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acquired immunodeficiency syndrome
acute intermittant porphyria
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
advances in neurology
adverse drug reaction
agitation
alcohol
alcoholism
aminoacidurias
anemia
anemia, megaloblastic
anesthesia, general
ankle, swelling of
anorexia
anticholinergic drugs
anticholinergic drugs, side effects of
areflexia
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
aspergillosis
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
azidodeoxythymidine
B 12 deficiency
B 12 deficiency, infants
brain natriuretic peptide
breast feeding
bulbar palsy
bulimia
bulimia nervosa
burning hands
burning paresthesia
calf hypertrophy
carbon monoxide poisoning
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, muscle
CAT scan, pelvis
catatonia
catatonia, lethal
cathartic
cerebrovascular accident
cervical spondylosis
children
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clofibrate
coenzyme Q10
coenzyme Q10 deficiency
colchicine
coma
compartment syndrome
compartment syndrome, gluteal
complications
compression neuropathy
confusion
confusional state, acute
congenital myopathy
conjunctivitis
contractures, joint
contraindications
cortisol, low
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
critical care unit
cultured skin fibroblasts
dantrolene sodium
deafness
delay in diagnosis
delirium
depression
dermatomyositis
developmental retardation
dexterity, impaired
diabetes insipidus
diagnostic criteria
diamond on quadriceps
differential diagnosis
difficulty climbing stairs
drug abuse
drug abuse, neonatal abstinence syndrome with
drug abuse, neurologic complications of
drug addiction
drug induced neurologic disorders
drug induced neurologic disorders in children
drug interactions
drug withdrawal
dysphagia
dystonia
dystonia musculorum deformens
dystrophin
eating disorder
ecchymoses
ECHO virus
electrocardiogram, abnormal
electromyogram
emergencies, neurologic
encephalomyopathy
encephalopathy
encephalopathy, metabolic
endophthlamitis
enterovirus
enzyme, defect
enzyme, muscle disease
enzyme, serum
epsilon-aminocaproic acid(E.A.C.A.)
etonogestrel
exercise
exercise intolerance
eye, pain in
facial weakness
falling
familial
fatigue
fever
fibrillations
fine motor function, impaired
fungal infection
gait disorder
gait, waddling
gasoline sniffing
gene
gene mutation
genetic neurologic disorders
genetic screening
genetic testing
glycogen storage disease
Gowers maneuver
hand weakness
head injury
hearing loss
hematuria, microscopic
hepatolenticular degeneration(Wilson's disease)
histochemistry of muscle
HMGcoA reductase inhibitors
homocystinuria
hormone replacement
hormone therapy
human immunodeficiency virus type 1
hung reflex
hypercapnia
hypernatremia
hyperpigmentation of skin
hypersegmented polys
hyperthermia
hypokalemia
hyponatremia
hyponatremic encephalopathy
hyporeflexia
hypotension, systemic
hypothermia
hypothyroidism
hypotonia, infants
iatrogenic neurologic disorders
implant contraceptives
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
inclusion body myositis
injection neuropathy
intellectual deterioration
intravenous drug abuse
ischemic exercise test
jaundice
lactic acidemia
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukocytosis
level of consciousness, decreased
limb-girdle weakness
lipid lowering agent
lithium
liver function enzymes
malignant hyperpyrexia
McArdle's disease
McArdle's disease, adult onset
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methylmalonic acid, serum
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mononeuropathy
mononeuropathy multiplex
mood change
mortality
movement disorder
MRI
MRI, muscle
MRI, spine
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelopathy
myoclonus
myocytolysis
myoedema
myoglobinuria
myopathy
myopathy, acute
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, proximal
myopathy, toxic
myositis
myotonia dystrophica
myxedema, neurologic manifestations of
nausea and vomiting
nephrotic syndrome
neuroleptic
neuroleptic malignant syndrome
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, acute
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
ochronosis
osteoarthrosis
osteoporosis
pain
pain, abdominal
pain, buttock
pain, leg
paraparesis, spastic
paresthesias
paresthesias, hands
PAS positive
periarteritis nodosa
periodic paralysis
peripheral blood smear, abnormal
pernicious anemia
personality change
phosphorylase b kinase deficiency
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
porphyria
precipitating factors
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
pruritus
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
quadriplegia
recurrent
red eye
renal failure
renal failure, acute
renal stones
respiratory failure
review article
rhabdomyolysis
rigidity
risk factors
Romberg's sign
sarcoglycan
sarcoglycanopathy
sciatic neuropathy
sclerae, hyperpigmented
second wind phenomena
seizure
seizure, neonatal
seizure, neonatal abstenence syndrome
selective serotonin reuptake inhibitors
sensorineural hearing loss
serotonin syndrome
serum alanine aminotransferase
sex reassignment surgery
sleep apnea
somnolence
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spondylolysis
statin therapy
status epilepticus
strychnine poisoning
stuporous
subdural hematoma
systemic illness
tachycardia
tachypnea
tetanus
toe walking
toilet seat neuropathy
tongue, smooth
tongue, swelling
transgender
treatment of neurologic disorder
tremor
trifluoperazine
tripping
unconsciousness
undiagnosed
urinary incontinence
urine osmolality, elevated
urine test in toxic screen
urine, dark
uveitis
vegetarianism
viral infection
viral myopathy
vision, blurred
visual acuity, decreased, monocular
visual loss
vitamin deficiency
vitritis
vomiting, recurrent
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
winging of scapula
workup
Showing articles 150 to 200 of 231 << Previous Next >>

Cranial Neuropathy Associated with Primary Amyloidosis
Ann Neurol 29:451-454, Traynor,A.E.,et al, 1991

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

Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991

VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991

Cerebral Edema Causing Death in Children with Maple Syrup Urine Disease
J Pediatr 119:42-45, Riviello,J.J.,et al, 1991

Intellectual Outcome in Children with Maple Syrup Urine Disease
J Pediatr 119:46-50, Kaplan,P.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Emergence of Recreational Drug Abuse as a Major Risk Factor for Stroke in Young Adults
Ann Int Med 113:821-827, Kaku,D.A.&Lowenstein,D.H., 1990

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

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

Cerebrovascular Complications of the Use of the"Crack"Form of Alkaloidal Cocaine
NEJM 323:699-704, Levine,S.R.,et al, 1990

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

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,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

Pituitary Adenoma in McCune-Albright Syndrome:MR Demonstration
J Comput Assist Tomogr 13:685-688, O'Laughlin,R.L.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

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

CT & MRI in Maple Syrup Urine Disease
Neurol 38:486-488, Uziel,G.,et al, 1988

Brain Malformations in Linear Nevus Sebaceous Syndrome:An MR Study
J Comput Assist Tomogr 12:338-340, Sarwar,M.&Schafer,M.E., 1988

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Clinicopath Conf
Pheochromocytoma with Hemorrhagic Infarct, Catecholamine-Induced Dilated Cardiomyopathy, Case Record, 15988,NEJM 318:970-981,1988., 1988

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Clinicopath Conf
Castleman's Disease, Synd of Polyneuropathy, Organomegally, Endocrinopathy, Monoclonal Gammopathy, &, Skin CPOEM Synd),NEJM 316:606-618,1987., 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Peripheral Neuropathy Associated with Dysproteinaemia, Skin Changes, & Endocrinopathy
BMJ 292:1415-1416, Burton,J.L., 1986

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

Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985

Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome
Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984

Cerebral Computed Tomography in Maple Syrup Urine Disease
J Comput Assist Tomogr 8:410-411, Romero,F.J.,et al, 1984

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

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

The Spectrum of Peripheral Neuropathy in Myeloma
Neurol 31:24-31, Kelly,J.J.,et al, 1981

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 1980

Detection of Phenylketonuria in Autistic & Psychotic Children
JAMA 243:126-128, Lowe,T.L.,et al, 1980

Plasma Cell Dyscrasia with Polyneuropathy, Organomegaly, Endocrinopathy, M Protein, & Skin Changes:The POEMS Syndrome
Medicine 59:311-322, Bardwick,P.A., 1980

Ophthalmoplegia & Bulbar Palsy in Variant Form of Maple Syrup Urine Disease
Ann Neurol 6:71-72, Chhabria,S.,et al, 1979

Conversion of Photosensitive to Scotosensitive Epilepsy:Report of a Case
Neurol 29:1550-1554, Panayiotopoulos,C.P., 1979

Clinical Pathological Conference
Adrenoleukodystrophy, with Peripheral Neuropathy, Case Record 18-1979, NEJM 300:1037-104579., , 1979

Free Amino Acid Levels in Amyotrophic Lateral Sclerosis
Ann Neurol 3:305, Patten,B.M.,et al, 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Celiac Sprue & Refractory Sprue
Gastroenter. 75:3071978., Trier,J.S.,et al, 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Subarachnoid Hemorrhage Complicating Acute Poststreptococcal Glomerulonephritis
Arch Neurol 35:473, DeBeukelaer,M.M.,et al, 1978

Extreme Insulin Resistance in Ataxia Telangiectasia
NEJM 298:1164, Bar,R.S.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

Ophthalmoplegia as a Sign of Metabolic Disease in the Newborn
Neurol 27:971, MacDonald,J.T.,et al, 1977



Showing articles 150 to 200 of 231 << Previous Next >>