroke 18:2-12, Babikian,V.&Ropper,A.H., 1987

White Matter Lucencies on CT, Subacute Arteriosclerotic Enceph (Binswanger's Disease) , & Blood Pressure
Stroke 18:900-905, McQuinn,B.A.&O'Leary,D.H., 1987

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Cogan's Syndrome:18 Cases & a Review of the Literature
Mayo Clin Proc 61:344-361, Vollertsen,R.S.,et al, 1986

Bone-Marrow Transplantation for Neurovisceral Storage Disorders
Editorial, Lancet 2:788-7891986., , 1986

Enzyme Replacement in Nervous Tissue After Allogeneic Bone-Marrow Transplantation for Fucosidoisis in Dogs
Lancet 2:772-774, Taylor,R.M.,et al, 1986

Azathioprine Toxicity in Neuromuscular Disease
Neurol 36:35-39, Kissel,J.T.,et al, 1986

Meningovascular Syphilis: CT and MR Findings
Radiology 158:439-442, Holland,B.A.,et al, 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

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

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985



Showing articles 250 to 300 of 3460 << Previous Next >>