Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis, bilateral
acetazolamide
aciduria
acute ataxia of childhood
acute cerebellar ataxia
acute disseminated encephalomyelitis
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
aggression
agitation
alcohol intolerance
algorithm
alkalosis
alkalosis, respiratory
alopecia
alpha-fetoprotein
altered states of consciousness
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
Alzheimer's disease
aminoacidurias
AMPA receptor antibodies
amyotrophic lateral sclerosis
anemia
aneurysm
aneurysm, children
aneurysm, fusiform
aneurysm, vertebral basilar system
Angelman syndrome
angiitis
angiitis, granulomatous of CNS
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, posterior fossa
angiotensin-converting enzyme
animal exposure
aniridia
ankle reflex, absent
anorexia
anti GQ1b IgG antibody
antibodies to measles
anticonvulsants
anticonvulsants, effectiveness
antithyroid antibodies
anxiety
aphasia
apnea
apraxia
apraxia of eye movements
areflexia
Arnold Chiari malformation
arterial dissection
arterial dissection, intracranial
arterial dissection, ruptured
arterial dissection, vertebral
arthralgia
arthritis
arylsulfatase A
ascending paralysis
Asia
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, congenital
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
ATP1A3 gene
attention span
autism
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
automobile accidents
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
bacterial infection
bacterial infection, CNS
ballismus, bilateral
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery migraine
basilar artery occlusion
basophilic stippling of red blood cells
Bassen-Kornzweig syndrome
behavior, combative
behavioral disorder
behavioral disorder, acute
biotin deficiency
biotinidase deficiency
blindness
blindness, monocular
blindness, transient
blood dyscrasias, neurologic findings with
bone marrow biopsy
brachycephaly
brain biopsy
brain biopsy, stereotaxic
brainstem, atrophy
brainstem, dysfunction
brainstem, glioma in children
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
bruxism
CAG repeats
calcification, intracranial
calcium antagonist
carcinoembryonic antigen
carcinoma
carcinoma of pancreas
cardiomyopathy
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, dense artery sign
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, pelvis
catalepsy
cataplexy
cataracts
cataracts, congenital
cat-scratch disease
cauda equina, enhancement
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar pontine angle
cerebellar pontine angle tumor
cerebellar vermis
cerebellitis
cerebellitis, autoimmune
cerebellum
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral embolism
cerebral embolism, mechanical extraction
cerebral folate deficiency syndrome
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, bilateral
cerebrovascular accident, prognosis in
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
cerebrovascular disease, surgical treatment of
channelopathy
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
chickenpox
children
choking
chorea
choreoathetosis
chorioretinitis
choroid plexus
chromosomal abnormality
chromosome 11
chromosome 15
chromosome 2
chromosome 6
chronic progressive external ophthalmoplegia
Chvostek sign
cisterna magna
Clinical Pathologic Conference(C.P.C.)
clonus
clot retrieval
cocaine
coenzyme Q10
coenzyme Q10 deficiency
cognition
cognitive delay
coma
coma, episodic
complications
confusion
conjunctival biopsy
conjunctivitis
consanguinity
corpus callosum, thinning
cortical ribbon sign
cough
counterimmunoelectrophoresis
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying
cultured skin fibroblasts
cyanide poison
cyst
cyst, parenchymal
cyst, subcortical
deafness
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delayed dentition
delirium
dementia
dementia, childhood
dementia, presenile
dementia, reversible
dementia, treatment of
demyelinating disease
dense basilar artery sign
dense middle cerebral artery sign
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dermatitis herpetiformis
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
digital subtraction angiography
dilantin
diplopia
disability, neurological
disease modifying agents
diurnal variation
dizziness
doll's head maneuver
down-beat nystagmus
Dravet syndrome
drooling
drowsiness
drug induced neurologic disorders
drug induced neurologic disorders in children
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmetria
dysmorphic
dysphagia
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electromyogram
electron microscopy
embolism, paradoxical
embolism, vertebral-basilar artery
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, postinfectious
encephalomyopathy
encephalopathy
encephalopathy, acute
encephalopathy, Hashimoto's
endovascular therapy
enterovirus
enterovirus infection of CNS
enzyme, defect
ependymoma
epicanthal folds
epidemic
epidemiology of neurology
epinephrine
episodic disorders
episodic neurologic deficits
Epstein-Barr virus
erethism
evoked potentials
excitotoxin
exercise intolerance
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
falling
familial
fasciculation
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fish
Fisher's syndrome
flaccid paralysis
fluorescene in situ hybridization
folic acid
folic acid deficiency
foot deformity
fornix, lesion of
fourth ventricle, enlargement of
fourth ventricle, neoplasm of
fragile-X syndrome
Friedreich's ataxia
fundus, abnormality of
gait disorder
gait, apraxic
gait, spastic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gastrointestinal disease, neurologic complications
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gillespie syndrome
glioblastoma multiforme(astrocytoma Gr.III)
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucagonoma
GluD2
glutamic acid
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
gram negative rod
granulomatous disease
gray matter
growth hormone
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, etiology of
Guillain Barre syndrome, infantile and childhood form
Guillain Barre syndrome, variant forms of
hallucination
hallucination, visual
hammertoes
hand flapping
hand-foot-mouth disease
handwriting
Hartnup's disease
head injury
head lag
head tilt
headache
headache, bifrontal
headache, occipital
headache, recurrent
headache, severe
headache, sudden onset of
hearing loss
hearing problems in children
heart block
heavy metal intoxication
heel-knee-shin test
hemiparesis
hemiplegia
hemosiderosis of CNS, superficial
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
HLA
hoarseness
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
huntingtin
Huntington's chorea
hydroxyglutaric aciduria
hyperactivity
hyperintense vessel sign
hyperosmolality
hyperreflexia
hypertension
hypertension, cerebrovascular disease with
hyperventilation
hypocalcemia
hypocalcemia, causes of
hypodontia
hypoglycemia
hypogonadism
hypomagnesemia
hypomyelination
hypoparathyroidism
hypopigmentation of skin
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
hypoxia
iatrogenic neurologic disorders
imbalance
immunization, neurologic complications with
immunodeficiency
immunosuppression
immunotherapy
inappropriate antidiuretic(A.D.H.)hormone
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic intranuclear
incoordination
industrial neurologic disorders
infection
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
internal capsule
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, young adult
intracranial hypertension, benign
intracranial pressure, increased
intrathecal medication
iris, abnormal
irritability
Jakob-Creutzfeldt disease
jaundice
Kearns-Sayre syndrome
lactic acidemia
language disorders in children
laryngismus stridulus
laughing, pathologic
lead and the nervous system
lead line, gingival
lead poisoning
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
lipid storage disorder of CNS
liver disease
liver function enzymes
locked-in syndrome
low back pain
lymphadenopathy
lymphoma
lysosomal storage disease
macrocephaly
macrognathia
macular degeneration
malabsorption
maple syrup urine disease
marche a petits pas
Marinesco-Sjogren syndrome
masked facies
mediastinum, mass of
megalencephaly
MELAS syndrome
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, recurrent
meningoencephalitis
meningoencephalitis, mumps
meningovascular syphilis
mental retardation
mental status, abnormal
MERCI trial
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methotrexate
microcephaly
microdontia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
miglustat
migraine
migraine, children
migraine, visual symptoms in
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
monoparesis
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR, hyperintense vessels
MRI, high signal foci on
MRI, negative
MRI, pelvis
MRI, serial
MRI, spinal cord
MRI, volumetry
MRS
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, children
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sclerosis, presenting manifestations
multiple sclerosis, prognosis
multiple system atrophy
mumps virus
muscle biopsy
muscle cramp
muscle pain
muscle weakness
mycoplasma
mycoplasma pneumoniae
myelinolysis, extrapontine
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myokymia
myopathy
myopathy, mitochondrial
myopia
myotonia dystrophica
nausea and vomiting
negative
neonatal screening, genetic neurologic disorders
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-treatment of
nephrotic syndrome
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurologic complications
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
neurologic symptoms
neuromyotonia
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
neuropathy
neuropathy, acute
neurosyphilis
neurotoxic
neurotoxicity, acute
neurotoxin
neurotransmitter
Niemann-Pick disease
NMDA antagonists
nystagmus
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, rotary
nystagmus, vertical
octreotide
ocular motility, disorders of
oculodentodigital dysplasia
ophelia syndrome
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic disc edema
optic nerve
optic neuritis
optic neuritis, children
optic neuropathy
optical coherence tomography
oral ulcerations
oscillopsia
osmotic demyelination syndrome
osteoporosis
ovarian tumor
ovary, enlarged
pain
pain, abdominal
pain, back
pain, leg
pancytopenia
panic attacks
papilledema
paralysis, acute
paralysis, acute areflexic
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
parotitis
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
past pointing
patent foramen ovale
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
Penumbra System
personality change
pica
pigmentary retinopathy
piperazine
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
poison, mercury
POLG1 gene
POLR3B
polymerase chain reaction
polyneuritis
polyneuropathy
pons, infarction of
pons, lesion of
pontine glioma
Poretti-Boltshauser syndrome
posterior leukoencephalopathy syndrome
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prevention of neurologic disorders
primary episodic ataxia
progeria
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
puberty
puberty, delayed
pulmonary edema
pulmonary infection
pulmonary infiltrates
Purkinje cell
Purkinje cell surface antibody
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation hypersensitivity
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
rash, hand
rectal biopsy
recurrent
Refsum's disease
remote effect of cancer on the nervous system
renal failure
respirations in CNS disease
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinitis pigmentosa
retinopathy
Rett's syndrome
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rhinorrhea
risk factors
rituximab
rocking
rubella encephalitis, progressive
rubeola virus
safety
salivation, excessive
sarcoidosis
sarcoidosis, CNS
schizophrenia
SCN1A gene
scoliosis
screening
seizure
seizure, children
seizure, differential diagnosis of
seizure, drug-induced
seizure, familial
seizure, febrile
seizure, intractable
seizure, laughing as manifestation
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
self-mutilation
semialdehyde dehydrogenase deficiency
sensorineural hearing loss
serologic testing
serologic testing, false negative
seronegative
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep pathology and physiology
slurred speech
smiling
sodium channel dysfunction
somnolence
spasmophilia
spastic ataxia
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
speech, loss of
spinal cord
spinal cord, lesion of
spinal cord, pathologic exam of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
splenomegaly
spongy degeneration of brain
startle myoclonus
status epilepticus
status tetanicus
steroid
steroid therapy, CNS treatment and complications with
strabismus
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuporous
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
subarachnoid hemorrhage, recurrent
suck, poor
symmetric brain lesions
syndactyly
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
teeth, wide-spaced
telangiectases
temporal lobe, lesion
teratoma
teratoma, ovarian
term infant
tetany
tetany, latent
tetany, normocalcemic
thalamus, lesion of
thrombectomy
tick bite
tick paralysis
tinnitus
titubation
tongue, protrusion of
tonic spasms
topiramate
torticollis
toxins, nervous system
transient ischemic attack
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremulousness
trinucleotide repeats
Trousseau's sign
upgaze
upgaze, paralysis of
upgaze, sustained
urinary incontinence
urinary retention
urine test for metabolic disorders
urine test in toxic screen
urticaria
vaccination, neurologic complications with
vaccine
vasculopathy
vasospasm, cerebral
vertebral-basilar insufficiency
vertigo
vertigo, episodic
violent behavior
viral infection
viral infection, CNS
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden-unilateral
visual loss, transient
visual obscurations, transient
visuospatial disturbance
von Bonsdorff's sign
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
web sites
weight loss
wheelchair
white matter disease
wide based gait
Wolfram syndrome
workup
X-linked bulbospinal neuronopathy
Showing articles 1200 to 1250 of 4289 << Previous Next >>

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Wyburn-Mason Syndrome
BMJ 360:k639, Guo, H.P,.et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

An Interdisciplinary Response to Contemporary Concerns About Brain Death Determination
Neurol 90:423-426, Lewis, A.,et al, 2018

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

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

Teaching NeuroImages: Acute Necrotizing Encephalopathy of Childhood
Neurol 90:e177-e178, Biswas, A.,et al, 2018

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

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018

Recurrent Ischemic and Hemorrhagic Strokes in a Young Adult
JAMA Neurol 75:628-629, Rocha, E.A. & Singhal, A.B., 2018

Coma
Neurol 90:e1638-e1645, Schievink, W.I.,et al, 2018

Essential Tremor
NEJM 378:1802-1810, Haubenberger, D.,et al, 2018

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

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

Brain Imaging in Cases with Positive Serology for Dengue with Neurologic Symtoms: A Clinicoradiologic Correlation
AJNR 39:699-703, Vanjare, H.A.,et al, 2018

Facial Ulceration in stroke
Neurol 90:e1448-e1449, May, L.M.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

Isolated Gait Dysfunction Due to Intracranial Hypotension
Neurol 91:271-272, Sasikumar,S.,et al, 2018

Coxa Saltans Misdiagnosed as Functional Gait Disorder
Neurol 91:276-277, Gilbert,D.L.,et al, 2018

An Infant with Episodic Facial Flushing
Neurol 91:278-281, Kang,J.H.,et al, 2018

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

Bow Hunter Syndrome:A Rare Cause of Posterior Circulation Stroke
Neurol 91:329-331, Jadeja,N. and Nalleballe,K., 2018

The Dangers of Playing Squash
BMJ 362:K3062, Marrinan,E.,et al, 2018

Risk of Ischemic and Hemorrhagic Strokes in Occult and Manifest Cancers
Stroke 49:1585-1592, Andersen, K.K. & Olsen, T.S., 2018

Incidence of Sudden Unexpected Death in Epilepsy in Children is Similar to Adults
Neurol 91:e107-e111, Keller, A.E.,et al, 2018

Autoimmune Pancerebellitis Associated with Pembrolizumab Therapy
Neurol 91:91-93, Vitt, J.R.,et al, 2018

Neurologic Outcomes in Pediatric Cardiac Arrest Survivors Enrolled in the THAPCA trials
Neurol 91:e123-e131, Ichord, R.,et al, 2018

Cerebrovascular Manifestations of Neurosarcoidosis: An Underrecognized Aspect of the Imaging Spectrum
AJNR 39:1194-1200, Bathla, G.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Unique Gadolinium Enhancement Pattern in Spinal Dural Arteriovenous Fistulas
JAMA Neurol 75:1542-1545, Zalewski, N.L.,et al, 2018

Papillary Fibroelastoma, Unusual Cause of Stroke in a Young Man
J Cardiothorac Surg 12:33, Grolla, E.,et al, 2017

Intracranial and Extracranial Neurovascular Manifestations of Takayasu Arteritis
AJNR 38:766-772, Bond, K.M.,et al, 2017

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Guillain-Barre Syndrome following tuberculosis: A rare association
J Neurosci Rural Pract 8:296-299, Lakhotia, A.N.,et al, 2017

Imaging Characteristics of Venous Parenchymal Abnormalities
Stroke 48:3258-3265, Arnoux, A.,et al, 2017

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

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

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

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017



Showing articles 1200 to 1250 of 4289 << Previous Next >>