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Differential
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acanthocytosis
acral sensory symptoms
Addison's disease
Adies pupil
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
allodynia
alternating rapid movement
alternating rapid movement, impaired
ammonia
amyotrophic lateral sclerosis, differential diagnosis
ANA
anemia
angiography, cerebral, beaded vessels
angiography, cerebral
ankle edema
ankle reflex, absent
anorexia
anorexia nervosa
anti citrullinated antibody
anti MAG antibodies
anticonvulsants
anticonvulsants, untoward effects of
areflexia
arrhythmia, cardiac
arsenic
arteritides
arthralgia
ascending paralysis
ascites
astereognosis
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
athetosis
atrophy, muscle
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonopathy, distal
B 12 deficiency
Babinski sign
BAL
basal ganglia, lesion of
basophilic stippling of red blood cells
bedridden
beriberi
biologic markers
bladder dysfunction
blink reflex
bone marrow suppression
bradykinesia
brainstem, infarction of
bulbar palsy
burning paresthesia
cachexia
calf atrophy
carcinoma
cardiac arrest
cardiac arrest and resuscitation
cardiomegaly
cardiomyopathy
cast
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar lesion
cerebellum, disease of
cerebrospinal fluid, abnormal
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, mimics
Charcot-Marie-Tooth
chest x-ray, abnormal
children
cholestanol
chorea
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
compression neuropathy
conduction block
confusion
congenital myopathy
congestive heart failure
corneal reflex, abnormal
corneal reflex, absent
cough
cranial nerve enhancement
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
deep gray nuclei
dementia
demyelinating disease
denervation potentials
dermatitis
descending paralysis
dexterity, impaired
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetic mononeuropathy
diarrhea
differential diagnosis
difficulty climbing stairs
digital health, wearable technology
diplopia
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
edema, pedal
edema, periorbital
efficacy
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, inflammatory disease
electromyogram
electromyogram, decremental response
electron microscopy
encephalopathy
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
eosinophilia
erythrocyte
ethylene oxide
evoked potentials
exercise
exome sequencing
eye movement, disorders of
face, numbness of
facial pain
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failed medical management
fall prevention
fall risk
falling
familial
fasciculation
fatigue
fever
fibrillations
fine motor function, impaired
fingernails, abnormal
flaccid paralysis
foot deformity
foot drop
foot, swollen
Friedreich's ataxia
F-wave response
gadolinium
gait disorder
gait speed
gait, waddling
gammaglobulin therapy, intravenous
ganglionitis
gastroenteritis
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glioma
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, sensory
hammertoes
hand deformity
hand numbness
hand swelling
hand weakness
headache
headache, severe
hearing loss
heavy metal intoxication
heel-knee-shin test
hemoglobinuria
hepatitis
hepatosplenomegaly
heralding manifestation
herpes simplex virus
herpes virus
herpes virus infection
herpes, genital
high arched feet
hip flexor weakness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
hot cross bun sign
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, treatment of
hyperamylasemia
hyperkeratosis
hypersomnia
hypogonadism
hyponatremia
hypophosphatemia
hypopigmentation of skin
hyporeflexia
hypotonia
imbalance
imbalance, postural
immunoelectrophoresis, serum
immunohistochemistry
immunomodulation
immunosuppression
immunosuppressive agents
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
incoordination
industrial neurologic disorders
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
jaw pain
Jewish
lactic dehydrogenase(LDH)
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
leukopenia
lid closure, weakness of
liver disease
liver function enzymes
long bone lesion
lumbosacral plexopathy
lymphadenopathy
lymphoma
McLeod syndrome
mediastinum, mass of
Mees lines
memory, impairment of
meningeal enhancement
meningismus
mental status, abnormal
midbrain, atrophy
midbrain, infarction of
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
mononeuropathy, children
mortality
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, lumbosacral plexus
MRI, muscle
MRI, negative
MRI, peripheral nerve
MRI, spinal cord
multiple myeloma
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, facioscapulohumeral
myasthenia gravis
myasthenia gravis, late-onset
myasthenia gravis, misdiagnosis of
myasthenia gravis, presenting manifestations
myelin protein zero gene
myeloma, osteosclerotic
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myopathy
myopathy, focal
myopathy, monomelic
nausea and vomiting
neoplasm, primary intracerebral
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve enlargement
nerve hypertrophy
nerve root biopsy
nerve root enhancement
nerve root hypertrophy
neuritis, heavy metals causing
neuroendocrinology
neurogenic bladder
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuronopathy
neuronopathy, sensory
neuronopathy, sensory and motor
neuropathology, brain
neuropathy
neuropathy, chronic
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, toxic
neuropathy, vasculitic, systemic
night blindness
numbness, extremity
numbness, generalized
nystagmus
occupational neuropathies
old age, neurology of
opportunistic infection
organomegaly
ornithine transcarbamylase deficiency
orthostatic hypotension
pain
pain, abdominal
pain, back
pain, calf
pain, foot
pain, leg
pain, thigh
pain, total body
pancreatitis
pancytopenia
papilledema
paraneoplastic ganglionopathy
paraparesis
paraparesis, spastic
paraproteinemia
parenteral alimentation
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, early symptoms
Parkinson disease, presymptomatic detection
periarteritis nodosa
pericardial effusion
pericarditis
perioral numbness
peripheral blood smear
peripheral blood smear, abnormal
peroneal nerve
peroneal nerve palsy
peroneal nerve palsy, bilateral
peroneal nerve, lesion of
pes cavus
plasmacytoma
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
POEMS syndrome
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, childhood
polyradiculoneuropathy
position sensation, abnormal
positional head-hanging test
posterior column disease
postoperative neurologic complications
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proprioception
proprioception, abnormal
pruritus
pseudohypertrophy
psychological testing
pulmonary infiltrates
pupil
pupil, dilated and fixed, bilateral
pyramidal
pyramidal tract dysfunction
quadriceps atrophy
quadriparesis
quadriplegia
reading disorder, acquired
real-time quaking-induced conversion
remote effect of cancer on the nervous system
renal cell carcinoma
repetitive nerve stimulation
respiratory failure
retroperitoneal mass
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rheumatoid vasculitis
risk factors
rituximab
Romberg's sign
Sabin-Feldman dye test
saccadic eye movements, abnormal
scannig speech
sciatic neuropathy
sclerosis, bone
sedimentation rate
sedimentation rate, elevated
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, asymmetric
sensory loss, band distribution
sensory polyneuropathy
serum glutamic oxaloacetic transaminase
shooting pain
shoulder-girdle wasting
shunt procedure, ventricular
Sjogren's syndrome
skin, lesions in neurologic disorders
slurred speech
sodium valproate
sodium valproate, toxicity
somatosensory evoked potentials
spasticity
speech disorder
speech disorder, non aphasic
splenomegaly
staggering
steppage gait
steroid
steroid therapy, CNS treatment and complications with
suspended sensory loss
sweating, abnormality of
synovitis
systemic illness
Tai chi
tandem gait, ataxic
tauopathy
telangiectases
temporalis muscle wasting
thiamine deficiency
thrombocytopenia
thrombocytosis
thrush
tongue, fasciculations of
toxoplasma complement fixation test
toxoplasmosis, acquired
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
trigeminal nerve, abnormality of
turning slowly
urea-cycle enzymopathies
uremia
urinary incontinence
urine test in toxic screen
uveitis
varicella zoster virus
vascular endothelial growth factor
vasculitides
vestibular migraine
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual impairment
vitamin deficiency
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weight loss
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
zoster sine herpete
Showing articles 300 to 350 of 2661 << Previous Next >>

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

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

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,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

Degenerative Cervical Myelopathy
BMJ 360:k186, Davies, B.M.,et al, 2018

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
Neurol 88:e26-e29, Qin, C.,et al, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Infratentorial Dural Arteriovenous Fistula Resulting in Brainstem Edema and Enhancement
Neurol 88:503-504, Emmer, B.J.,et al, 2017

A 74-year-old Woman with Bilateral Foot Pain and a Palmar Rash
Neurol 88:e44-e50, Wynn, D.P.,et al, 2017

Cranial Nerve Hypertrophy in IgG4 Anti-Neurofascin 155 Antibody-Positive Polyneuropathy
Neurol 88:e52, Franques, J.,et al, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

Monitoring long-term Efficacy of Fampridine in Gait-Impaired Patients with Multiple Sclerosis
Neurol 88:832-841, Filli, L.,et al, 2017

Blood-based NfL - A biomarker for differential diagnosis of parkinsonian disorder
Neurol 88:930-937,922, Hansson, O.,et al, 2017

A Woman in Her 60s with Chronic Meningitis from Aspergillus
JAMA Neurol 74:348-352, Pichler, M.R.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Reversible Gait Ataxia
Neurol 88:e145-e149, Abkur, T.M. & Bede, P., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Viral Hepatitis and Parkinson Disease
Neurol 88:1630-1633, Pakpoor, J.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

Acute Bilateral Isolated Foot Drop: Changing the Paradigm in Management of Degenerative Spine Surgery with Percutaneous Endoscopy
World Neurosurg 110:319-322, Adsul, N.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

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

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma Consistent with Neurolymphomatosis
NEJM 376:2471-2481, Case 19-2017, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

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

CNS Posttransplant Lymphoproliferative Disorder
Neurol 89:e32-e37, Kesari, N.K.,et al, 2017

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

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Conversion to Parkinson Disease in the PARS Hyposmic and Dopamine Transporter-Deficit Prodromal Court
JAMA Neurol 74:933-940,901, Jennings, D.,et al, 2017

Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
Neurol 89:1416-1423, Cury, R.G.,et al, 2017

National Randomized Controlled Trial of Virtual House Calls for Parkinson Disease
Neurol 89:1152-1161,1103, Beck, C.A.,et al, 2017

MRI of the Swallow Tail Sign: A Useful Marker in the Diagnosis of Lewy Body Dementia?
AJNR 38:1737-1741, Shams, S.,et al, 2017

Management of Parkinson Disease in 2017
JAMA 318:791-792, Okun, M.S.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

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

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017



Showing articles 300 to 350 of 2661 << Previous Next >>