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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 950 to 1000 of 5708 << Previous Next >>

Acute Viral Encephalitis
NEJM 379:357-366, Tyler,K.L., 2018

Nonconvulsive Status Epilepticus in Acute Intracerebral Hemorrhage
Stroke 49:1759-1761, Matsubara, S.,et al, 2018

Management of Acute Retinal Ischemia
Ophthalmol 125:1597-1607, Viousse, V.,et al, 2018

Progressive Multifocal Leukoencephalopathy: Epidemiology, Clinical Manifestations, and Diagnosis
www.UptoDate.com, May, Koralnik, I.J., 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Clinicopathologic Conference, Intracranial Hypertension Associated with Systemic Lupus Erythematosus and Steroid Use
NEJM 378:282-289, Case 2-2018, 2018

Clinical Reasoning: A 66-year-old Woman with Seizures and Progressive Right-Sided Weakness
Neurol 90:e435-e439, St-Pierre, B.D.,et al, 2018

Five and 10 Minute Apgar Scores and Risks of Cerebral Palsy and Epilepsy: Population Based Cohort Study in Sweden
BMJ 360:k207, Persson, M.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

The Laser Shoes
Neurol 90:e164-e171, Barthel, C.,et al, 2018

Mixed-Location Cerebral Hemorrhage/Microbleeds
Neurol 90:e119-e126, Pasi, M.,et al, 2018

Maternal and Fetal Risks of Natalizumab Exposure in Utero
Neurol 90:443-444, Marrie, R.A.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
Neurol 90:518-519, Peddawad, D.,et al, 2018

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

Cannabidiol in Patients with Seizures Associated with Lennox-Gastaut Syndrome (GWPCARE4): A Randomised, Double-Blind, Placebo-Controlled Phase 3 Trial
Lancet 391:1085-1096, Thiele, E.A.,et al, 2018

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

Neonatal Abstinence Syndrome
JAMA 319:1362-1374, Wachman, E.,et al, 2018

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
NEJM 376:2011-2020, Devinsky, O.,et al, 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Myeloperoxidase-Anti-Neutrophil Cytoplasmic Antibody-Positive Hypertrophic Pachymeningitis
Neurol 89:e253-e254, Culbertson, C.J.,et al, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

A Man with Paraesthesia, Headache, and Vertigo
BMJ 359:j5165, ODay, J. & Bhatt, P., 2017

High Risk of Postpartum Relapses in Neuromyelitis Optica Spectrum Disorder
Neurol 89:2238-2244, Klawiter, E.C.,et al, 2017

A 61-year-old woman with Lower Extremity Paralysis and Sensory Loss
Neurol 89:e257-e263, Manners, J.,et al, 2017

Subarachnoid Hemorrhage
NEJM 377:257-266, Lawton, M.T. & Vates, G.E., 2017

TIPIC Syndrome: Beyond the Myth of Carotidynia, a New Distinct Unclassified Entity
AJNR 38:1391-1398, Lecler, A.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Effect of Gluten-Free Diet on Cerebellar MR Spectroscopy in Gluten Ataxia
Neurol 89:705-709, Hadjivassiliou, M.,et al, 2017

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

A 50-year-old Woman with SLE and a Tumefactive Lesion
Neurol 89:e140-e145, Choi, J.H.,et al, 2017

Thalamic Deep Brain Stimulation for Tremor in Parkinson Disease, Essential Tremor, and Dystonia
Neurol 89:1416-1423, Cury, R.G.,et al, 2017

Recrudescence of Deficits After Stroke
JAMA Neurol 74:1048-1055, Topcuoglu, M.A.,et al, 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Pure Sensory Ganglionopathy as the First Sign of Relapse in Non-Hodgkin Lymphoma
Neurol 88:1976-1977, Hossack, M. & McClean, J., 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

Recurrence Risk of Ictal Asystole in Epilepsy
Neurol 89:785-791, Hampel, K.G.,et al, 2017



Showing articles 950 to 1000 of 5708 << Previous Next >>