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Differential
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abdominal distention
acetazolamide
aciduria
acyl CoA dehydrogenase deficiency
addiction, heroin
adverse drug reaction
aggression
agitation
alcohol intoxication
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
alkalosis, respiratory
alopecia
aminoacidopathies
aminoacidurias
ammonia
amyloidosis
anemia
anesthesia, general
anion gap
anorexia
anorexia nervosa
antibiotics
antibiotics, neurologic complications with
Apgar score
aphasia
areflexia
arm weakness
arrhythmia, cardiac
Asians
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bat bite
bath salts, psychoactive
behavior, combative
behavioral disorder
behavioral disorder, acute
beriberi
beta-D-glucon
biotin
biotin deficiency
biotin deficiency, juvenile form
biotinidase deficiency
blindness
blindness, sudden
bradykinesia
brain biopsy
BUN, elevated
buried bumper syndrome
cachexia
calcification, intracranial
carbonic anhydrase II deficiency
carcinoma
cardiac arrest
cardiomegaly
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, disappearing lesion on
CAT scan, false negative
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral infarction
cerebral palsy
cerebral palsy, risk factors
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
children
chorea
chromosome 19
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cocaine
coenzyme Q10
coenzyme Q10 deficiency
coma
coma, sudden onset
compartment syndrome
compartment syndrome, abdominal
complications
compression fracture
confusion
conjunctival biopsy
conjunctivitis
cornea, abnormal
cortical blindness
cranial nerve palsies
creatine phosphokinase(CPK)elevated
creatinine, elevated
cultured skin fibroblasts
cyanide poison
cyanosis
D-dimer
deafness
deep gray nuclei
degenerative diseases of CNS
delirium
dementia
dementia, rapidly progressive
depressants
depression
dermatitis
designer drugs
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes dialysis basal ganglia syndrome
diabetes mellitus
diabetes mellitus, neurologic manifestations of
dialysis
diarrhea
differential diagnosis
diplopia
disability, neurological
disorientation
disseminated intravascular coagulation(DIC)
disulfiram
dizziness
D-lactate acidosis
downward deviation of eyes
drug abuse
drug abuse, toxic screen In
drug induced neurologic disorders
drug overdose
dysarthria
dysphagia
dyspnea
dystonia
echocardiogram
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
encephalitis
encephalitis, viral
encephalomyopathy
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endocarditis
endocarditis, marantic
enzyme, defect
episodic neurologic deficits
ethylene glycol
exercise
exercise intolerance
exercise-induced neurologic dysfunction
eye movement, disorders of
facial asymmetry
facial weakness
failure to thrive
falling
false negative
familial
fatigue
fetal distress
fever
fingerprint bodies
fluctuate
formication
fracture, pathologic
gait disorder
gastrointestinal bleeding
gastrostomy, percutaneous endoscopic
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, hemorrhage
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
growth retardation
hallucination
hallucination, auditory
headache
headache, severe
hearing loss
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hemorrhagic diathesis
hemorrhagic shock encephalopathy syndrome
hepatic failure
hepatomegaly
heralding manifestation
herniated disc, differential diagnosis of
herpes simplex encephalitis
hirsutism
Hispanics
histochemistry of muscle
hydrophobia
hyperammonemic encephalopathy
hypercapnia
hypercoagulable state
hyperkalemia
hyperreflexia
hypertension
hyperthermia
hypoglycemia
hypokalemia
hypotonia
hypoxia
hypoxia, newborn
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunofluorescence
impulsivity
inborn errors of metabolism
inclusion bodies
infection
in-hospital
intellectual deficit
intellectual deterioration
internal capsule
intracranial pressure, increased
intravenous drug abuse
isoniazid
isopropyl alcohol
jaundice
kaliuresis
Kearns-Sayre syndrome
keratoconjunctivitis
ketoacidosis
ketonuria
lactic acidemia
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lentiform fork sign
lethargy
leukocytosis
leukodystrophy
level of consciousness, decreased
level of consciousness, decreased acute
lipid storage myopathy
liver function enzymes
Lowe's syndrome
lysosomal storage disease
malabsorption
malignant hyperpyrexia
marche a petits pas
MELAS syndrome
memory, impairment of
meningitis
meningitis, aseptic
mental retardation
mental status, abnormal
mental status, abnormal, acute
metabolic acidosis
metabolic disorder, primary
metformin
methcathinone
methylmalonic acidemia
methylmalonic aciduria
microangiopathic hemolytic anemia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, serial
MRI, susceptibility weighted
mucormycosis
multiple organ failure
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle pain
muscle relaxant
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelopathy
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, mitochondrial
myopathy, proximal
myotonia
myotonia congenita
myotonia, treatment of
nausea and vomiting
neck weakness
negative
Negri bodies
neonatal epileptic encephalopathy
nephrotic syndrome
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuromuscular blockade
neuronal ceroid-lipofuscinosis
neurons
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy, peripheral
neurotoxic
neurotoxicity, acute
neurotoxin
normal
nutritional deficiency
nystagmus
nystagmus, rotary
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic foramina
optic foramina, abnormal
ornithine transcarbamylase deficiency
osteopetrosis
osteoporosis
pain
pain, abdominal
pain, arm
paramyotonia congenita
paranoia
paraplegia
paresthesias
Parkinsonism syndrome
paroxysmal neurologic deficits
partial thromboplastin time, prolonged
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
polymerase chain reaction
posterior cerebral artery territory infarction
precipitating factors
prevention of neurologic disorders
prognosis
progressive neurologic disorder
propionic aciduria
propofol
proptosis
proteinuria
pruritus
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
pulmonary edema
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyridoxine
pyridoxine deficiency
pyruvate metabolism, abnormality of
quadriparesis
rabies prophylaxis
rabies, nervous system involvement with
ragged-red fibers
rapidly progressing neurologic illness
rash
renal biopsy
renal failure
renal failure, acute
renal tubular acidosis
retina, abnormal
retinitis pigmentosa
reversible neurologic disorder
review article
rhabdomyolysis
rickets
rigidity
risk factors
salicylate intoxication
schistocytes
sedation
seizure
seizure, children
seizure, drug-induced
seizure, intractable
seizure, intractable, treatment of
seizure, neonatal
seizure, treatment of
self harm
sensorineural hearing loss
shock, hypovolemic
short stature
skin, biopsy
skin, lesions in neurologic disorders
skin, pink
skull x-ray, abnormal
slurred speech
small-bowel bypass
somnolence
spasticity
speech, loss of
speech, slowed
spinal cord, infarction of
splenomegaly
spontaneous remission
status epilepticus
stimulant drugs
stool, guaiac positive
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuporous
sudden death
suicide
sweating
symmetric brain lesions
sympathomimetic drugs
systemic illness
tachycardia
tachypnea
temporal lobe, lesion
tetany
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thiamine deficiency
thrombocytopenia
thrombotic microangiopathy
thyroxine, low
tinnitus
titubation
toxic encephalopathy
toxins, nervous system
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
Trousseau's syndrome
uncal herniation
undiagnosed
upgaze, paralysis of
urea-cycle enzymopathies
uremia
uremic encephalopathy
urinalysis, abnormal
urine sediment
urine test for metabolic disorders
urine test in toxic screen
vecuronium
violent behavior
viral infection
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
walking, difficulty with
weakness
weakness, fluctuating
weakness, generalized
weakness, proximal
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, subcortical
workup
x-linked mental retardation
Showing articles 0 to 50 of 129 Next >>

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

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

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

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

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

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

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

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

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

Confusion After Antibiotics
Lancet 357:1410, Gavazzi,C.,et al, 2001

Mitochondrial Disease and Stroke
Stroke 32:2507-2510, Martinez-Fernandez,E.,et al, 2001

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999

Rhabdomyolysis and Hypoxia Associated with Prolonged Propofol Infusion in Children
Neurol 50:301-303, Hanna,J.P.&Ramundo,M.L., 1998

Recurrent Strokes in a 34-Year-Old Man
Lancet 350:560, Chinnery,P.F.,et al, 1997

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Ophthalmologic Manifestations in MELAS Syndrome
Arch Neurol 50:977-980, Fang,W.,et al, 1993

Clinicopath Conf, Herpes Simplex Encephalitis
Am J Med 93:327-334, Krogstad,D., 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Persistent Paralysis in Critically Ill Patients after Long-Term Administration of Vecuronium
NEJM 327:524-528, Segredo,V.,et al, 1992

Reversal of Prolonged Isoniazid-Induced Coma by Pyridoxine
Arch Int Med 150:1751-1753, Brent,J.,et al, 1990

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
J Pediatr 114:194-203, Levin,M.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Perinatal Brain Damage:Predictive Value of Metabolic Acidosis & The Apgar Score
BMJ 297:24-27, Ruth,V.J.&Raivio,K.O., 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987



Showing articles 0 to 50 of 129 Next >>