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acrocyanosis
advances in neurology
adverse drug reaction
akinetic mute
alien hand syndrome
alpha-synuclein
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis-like syndrome
ANA
anemia
anemia, megaloblastic
anorexia
anterior horn cell disease
anti citrullinated antibody
anti IgLON5
anti Tr antibodies
anticonvulsants
anticonvulsants, untoward effects of
apnea
applause sign
apraxia
apraxia, constructional
areflexia
arm swing, reduced
arm weakness
arrhythmia, cardiac
arthralgia
astereognosis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxic gait
athetosis
autoantibodies
autoimmune cerebellar ataxia
axonal degeneration
B 12 deficiency
Babinski sign
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
benign essential tremor, refractory
blepharospasm
blindness
blinking, reduced
brachial neuritis
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
bradykinesia
brain atrophy
breast feeding
bulbar palsy
burning hands
burning paresthesia
calf hypertrophy
cardiomyopathy
CAT scan, emission, abnormal
central cord syndrome
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cervical myelopathy
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coin rotation test
cold intolerance
coma, episodic
complications
conduction block
congestive heart failure
consanguinity
cortical-basal ganglionic degeneration
creatine phosphokinase(CPK)elevated
cyclophosphamide
deep gray nuclei
degenerative cervical myelopathy
degenerative diseases of CNS
delay in diagnosis
delayed muscle relaxation
dementia
dementia, rapidly progressive
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplegia, brachial
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dopamine agonist
downward gaze
drug abuse
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystrophin
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalopathy
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
failed medical management
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
fetal tissue
fibrillations
fine motor function, impaired
finger numbness
foot deformity
foot drop
Friedreich's ataxia
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
ganglionitis
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
Gowers maneuver
granular osmiphilic material
hammertoes
hand deformity
hand numbness
hand weakness
handwriting
head nodding
hearing loss
heralding manifestation
herniated disc
herniated disc, central
herniated disc, cervical
high arched feet
hoarseness
homocysteine, serum
Horner's syndrome
hydrocephalus
hyperhomocysteinemia
hyperreflexia
hypersegmented polys
hypersomnia
hypometric saccades
hypophonia
hyporeflexia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunologic disease
immunosuppressive agents
immunotherapy
incoordination
infant, evaluation of
inferior olivary nucleus
intellectual deficit
intellectual deterioration
intelligence quotient
intrauterine
intrinsic hand muscles, wasting of
introverted
jaundice
lactic dehydrogenase(LDH)
laminectomy
laminectomy, cervical
lateropulsion
L-dopa
learning disability
learning disability, in children
leg numbness
leg weakness, bilateral
Lewy body
Lhermitte's sign
liver disease
liver function enzymes
lobar atrophy
low birth weight
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
masked facies
memory, defect of recent
memory, impairment of
meningitis
meningitis, bacterial
meningitis, children
meningitis, CSF cell count-normal
meningitis, factors influencing mortality in
meningitis, late neurologic sequelae in
meningitis, neurologic aspects and complications of
methylmalonic acid, serum
methylmalonic acidemia
microcephaly
midbrain
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor development
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
motor symptoms
motor system
movement disorder
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, spinal cord
MRI, spine
multiple sclerosis
muscle cramp
muscle stiffness
muscle twitching
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
musicians
myelitis, longitudinal
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonus
myoglobinuria
mysoline
neck pain
neck stiffness
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve hypertrophy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic testing
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuromyotonia and axonal neuropathy
neuronal ceroid-lipofuscinosis
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, sensory
neuropathy, toxic
neurotoxic
next-generation sequencing
nitrous oxide
numb clumsy hands syndrome
numbness, extremity
nystagmus
occupational neurologic disorders
olivary degeneration, hypertrophic
overuse syndrome
pain
pain, abdominal
pain, arm
pain, severe
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, diagnosis
Parkinson disease, nonmotor problems of
Parkinson disease, pathogenesis of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
penguin silhouette sign
peripheral blood smear, abnormal
pernicious anemia
pes cavus
pianist
placebo effect
position sensation
positive sharp waves
posterior column disease
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
prenatal
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
propranolol
proprioception
protein 14-3-3, cerebrospinal fluid
pseudoathetosis
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
pyramidal tract dysfunction
rapidly progressing neurologic illness
recruitment
recruitment, reduced
recurrent
REM sleep behavior disorder
remote effect of cancer on the nervous system
respiratory tract infection
retrocollis
retropulsion
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rheumatoid arthritis, neurologic complications of
rigidity
rigidity, axial
risk factors
Romberg's sign
saccadic eye movements, abnormal
scoliosis
sedimentation rate, elevated
seizure
seizure, children
seizure, treatment of, polytherapy
sensorineural hearing loss
sensory loss
sensory loss, asymmetric
sequencing difficulty
shooting pain
sinemet
Sjogren's syndrome
sleep pathology and physiology
slurred speech
spastic diplegia
spasticity
speech disorder, childhood
speech, delayed development of
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia
spontaneous remission
stem cell transplantation
steppage gait
stimulation, deep brain
systemic illness
tandem gait, ataxic
tau protein
tauopathy
thalamotomy
thalamus, focused ultrasound ablation
toe walking
tone, muscle, increased
tongue, smooth
tongue, swelling
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, surgical treatment of
tremor, treatment of
trinucleotide repeats
tripping
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
urinary incontinence
urine, dark
useless hand
vibratory sensation
vibratory sensation, abnormal
violinist
vision, blurred
visual loss
visual symptoms
visuospatial disturbance
vitamin deficiency
vitiligo
vocalizations
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
wide based gait
winging of scapula
writing
Showing articles 450 to 500 of 4134 << Previous Next >>

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

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Optic Nerve Head Edema Among Patients Presenting to the Emergency Department
Neurol 90:e373-e379, Sachdeva, V.,et al, 2018

Hemorrhagic Encephalitis Associated with H3N2 Influenza A Viral Pneumonia
Neurol 90:336-337, AbdelRazek, M.A.,et al, 2018

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

Clinicopathologic Conference, Human Herpesvirus 6-Related Meningoencephalitis
NEJM 378:659-669, Case 5-2018, 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

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

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Convexal subarachnoid hemorrhage accompanied by transient global amnesia
Neurol 90:e1933-e1934, Beitzke, M.,et al, 2018

Bilateral temporal crescent sparing after cardiac arrest
Neurol 90:1035-1036, Lindegger, D.J.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Maternal and Fetal Risks of Natalizumab Exposure in Utero
Neurol 90:443-444, Marrie, R.A.,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

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Isolated Mammillary Body Infarction Presenting with Memory Impairment
Neurol 90:e1093-e1094, Park, K.M.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

Tinnitus
NEJM 378:1224-1231, Bauer, C.A., 2018

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

Acute Amnestic Syndrome Associated with Fentanyl Overdose
NEJM 378:1157-1158, Barash, J.A., et al, 2018

Acute amnesia associated with damaged fiber tracts following anterior fornix infarction
Neurol 90:706-707, Zhu, Q.Y.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

Facial Ulceration in stroke
Neurol 90:e1448-e1449, May, L.M.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Orbital Apex Syndrome
NEJM 378:18, Sacks. C.A., 2018

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

Coma
Neurol 90:e1638-e1645, Schievink, W.I.,et al, 2018

A 48-year-old woman with confusion, personality change, and multiple enhancing brain lesions
Neurol 90:e1724-e1729, Hills, J.M.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Inflammatory Demyelinating Polyneuropathy Versus Leptomeningeal Disease Following Ipilimumab
J Immunother Cancer 6:11, Cafuir, L.,et al, 2018

Numb Chin Syndrome
UptoDate.com Sept, Robertson, C.E., 2018

Bilateral Ageusia and Tongue Anesthesia Following Unilateral Brainstem Infarct: A Case Report with a Brief Review of the Literature
Case Rep Neurol 10:60-65, Saleh, C.,et al, 2018

Ophthalmic Manifestations of Giant Cell Arteritis
Rheumatology 57:ii63-1172, Vodopivec, I. & Rizzo, J.F. III, 2018

Cerebral Fat Embolism Syndrome in Sickle Cell Disease Without Evidence of Shunt
eNeurologicSci 14:19-20, Nathan, C.L.,et al, 2018

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

Bilateral Basal Ganglia Necrosis Secondary to Methamphetamine
MDCP 5:55-556, Sanchez,A. et al, 2018

Optic Neuritis in a Patient with Celiac Disease
Neurol Neurochir Pol 51:534-536, Baghbanian, S.M. & Moghadasi, A.N., 2017

Simultaneous Bilateral Posterior Ischemic Optic Neuropathy Secondary to Giant Cell Arteritis
BMC Ophthalmology 18:317, Albarrak, A.A.,et al, 2017

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

A Rare Case of Bilateral Optic Neuritis and Guillain-Barre Syndrome Post Mycoplasma Pneumoniae Infection
Neuro Opth 41:41-47, Baheerathan, A.,et al, 2017

IGG4-Related Hypertrophic Pachymeningitis Coexpressing Antineutrophil Cytoplasmic Antibodies
Neurol 4:e341-e343, Massey, J., 2017

Rosai-Dorfman Disease: Rare Presentation as Isolated Mediastinal and Hilar Lymphadenopathy
Cureus DOI 10.7759/cureus, Lateef, N.,et al, 2017

Posterior Ischemic Optic Neuropathy
UptoDate Aug, Tamhankar, M. & Volpe, N., 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017



Showing articles 450 to 500 of 4134 << Previous Next >>