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Differential
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accommodation
accomodation, abnormal
advances in neurology
adverse drug reaction
ammonia
ANA
anasarca
anesthesia, general
angiokeratoma
ankle edema
anorexia
anterior tibial muscle weakness
antiviral agents
areflexia
arrhythmia, cardiac
arthralgia
arthritis
arthrogryposis multiplex
ascites
ataxia
ataxic gait
atrial fibrillation
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
biopterin deficiency
blinking
blinking, reduced
bone marrow transplantation
bradycardia
bradykinesia
brain atrophy
brainstem, atrophy
Brown-Vialetto-Van Laere syndrome
burning paresthesia
cachexia
calcification, intracranial
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
caries
carpal tunnel syndrome
CAT scan, abnormal
cataracts
causalgia
central core disease
cerebellar atrophy, primary
cerebral cortical atrophy
cerebral embolism
cerebral embolism, carotid origin
cerebral palsy
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
ceruloplasmin, serum
cervical spine
cervical spine abnormality
Charcot-Marie-Tooth
children
cholelithiasis
chorea
chromosomal abnormality
chromosome 14
chromosome 17
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
cogwheel rigidty
congenital infection, CNS
congenital myopathy
congenital myopathy, inflammatory
congestive heart failure
consanguinity
contractures, joint
contrast agents, neurotoxicity of
convergence
convergence, impaired
cornea, opacity of
corpus callosum, lesion of
cough
cranial neuropathy
cranial neuropathy, multiple
crawl regression
C-reactive protein, elevated
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
cytomegalovirus infection
cytomegalovirus infection, congenital
D-dimer
decision analysis
dementia
dermatomyositis
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
dialysis
diamond on quadriceps
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
disability rating scale, neurological
disability, neurological
dislocated hip, congenital
distal muscle atrophy
distal muscle weakness
diurnal variation
dopa responsive dystonia
drooling
drug induced neurologic disorders
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonia, treatment of
dystrophic calcification
dystrophin
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
endemic area
enzyme, defect
enzyme, muscle disease
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epileptic encephalopathy
equinovarus
exercise
exome sequencing
eyes, sunken
facial appearance, abnormal
facial weakness
failure to thrive
falling
familial
FARS2 deficiency
fasciculation
fatigue
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
fine motor function, impaired
floppy infant
foot deformity
foot drop
fracture, long bone
fucosidosis
gadolinium
gait disorder
gait, festinating
gait, spastic
gait, waddling
galactorrhea
gamma amino butyric acid
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
glutamic acid decarboxylase, antibody
glycoprotein
Gowers maneuver
grimacing
groove sign
growth retardation
Guillain Barre syndrome
hammertoes
hand deformity
hand pain
hand weakness
handwriting
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
high arched feet
histochemistry
histochemistry of muscle
hyperpigmentation of skin
hyperreflexia
hypertonia
hypogonadism
hypoparathyroidism
hypophonia
hyporeflexia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
implantable cardioverter defibrillator
inclusion body myositis
infection, recurrent
influenza A virus
influenza B virus
injection neuropathy
intellectual deficit
intellectual deterioration
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intrinsic hand muscles, wasting of
jaw contractures
joint hypermobility
Kayser-Fleischer ring
kinesia paradoxica
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
lateral cutaneous nerve of forearm
L-dopa
leg dragging
leg swelling
leprosy
leukocytosis
leukodystrophy
life expectancy
limb-girdle weakness
liver disease
liver function enzymes
liver transplantation
lordosis
L-tryptophan
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
malignant hyperpyrexia
marche a petits pas
masked facies
median neuropathy
meningitis, CSF cell count-normal
mental retardation
merosin
microcephaly
micrographia
misdiagnosis
mitochondrial disease
mitral valve prolapse
molecular genetics
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, complications with
MRI, contraindications
MRI, contrast enhanced
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myocardial biopsy
myocarditis
myoglobinuria
myopathy
myopathy, hypocalcemic
myopathy, quadriceps
myositis
myositis, acute of childhood
myositis, post infectious
myotonia dystrophica
myotonic discharges
neck extension
neck weakness
nephrogenic systemic fibrosis
nerve conduction studies
nerve enlargement
nerve hypertrophy
nerve injury
neurocutaneous disease
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, iatrogenic
neuropathy, peripheral
neurotoxic
nystagmus
optic atrophy
optic neuropathy
orange peel appearance of skin
overlap syndrome
pacemaker, cardiac-transvenous
pain
pain, calf
pain, leg
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinsonism syndrome
periventricular leukomalacia
personality change
pes cavus
phlebotomy
photosensitivity, skin
pigmentary retinopathy
pneumonia
polymerase chain reaction
polymyalgia rheumatica
polymyositis
pons, atrophy
positive sharp waves
practice guidelines
prayer sign
premature infant
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
prolactin, elevated
proximal muscle atrophy
pruritus
pseudohypertrophy
psychiatric problems in neurologic disorders
psychomotor retardation
pulmonary infiltrates
pyramidal tract dysfunction
rash
Red flags
reflex sympathetic dystrophy
renal failure
renal tubular acidosis
repetitive nerve stimulation
respiratory failure
retinopathy
retropulsion
review article
rhabdomyolysis
riboflavin transporter deficiency
rickets
rigid spine syndrome
rigidity
rippling muscle disease
safety
Samoa
sarcoglycan
sarcoglycanopathy
sarilumab
scoliosis
scoliosis, neurologic association with
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
serositis
short stature
shoulder, pain in
sinemet
skin, biopsy
skin, lesions in neurologic disorders
skin, thickened
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
splenomegaly
stare
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff joints
stiff man syndrome
stillbirth
stooped posture
suck, poor
sudden death
systemic illness
systemic juvenile idiopathic arthritis
tandem gait, ataxic
tenderness
thrombocytosis
tocilizumab
toe walking
toxic oil syndrome
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
tremor, resting
tripping
type 1 muscle fiber
type 2 muscle fiber
tyrosine hydroxylase deficiency
urea-cycle enzymopathies
uremia
urine test for metabolic disorders
urine, dark
viral infection
viral myopathy
vital capacity
voice, abnormality of
Walker-Warburg syndrome
walking
walking frame
walking, delayed
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
workup
wrist drop
x-ray, cervical spine
Showing articles 250 to 300 of 854 << Previous Next >>

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

Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
Neurol 79:1466-1473, Weissenborn, K.,et al, 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Teaching NeuroImages: Isolated Sensory Loss of the Arm Sparing Hand in Cortical Infarction
Neurol 76:e3, Cha,M.-J.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Fulminant Encephalopathy With Basal Ganglia Hyperintensities in HIV-Infected Drug Users
Neurol 76:787-794, Newsome,S.D.,et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

Fulminant Encephalopathy with Basal Ganglia Hyperintensities in HIV-infected Drug Users
Neurol 77:923, Finelli, P.F., 2011

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

An Unusual Cause of Pseudomedian Nerve Palsy
Case Reports Neurol Med doi:10.1155/2011/474271, Manjaly, Z.M.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

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

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Clinicopath Conf, Intravascular Large-B-Cell Lympoma
NEJM 362:1129-1138, Case 9-2010, 2010

Is the Diagnosis at Hand?
The Lancet 375:1134, Holmes,M.V., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

Validation of the Coin Rotation Test: A Simple, Inexpensive, and Convenient Screening Tool for Impaired Psychomotor Processing Speed
Neurologist 16:249-253, Hill,B.D., et al, 2010

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

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

Diffusion Abnormalities in the Primary Sensorimotor Pathways in Writers Cramp
Arch Neurol 66:502-508, Delmaire,C.,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

Motor Development in Very Preterm and Very Low-Birth-Weight Children From Birth to Adolescence: A Meta-Analysis
JAMA 302:2235-2242, 2257, De Kieviet,J.,et al, 2009

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

Frequency, Characteristics, and Risk Factors for Amiodarone Neurotoxicity
Arch Neurol 66:865-869, Orr,C.F. &Ahlskog,E., 2009

Parkinsons Disease
Lancet 373:2055-2066, Lees,A.J.,et al, 2009

Ischemic Stroke of the Cortical "Hand Knob" Area: Stroke Mechanisms and Prognosis
J Neurol 256:1146-1151, Peters, N.,et al, 2009

Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
J Natl Cancer Inst 101:946-958, Armstrong,G.T.,et al, 2009

Psychogenic Tremor Occurring After Deep Brain Stimulation Surgery for Essential Tremor
Neurol 70:1498-1499, McKeon,A.,et al, 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

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

Changes in the Incidence and Predictors of Human Immunodeficiency Virus-Associated Dementia in the Era of Highly Active Antiretroviral Therapy
Ann Neurol 63:213-221, Bhaskaran,K.,et al, 2008

In-Laws, Insecticide--And a Mimic of Brain Death
Lancet 371:622, Peter,J.V.,et al, 2008

Viral Meningitis
BMJ 336:36-40, Logan,S.A. &MacMahon,E., 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

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

Neurodevelopment and Cognition in Children After Enterovirus 71 Infection
NEJM 356:1226-1234, Chang,L.-Y.,et al, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Clinicopath Conf., Multifocal Motor Neuropathy With Conduction Block
NEJM 357: 2707-2715, Case 40-2007, 2007

Clinical Update:Diagnosis and Treatment of Essential Tremor
Lancet 369:1152-1154, Benito-Leon,J&Louis,E.D., 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Deep Brain Stimulation
Neurologist 13:237-252, Kem,DS. &Kumar,R., 2007

A 75-Year-Old Man With Cognitive Impairment and Gait Changes, Lewy Body Disease
Neurol 69:1183-1189, Lippa,C.F.,et al, 2007

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

Multifocal Motor Neuropathy: The Diagnostic Spectrum and Response to Treatment
Neurol 69:1680-1687, Slee,M.,et al, 2007

Primary Episodic Ataxias:Diagnosis, Pathogenesis and Treatment
Brain 130:2484-2493, Jen, J.C.,et al, 2007

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Topiramate in Essential Tremor, A Double-Blind, Placebo-Controlled Trial
Neurol 66:672-677, Ondo,W.G.,et al, 2006

Benign Tremulous Parkinsonism
Arch Neurol 63:354-357,321, Josephs,K.A.,et al, 2006

Valproic Acid Adjunctive Therapy for HIV-Associated Cognitive Impairment: A First Report
Neurol 66:919-921, Schifitto,G.,et al, 2006



Showing articles 250 to 300 of 854 << Previous Next >>