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Differential
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abducens nerve paralysis
acanthocytosis
acetazolamide
acoustic nerve
acromicria
acyl CoA dehydrogenase deficiency
Addison's disease
adrenoleukodystrophy
aggression
alcohol
alcohol intolerance
algorithm
alkylating agents
alopecia
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidopathies
aminoacidurias
amniocentesis
anemia
Angelman syndrome
anosmia
antibodies to voltage-gated calcium channels
anticonvulsants
anticonvulsants, effectiveness
anticonvulsants, selection of
antimetabolite
aphasia
apnea
apnea, primary central
apraxia
areflexia
arthralgia
arylsulfatase A
asparginase
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
atonic bladder
ATP1A3 gene
attention span
autism
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
Bassen-Kornzweig syndrome
behavior, combative
behavioral disorder
biotin deficiency
biotinidase deficiency
blindness
blood dyscrasias, neurologic findings with
brachycephaly
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
calcium channel dysfunction
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
caudate nucleus, atrophy
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral edema
cerebral infarction, subcortical
cerebral palsy
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure low
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
cherry red spot-myoclonus syndrome
children
chloride channel dysfunction
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 15
chromosome 19
chromosome 2
chromosome 6
chronic progressive external ophthalmoplegia
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
clonus
cobalamin C deficiency
Cockayne's syndrome
cognition
cogwheel rigidty
color vision, impaired
coma
coma, episodic
conjunctivitis
consanguinity
contractures, joint
cornea, abnormal
corpus callosum, lesion of
cortical blindness
cranial nerve palsies
cranial neuropathy, multiple
cry, abnormal
cry, weak
cryopyrin-associated periodic syndrome
cultured skin fibroblasts
cyclic vomiting
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, rapidly progressive
demyelinating disease
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
Dravet syndrome
drooling
dropped head syndrome
dwarfism
dysarthria
dysmorphic
dysphagia
dyspnea
dyssynergia cerebellaris myoclonica
dystonia
EAST syndrome
eating disorder
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, progressive
enzyme, defect
epicanthal folds
epileptic encephalopathy
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
facial expression abnormality
facial nerve palsy, bilateral
facial pain
failure to thrive
false negative
familial
familial hemiplegic migraine
familial periodic ataxia
FARS2 deficiency
fatigue
feeding disorder
fever
fever, recurrent
fine motor function, impaired
fingerprint bodies
fish
fluorescene in situ hybridization
fluorouracil
flush syndrome
foot drop
Friedreich's ataxia
frontal bossing
gait disorder
gait, apraxic
galactosemia
gargoylism
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glaucoma
gliosis
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
gout
granular osmiphilic material
growth hormone deficiency
Hallervorden Spatz disease
Hallgren's syndrome
hallucination
hand clapping
hand flapping
hand wringing
head circumference
headache
hearing loss
heart block
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatic failure
hepatomegaly
hepatosplenomegaly
homocystinuria
Huntington's chorea
Huntington's disease, children
Hurler's syndrome
hyperactivity
hyperhomocysteinemia
hyperphagia
hyperreflexia
hypertriglyceridemia
hypertrophic intracranial pachymeningitis
hypofibrinogenemia
hypogonadism
hypokalemia
hypokalemic periodic paralysis
hypomyelination
hyponatremia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunologic disease
impotence
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inappropriate behavior
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incoordination
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracranial pressure, increased
iron, brain
irritability
isoniazid
jaw pain
Kearns-Sayre syndrome
keratoconus
Korsakoff's psychosis
lactic acidemia
lacunar infarction
Lafora's disease
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of, bilateral
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
lymphadenopathy
lysosomal storage disease
macrognathia
macular degeneration
malformation, CNS, congenital
malignant hyperpyrexia
maple syrup urine disease
MELAS syndrome
memory, impairment of
meningismus
meningitis, aseptic
meningitis, carcinomatous
meningitis, CSF cell count-normal
meningoencephalopathy
mental retardation
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methotrexate
methylhydrazine derivatives
methylmalonic acidemia
Mexican
microcephaly
microdontia
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
Minamata disease
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
molecular genetics
monoamine oxidase inhibitors
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, muscle
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle pain
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myoclonic jerks
myoclonus
myoclonus, epilepsy
myokymia
myopathy
myopathy, genetic
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
myotonia
myotonia congenita
nausea and vomiting
negative
nerve biopsy
neuritis
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotoxin
neutropenia
next-generation sequencing
Niemann-Pick disease
nitrogen mustard
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, rotary
nystagmus, vertical
obesity
ocular myopathy
oculodentodigital dysplasia
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optokinetic nystagmus, abnormal
orthostatic hypotension
oscillopsia
pain
pancytopenia
papilledema
paralysis
paramyotonia congenita
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
patient information and support
periodic paralysis
peroxisomal disease
personality change
pleocytosis of cerebrospinal fluid
poison, mercury
poison, neurologic problems with
POLG1 gene
polydactyly
polymerase chain reaction
pons, atrophy
pons, lesion of
pontocerebellar atrophy
postural abnormality
potassium channel antibodies
potassium channel dysfunction
Prader-Labhart-Willi syndrome
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
pretectal syndrome
primary episodic ataxia
procarbazine
prognathism
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
proteinuria
pseudobulbar palsy
pseudoretinitis pigmentosa
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
pulmonary embolism
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
renal failure
respiratory failure
respiratory tract infection
retinal degeneration
retinitis pigmentosa
retinopathy
Rett's syndrome
review article
riboflavin
rigidity
schizophrenia
SCN1A gene
scoliosis
screaming
screening
sea-blue histiocytes
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, psychomotor-temporal lobe
seizure, tonic-clonic
seizure, treatment of
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
short stature
skin, lesions in neurologic disorders
skull bone, thickening
slurred speech
small vessel disease
small vessel disease, cerebral
smiling
sodium channel dysfunction
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
Spielmeyer Vogt syndrome
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 10
spinocerebellar ataxia type 6
spinocerebellar degeneration
splenomegaly
status epilepticus
stereotyped behavior
stereotypy
steroid therapy, CNS treatment and complications with
storage disease of CNS
strabismus
stress, emotional
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuttering
subarachnoid hemorrhage
substantia nigra
suck, poor
symmetric brain lesions
syndactyly
teeth, abnormal
teeth, wide-spaced
temper tantrums
temporal lobe, lesion
thrombocytopenia
thrombophlebitis
tinnitus
titubation
toe walking
tongue, protrusion of
topiramate
toxins, nervous system
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
trinucleotide repeats
tubulopathy
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
urea-cycle enzymopathies
urinary incontinence
urine test for metabolic disorders
Usher's syndrome
vasculopathy
venous thrombosis, non-cerebral
vertigo
vertigo, episodic
vertigo, treatment of
vinblastine
vincristine neurotoxicity
violent behavior
visual evoked response
visual field defect
visual fields, constricted
vitamin E deficiency
vocal cord paralysis
walking, difficulty with
weakness
weakness, progressive
web sites
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
Wolfram syndrome
wrist drop
Showing articles 1550 to 1600 of 5708 << Previous Next >>

Status Epilepticus Migrainosus: Clinical, Electrophysiologic, and Imaging Characteristics
Neurol 75:373-374, Perucca,P., et al, 2010

Clinicopath Conf, Inflamatory Cerebral Amyloid Angiopathy,
NEJM 363:373-381, Case 22-2010, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Neurosacrcoidosis: Presentations and Management
Neurologist 16:2-15, Terushkin,V.,et al, 2010

Cerebral Amyloid Angiopathy as Cause of Convexity SAH in the Elderly
Neurologist 16:37-40, Finelli,P., 2010

Opsoclonus-Myoclonus Syndrome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis
Arch Neurol 67:118-121, Kurian,M.,et al, 2010

New-Onset Aferbrile Seizures in Infants: Role of Neuroimaging
Neurol 74:150-158, Hsieh,D.,et al, 2010

MR Imaging in Novel Influenza A(H1N1)-Associated Meningoencephalitis
AJNR 31:394-395, 393, Haktanir,A., 2010

Acute Necrotizing Encephalopathy in a Child during the 2009 Influenza A(H1N1) Pandemia: MR Imaging in Diagnosis and Follow-up
AJNR 31:396-400, 393, Ormitti,F.,et al, 2010

Epilepsy and the Natural History of Rett Syndrome
Neurol 74:909-912, Glaze,D.G.,et al, 2010

Hot Water Epilepsy: Seizure Type, Water Temperature, EEG Findings and Treatment
The Neurologist 16:109-112, Gokcil,Z.,et al, 2010

Subclinical Hypothyroidism Presenting with Gait Abnormality
The Neurologist 16:115-116, Edvardsson,B. &Persson,S., 2010

A 31-Year-Old Woman with a Transformed Low-Grade Glioma
JAMA 303:967-976, Warnke,P.C., 2010

Horners Syndrome-Not To Be Sneezed At
Lancet 375:776, Bazari,F.,et al, 2010

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy
NEJM 362:790-799, Glauser,T.A.,et al, 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
Neurol 74:691-696, Katzberg,H.D.,et al, 2010

Prospective Study of New-Onset Seizures Presenting as Status Epilepticus in Childhood
Neurol 74:636-642, 624, Singh,R.K.,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

Randomized Trial of Adjunctive Topiramate Therapy in Infants with Refractory Partial Seizures
Neurol 74:714-720, Novotny,E.,et al, 2010

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
AJNR 31:377-382, Petersen,T.A.,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

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

Hyperfamiliarity for Faces
Neurol 74:970-974, Devinsky,O.,et al, 2010

New-Onset Refractory Status Epilepticus with Restricted DWI and Neuronophagia in the Pulvinar
Neurol 74:1003-1005, Boyd,J.G.,et al, 2010

Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
Medicine 89:75-84, Kalyoncu,U.,et al, 2010

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

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

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

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

Tumefactive Multiple Sclerosis
www.medlink.com, JUne, Bunyan, R.F. and Lucchinetti, C.F., 2010

Pathophysiology of Thrombotic Thrombocytopenic Purpura
Int J Hematol 91:1-30, Tsai, H.M., 2010

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

Paraneoplastic Extra Limbic Encephalitis Associated with Thymoma
ICVTS 9:755-756, Rizzardi,G.,et al, 2009

Reversible Extralimbic Paraneoplastic Encephalopathies with Large Abnormalities on Magnetic Resonance Images
Arch Neurol 66:268-271, McKeon,A.,et al, 2009

Tempo of Disease. In Merritts Neurology. Signs and symptoms in neurologic diagnosis: Approach to the patient
, Rowland, L.P.,et al, 2009

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

Acute Limbic Encephalitis and Glutamic Acid Decarboxylase Antibodies:A Reality?
J Neurosci 287:69-71, Blanc,F.,et al, 2009

Limbic Encephalitis Associated with Anti-GAD Antibody and Common Variable Immune Deficiency
Dev Med Child Neurol 51:563-567, Akman,C.I.,et al, 2009

Voltage-gated Potassium Channel-associated Limbic Encepahlitis in the West of Scotland:Case Reports and Literature Review
Scott Med J 54:27-31, Reid,J.M.,et al, 2009

Obesity Is a Common Comorbidity for Pediatric Patients with Untreated, Newly Diagnosed Epilepsy
Neurol 73:658-664, 654, Daniels, Z.S.,et al, 2009

Intracranial Atherosclerotic Disease: An Update
Ann Neurol 66:730-738, Qureshi,A.,et al, 2009

Case 38-2009: A 16-Year-Old Boy with Paroxysmal Headaches and Visual Changes
NEJM 361:2367-2378, Brass,S.,et al, 2009

A Woman With Acute Myelopathy in Pregnancy: Case Outcome
BMJ 339:1372-1376, Reu�,R.,et al, 2009

Association of Parental Dementia With Cognitive and Brain MRI Measures in Middle-Aged Adults
Neurol 73:2071-2078, 2054, Debette,S.,et al, 2009

Functional and Cognitive Outcome in Prolonged Refractory Status Epilepticus
Arch Neurol 66:1505-1509, Cooper,A.,et al, 2009

Crescendo Transient Aura Attacks: A Transient Ischemic Attack Mimic Caused by Focal Subarachnoid Hemorrhage
Stroke 40:3725-3729, Izenberg,A.,et al, 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009



Showing articles 1550 to 1600 of 5708 << Previous Next >>