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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
aciduria
acquired immunodeficiency syndrome
activities of daily living scale
addiction, heroin-neurologic complications with
adenosine deaminase deficiency
adult polyglucosan body disease
advances in neurology
adverse drug reaction
agitation
alcohol, neurologic complications with
alcoholism
aldolase
alopecia
alpha glucosidase
altered states of consciousness
alveolar hypoventilation
amantadine
amenorrhea
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
anemia, hemolytic
anemia, megaloblastic
aneurysm
angina pectoris
angiography, neurologic complications with
angiokeratoma
angiotensin-converting enzyme
animal bite
animal exposure
ankle edema
anorexia
anosmia
anterior horn cell disease
anti signal recognition particle antibody
anticholinergic drugs
anticoagulant, complications of
anticonvulsants
anticonvulsants, hypersensitivity syndrome
anticonvulsants, untoward effects of
antihistamines
antiphospholipid antibodies
antithyroid antibodies
antiviral agents
aphasia
arachnoiditis
arbovirus
areflexia
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
arsenic
arteritides
arteritis, temporal
arthralgia
arthritis
ascending paralysis
ascites
aspartate aminotransferase
aspartocyclase
aspiration
asplenia
ataxia
ataxia, cerebellar
ataxic gait
atherosclerosis, generalized
athetosis
atrial fibrillation
atrial myxoma
atrioventricular block
autism
autoantibodies
autoimmune disease
autonomic dysfunction
B 12 deficiency
babesiosis
Babinski sign
bacterial infection
BAL
basal cistern
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
behavioral disorder
biotin deficiency
biotinidase deficiency
blacks
bladder dysfunction
blindness
blindness, monocular
blood dyscrasias, neurologic findings with
bone age
bone demineralization
bone marrow infarction
bone marrow necrosis
bone marrow suppression
bone marrow transplantation
bradykinesia
brain atrophy
brain biopsy
brain biopsy, false negative
brain natriuretic peptide
brain purpura
brainstem, lesion of
breast feeding
bulimia
bulimia nervosa
BUN, elevated
burning hands
burning paresthesia
cachexia
calcification, liver
calcification, lymph node
calf hypertrophy
California
Canavan's disease
carbamazepine
carbidopa
carcinoma
cardiac enzymes
cardiac surgery, neurologic complications with
cardiac tumor
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
cat exposure
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission, abnormal
cataracts
catatonia
cathartic
cauda equina, lesion of
CD4 counts
central nervous system, infection of
central nuclei, muscle
cerebellar infarction
cerebellar lesion
cerebral cortical atrophy
cerebral edema
cerebral embolism
cerebral embolism, cardiac origin
cerebral infarction, hemorrhagic
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, gold sol.curve of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, complications with
cerebrovascular accident, multiple
cerebrovascular accident, prognosis in
cerebrovascular accident, seizure with
cerebrovascular disease, cardiovascular disease with
ceruloplasmin, serum
chelation therapy
chemosis
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
chest pain
chest x-ray, abnormal
children
cholelithiasis
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
clofibrate
cogwheel rigidty
coinfection
collagen vascular disease
coma
complications
confusion
congenital infection, CNS
congenital infection, viral
congenital myopathy
congestive heart failure
conjunctival injection
conjunctivitis
consanguinity
contractures, joint
coronary artery bypass
corpus callosum, infarction of
corpus callosum, lesion of
cough
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
C-reactive protein, elevated
creatine kinase
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
critical care unit
cry, abnormal
cultured skin fibroblasts
cyclophosphamide
cyst, bone
cystoisospora belli
cytochrome c oxidase
cytochrome c oxidase, deficiency
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
D-dimer
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dentate nuclei
dentate nuclei, lesion of
depression
dermatitis
dermatomyositis
developmental disability
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diagnostic criteria
dialysis
diaphragmatic paralysis
diarrhea
diet
differential diagnosis
difficulty climbing stairs
dilantin
dilantin, hypersensitivity to
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
DNA sequencing
dopa responsive dystonia
doxycycline
drooling
dropped head syndrome
drug abuse
drug induced neurologic disorders
drug interactions
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dystonia
dystonia, children
dystrophic calcification
dystrophin
eating disorder
echocardiogram
echocardiogram, transesophageal
edema, pedal
edema, periorbital
efficacy
ehrlichiosis
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
embolism
embolism, atheromatous
embolism, cholesterol
embolism, fat
embolism, retinal
embolism, systemic
embolism, tumor
emergencies, neurologic
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalomyelitis
encephalopathy
encephalopathy, acute
encephalopathy, Hashimoto's
encephalopathy, neonatal
encephalopathy, progressive
endemic area
enteritis
enuresis
enzyme activity
enzyme inhibition
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
eosinophilia-myalgia syndrome
epidemiology of neurology
epistaxis
Epstein-Barr virus
Epstein-Barr virus, negative
erythrocyte
esophageal varices
evoked potentials
exercise
exercise intolerance
extraocular muscle enlargement
extraocular muscle lesion
eye movement, disorders of
face, numbness of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
femoral artery catheterization
femoral neuropathy
ferritin, elevated
fever
fibrillations
fine motor function, impaired
fingernails, abnormal
flaccid paralysis
flea bite
fleas
floppy infant
flu-like illness
food allergy
fucosidosis
fundus, abnormality of
gadolinium
gait disorder
gait, waddling
galactorrhea
galactosemia
gallium scan
gammaglobulin therapy, intravenous
gangliosidosis GM1
gangliosidosis GM2
gastroenteritis
gastrointestinal bleeding
gaze deviation
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
geographic location
globoid cells
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
Gowers maneuver
granulomatous disease
growth retardation
grunting
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
guinea pigs
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hamster
hand pain
hand weakness
hands, fisted
head lag
headache
headache, new onset
headache, persistent
headache, retro-orbital
hearing loss
hearing loss, unilateral
heart block
heart murmur
heavy metal intoxication
hematuria, microscopic
hemiparesis
hemoglobin abnormality, neurologic complications of
hemoglobinuria
hemolytic-uremic syndrome
hemophilia
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatitis
hepatitis B virus
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
herniation syndromes, intracranial
heterophile antibody test
hexosaminidase-A
hip flexor weakness
hippocampus
histochemistry
histochemistry of muscle
HMGcoA reductase inhibitors
hoarseness
homosexual
human granulocytic anaplasmosis
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
hydrocephalus
hyperamylasemia
hyperbilirubinemia
hypercalcemia
hyperglycemia
hyperkalemia
hyperkeratosis
hyperparathyroidism, secondary
hyperphosphatasia
hyperreflexia
hypersegmented polys
hypersensitivity reaction
hypertension
hypertensive encephalopathy
hypertonia
hypertrophic intracranial pachymeningitis
hypoalbuminemia
hypocalcemia
hypoglycemia
hypoglycorrhachia
hypokalemia
hypokalemic paralysis
hypomyelination
hyponatremia
hypoparathyroidism
hypoparathyroidism, idiopathic
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypothalamus, lesion of
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
IFA
ileus, paralytic
imbalance
immunologic disease
immunosuppression
immunosuppressive agents
inappropriate antidiuretic(A.D.H.)hormone
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inclusion body myositis
infection
infection, recurrent
infectious mononucleosis
insulin
intellectual deficit
intellectual deterioration
interferon
interferon antibodies
interferon beta 1-a
interferon beta 1-b
intracerebral hemorrhage
intracranial pressure, increased
intrauterine infection
intrauterine infection, viral
iritis
iron, brain
irritability
ischemic exercise test
jaundice
jaw claudication
jaw pain
Jewish
Kayser-Fleischer ring
Krabbe's disease
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
L-dopa
L-dopa, drug interactions with and side effects of
L-dopa, potentiators of
learning disability
learning disability, in children
leg weakness, bilateral
Legionella pneumophilia
Legionnaires'disease
Leigh's disease
leptospirosis
lethargy
leukemia
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
life expectancy
limbic encephalitis
lipid lowering agent
lipid storage disorder of CNS
livedo reticularis
liver biopsy
liver disease
liver function enzymes
long bone lesion
low back pain
Lowe's syndrome
L-tryptophan
lymphadenopathy
lymphadenopathy, cervical
lymphadenopathy, hilar
lymphadenopathy, paraaortic
lymphocytic choriomeningitis
lymphocytosis
lymphoma
lymphoma involving CNS
lymphopenia
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malaise
masked facies
Massachusetts
McArdle's disease
meconium staining
Mees lines
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, basilar
meningitis, chronic
meningitis, leptospira
meningitis, neutrophilic
meningitis, plasma cell
meningitis, recurrent
meningoencephalitis
meningomyelitis
menses
menses, irregular
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
methylmalonic acid, serum
microcephaly
microhemorrhage, intracerebral
migraine, seizures in
mimics
misdiagnosis
mitochondrial disease
mitoxantrone
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
mononeuropathy multiplex
mortality
mosquito
motor neuron disease
mouse
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, cardiac
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, muscle
MRI, negative
MRI, orbit
MRI, paramagnetic effect
MRI, pelvis
MRI, spine
MRI, sulcal hyperintensity
MRI, susceptibility weighted
MRS
multinucleated giant cell
multiple sclerosis
multiple sclerosis, treatment of
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, intermediate onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
myelitis, longitudinal
myelomalacia
myeloneuropathy
myelopathy
myocardial infarction
myocardial infarction, acute
myocardial injury
myocardial ischemia
myocarditis
myoclonic jerks
myoclonus
myocytolysis
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, centronuclear
myopathy, critically ill
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, genetic
myopathy, hypocalcemic
myopathy, hypokalemic
myopathy, inflammatory
myopathy, metabolic
myopathy, necrotizing
myopathy, necrotizing, autoimmune
myopathy, vacuolar
myositis
myotonic discharges
nausea and vomiting
neck pain
neck stiffness
neck weakness
necrotizing granuloma
negative
neonatal infection, viral
neonatal screening, genetic neurologic disorders
neoplastic angioendotheliosis
nephritis
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neuritis, heavy metals causing
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neuropathy, toxic
neurotransmitter
neutropenia
NMDA antagonists
nonsteroidal anti-inflammatory drug
nutritional deficiency
nystagmus
occupational neurologic disorders
oculogyric crisis
oculopharyngeal muscular dystrophy
odynophagia
ophthalmoplegia
opisthotonus
optic atrophy
optic chiasm, enlarged
optic disc edema
optic nerve
optic nerve, enlarged
optic nerve, lesion of
optic neuritis
optic neuropathy
oral ulcerations
orbit, mass
orthopnea
osteomalacia
overlap syndrome
pain
pain, abdominal
pain, back
pain, foot
pain, head
pain, leg
pain, thigh
palilalia
pancreatitis
pancytopenia
PANK2 mutation
papilledema
paralysis, acute
paralysis, acute areflexic
paraparesis
paraparesis, spastic
parasitic infection
parasitic infection, CNS
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, on-off phenomena in
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathology
pediatric neurology
penicillamine
periarteritis nodosa
pericardial effusion
pericarditis
peripheral blood smear
peripheral blood smear, abnormal
pernicious anemia
personality change
petechiae
phenobarbital
phenothiazine
phosphorylase b kinase deficiency
photophobia
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
pneumonia
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polyneuropathy
Pompe's disease of glycogen storage
position sensation, abnormal
positive sharp waves
postural abnormality
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
pressure sores
prevention of neurologic disorders
procyclidine
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
prolactin, elevated
proprioception, abnormal
proteinuria
protozoan infection
pruritus
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis, unilateral
pulmonary embolism
pulmonary function tests
pulmonary hypertension
pulmonary infiltrates
pyloric stenosis
pyramidal tract
pyridoxine
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
quinidine
race
rapidly progressing neurologic illness
rash
rat exposure
Raynaud's phenomenon
recurrent
release phenomena
remote effect of cancer on the nervous system
renal biopsy
renal failure
renal failure, acute
renal stones
reptiles
reserpine and reserpine like drugs
respirator
respiratory distress syndrome, neurologic status with
respiratory failure
reticulum cell sarcoma
retinal degeneration
retinopathy
retro-orbital pain
review article
rhabdomyolysis
rickets
rickettsial organism
rigidity
riluzole
risk factors
risus sardonicus
rodents
Romberg's sign
Sabin-Feldman dye test
sarcoidosis
sarcoidosis, CNS
scalp swelling
scalp tenderness
sclerodactyly
scleroderma
scoliosis
scoliosis, neurologic association with
screening
second wind phenomena
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
sensory loss
seroconversion
serologic testing
seronegative
serum alanine aminotransferase
serum glutamic oxaloacetic transaminase
serum glutamic pyruvic transaminase
serum lipase, elevated
serum sickness
severe acute respiratory syndrome
sex reassignment surgery
sexual behavior, disorder of
short stature
sickle cell disease
sinemet
skew deviation
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
small for dates infant, problems in
somnolence
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spirochete infection
splenectomy
splenomegaly
spongy degeneration of brain
standing difficulty
startle reaction
statin therapy
steroid
steroid therapy, CNS treatment and complications with
stiff joints
stuporous
subarachnoid hemorrhage
subcutaneous nodules
sudden death
sweating
sweating, abnormality of
symmetric brain lesions
syncope
systemic illness
tachycardia
Tay-Sachs disease
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
term infant
Texas
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
tick bite
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, smooth
tongue, swelling
tongue, weakness
toxoplasma complement fixation test
toxoplasma gondii
toxoplasmosis, acquired
toxoplasmosis, CNS
toxoplasmosis, muscle
transgender
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, intention
trientine dihydrochloride
tripping
troponin T
tumor necrosis factor inhibitor
type 2 muscle fiber
typhus, murine
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
ultrasonography, head
uncal herniation
unconsciousness
uremia
urinary casts
urinary incontinence
urinary tract infection
urine test for metabolic disorders
urine test in toxic screen
urine, dark
uveitis
vasculitides
vectors of infection
vegetarianism
vertebral infarction
vertigo
viral infection
viral infection, CNS
viral load
vision, blurred, monocular
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual impairment
visual loss
visual loss, sudden-unilateral
visual loss, transient
vital capacity
vitamin D
vitamin D deficiency
vitamin deficiency
vitamin, multiple
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weakness, severe
weight loss
West Nile fever
Western immunoblot test
wheelchair
white matter disease
winging of scapula
X-linked myopathy
zinc
Showing articles 700 to 750 of 3112 << Previous Next >>

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

Spinal Muscular Atrophy A Timely Review
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"Im fine; Im just waiting for my disease" The New and Growing Class of Presymptomatic Patients
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Progressive Encephalomyelitis with Rigidity and Myoclonus Gycine and NMDA Receptor Antibodies
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The "Million Hearts" Initiative - Preventing Heart Attacks and Strokes
NEJM 365:e27, Frieden, T.R.,et al, 2011

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Pure Motor Monoparesis Due to Ischemic Stroke
The Neurologist 17:301-308, Hiraga, A., 2011

Epidemic Profile of Shiga-Toxin-Producing Escherichia coli O104:H4 Outbreak in Germany
NEJM 365:1771-1780, Frank, C.,et al, 2011

Diagnosis and Management of Lumbar Spine Stenosis
JAMA 303:71-72, Haig,A. &Tomkins,C., 2010

Neurosacrcoidosis: Presentations and Management
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Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
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Chronic Inflammatory Demyelinating Polyneuropathy: Etiology, Clinical Features, and Diagnosis
UpToDate, Sept, Lewis, R., 2010

Acute Hyperammonemic Encephalopathy in Adults: Imaging Findings
AJNR 32:413-418, U-King-Im,J.M.,et al, 2010

The Patient Has the Diagnosis
Lancet 378:1436, Jubany,L.I.,et al, 2010

Clinical Features of Facioscapulohumeral Muscular Dystrophy 2
Neurol 75:1548-1554, Greef,J.C.,et al, 2010

Tricyclic Antidepressants and Headaches: Systematic Review and Meta-Analysis
BMJ 341:c5222, Jackson,J.L.,et al, 2010

Tired Legs - A Gut Diagnosis
Lancet 376:1798, Di Lazzaro,V.,et al, 2010

Recurrent Ischemic Events in Young Adults After First-Ever Ischemic Stroke
Ann Neurol 68:661-671, Putaala,J.,et al, 2010

Predictors of Neurologic Outcome in Hypothermia After Cardiac Arrest
Ann Neurol 68:907-914, Fugate,J.E.,et al, 2010

Acute Hepatic Encephalopathy: Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Findings, and Correlation With Plasma Ammonia Level and Clinical Outcome
AJNR 31:1471-1479, McKinney,A.M.,et al, 2010

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

Neuromuscular Symptoms and Elevated Creatine Kinase After Statin Withdrawal
NEJM 362:564-565, Echaniz-Laguna,A.,et al, 2010

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

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

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

Oral Fingolimod or Intramuscular Interferon for Relapsing Multiple Sclerosis
NEJM 362:402-415, 456, Cohen,J.A.,et al, 2010

A Placebo-Controlled Trial of Oral Fingolimod in Relapsing Multiple Sclerosis
NEJM 362:387-401, 456, Kappos, L.,et al, 2010

Cancer-Associated Myositis and Anti-p155 Autoantibody in a Series of 85 Patients with Idiopathic Inflammatory Myopathy
Medicine 89:47-52, Trallero-Araguas,E.,et al, 2010

Practice Parameter: Pharmacologic Treatment of Spasticity in Children and Adolescents with Cerebral Palsy (an Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 74:336-343, Delgado,M.R.,et al, 2010

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

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

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

Medical Complications Among Hospitalizations for Ischemic Stroke in the United States from 1998 to 2007
Stroke 41:980-986, Tong,X., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

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

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

Risk of Acute Myocardial Infarction, Stroke, Heart Failure, and Death in Elderly Medicare Patients Treated with Rosiglitazone or Pioglitazone
JAMA 304:411-418,469, Graham,D.J., 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

Glucosamine and the Ongoing Enigma of Chronic Low Back Pain
JAMA 304:93-94, 114, Avins,A.L., 2010

Stenting Versus Endarterectomy for Treatment of Carotid-Artery Stenosis
NEJM 363:11-23, 80, Brott,T.G., 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

Cogan Syndrome
www.medlink.com, Feb, Ramachandran, T.S., 2010

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

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Evaluation and Treatment of Inflammatory Myopathies
JNNP 80:1060-1068, Amato,A. &Barohn,R.J., 2009



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