Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
acoustic nerve
acral sensory symptoms
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcohol intolerance
alkylating agents
altered states of consciousness
alternating rapid movement
amitriptyline
amyloid
amyloid angiopathy, cerebral
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ankle reflex, absent
anterior interosseous neuropathy
anterior tibial muscle weakness
antimetabolite
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
arthropathy
arthropathy, neuropathic
arylsulfatase B
asparginase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
atonic bladder
auditory evoked brainstem potentials
autonomic dysfunction
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
Babinski sign
bacterial infection
Bassen-Kornzweig syndrome
benign essential tremor
blacks
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial neuritis, prognosis of
brachial plexus
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
burning paresthesia
caloric testing
cardiomyopathy
case studies
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
cataracts
cataracts, congenital
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central core disease
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, secondary
cerebellar lesion
cerebellum, disease of
cerebro hepato renal syndrome
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
cholesterol
cholesterol, HDL
chorea
chromosomal abnormality
chromosome 16
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
cold temperature
coloboma
compression neuropathy
compression neuropathy, recurrent
cornea, abnormal
cornea, opacity of
corpus callosum, lesion of
cough
cranial nerve enhancement
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
deafness
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
demyelinating disease
denervation of muscle
dermatomyositis
diabetes mellitus
diarrhea
differential diagnosis
diplegia, brachial
diplopia
diplopia, transient
disability, neurological
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
DNA probes
down-beat nystagmus
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
electrocardiogram, abnormal
electroencephalogram, inflammatory disease
electromyogram
electronystagmography
electroretinograph
encephalopathy
entrapment neuropathy
enzyme, muscle disease
epidemiology of neurology
episodic neurologic deficits
erythromelalgia
evoked potentials
eye movement, disorders of
face, numbness of
facial nerve palsy, bilateral
facial pain
facial weakness
facial weakness, bilateral
falling
familial
family planning
fasciculation
Fazio-Londe's disease
fever
fibrillations
fine motor function, impaired
fluorouracil
flush syndrome
foot deformity
foot drop
foot numbness
Friedreich's ataxia
fundus, abnormality of
gadolinium
gait disorder
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genu of corpus callosum
giant axonal neuropathy
Guillain Barre syndrome
hair analysis
Hallervorden Spatz disease
hallucination
hammertoes
hand deformity
hand numbness
hand weakness
headache
hearing loss
heavy metal intoxication
heel-knee-shin test
hemiparesis
hemiparesis, transient
hepatitis C virus
hepatomegaly
hepatosplenomegaly
Hicks disease
high arched feet
human genome
human immunodeficiency virus type 1
hydrocephalus
hyperreflexia
hyperthyroidism
hyponatremia
hyporeflexia
hypotelorism
idiopathic polyneuropathy
imbalance
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intellectual deficit
internuclear ophthalmoplegia
intracerebral hemorrhage
intracerebral hemorrhage, familial
intrinsic hand muscles, wasting of
Isaacs syndrome
isoniazid
jaw pain
Jewish
Kearns-Sayre syndrome
keratitis
klippel feil syndrome
Korsakoff's psychosis
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
kyphosis
laminectomy, cervical
laminectomy, lumbar
Laurence-Moon-Bardet-Biedl syndrome
Leber's congenital amaurosis
leg weakness, bilateral
leprosy
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
light-near dissociation, causes of
liver transplantation
lumbosacral plexopathy
lumbosacral plexus
lymphadenopathy
macular degeneration
magnetic stimulation
magnetic stimulation, brain
median neuropathy
meningismus
meningoencephalopathy
mental retardation
methotrexate
methylhydrazine derivatives
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
mononeuropathy multiplex
mononeuropathy, children
mononeuropathy, recurrent
monoparesis
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
mucopolysaccharidoses
multiple system atrophy
muscle atrophy, focal
muscle atrophy, progressive
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myasthenic crisis
myelin protein zero gene
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myeloradiculopathy
myokymia
myopathy
myopathy, carcinomatous
myopathy, mitochondrial
myopathy, thyroid disease causing
myopia
myositis
myotonia dystrophica
nausea and vomiting
neck pain
nerve biopsy
nerve biopsy, indication
nerve conduction studies
nerve conduction studies, sensory
nerve growth factor
nerve growth stimulating activity
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuritis, causes of
neuroblastoma
neurofibrillary degeneration
neurofibromatosis 1
neurogenic bladder
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronopathy, sensory
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, onion bulb
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, recurrent
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, work up for
neurotoxin
neurotrophin-3
next-generation sequencing
night blindness
nitrogen mustard
numbness, extremity
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, monocular
optic atrophy
optic atrophy, hereditary
optic nerve
optic neuropathy
orthostatic hypotension
orthostatic hypotension, idiopathic
pain
pain, arm
pain, foot
pain, severe
pain, wrist
papilledema
paralysis
paralysis, recurrent
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, lower extremity
patient information and support
peroneal muscle atrophy, causes of
peroneal nerve
peroneal nerve, lesion of
peroxisomal disease
pes cavus
pheochromocytoma
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
POLG1 gene
poliomyelitis
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
porphyria
positional head-hanging test
positive sharp waves
post polio syndrome
precipitating factors
pregnancy, neurologic complications in
procarbazine
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudointernuclear ophthalmoplegia
psychological testing
psychosis
ptosis
ptosis, bilateral
puerperium
pulmonary function tests
pupil
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, scalloped
pyramidal
pyramidal tract dysfunction
quadriparesis
quadriplegia, transient
quality of life
radial nerve, palsy of
radiculopathy
reading disorder, acquired
recombinant DNA
recruitment
recruitment, reduced
recurrent
refractive errors
Refsum's disease
respiratory failure
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFC1 gene
RFLPs
Riley-Day syndrome
risk factors
Romberg's sign
root lesion, nerve
Roussy Levy syndrome
saccadic eye movements, abnormal
sarcoidosis
scoliosis
seizure
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, leg
sensory loss, truncal
sensory nerve action potentials
sensory polyneuropathy
short stature
shoulder, numbness
shoulder, pain in
Shy-Drager syndrome
skin, lesions in neurologic disorders
somatosensory evoked potentials
spasticity
speech disorder
speech disorder, non aphasic
spinal cord, compression of
spinal muscular atrophy
spinal stenosis
spinal stenosis, familial
spinocerebellar ataxia
spinocerebellar degeneration
splenium of corpus callosum
splenomegaly
spontaneous muscle activity
spontaneous remission
steppage gait
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
subdural hematoma
sudden death
suprascapular neuropathy
symmetric brain lesions
syncope
tandem gait, ataxic
Tangier's disease
tapetoretinal degeneration
tauopathy
tensilon test
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thyrotoxicosis
tinnitus
toe walking
tomaculous neuropathy
tongue, enlarged
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
ulnar neuropathy
ultrasonography, nerve
urinary incontinence
Usher's syndrome
vestibular areflexia
vestibular function, tests of
vestibulopathy
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
viral infection
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
visual loss, congenital
vitreous opacities
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
wheelchair
white matter disease
wide based gait
winging of scapula
wrist drop
X-linked neuropathy
x-ray, spine
Showing articles 650 to 700 of 5288 << Previous Next >>

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Diagnosis of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease:International MOGAD Panel Proposed Criteria
Lancet Neurol doi.org110.1016/51474-4422(22)00431-8, Banwell,B.,et al, 2023

Neuromyelitis Optica: A Case Report From a Radiological Perspective
Cureus doi:10.7759/cureus.38945, Rentiya,Z.S.,et al, 2023

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Idiopathic Orbital Inflammation and Tolosa-Hunt Syndrome with Intracranial Extension
Neurol 101:371-374, Yu,S. & Chen,T., 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

A Septuagenarian With Painless Ulceration on the Fingertip
Neurol 101:e1473 - e1477, Iyer,V.G., 2023

Age-Related Changes in Neurologic Examination and Sensory Nerve Amplitude in the General Population, Aging of the Peripheral Nervous System
Neurol 101:e1351-e1358, Taams,N.E.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Trial of Botulinum Toxin for Isolated or Essential Head Tremor
NEJM 389:1753-1765, Marques,A.,et al, 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

Consensus Practice Guidelines on Postdural Puncture Headache from a Multisociety, International Working Group
JAMA Network Open 6:e2325387, Uppal,V.,et al, 2023

Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
Neurol 100:1025-1031, Sharma,V. & Soto,O, 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Woman With Acute Bilateral Ophthalmoplegia
Neurol 101:140-144, Giacobbe,Alket al, 2023

Brain Abscess and Stroke in Children and Adults with Hereditary Hemorrhagic Telangiectasia
Neurol 100:e2324-e2330, White,A.J.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023

Management of Possible Multiple Sclerosis
NEJM 388:2195-2190, , 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

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

Glucose Hypermetabolism in the Basal Ganglia
Neurol 101:90-91, Kim,Y.E.,et al, 2023

Risk of Parkinson Disease Among Service Members at Marine Corps Base Camp Lejeune
JAMA Neurol 80:673-681, Goldman,S.M.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Early Surgery for Sciatics, Does New Evidence Challenge a Stepped Care Approach for all Patients?
BMJ 381:791, Schmid,A.B.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

Lead Poisoning
NEJM 388:e63, Dhar,S. & Garg,D., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Extrapulmonary Manifestations of Sarcoidosis
Rheum Dis Clin North Am 39:277-297, Rao,D.A. & Dellaripa,P.F., 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Wrist Drop After a Fall Onto the Shoulder
BMJ 380:e070708, Ali,M.A. & Freilich,S., 2023

A 67-Year-Old Woman with Progressive Tingling Sensations and Imlalance
Neurol 100:151-157, Horta,L.F.B.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Ann Neurol 91:889-890, Gollion, C.,et al, 2022

Neurological Events Reported after COVID-19 Vaccines: An Analysis of Vaccine Adverse Event Reporting System
Ann Neurol 91:756-771, Frontera, J.A.,et al, 2022

Bilateral Trigeminal Neuralgia - A Condition of the Upper Neck
Head Pain Disorder, Jan, , 2022

Vision Loss in Giant Cell Arteritis
Pract Neurol 22:138-140, Donaldson, L. & Margolin, E., 2022

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

A 67-Year-Old Woman with Abdominal Pain, Constipation, and Urinary Retention
Neurol 99:117-122, Hanna, S.S.,et al, 2022

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022



Showing articles 650 to 700 of 5288 << Previous Next >>