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Differential
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abdominal cramps
acalculia
acetaminophen
aciduria
acyl CoA dehydrogenase deficiency
adult T-cell leukemia-lymphoma
aldolase
alexia
alexia with agraphia
algorithm
ammonia
ANA
anemia
anemia, hemolytic
anemia, megaloblastic
aneurysm, intracranial
aneurysm, multiple intracranial
angiography, cerebral, negative
anorexia
antineutrophil cytoplasmic autoantibodies
antiphospholipid antibodies
aphasia
areflexia
arm weakness
arterial dissection, carotid
arteriopathy
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
atypical lymphocytes
B 12 deficiency
B cell lymphoma
B12
B12, elevated
bacterial infection
basal ganglia, calcification of
basophilic stippling of red blood cells
behavioral disorder, acute
blacks
blood transfusion
bone marrow biopsy
bone marrow infarction
bone marrow necrosis
bone pain
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain purpura
BUN, elevated
burning hands
burning paresthesia
calcification, intracranial
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
carotid angiogram
carotid artery occlusion, neck
carpal tunnel syndrome
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, angiography
CAT scan, chest
CAT scan, dense artery sign
cataracts
cauda equina
cauda equina, lesion of
caudate nucleus, lesion of
CD4 counts
cerebellar lesion
cerebral arteries
cerebral cortex
cerebral edema
cerebral edema, cytotoxic
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, multiple
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, subcortical
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count, normal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, adolescent
cerebrovascular accident, bilateral
cerebrovascular accident, cryptogenic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
cerebrovascular disease, rapidly progressive
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
Cheyne Stokes respirations
children
chin numbness
Clinical Pathologic Conference(C.P.C.)
coagulopathy
coma
complications
confusion
confusional state, acute
conus medullaris, lesion of
corneal dystrophy
corpus callosum, infarction of
cortical blindness
cough
cranial nerve palsies
cranial neuropathy, multiple
C-reactive protein
C-reactive protein, elevated
creatine phosphokinase isoenzyme elevation
creatine phosphokinase(CPK)elevated
D-dimer
decerebrate posture
deep gray nuclei
delay in diagnosis
delusion
dementia
dementia, rapidly progressive
dexterity, impaired
diagnostic criteria
diarrhea
diarrhea, bloody
diplopia
disability, neurological
disorientation
disseminated intravascular coagulation(DIC)
drug overdose
dyspnea
ecchymoses
echocardiogram, transesophageal
eclampsia
eclampsia, postpartum
eculizumab
electrical sensation
electroencephalogram
electroencephalogram, abnormalities of
electrophoretic pattern, serum
embolic stroke of unknown source
embolism
embolism, fat
emotional lability
encephalitis, viral
encephalopathy
encephalopathy, acute
endocarditis
endocarditis, marantic
endovascular therapy
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
epistaxis
Epstein-Barr virus
Epstein-Barr virus, negative
escherichia coli
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exome sequencing
eye movement, painful
fasciculation
fatigue
ferritin, elevated
ferritinemia
fever
fibrin split products
fibrinolytic agents
fluctuate
food poisoning
fundus, abnormality of
gait disorder
gastroenteritis
gene mutation
genetic neurologic disorders
genetic testing
Gerstmann syndrome
granulomatous disease
Haiti
hand pain
hand weakness
headache
headache, severe
heart murmur
hematuria, microscopic
hemianopia
hemiparesis
hemiplegia
hemoglobin abnormality, neurologic complications of
hemoglobinuria
hemolysis
hemolytic-uremic syndrome
hepatic failure
hepatic failure, acute
hepatitis
hepatomegaly
heralding manifestation
hoarseness
hot, red, angry babies
Howell-Jolly bodies
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
human parechovirus
human T-lymphotropic virus type I(HTLV-I)
hyperammonemic encephalopathy
hyperbilirubinemia
hypercalcemia
hyperhomocysteinemia
hyperkalemia
hypersegmented polys
hyperuricemia
hypocalcemia
hypoglycemia
hypoglycorrhachia
hyponatremia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypopituitarism
hyporeflexia
hypothyroidism
hypotonia
hypoxia
immunosuppression
inappropriate antidiuretic(A.D.H.)hormone
inattention
inborn errors of metabolism
infection
infectious mononucleosis
intracerebral hemorrhage
intracranial pressure, increased
iron, serum, elevated
irritability
jaundice
lactic acidemia
lactic dehydrogenase(LDH)
left-right orientation
leg weakness, bilateral
Legionella pneumophilia
Legionnaires'disease
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukopenia
level of consciousness, decreased
lipid storage myopathy
liver disease
liver function enzymes
liver nodules
liver scan
lung nodule
lymph node biopsy
lymphadenopathy
lymphadenopathy, cervical
lymphadenopathy, hilar
lymphadenopathy, paraaortic
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lymphoma, systemic
lymphopenia
malabsorption
memory, defect of recent
meningeal biopsy
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, leukemic
meningitis, plasma cell
meningoencephalitis
mental status, abnormal
mental status, abnormal, acute
metabolic acidosis
methylmalonic acid, serum
methylmalonic acidemia
microangiopathic hemolytic anemia
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
misdiagnosis
mitral valve lesion
mitral valve vegetation
monoclonal antibodies
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
MRI
MRI pattern
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, FLAIR
MRI, gradient-echo
MRI, negative
MRI, repeat
MRI, spinal cord
MRI, spine
MRI, starfield pattern
MRI, susceptibility weighted
MRI, vertebral bone marrow
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne, carrier
myelitis, longitudinal
myelopathy
myoclonus
myoglobinuria
myopathy
myopathy, hypocalcemic
myopathy, metabolic
myopathy, proximal
nausea and vomiting
neck weakness
neoplasm, pituitary
neoplastic angioendotheliosis
nerve conduction studies
neuroendocrinology
neurologic complications
neurologic complications of, surgery
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic symptoms
neuropathology
neuropathy
neuropathy, peripheral
neuropathy, sensory
night sweats
numb chin syndrome
odynophagia
oral contraceptives
overlap syndrome
pain
pain, abdominal
pain, arm
pain, back
pain, leg
pain, severe
pain, thigh
pancytopenia
papilledema
paraparesis
paraparesis, flaccid
paraplegia
parechovirus encephalitis
paresthesias
paresthesias, feet
paresthesias, hands
paroxysmal nocturnal hemoglobinuria
parvovirus
pediatric neurology
pericarditis
peripheral blood smear, abnormal
pernicious anemia
perseveration
petechiae
pituitary
pituitary, enlargement
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
polymerase chain reaction
polymyositis
pons, lesion of
posterior leukoencephalopathy syndrome
posterior leukoencephalopathy syndrome, location
precipitating factors
preclinical
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proteinuria
proteomics
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
pulmonary embolism
pulmonary infiltrates
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
rash
rash, hand
recurrent
Red flags
renal failure
renal failure, acute
respiratory failure
respiratory tract infection
reticulum cell sarcoma
retinal artery occlusion
retinal hemorrhages
retinopathy
reversible cerebral vasoconstrictive syndromes
review article
rhabdomyolysis
rituximab
Romberg's sign
Roth spots
Sabin-Feldman dye test
saddle anesthesia
salivary gland biopsy
sarcoidosis
sarcoidosis, CNS
sarcoma
sarcoma, osteogenic
schistocytes
screening
season
sedimentation rate
sedimentation rate, elevated
seizure
seizure, neonatal
sella turcica, enlargement of
sensory loss
septicemia
seronegative
serum alanine aminotransferase
serum glutamic oxaloacetic transaminase
serum lipase, elevated
Shiga toxin
sickle cell crisis
sickle cell disease
skew deviation
skin, biopsy
skin, lesions in neurologic disorders
small vessel disease
soluble interlukin 2 receptor
somnolence
sore throat
speech, pressured
spinal cord
spinal cord, enlargement
spinal cord, lesion of
spine, metastasis to
splenic-vein thrombosis
splenomegaly
splinter hemorrhages
sprouts
status epilepticus
stiff joints
strokelike episodes
suck, poor
suicide
symmetric brain lesions
systemic illness
tangential
target red cells
term infant
thalamus, lesion of-bilateral
Three territory sign
thrombocytopenia
thrombocytopenia, differential diagnosis of
thrombotic microangiopathy
thrombotic thrombocytopenia purpura
tissue plasminogen activator, intravenous
tongue, smooth
tongue, swelling
toxoplasma complement fixation test
toxoplasmosis, acquired
toxoplasmosis, CNS
transient ischemic attack
treatment of neurologic disorder
tremor
tremor, intention
ultrasonography, testes
unconsciousness
urinary casts
urine, dark
uveitis
vasculopathy
vertebral infarction
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
vitamin deficiency
vitreous biopsy
weakness
weakness, fluctuating
weakness, progressive
weakness, proximal
weight loss
white matter disease
workup
Showing articles 50 to 100 of 138 << Previous Next >>

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Clinicopath Conf, Chronic Salicylate Toxicity
NEJM 388:264-272, Case Record 2, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Lentiform Fork Sign in Metabolic Acidosis
Ann Neurol 89:188-189, Kumar, N. & Kumar, D., 2021

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Clinicopathologic Conference, Ingestion of Isopropyl Alcohol
NEJM 380:1657-1665, Case 13-2019, 2019

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Uremic Encephalopathy: MR Imaging Findings and Clinical Correlation
AJNR 37:1604-1609, Kim, D.M.,et al, 2016

Clinicopathologic Conference, Ethylene Glycol Ingestion
NEJM 372:465-473, Case 4-2015, 2015

The Lentiform Fork Sign
Neurol 84: e15, Fernandes, G.C.,et al, 2015

Encephalopathy and High Anion Gap Metabolic Acidosis: An Unusual Herald of Buried Bumper Syndrome
Lancet 385:744, Lopez, E.M.J.,et al, 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

Clinical Features, Diagnosis, and Treatment of Disseminated Intravascular Coagulation in Adults
UptoDate, Leung, L.L.K., 2015

A 49-year-old Man with Fever and Proximal Weakness in his Arms
Neurol 82:e65-e69, Seliger, C.,et al, 2014

A Syndrome of Bilateral Symmetrical Basal Ganglia Lesions in Diabetic Dialysis Patients
Am J Kidney Dis 63: 286-288, Finelli, P.F. & Singh, J.U., 2014

Clinicopathologic Conference, Rabies Encephalitis
NEJM 368:172-180, Case 1-2013, 2013

Clinicopathologic Conference, Toxic Effects of Metformin
NEJM 369:374-382, Case 23-2013, 2013

Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome
JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013

Clinicopathologic Conference, Methcathinone (Bath Salts) Intoxication
NEJM 369:2536-2545, Case 40-2013, 2013

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Heterogeneity of Coenzyme Q10 Deficiency
Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012

Dilemmas in the Diagnosis of Acute Community-Acquired Bacterial Meningitis
Lancet 380:1684-1692,1623, Brouwer, M.,et al, 2012

MELAS
MedLink.com, August, Klopstock, T., 2012

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Painful Paraplegia Caused by Spontaneous Abdominal Compartment Syndrome
Neurol 74:1833-1834, Hermann,A., et al, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Ethylene Glycol Toxicity: Chemistry, Pathogenesis, and Imaging
Radiology Case Reports 3, Moore, M.M.,et al, 2008

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007

Vigabatrin Improves Paroxysmal Dystonia in Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 68:1320-1321, Leuzzi,V.,et al, 2007

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Frequently Missed Diagnosis?
Neurol 67:1519, Koppel,S.,et al, 2006

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Neonatal Epileptic Encephalopathy
Lancet 361:1614, Clayton,P.T.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002



Showing articles 50 to 100 of 138 << Previous Next >>