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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 250 to 300 of 2661 << Previous Next >>

Toxic Diffuse Isolated Cerebellar Edema from Over-the-Counter Health Supplements
Neurol 92:965-966, Kim, D.D.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Kelch-Like Protein 11 Antibodies in Seminoma-Associated Paraneoplastic Encephalitis
NEJM 381:47-54, Mandel-Brehm, C.,et al, 2019

Suicide and Suicide Attempts after Subthalamic Nucleus Stimulation in Parkinson Disease
Neurol 93:e97-e105, Giannini, G.,et al, 2019

Vestibular Migraine
BMJ 366:L4213, Li, V.,et al, 2019

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

A 78-year-old Man with a Gait Disorder
Neurol 93:223-227, Saucedo, M.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

MR Imaging of the Brain in Neurologic Wilson Disease
AJNR 40:178-183, Yu, X.-E.,et al, 2019

Compressive Lateral Femoral Cutaneous Neuropathy Secondary to Sartorius Muscle Fibrosis
JAMA Neurol 76:109-110, Triplett, J.D.,et al, 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Clinical Features of Syphilitic Myelitis with Longitudinally Extensive Myelopathy on Spinal Magnetic Resonance Imaging
World J Clin Cases 7:1282-1290, Yuang,J-L.,et al, 2019

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

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

Bilateral Basal Ganglia Necrosis Secondary to Methamphetamine
MDCP 5:55-556, Sanchez,A. 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

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

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

Neuronal Intranuclear Inclusion Disease Showing Intranuclear Inclusions in Renal Biopsy 12 Years Earlier
Neurol 91:884-886, Motoki, M.,et al, 2018

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

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Foot Drop
WebMD, Bernstein, L., 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Neuro-Sweet Disease Presenting as Ischemic Stroke and Aseptic Meningitis
Neurol 91:e2197-e2199, Das, A.S.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 75-year-old man with parkinsonism, mood depression, and weight loss
Neurol 90:572-575, Frattini, E.,et al, 2018

A 60-year-old woman with ataxia
Neurol 90:e1627-e1630, Dandapat, S.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Review of the Neurological Implications of von Hippel-Lindau Disease
JAMA Neurol 75:620-627, Dornbos, D.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

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

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

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

The Parkinson Pandemic - A Call to Action
JAMA Neurol 75:9-10, Dorsey, E.R. & Bloem, B.R., 2018

Recurrent Dysarthria and Ataxia in a Young Girl
JAMA Neurol 75:125-126, Romba, M.,et al, 2018



Showing articles 250 to 300 of 2661 << Previous Next >>