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Differential
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abdominal distention
acoustic nerve
advances in neurology
aggression
agitation
alcohol intoxication
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
algorithm
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
anemia
anesthesia, general
anion gap
anorexia
anticoagulant, treatment
aphasia
aphasia, children
aphasia, global
apraxia, speech
arachnodactyly
areflexia
arrhythmia, cardiac
arsenic
ascending paralysis
ascites
aspartocyclase
asterixis
asymptomatic
ataxia
ataxia, cerebellar
athetosis
attention deficit disorder with hyperactivity
autism
autonomic dysfunction
BAL
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
bath salts, psychoactive
behavior, combative
behavioral disorder
behavioral disorder, acute
Benedict's solution test
bifid uvula
biotin
biotin deficiency
biotinidase deficiency
bismuth
body odor
bone marrow suppression
burn injury
calcification, intracranial
calcium oxalate crystals
Canavan's disease
cardiomegaly
cardiomyopathy
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
ceruloplasmin, serum
cervical spondylosis
cherry red spot
children
cholelithiasis
chromosomal abnormality
chromosome 19
chromosome 6
cirrhosis, infancy
cleft palate
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
cocaine
coenzyme Q10
coenzyme Q10 deficiency
cogwheel rigidty
coma
complications
confusion
congenital deformities
congenital myopathy
cornea, abnormal
cortical vein thrombosis
cranial nerve palsies
creatine phosphokinase(CPK)elevated
creatinine, elevated
cultured skin fibroblasts
cystinuria
deafness
deafness, bilateral
delirium
demyelinating disease
dermatitis
designer drugs
developmental evaluation
developmental milestones, loss of
developmental retardation
diabetes insipidus
diarrhea
diet
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
disorientation
distal muscle weakness
drooling
drug abuse
drug abuse, neurologic complications of
drug abuse, toxic screen In
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysplasia of C.N.S.
dystonia
edema, pedal
electrocardiogram, abnormal
electroconvulsive therapy
electroencephalogram
electromyogram
encephalomyopathy
encephalopathy
encephalopathy, acute
encephalopathy, metabolic
encephalopathy, neonatal
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
erythrocyte
ethylene glycol
exercise
exercise intolerance
eye color
eye movement, disorders of
Fabry's disease
facial nerve palsy, bilateral
failure to thrive
familial
fatigue
feeding disorder
ferric chloride test
fever
fingernails, abnormal
formication
fracture, long bone
fragile-X syndrome
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gastroenteritis
gastrointestinal bleeding
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
glycogen storage disease
grimacing
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guthrie test
hallucination
hallucination, auditory
hand weakness
head injury
head lag
headache
hearing loss
hearing problems in children
heavy metal intoxication
hemiparesis
hemoglobinuria
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
homocystinuria
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hypercapnia
hyperglycinemia
hyperhomocysteinemia
hyperkeratosis
hypernatremia
hypertension
hyperthermia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
imbalance
inborn errors of metabolism
inclusion body myositis
incoordination
infection
in-hospital
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia, bilateral
ischemic exercise test
isopropyl alcohol
jaw contractures
karyotyping
Kayser-Fleischer ring
ketoacidosis
ketonuria
klippel feil syndrome
lactic acidemia
lactic dehydrogenase(LDH)
language disorders in children
lead poisoning
leg weakness, bilateral
Leigh's disease
lens, dislocation of
lens, ectopic
lethargy
leucine
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
leukopenia
levamisole
level of consciousness, decreased
level of consciousness, decreased acute
lipid storage disorder of CNS
liver disease
liver function enzymes
liver transplantation
Lowe's syndrome
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
marfanoid skeletal abnormalities
McArdle's disease
Mees lines
meningitis, aseptic
mental retardation
mental status, abnormal
mental status, abnormal, acute
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
methcathinone
midline defect in children
misdiagnosis
mitochondrial disease
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, muscle
MRI, ring sign
MRI, serial
MRI, spine
MRI, venography
mucopolysaccharidoses
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Duchenne
myelodysplasia
myelopathy
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopia
myotonia dystrophica
nasal speech
nausea and vomiting
nephrotic syndrome
nerve conduction studies
neuritis, heavy metals causing
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, peripheral
neuropathy, toxic
neurotoxic
neurotoxin
neurotransmitter
ochronosis
ophthalmoplegia
ophthalmoplegia, neonatal
opisthotonus
optic atrophy
ornithine transcarbamylase deficiency
osteoarthrosis
osteoporosis
pain, leg
palatopharyngeal incompetence
pancreatitis
pancytopenia
paranoia
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
Parkinsonism syndrome
PAS positive
pectus excavatum
pericardial effusion
periodic paralysis
peripheral blood smear
peripheral blood smear, abnormal
personality change
phenylketonuria
phenylketonuria, adult onset
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pleural effusion
polyneuropathy
position sensation, abnormal
practice guidelines
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
psychotic behavior
pyridoxine
pyridoxine deficiency
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
recurrent
renal failure
renal failure, acute
renal stones
respiratory failure
Rett's syndrome
review article
rhabdomyolysis
rickets
rigidity
risk factors
Sandhoff's disease
schizophrenia
sclerae, hyperpigmented
screaming
second wind phenomena
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, neonatal
seizure, psychosocial aspects of
seizure, pyridoxine dependent
seizure, treatment of
self harm
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
skin, biopsy
skin, lesions in neurologic disorders
skin, pink
speech disorder, childhood
spina bifida
spondylolysis
spongy degeneration of brain
steroid therapy, CNS treatment and complications with
stimulant drugs
stool, guaiac positive
stuporous
stuttering
subdural hematoma
suicide
sweating
sweating, abnormality of
sympathomimetic drugs
tachycardia
tachypnea
thrombocytopenia
toxic encephalopathy
toxins, nervous system
treatment of neurologic disorder
tremor
tremulousness
urea-cycle enzymopathies
uremia
urinalysis, abnormal
urinary incontinence
urine sediment
urine test for metabolic disorders
urine test in toxic screen
urine, dark
violent behavior
vitamin deficiency
weakness
weakness, generalized
weakness, progressive
weight loss
white matter disease
x-linked mental retardation
Showing articles 150 to 200 of 17368 << Previous Next >>

Treatment of Brain Metastases
J Clin Oncol 33:3475-3484, Lin, X. & DeAngelis, L.M., 2015

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Central Nervous System Involvement in Adult Acute Lymphoblastic Leukemia at Diagnosis: Results from the International ALL trial MRC UKALL XII/ECOG E2993
Blood 108:465-472, Lazarus, H.M.,et al, 2015

Maintenance Therapy with Tumor-Treating Fields Plus Temozolomide vs Temozolomide Alone for Glioblastoma
JAMA 314:2535-2543,2511, Stupp, R.,et al, 2015

Clinical Features, Diagnosis, and Treatment of Disseminated Intravascular Coagulation in Adults
UptoDate, Leung, L.L.K., 2015

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Clinicopathologic Conference, Primary Central Nervous System Diffuse Large B-cell Lymphoma
NEJM 373:367-377, Case 23-2015, 2015

Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm
JNNP 86:774-781, Van Egmond, M.E.,et al, 2015

Worsening Neurologic Symptoms in a Brain Tumor Patient
Neurol 85:e57-e61, Faivre, G.,et al, 2015

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

The Lentiform Fork Sign
Neurol 84: e15, Fernandes, G.C.,et al, 2015

MRI Characteristics of Globus Pallidus Infarcts in Isolated Methylmalonic Acidemia
AJNR 36:194-201, Baker, E.H.,et al, 2015

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

Randomized Phase III Study of Whole-Brain Radiotherapy for Primary CNS Lymphoma
Neurol 84:1242-1248, Korfel, A.,et al, 2015

Treatment of Langerhans Cell Histiocytosis
UptoDate Oct. 2014, McClain, K.L., 2014

A 47-year-old Woman with Left Shoulder Pain after a Fall
Neurol 83:e112-e116, Jerath, N.U.,et al, 2014

Sustained Downgaze as the only remained sign after regaining consciousness in hepatic encephalopathy
Neurol Asia 19:105-106, Park, D.G.,et al, 2014

Diseases of the Nervous System Caused by Nutritional Deficiency, Pyridoxine (Vitamin B6 Deficiency)
Adams & Victors Principles of Neurology Chp 41, pg 1171, Ropper, A.H.,et al, 2014

A Syndrome of Bilateral Symmetrical Basal Ganglia Lesions in Diabetic Dialysis Patients
Am J Kidney Dis 63: 286-288, Finelli, P.F. & Singh, J.U., 2014

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

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

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

MATILDE Chemotherapy Regimen for Primary CNS Lymphoma
Neurol 82:1370-1373, Ferreri, A.J.M.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

A 20-year-old Woman with Rapidly Progressive Weakness
Neurol 82:e200-e204, Paganoni, S.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Biopterine Deficiency
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Galactosemia
Adams & Victors Principles of Neurology, Chp 37, pg 951, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 960, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Metachromatic Leukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 971, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Infantile Gaucher Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hyperglycemia
Adams & Victors Principles of Neurology Chp 40, pg 1141, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
Adams & Victors Principles of Neurology Chp 40, pg 1142, Ropper, A.H.,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, Dialysis Disequilibrium Syndrome
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Dialysis Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hyponatremia and Syndrome of Inappropriate Antidiuretic Hormone
Adams & Victors Principles of Neurology Chp 40, pg 1148, , 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Arsenic
Adams & Victors Principles of Neurology Chp 43, pg 1222, Ropper, A.H.,et al, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Oligodendroglioma
Adams & Victors Principles of Neurology, Chp 31, pg 654, Ropper, A.H.,et al, 2014

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

Primary CNS Posttransplant Lymphoproliferative Disease (PTLD): An International Report of 84 Cases in the Modern Era
Am J Transplant 13:1512-1522, Evens, A.M.,et al, 2013

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

The 2012 West Nile Encephalitis Epidemic in Dallas, Texas
JAMA 310:297-307,267, Chung, W.M.,et al, 2013

Clinicopathologic Conference, Toxic Effects of Metformin
NEJM 369:374-382, Case 23-2013, 2013

Primary Leptomeningeal Lymphoma
Neurol 81:1690-1696, Taylor, J.W.,et al, 2013

Cognitive Delay in a 7-year-old Girl
Neurol 81: e148-e150, Cachia, D. & Stine, C., 2013

Cerebrospinal Fluid Analysis in the Workup of GLUT1 Deficiency Syndrome
JAMA Neurol 70:1440-1444, Leen, W.G.,et al, 2013

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

A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013



Showing articles 150 to 200 of 17368 << Previous Next >>