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acoustic nerve
acute intermittant porphyria
Adies pupil
adrenergic blocker
adult polyglucosan body disease
adverse drug reaction
agitation
akathisia
alcoholism
allodynia
alopecia
alpha adrenergic blocker
aluminum
Alzheimer's disease
amphiphysin antibodies
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anisocoria
anorexia
antibodies to voltage-gated calcium channels
antiganglioside antibodies
antitoxin
areflexia
arm weakness
ataxia
ataxia, progressive
atypical
autoantibodies
autoimmune disease
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
axonal degeneration
Babinski sign
bladder dysfunction
bone scanning
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
bradykinesia
bulbar palsy
bulbar palsy, acute
burning paresthesia
cachexia
calf atrophy
campylobacter infection
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
cerebellar degeneration
cerebellar lesion
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
chest pain
chewing movements
chorea
cingulate island sign
Clinical Pathologic Conference(C.P.C.)
coat-hanger pain
cognition
cogwheel rigidty
coinfection
collapsin response mediator protein 5 IgG
complications
confabulation
confusion
constipation
contactin associated protein like 2 antibodies
corpus callosum
corpus callosum, lesion of
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cry, abnormal
cry, weak
crying
cyanosis
cyst, arachnoid, infant
deep tendon reflexes
degenerative diseases of CNS
dementia
dementia, familial
dementia, rapidly progressive
depression
dermatomyositis
diabetes mellitus
diabetes mellitus, chemical
dialysis
dialysis dementia
dialysis disequilibrium syndrome
diplopia
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
dysarthria
dysphagia
dyspnea
edema, pedal
electroencephalogram, abnormalities of
electromyogram
electromyogram, incremental response
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalomyelitis
encephalopathy
ephedrine
epidemiology of neurology
erectile dysfunction
exercise
exercise-related muscle strength increase
exome sequencing
extrapyramidal movement disorder, progressive
facial asymmetry
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fibrillations
Fisher's syndrome
flaccid paralysis
fludrocortisone
food poisoning
food-borne infection
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gastroparesis
gene mutation
genetic neurologic disorders
genetic testing
glaucoma
glucose tolerance test, abnormal
glycogen storage disease
guanethidine
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, complications
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, prognosis of
Guillain Barre syndrome, variant forms of
hallucination, auditory
head bobbing
heat intolerance
hemifacial atrophy
hemiparesis
heralding manifestation
hoarseness
honey
Horner's syndrome
hot bath test
H-reflex testing
hyperamylasemia
hyperhidrosis
hyperreflexia
hypertension
hypohidrosis
hypokalemic paralysis
hyponatremia
hypoosmolality of serum
hypophonia
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypothermia
hypotonia
hypotonia, infants
ileus, paralytic
imbalance
imbalance, postural
immunologic disease
immunology and the nervous system
immunotherapy
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
infant, evaluation of
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intrinsic hand muscles, wasting of
irritability
irritable baby
Jewish
juvenile distal and segmental muscular atrophy
laughing
laughing, pathologic
L-dopa
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukoencephalopathy
life expectancy
lightheaded
light-near dissociation, causes of
limbic encephalitis
livedo reticularis
malignancy screen
malignancy, occult
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
mental status, abnormal
metabolic disorder, primary
midodrine
mimics
Mini Mental Status Examination
misdiagnosis
monoamine oxidase inhibitors
mortality
Morvan's fibrillary chorea
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle cramp
muscle pain
muscle strength, testing
muscle twitching
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenic syndrome
myelomalacia
myeloneuropathy
myoclonic jerks
myokymia
nausea and vomiting
neck pain
neck weakness
nerve conduction studies
nerve growth factor
nerve growth stimulating activity
neuroblastoma
neurofibromatosis 1
neurogenic bladder
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuromyotonia
neuronal cell surface antigen
neuronal intranuclear inclusion disease
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, paraneoplastic
neuropathy, sensory
neuropathy, sensory, hereditary
neuroprotective agents
neurotoxin
next-generation sequencing
NMDA antagonists
NOTCH2NLC
onconeural antibodies
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, total
opsoclonus-myoclonus syndrome
optic neuropathy
oral contraceptives
orthostatic hypotension
orthostatic hypotension, idiopathic
orthostatic hypotension, treatment of
osteoporosis
pain
pain, abdominal
pain, leg
palate, paralysis
pancreatitis
paralysis
paralysis, acute areflexic
paraneoplastic cerebellar degeneration
paresthesias
Parkinson disease
Parkinson disease, atypical
Parkinson disease, differential diagnosis of
Parkinson disease, familial
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
peripheral nerve, lesion of
pheochromocytoma
physical therapy
plasmapheresis
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
polyneuropathy, uremic
porphyria
posterior leukoencephalopathy syndrome
postural abnormality
prevention of neurologic disorders
prion disease
prognosis
progressive hemifacial atrophy
progressive neurologic disorder
progressive supranuclear palsy
pruritus
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychosis, acute
psychotic behavior
ptosis
ptosis, bilateral
pulmonary embolism
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated, bilateral
pupil, light reflex, abnormal
pupil, oval
pupil, tonic
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
Red flags
reflex sympathetic dystrophy
reflex sympathetic dystrophy, children
remote effect of cancer on the nervous system
renal failure
renal transplantation
renal tubular acidosis
repetitive nerve stimulation
respirator
respiratory failure
retinopathy
review article
rigidity
Riley-Day syndrome
risk factors
Romberg's sign
salivation, excessive
schizophrenia
scleroderma
scleroderma, neurologic involvement with
screening
seizure
sensory ganglia
serum lipase, elevated
shoulder, pain in
Shy-Drager syndrome
sicca syndrome
single-fiber electromyography
Sjogren's syndrome
skin, temperature difference
sleep pathology and physiology
SNCA duplication
spasticity
spinal cord, lesion of
stare
steroid
steroid therapy, CNS treatment and complications with
suck, poor
sweating
sweating, abnormality of
sympathetic block
sympathetic nervous system
sympathomimetic drugs
syncope
synucleinopathy
systemic illness
tachycardia
tandem gait, ataxic
tensilon test, false positive
thermography
thymoma
tongue, impaired movements of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
uremia
uremic encephalopathy
urinary incontinence
urine osmolality, elevated
vasopressin
viral infection
vision, blurred
visual loss
vocal cord paralysis
walking, difficulty with
Watson-Schwartz reaction
weakness
weakness, acute
weakness, generalized
weakness, infant
weakness, progressive
weakness, proximal
weight loss
wheelchair
white hair
white matter disease
wide based gait
workup
xerostomia
Showing articles 100 to 150 of 3653 << Previous Next >>

Clinical Manifestations of Myasthenia Gravis
UptoDate Aug 2016, Bird, S.J., 2016

A 64-year-old Man with Progressive Paraspinal Muscle Weakness
Neurol 86:e4-e9, Schneider, R.,et al, 2016

Cardiovascular Dysfunction in Multiple Sclerosis
Neurologist 20:108-114, Kaplan, T.B.,et al, 2015

A 44-year-old Woman with Rapidly Progressive Weakness and Ophthalmoplegia
Neurol 85:e22-e27, Schreck, K.C.,et al, 2015

Progressive Development of Cardiomyopathy Following Altered Autonomic Activity in Status Epilepticus
Am J Physiol Heart Circ 309:1554-1564, Read, M.I.,et al, 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Cyclical Konzo Epidemics and Climate Variability
Ann Neurol 77:371-380, Oluwole, O.S.A., 2015

Efficacy of Idebenone on Respiratory Function in Patients with Duchenne Muscular Dystrophy not using Glucocorticoids (DELOS): A Double-Blind Randomised Placebo-Controlled Phase 3 Trial
Lancet 385:1748-1757,1704, Buyse, G.M.,et al, 2015

Clinicopathologic Conference, Infective Endocarditis and Infectious Aortitis due to Staphylococcus Aureus
NEJM 370:651-660, Case 5-2014, 2014

A 14-Year-Boy with Spells of Somnolence and Cognitive Changes
Neurol 82:e142-e146, de Gusmao, C.M.,et al, 2014

Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
Neurol 82:1813-1821, Araki, A.,et al, 2014

Clinicopathologic Conference, Dermatomyositis. Malignant Atrophic Papulosis (Degoss Disease), Involving the Skin and Gastrointestinal Tract
NEJM 370:2327-2337, Case 18-2014, 2014

Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

Clinicopathologic Conference, Chronic Meningoencephalitis Consistent with Rasmussens Encephalitis
NEJM 371:1737-1746, Case 34-2014, 2014

Clinical Radiologic Features of Encephalopathy during 2011 E Coli O111 outbreak in Japan
Neurol 82:564-572, Takanashi, J.,et al, 2014

Serotonin Syndrome
BMJ 348:g1626, Buckley, N.A.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Uremic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1145, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Ischemic-Hypoxic Encephalopathy
Adams & Victors Principles of Neurology Chp 40, pg 1133, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Anterior Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 763, Ropper, A.H.,et al, 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Normal Pressure Hydrocephalus
Adams & Victors Principles of Neurology, Chp 30, pg 624, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Multiple System Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1095, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Vitamin B12 Deficiency Causing Night Sweats
Scott Med J 59:e8-e11, Rehman,H.U., 2014

Clinicopathologic Conference, Methcathinone (Bath Salts) Intoxication
NEJM 369:2536-2545, Case 40-2013, 2013

Clinicopathologic Conference, Rabies Encephalitis
NEJM 368:172-180, Case 1-2013, 2013

Cholinergic Autonomic Dysfunction in Veterans with Gulf War Illness
JAMA Neurol 70:191-200, Haley, R.,et al, 2013

Clinical Features of Dopamine Agonist Withdrawal Syndrome in a Movement Disorders Clinic
JNNP 84:130-135, Pondal, M.,et al, 2013

Diagnosis of Lambert-Eaton Myasthenic Syndrome in Children
Neurol 80:e220-e222, Morgan-Followell,B.& de los Reyes,E., 2013

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Neurological Disorders in Primary Sjogrens Syndrome
Autoimmune Dis: DOI: ID.1152012/645967, Tobon, G.J.,et al, 2012

Clinical Reasoning: Encephalopathy in a 10-year-old boy
Neurol 79:e12-e18, Rodan, L. & Tein, I., 2012

Morvan Syndrome: Clinical and Serological Observations in 29 Cases
Ann Neurol 72:241-255, Irani, S.R.,et al, 2012

Clinicopathologic Conference,Necrotizing Noninflammatory Myopathy Consistent with Exposure to Statins
NEJM 36:944-954, Case 7-2012, 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Cluster Headache
BMJ 344:e2407, Nesbitt,A.D.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Autonomic Dysfuntion in Chronic Inflammatory Demyelinating Polyradiculoneuropathy
Neurol 78:702-708, Figueroa,J.J.,et al, 2012

The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Project
Clin Inf Dis 54:899-904, Gable, M.S.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

A Middle-Aged Woman with Nausea, Weight Loss, and Orthostatic Hypotension
Neurol 77:489-495, Singer, W.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Intravenous Dihydroergotamine for Inpatient Management of Refractory Primary Headaches
Neurol 77:1827-1832, Nagy, A.J.,et al, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy
Neurol 77:62-66, Schade van Westrum, S.M.,et al, 2011

Clinical Presentation, Pathologic Features, and Diagnosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Progressive Multifocal Leukoencephalopathy in Individuals with Minimal or Occult Immunosuppression
JNNP 81:247-254, Gheuens,S., et al, 2010

Vitamin B12-Responsive Severe Leukoencephalopathy and Autonomic Dysfunction in a Patient With "Normal" Serum B12 Levels
JNNP 81:1369-1371, Graber,J.J.,et al, 2010

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010



Showing articles 100 to 150 of 3653 << Previous Next >>