Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal muscle paralysis
acetylcholine
acetylcholine in CNS
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
activities of daily living scale
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
Africa
agalsidase alfa
alopecia
alpha galactosidase A deficiency
alpha glucosidase
Alzheimer's disease
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
anemia
anemia, hemolytic
anemia, megaloblastic
aneurysm
angiokeratoma
angiotensin-converting enzyme
ankle edema
anorexia
anorexia nervosa
anterior horn cell disease
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, untoward effects of
antiviral agents
apraxia
apraxia of eye movements
aromatic amino acid decarboxylase deficiency
arthralgia
arthropathy
arthropathy, neuropathic
arylsulfatase A
ascites
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
athetosis
autism
autonomic dysfunction
B 12 deficiency
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biotin deficiency
biotinidase deficiency
blindness
blood dyscrasias, neurologic findings with
bone demineralization
bone loss
bone marrow transplantation
brain atrophy
brain biopsy
brain purpura
brainstem
brainstem, infarction of
brainstem, lesion of
breast feeding
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
cardiopulmonary bypass
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
caudate nucleus, lesion of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, glycine
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
ceruloplasmin, serum
cherry red spot
cherry red spot-myoclonus syndrome
chest x-ray, abnormal
children
cholesterol
choline acetyltransferase
choline chloride
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
codfish vertebrae
coenzyme Q10 deficiency
coma
complications
compression fracture
confusion
congenital infection, CNS
congenital infection, viral
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
coprolalia
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
cranial nerve enlargement
cranial nerve palsies
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
crying
cultured skin fibroblasts
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
developmental disability
developmental milestones, loss of
developmental retardation
dexterity, impaired
diaphragmatic paralysis
diet
differential diagnosis
difficulty climbing stairs
dilantin
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
dopamine
drooling
dropped head syndrome
dysarthria
dysdiadochokinesia
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
echolalia
edema, pedal
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emergencies, neurologic
emotional lability
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme inhibition
enzyme treatment
enzyme, defect
enzyme, induction
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
esophageal varices
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial hypoplasia
facial weakness
failure to thrive
falling
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
femoral neuropathy
fever
fibrillations
floppy infant
flow study, carotid artery
folic acid
fontanel, bulging
food allergy
fornix, lesion of
fracture, pathologic
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gait disorder
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis GM2-AB variant
Gaucher's disease
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
growth retardation
grunting
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hand pain
hand weakness
hands, fisted
head lag
headache
headache, progressive
headache, thunderclap
headbanging
hearing loss
heart murmur
hematopoietic tissue, extramedullary
hemianopia, homonymous
hemophilia
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
hexosaminidase-A
hexosaminidase-A and B
hip flexor weakness
histochemistry
histochemistry of muscle
homocystinuria
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperbilirubinemia
hyperglycinemia
hyperhomocysteinemia
hyperphosphatasia
hyperreflexia
hypersegmented polys
hypertension
hypertonia
hypoalbuminemia
hypocalcemia
hypogammaglobulinemia
hypoglycemia
hypomyelination
hyponatremia
hypoparathyroidism
hypoparathyroidism, idiopathic
hypophosphatemia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
hypoxia
ileus, paralytic
imbalance
immunosuppression
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
infection
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
iron, brain
irritability
ischemic exercise test
jaundice
Jewish
Kayser-Fleischer ring
Kearns-Sayre syndrome
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic dehydrogenase(LDH)
lacunar infarction
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukopenia
life expectancy
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
long bone lesion
low back pain
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malabsorption
marihuana
McArdle's disease
meconium staining
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
methylmalonic acid, serum
methylmalonic acidemia
microcephaly
microspherophakia
migraine, seizures in
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, hypointense signal foci on
MRI, muscle
MRI, paramagnetic effect
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
myelopathy
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myopia
myotonic discharges
nausea and vomiting
neck weakness
neonatal infection, viral
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neuroendocrinology
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, iatrogenic
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neurotransmitter
night sweats
nutritional deficiency
nystagmus
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
pain, abdominal
pain, back
pain, leg
palilalia
pancytopenia
PANK2 mutation
papilledema
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, hands
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
patient in waiting
pectus excavatum
pediatric neurology
penicillamine
peripheral blood smear, abnormal
pernicious anemia
peroxisomal disease
peroxisomes
personality change
petechiae
phenelzine
phenobarbital
phenylketonuria
phosphorylase b kinase deficiency
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
porphyria
postpartum
postpartum coma
postural abnormality
practice guidelines
precipitating factors
preclinical
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
proteinuria
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychotic behavior
pulmonary function tests
pulmonary hypertension
putamen, lesion of
pyramidal tract
pyridoxine
pyridoxine deficiency
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
rash
recurrent
renal failure
renal stones
renal tubular acidosis
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
rhabdomyolysis
rickets
rigidity
Romberg's sign
Sandhoff's disease
Sanfilippo syndrome
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
seizure
seizure, children
seizure, neonatal
seizure, pregnancy
seizure, psychomotor-temporal lobe
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
serum alanine aminotransferase
short stature
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
small for dates infant, problems in
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
spasticity
speech disorder
speech disorder, childhood
speech, pressured
sphingolipodoses
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
striatum, lesion of
stuporous
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
tangential
Tay-Sachs disease
temporal lobe, lesion
term infant
tetrahydrobiopterin
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thrombocytopenia
thyroid function tests
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, smooth
tongue, swelling
tongue, weakness
transketolase
treatment of neurologic disorder
tremor
trientine dihydrochloride
type 2 muscle fiber
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
ultrasonography, head
umbilical-cord blood transplantation
urea
urea-cycle enzymopathies
uremia
urinary incontinence
urine test for metabolic disorders
urine, dark
vasculitides
vasculopathy
vegetarianism
vertebral-basilar insufficiency
vertigo
vertigo, episodic
visual impairment
visual loss
vital capacity
vitamin D
vitamin D deficiency
vitamin deficiency
vitamin, multiple
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
winging of scapula
workup
zinc
Showing articles 200 to 250 of 1593 << Previous Next >>

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020

Fat Embolism Syndrome in Sickle Cell Disease
J Clin Med 9:1-12, Tsitsikas, D.A.,et al, 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

A Patient with Psychiatric Illness and Multiple Hemorrhages
JAMA 322:2437-2438, Van Baalen, E.,et al, 2019

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

A Pregnant Woman with Chin Numbness
Neurol 92:e996-e999, Arnold, A.J.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Neurologic IgG4-Related Disease
Neurohospitalist 9:118-119, Topiwala, K.,et al, 2019

Subacute Progressive Sensorimotor Symptoms
BMJ 365:doi:10.1136/bmj.l1923, Francis, A.,et al, 2019

Clinicopathologic Conference, Statin-Associated Autoimmune Myopathy
NEJM 381:275-283, Case 22-2019, 2019

A Middle Aged Man with Back Pain and Heavy Legs
BMJ 366:e2420, Chanchlani, N. & Reading, N.G., 2019

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Clinicopathologic Conference, Lymphocytic Choriomeningitis Virus Infection
NEJM 381:2553-2560, Case Record 40-2019, 2019

Cognitive Impairment Before Intracerebral Hemorrhage is Associated with Cerebral Amyloid Angiopathy
Stroke 49:40-45, Banerjee, G.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Neurological Manifestations Among US Government Personnel Reporting Directional Audible and Sensory Phenomena in Havana, Cuba
JAMA 319:1125-1133, 1098, 1079, Swanson, R.L.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

Hemophagocytic Lymphohistiocytosis in 2 patients with multiple sclerosis treated with alemtuzumab
Neurol 90:849-851, Saarela, M.,et al, 2018

Recurrent Ischemic and Hemorrhagic Strokes in a Young Adult
JAMA Neurol 75:628-629, Rocha, E.A. & Singhal, A.B., 2018

Effect of Cannabidiol on Drop Seizures in the Lennox-Gastaut Syndrome
NEJM 378:1888-1897, Devinsky, O.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Clinicopathologic Conference, Vitamin C Deficiency (Scurvey), Vitamin B6 & Folate Deficiencies
NEJM 379:282-289, Case 22-2018, 2018

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

A Headache of a Diagnosis
NEJM 379:475-479, Stern,R.M.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Clinicopathologic Conference, Lyme Meningoradiculitis
NEJM 379:1862-1868, Case 34-2018, 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

IgG4-Related Disease and Intracranial Hypertension: Case Report of a Novel Mechanistic Association
J Neurol Sci 385:75-77, Healy, J.,et al, 2018

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Sarcoidosis Limbic Encephalitis
Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017

Basal Ganglia T1 Hyperintensity in Hereditary Hemorrhagic Telangiectasia
AJNR 38:1929-1933, Parvinian, A.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Clinicopathologic Conference, Atypical Immunoblastic Reaction that was consistent with Primary Epstein-Barr virus Infecton
NEJM 377:677-688, Case 25-2017, 2017



Showing articles 200 to 250 of 1593 << Previous Next >>