Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal migraine
acrochordon
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
affect, inappropriate
agnosia, color
agnosia, visual
akathisia
alcoholism
alexia
alexia without agraphia
Alzheimer's disease
Alzheimer's disease, visual variant
amnesic stroke
anatomy of
anemia
anemia, megaloblastic
angiotensin-converting enzyme
ankle, swelling of
anorexia
anosmia
aphasia
argyria
arrhythmia, cardiac
arthralgia
ascites
aspartate aminotransferase
ataxia
ataxia, cerebellar
ataxic gait
autoantibodies
autonomic dysfunction
B 12 deficiency
behavioral disorder
bladder dysfunction
blindness
bone marrow transplantation
brain biopsy
brain natriuretic peptide
burning hands
burning legs
burning paresthesia
burning skin
calf hypertrophy
carbon monoxide poisoning
cardiomyopathy
cardiovascular disease
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission
CAT scan, emission, abnormal
cerebellum, disease of
cerebral artery, encasement
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral peduncle
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, women
cervical spondylosis
children
cirrhosis
Clinical Pathologic Conference(C.P.C.)
color desaturation
color vision
color vision, impaired
color vision, impaired, cerebral
color vision, impaired, sudden onset
coma
complications
confusion
contractures, joint
corpus callosum
corpus callosum, infarction of
cortical blindness
creatine phosphokinase(CPK)elevated
critical care unit
crying, pathologic
cultured skin fibroblasts
cyclic vomiting
cyclic vomiting syndrome
dantrolene sodium
deafness
decerebrate posture
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
depression
depth perception, impaired
dermal sinus tract
dermoid
developmental retardation
dexterity, impaired
diabetes insipidus
diagnostic criteria
diamond on quadriceps
diastematomyelia
diet
differential diagnosis
difficulty climbing stairs
dimple
disconnection syndrome
dizziness
drug induced neurologic disorders
drug interactions
dysarthria
dyschromatopsia
dysphagia
dyspnea
dyspraxia
dysraphism, spinal
dystonia
dystrophin
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, post anoxic
epidemiology of neurology
ergotamine
ergotism
erythromelalgia
exercise
facial weakness
falling
familial
fatigue
fatty acid, elevated plasma content
fever
fibrillations
fine motor function, impaired
gadolinium
gait disorder
gait, waddling
gangrene
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucose tolerance test, abnormal
Gowers maneuver
hand weakness
headache
headache, recurrent
hemiachromatopsia
hemiakathisia
hemianopia
hemianopia, homonymous
hemianopia, isolated homonymous
hemichorea
hemiplegia
hemochromatosis
hemochromatosis, primary
hepatic encephalopathy
hepatolenticular degeneration(Wilson's disease)
HMGcoA reductase inhibitors
hung reflex
hyperbaric oxygen
hypercoagulable state
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertrichosis
hypogonadism
hypopigmentation of skin
hypothermia
hypothyroidism
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deterioration
jaundice
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
lethargy
leukodystrophy
level of consciousness, decreased
limb ischemia
limb-girdle weakness
lipoma of CNS
lipoma of skin
liver function enzymes
Lorenzo's oil
Marcus Gunn pupil
memory, defect of recent
memory, impairment of
metabolic disorder, primary
methylmalonic acid, serum
midbrain, infarction of
migraine
migraine, children
migraine, equivalents
misdiagnosis
mood change
mortality
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, mass effect on
MRI, negative
MRI, spine
muscle biopsy
muscle pain
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
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
myoedema
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, necrotizing, autoimmune
myxedema, neurologic manifestations of
nausea and vomiting
nerve biopsy
neurocutaneous disease
neurofibromatosis 1
neuroleptic
neuroleptic malignant syndrome
neurologic complications
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, sensory
neuropathy, toxic
neurotoxin
nocturia
nutritional deficiency
occipital lobe, infarction
occipital lobe, infarction, bilateral
ochronosis
optic atrophy
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
osteoarthrosis
osteoporosis
pain, abdominal
palinopsia
papilledema
paraparesis
paraparesis, spastic
paresthesias
paresthesias, hands
Parkinsonism syndrome
peripheral blood smear, abnormal
peripheral pulse, absent
pernicious anemia
peroxisomal disease
personality change
phlebotomy
posterior cerebral artery
posterior cerebral artery embolism
posterior cerebral artery occlusion
posterior cerebral artery territory infarction
posterior cortical atrophy
postural abnormality
precipitating factors
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prosopagnosia
protease inhibitor, HIV-1
proximal muscle atrophy
pruritus
pseudobulbar palsy
ptosis
pure sensory stroke
quadrantanopsia, superior
quadriparesis
radiation therapy, CNS treatment and complications with
reading
reading disorder, acquired
Red flags
renal failure
renal stones
respiratory failure
review article
rhabdomyolysis
rigidity
ritonavir
Romberg's sign
sarcoglycan
sarcoglycanopathy
sarcoidosis
sarcoidosis, CNS
sclerae, hyperpigmented
seizure
sensorineural hearing loss
serum alanine aminotransferase
sex reassignment surgery
silver toxicity
simultanagnosia
skin, biopsy
skin, cherry-red
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
skin, pale
sleep apnea
speech disorder
speech disorder, childhood
speech, delayed development of
speech, slowed
spina bifida
splenium of corpus callosum
spondylolysis
statin therapy
steroid therapy, CNS treatment and complications with
stress, emotional
suicide
systemic illness
testicular atrophy
tethered spinal cord
thalamus, infarction of
toe walking
tongue, smooth
tongue, swelling
transgender
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trifluoperazine
tripping
Trousseau's syndrome
urinary frequency
urinary incontinence
urinary urgency
urine, dark
vasospasm
very long chain fatty acids
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual loss
visual loss, slow-unilateral
visuospatial disturbance
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
white matter disease
winging of scapula
work loss
workup
Showing articles 0 to 50 of 1604 Next >>

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Cervical Spondylotic Myelopathy Secondary to Ochronotic Vertebral Arthropathy
Neurol 96:627-628, Pinto, W.,et al, 2021

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Burning Pain in the Legs
NEJM 383:e18, Sacks, C.A., 2020

Peripheral Neuropathy Associated with Silver Toxicity
Neurol 92:481-483, Naddaf, E.,et al, 2019

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

Wilson Disease
NIDDK Oct2018, , 2018

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

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

The Acquired Metabolic Disorders of the Nervous System, Carbon Monoxide Poisoning
Adams & Victors Principles of Neurology Chp 40, pg 1138, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Clinicopath Conf
Noncaseating Granulomas Consistent with Sarcoidosis, Case 37-1996, NEJM 335:1668-1674996., , 1996

Haemorrhagic Stroke, Overall Stroke Risk & Combined Oral Contraceptives:Internat'l Multicentre Study
Lancet 348:505-510, Poulter,N.R.,et al, 1996

Cerebral Achromatopsia as a Presentation of Trousseaus Syndrome
Postgrad Med J 71:44-46, Orrell, R.W.,et al, 1995

Acquired Cerebral Achromatopsia
Neuro Ophthalmol 14:31-36, Setala, K. & Vesti, E., 1994

Skin Lesions of the Spinal Axis and Spinal Dysraphism:Fifteen Cases & Review of the Literature
Arch Pediatr Adolesc Med 148:740-748, McAtee-Smith,J.,et al, 1994

Missed Neuroleptic Malignant Syndrome
BMJ 304:831-832, Renwick,D.S.,et al, 1992

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

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

Acute Ventilatory Failure & Myoglobinuria
Neurol 34:369-371, Taverner,D.,et al, 1984

Central Achromatopsia:Behavioral, Anatomic, & Physiologic Aspects
Neurol 30:1064-1071, Damasio,A.,et al, 1980

Cerebral Color Blindness:An Acquired Defect in Hue Discrimination
Ann Neurol 5:253-261, Pearlman,A.L.,et al, 1979

Alexia without Agraphia & the Inferior Splenium
Neurol 27:685, Ajax,E.T.,et al, 1977

Reversible Cerebellocerebral Disorder in Primary Hemochromatosis
Arch Neurol 34:123, Singh,N.,et al, 1977

Associative Visual Agnosia
Arch Neurol 24:305, Rubens,A.,et al, 1971

Right Hemianopia with Memory & Color Deficits in Circumscribed Left Posterior Cerebral Artery Territory Infarction
Neurol 2l:1104-1113, 1971, Mohr,J.P.,et al, 1971

Color-Naming Defects in Association With Alexia
Arch Neurol 15:137-146, Geschwind,N.,et al, 1966

A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
Neurol 104:e213712, Crausaz,L.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

A 72-Year-Old Man With Meningoencephalitis
Neurol 104:e213658, Isaza-Pierotti,D.F.,et al, 2025

Addressing Systemic Complications of Acute Stroke: A Scientific Statement From the American Heart Association
Stroke 56:e15-e29, Kumar,S.,et al, 2025

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024



Showing articles 0 to 50 of 1604 Next >>