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Differential
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acquired immunodeficiency syndrome
adolescent medicine
adverse drug reaction
akathisia
akinesia of eyelid function
alcohol, neurologic complications with
alcoholism
algorithm
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, Parkinson-dementia-complex
ANA
anergy
anoxia
anti IgLON5
antibiotics
anticardiolipin antibodies
anticonvulsants, untoward effects of
antiphospholipid antibody syndrome
aphasia
aphasia, progressive, primary
apraxia
apraxia of eye movements
apraxia of eyelid opening
arbovirus
areflexia
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
ataxin
ataxin-2
athetosis
ATP1A3 gene
atypical
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
baclofen
bacterial infection
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
bilirubin encephalopathy
biologic markers
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blepharospasm
blinking
blinking, reduced
bone marrow transplantation
botulinum toxin
botulinum toxin, complications of
bradykinesia
bradykinesia, facial
bradyphrenia
brain atrophy
brain biopsy
brain damage
brainstem
brainstem, infarction of
brainstem, lesion of
Brueghel's syndrome
cachexia
CAG repeats
camptocormia
carcinoembryonic antigen
carcinoma
carcinoma of breast
cardiomyopathy
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, muscle
caudate nucleus, atrophy
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral hypoperfusion
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
Charcot's sign
chewing movements
children
chorea
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 11
chromosome 20
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
collagen vascular disease
concussion
confabulation
confusion
congenital infection, CNS
consanguinity
contractures, joint
controversies in neurology
conversion reaction
corpus callosum, thinning
cortical-basal ganglionic degeneration
cost
cost effectiveness
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Cuba
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, treatment of
Dengue fever
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
diplopia
disorientation
distal muscle atrophy
dopa responsive dystonia
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drug abuse
drug abuse, neurologic complications of
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonia, cervical
dystonia, children
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, episodic
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endarterectomy, carotid
endemic area
enolase
enzyme, defect
epidemiology of neurology
episodic neurologic deficits
evidence-based research
exercise intolerance
exome sequencing
extralimbic encephalitis
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial movement disorder
facial nerve palsy
falling
false negative
familial
fasciculation
fatal familial insomnia
fever
fluctuate
fluorescent treponema antibody absorption/false positive
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
frontal behavioral spatial syndrome
frontal lobe, anatomy and physiology
gait disorder
galactorrhea
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
granulomatous disease
growth retardation
Guillain Barre syndrome
gyrus, abnormal
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, visual
hammertoes
head injury
headache
hearing loss
hemifacial spasm
hemiparesis
hepatic failure
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
heralding manifestation
hippocampus
hippocampus, hyperintense
Horner's syndrome
human immunodeficiency virus type 1
Huntington's chorea
Huntington's disease, children
hydrocephalus
hyperammonemic encephalopathy
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypercalcemia
hyperesthesia
hyperreflexia
hypersomnia
hypertonia
hypocomplementemia
hypophonia
hyporeflexia
hyposmia
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypoxia
hypoxic encephalopathy
imbalance
imbalance, postural
immunocompetent
immunodeficiency
immunomodulation
immunosuppression
immunotherapy
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intranuclear
infection
insight, loss
insomnia
intellectual deficit
intellectual deterioration
internal capsule
intracranial hypertension, benign
intravenous
iron, brain
Isaacs syndrome
Jakob-Creutzfeldt disease
jaundice
jaw jerk, abnormal
kernicterus
ketoacidosis
kyphosis
Latvia
L-dopa
leg spasms
leg spasms, painful
lenticular nucleus, lesion of, bilateral
leukemia
leukoencephalopathy
Lewy body
Lewy body disease, diffuse
lid abnormalities
limbic encephalitis
liver disease
lordosis
low back pain
lymphadenopathy, hilar
lymphoma
maculopathy
manganese intoxication
marche a petits pas
masked facies
mediastinum, mass of
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, carcinomatous
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methcathinone
methylmalonic acidemia
microcephaly
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
molecular genetics
mononeuropathy
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, paroxysmal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, gradient-echo
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, paramagnetic effect
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle spasm
muscle stiffness
muscle weakness
muscular dystrophy
myasthenia gravis
myelitis
myelopathy
myelopathy, hepatic
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, segmental
myopathy
myopathy, metabolic
myositis
nausea and vomiting
neck weakness
neurocutaneous disease
neurodegeneration with brain iron accumulation
neuroendocrinology
neurologic complications of, systemic disease
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, tempo
neurologic signs
neuron specific enolase
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neurotoxic
neurotoxin
next-generation sequencing
NOTCH2NLC
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, monocular
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculomasticatory myorhythmia
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic neuritis
orthostatic hypotension
palilalia
PANK2 mutation
papilledema
paraparesis, spastic
parasomnia
paraspinal muscle
paraspinal muscle weakness
parenteral alimentation
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
Parkinsonism, freezing phenomena in
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathology
pericarditis
peripheral nerve, lesion of
personality change
pigmentary retinopathy
pituitary, lesion of
pleocytosis of cerebrospinal fluid
POLG1 gene
polymerase chain reaction
polyneuropathy
portal caval shunt
posterior inferior cerebellar artery syndrome
postural abnormality
precipitating factors
preclinical
premature infant
prevention of neurologic disorders
prion disease
PRKN gene
progeria
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinopathy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
recurrent
remote effect of cancer on the nervous system
renal stones
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
rigidity, axial
Romberg's sign
rubella encephalitis, progressive
rubella syndrome
rubella virus
Russia
saccadic eye movements
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
Saudi Arabia
scoliosis
screening
sea-blue histiocytes
seizure
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
shaking
sinemet
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray
skull x-ray, abnormal
sleep pathology and physiology
slow virus infection of CNS
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 2
splenomegaly
spongy degeneration of brain
standing difficulty
stare
startle reaction
status epilepticus
status epilepticus, intractable
steroid therapy, CNS treatment and complications with
stiff legs
stiff limb syndrome
stiff man syndrome
stimulant drugs
stooped posture
striatum, lesion of
striatum, lesion of, bilateral
stridor
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
substantia nigra
subthalamic nucleus
symmetric brain lesions
synucleinopathy
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
thalamus, lesion of
thalamus, lesion of-bilateral
Three territory sign
thrombophlebitis
thymoma
tinnitus
titubation
tonic foot response
torticollis
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
travel history
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, writing
trigeminal neuropathy
trinucleotide repeats
tyrosine hydroxylase deficiency
unconsciousness
unconsciousness, transient
uveitis
valium
vegetarianism
viral infection
viral infection, CNS
virus, slow
visual evoked response
visual impairment
vitamin deficiency
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
web sites
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
workup
writing
Showing articles 200 to 250 of 17967 << Previous Next >>

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

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
Neurol 79:195-196, Tofaris,G.K.,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

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

PANDAS
www.medlink.com,Feb, Erfe,M.C.B., 2011

Vertebral Artery Dissection Leading to Stroke Caused by Violent Neck Tics of Tourette Syndrome
Neurol 77:1706-1707, Lehman, L.L.,et al, 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

Movement Disorders Emergencies Part 1
, Robottom, B.J., et al, 2011

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

Retrospective Analysis of NMDA Receptor Antibodies in Encephalitis of Unknown Origin
Neurol 75:1735-1739, Pr�ss,H.,et al, 2010

Anti-N-Methyl-d-Aspartate Receptor Encephalitis: Characteristic Behavioral and Movement Disorder
Arch Neurol 67:250-251, Ferioli,S.,et al, 2010

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Response to Immunotherapy in a 20-Month-Old Boy With Anti-NMDA Receptor Encephalitis
Neurol 74:1550-1551, Wong-Kisiel,L.C., et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Essential Palatal Myoclonus
NEJM 362:e64, Scozzafava,J. &Yager,J., 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Hemichorea-Hemiballism after Diabetic Ketoacidosis
NEJM 363:e27, Duker,A.P. &Epsay,A.J., 2010

Tourettes Syndrome
NEJM 363:2332-2338, Kurlan,R., 2010

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

Cerebral Toxoplasmosis in Acquired Immunodeficiency Syndrome (AIDS) Patients also Provides Unifying Pathophysiologic Hypotheses for Holmes Tremor
BMC Neurol 10:37, Lekoubou, A.,et al, 2010

The Neurologic Manifestations of Systemic Lupus Erythematosus
The Neurologist 15:115-121, Greenberg,B.M., 2009

Long-Term Effects of Pallidal Deep Brain Stimulation in Tradive Dystonia
Neurol 73:53-58, Gruber,D.,et al, 2009

Parkinsonism in HIV-Infected Patients on Highly Active Antiretroviral Therapy
Neurol 73:401-403, Tisch,S. &Brew,B., 2009

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Diabetic Striatal Disease: Clinical Presentation, Neuroimaging, and Pathology
InterMed 48:1135-1141, Abe, Y.,et al, 2009

Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
Lancet Neurol 7:1091-1098, Dalmau,J.,et al, 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Restless Arms
Lancet 371:530, Horvath,J.,et al, 2008

Reversible Parkinsonism and Ataxia Associated With High-Dose Octreotide
Neurol 70:2345-2346, Espay,A.J., 2008

The Writing on the Wall
Lancet 372:344, Wilder-Smith,E.P. &Ng,E.S., 2008

Internal Pallidal and Thalamic Stimulation in Patients With Tourette Syndrome
Arch Neurol 65:952-957, Welter,M.-L.,et al., 2008

Clinicopath Conf., Anti-MNDAR Antibody Mediated Paraneoplastic Limbic Encephalitis Associated With Ovarian Teratoma
NEJM 359:842-853, Case 26-2008, 2008

Anti-NMDA-Receptor Encephalitis: Case Series and Analysis of the Effects of Antibodies
Lancet Neurol 7:1091-1098, Dalmau,J.,et al, 2008

Clinical and Radiological Characteristics of Methotrexate-Induced Acute Encephalopathy in Pediatric Patients with Cancer
Ann Oncol 19:178-184, Inaba, H.,et al, 2008

Bilateral Basal Ganglia Lesions in Patients with End-Stage Diabetic Nephropathy
Nephrology 13:68-72, Li, J.,et al, 2008

Acute Chorea and Bilateral Basal Ganglia Lesions in a Hemodialysis Patient
Kidney Int:73:1087-1091, Kiryluk, K.,et al, 2008

Secondary Motor Disturbances in 101 Patients With Musicians Dystonia
JNNP 78:949-953, Rosset-Llobet,J.,et al, 2007

A Genetic Risk Factor for Periodic Limb Movements in Sleep
NEJM 357:639-647, Stefansson,H.,et al, 2007



Showing articles 200 to 250 of 17967 << Previous Next >>