Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abstract reasoning
abulia
accommodation
accomodation, abnormal
aciduria
acquired immunodeficiency syndrome
acrocyanosis
acute cerebellar ataxia
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
affect, flat
affect, inappropriate
aggression
agitation
agnosia
agnosia, visual
Aicardi-Goutieres syndrome
akinetic mute
alcohol
alcohol intolerance
alcohol, neurologic complications with
alcoholism
Alexanders disease
alexia
algorithm
alpha-fetoprotein
alternating hemiplegia
alternating rapid movement
alternating rapid movement, impaired
aluminum
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, preclinical
Alzheimer's disease, visual variant
aminoacidurias
amnesia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
anemia
anemia, hemolytic
Angelman syndrome
angiography, cerebral
ankle edema
ankle, swelling of
anomic aphasia
anorexia
anti IgLON5
anti La antibody
anti Ro antibody
antibiotics, neurologic complications with
anticholinergic drugs
aphasia
aphasia, children
aphasia, progressive
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
aphonia
apraxia
apraxia of eye movements
apraxia, speech
areflexia
arm swing, reduced
arm weakness
arthritis
arthrogryposis multiplex
arylsulfatase A
ascites
aspiration
asterixis
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
ATP1A3 gene
attention deficit disorder with hyperactivity
attention span
atypical
auditory processing, impaired
autism
autoantibodies
automobile accidents
autonomic nervous system
axonal spheroid
B 12 deficiency
B cell lymphoma
Babinski sign
Balint's syndrome
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
Behcet's syndrome
belligerent
Benedict's solution test
bifid uvula
biologic markers
BiPAP
bladder dysfunction
blepharospasm
blindness
blinking
blinking, reduced
blood brain barrier
bone marrow biopsy
bone marrow transplantation
brachycephaly
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, infarction of
brainstem, lesion of
bruit
bruxism
bulbar palsy
bulbar palsy, progressive
burning feet
burning feet, differential diagnosis of
cafe au lait spots
CAG repeats
calcification, intracranial
calculations
calf hypertrophy
camptocormia
cane
carbon monoxide poisoning
carcinoembryonic antigen
carcinoid syndrome
carcinoid tumor
carcinoma
carcinoma of thymus
cardiomyopathy
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carotid siphon
carotid-siphon occlusion
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
cataplexy
cataracts
caudate nucleus
caudate nucleus, infarction
caudate nucleus, lesion of, bilateral
central hypoventilation
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar lesion
cerebellar vermis
cerebellitis
cerebellum
cerebellum, disease of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral dominance
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, complications with
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, silent
cerebrovascular disease
ceruloplasmin, serum
chasing the dragon
chelation therapy
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
chilbran skin lesions
children
choking
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 15
chromosome 17
chromosome 20
chromosome 9
cirrhosis
cleft palate
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
cognition
cognition, slowed
cognitive delay
cogwheel rigidty
coma
comorbidities
complications
comprehension, impaired
confusion
congenital bilateral perisylvian syndrome
congenital infection, CNS
congenital malformation
congenital myasthenic syndromes
conjunctival biopsy
consanguinity
constipation
contractures, joint
controversies in neurology
convergence
convergence, impaired
copper
copper metabolism, abnormal
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
crying
crying, pathologic
cryptococcal antigen
cryptococcal meningitis
cultured skin fibroblasts
cyanosis
cytomegalic inclusion disease
cytomegalovirus infection
deafmute
deafness
decerebrate posture
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, age at onset
dementia, childhood
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
dementia, thalamic
dementia, transmissible
demyelinating disease
denervation of muscle
denervation potentials
dentate nuclei
dentate nuclei, lesion of
depression
dermatitis
developmental abnormality of brain
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
dialysis
dialysis dementia
diarrhea
dichotic hearing
diet
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability rating scale, neurological
disability, neurological
disorientation
distal muscle weakness
dizziness
dopamine agonist
drooling
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
drug induced neurologic disorders
dural arteriovenous malformation
dying
dysarthria
dysdiadochokinesia
dysequilibrium syndrome
dyskinesia, buccal lingual facial
dyslexia
dysmetria
dysmorphic
dysnomia
dysphagia
dysphasia
dysphonia
dysplasia of C.N.S.
dyspnea
dyspraxia
dystonia
dystonia, children
dystrophin
ear, pain in
ears of the Lynx MR sign
echolalia
edema, pedal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electrophoretic pattern, CSF
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, viral
encephalomalacia
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, metabolic
enzyme, defect
epilepsia partialis continua
Epstein-Barr virus
equinovarus
esophageal varices
euphoria
executive dysfunction
exome sequencing
eye movement, disorders of
face, inexpressive
face, numbness of
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
fish
Fisher C.M.
fistula, arterio-venous, dural
fluency
fluorescene in situ hybridization
foam cells
folic acid
food-borne infection
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
frataxin
Friedreich's ataxia
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
fucosidosis
fungal infection
fungal infection, CNS
gag reflex, depressed
gait disorder
gait, apraxic
gait, festinating
gait, spastic
gammaglobulin therapy, intravenous
gastroenteritis
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genital ulcerations
Gerstmann syndrome
Gerstmann-Straussler-Scheinker disease
glabellar sign
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glossitis
GM1 ganglioside antibodies
Gowers maneuver
grandiosity
granular osmiphilic material
grasp reflex
gray matter
grimacing
growth retardation
gyrus, abnormal
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, visual
hand numbness
handwriting
head circumference
head lag
headache
headache, intermittent
headache, intractable
headache, severe
headache, sudden onset of
headache, vascular
hearing loss
hearing problems in children
heel-knee-shin test
hemianopia, homonymous
hemiballismus
hemifacial spasm
hemiparesis
hemiparesis, transient
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus
hiccoughs
high arched palate
hippocampus
HLA
hoarseness
hospice
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydroxyglutaric aciduria
hyperactivity
hyperkalemia
hyperlipoproteinemia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypersegmented polys
hypersomnia
hypertension
hypoalbuminemia
hypoglycorrhachia
hypometric saccades
hypophonia
hypopigmentation of skin
hyposmia
hypothyroidism
hypothyroidism, congenital
hypotonia
hypotonia, infants
illusions
imbalance
imbalance, postural
immunocompetent
immunodeficiency
immunohistochemistry
immunosuppression
impulsivity
inattention
inborn errors of metabolism
incarceration
inclusion bodies
inclusion bodies, intracytopasmic
incontinence, fecal
incoordination
infection, recurrent
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inflexibility, mental
initiative, lack of
insomnia
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
internal capsule
internuclear ophthalmoplegia
intracranial pressure, increased
intrauterine
intrinsic hand muscles, wasting of
introverted
iodine deficiency
iris, abnormal
iron, brain
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
jaw jerk, abnormal
karyotyping
Kayser-Fleischer ring
kinesia paradoxica
klippel feil syndrome
Kluver-Bucy syndrome
lactic acidemia
language
language delay
language development, neurologic basis of
language disorder in adults
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
left-right orientation
leg dragging
leg weakness, bilateral
leg weakness, unilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukemia
leukocyte alkaline phosphotase
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
leukopenia
Lewy body
life expectancy
limbic encephalitis
limbic system
lip biopsy
lipid storage disorder of CNS
Lisch nodules
listeria monocytogenes
listeriosis, CNS
lithium
liver disease
liver function enzymes
liver transplantation
lobar atrophy
locked-in syndrome
logopenia
long bone lesion
loss of sympathy
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
macrocephaly
macrognathia
magnetic source image
magnetoencephalography
malformation, CNS, congenital
mania
maple syrup urine disease
marche a petits pas
masked facies
masseter muscle wasting
mediastinum, mass of
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
meningeal enhancement
meningeal enhancement, nodular
meningismus
meningitis
meningitis, fungal
meningitis, neutrophilic
meningitis, neutrophilic, persistent
mental retardation
mental status, abnormal
mesial temporal lobe
mestinon
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microangiopathy, brain
microangiopathy, retina
microcephaly
micrographia
microhemorrhage, intracerebral
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
midline defect in children
migraine
mimics
misdiagnosis
mitochondrial disease
molecular genetics
monoclonal gammopathy
monoparesis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, false negative
MRI, FLAIR
MRI, functional
MRI, negative
MRI, nodular enhancement
MRI, paramagnetic effect
MRI, punctate pattern
MRI, serial
MRI, spinal cord
MRI, venography
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle cramp
muscle pain
muscle spasm, face
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myelodysplasia
myeloneuropathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoglobinuria
myxedema, neurologic manifestations of
nasal speech
nausea and vomiting
neck weakness
neoplasm, primary of CNS
neoplasm, primary of CNS-treatment of
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurofibroma
neurofibromatosis 1
neurologic complications
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic examination, non-focal
neurologic signs
neurologic symptoms
neurologic testing
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuroprotective agents
neurosyphilis
neurotoxic
neurotoxin
next-generation sequencing
Niemann-Pick disease
night sweats
nonverbal
Notch3 gene
nystagmus
ocular bobbing
ocular motility, disorders of
old age, neurology of
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
opsoclonus
optic atrophy
optokinetic nystagmus, abnormal
oral ulcerations
otitis, neurologic complications with
pain, increased response
palatal myoclonus
palatopharyngeal incompetence
palilalia
palmomental response
pancreatitis
pancytopenia
PANK2 mutation
papilledema
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, spastic
paraphasias
paraplegia
paraplegia, in flexion
parasomnia
paresthesias
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, freezing phenomena in
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
patent foramen ovale
pathologic reflex
pathology
pellagra
penicillamine
penicillin
peripheral blood smear
peripheral blood smear, abnormal
peroxisomal disease
perseveration
personality change
pes cavus
phenylketonuria
pheochromocytoma
Pick bodies
Pick's disease
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pneumoencephalogram(PEG)
polycythemia, primary
polymicrogyria
polyneuropathy
polyneuropathy, uremic
pons, infarction of
post infectious cerebellar ataxia
posterior cortical atrophy
postinfectious
postural abnormality
preclinical
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
primary lateral sclerosis
prion disease
prion protein gene
prisoner
progeria
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
protein 14-3-3, cerebrospinal fluid
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, bilateral
ptosis, unilateral
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiation hypersensitivity
rapidly progressing neurologic illness
real-time quaking-induced conversion
Red flags
rehabilitation for neurologic disorders
release phenomena
remote effect of cancer on the nervous system
renal failure
renal stones
renal transplantation
repetition, impaired
respirations in CNS disease
respirator
respiratory failure
restless leg syndrome
reticulum cell sarcoma
retina, abnormal
retinal branch artery occlusion
retinal infarction
retinitis pigmentosa
retinopathy
retropulsion
Rett's syndrome
review article
rigidity
rigidity, axial
riluzole
risk factors
roaming behavior
rocking
Romberg's sign
rooting reflex
Rosenthal fibers
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
saccadic eye movements, abnormal
salivation, excessive
Schirmer test
schizophrenia
scleritis
scoliosis
screening
sea-blue histiocytes
seizure
seizure, advice to parents and teachers regarding
seizure, focus
seizure, psychosocial aspects of
seizure, recurrent
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
semantic dementia
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
sign language
sinemet
single photon emission computed tomography
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skew deviation
skin, biopsy
skin, lesions in neurologic disorders
sleep
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
slow virus infection of CNS
slurred speech
smiling
snout reflex
spastic ataxia
spastic diplegia
spastic paraplegia, type 11
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, loss of
speech, pressured
speech, slowed
speech, soft
spina bifida
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinopontine atrophy, dominant
splenomegaly
spongy degeneration of brain
square wave jerks
stammering
stare
startle myoclonus
startle reaction
stem cell rescue
stem cell transplantation
stereotyped behavior
stooped posture
striopallidodentate calcifications, familial idiopathic
stuporous
stuttering
stuttering following CVA
subdural hematoma
substantia nigra
suck reflex
suck, poor
suicide
Susac's syndrome
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tachycardia
tandem gait, ataxic
tangential
tau protein
tauopathy
teeth, wide-spaced
telangiectases
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
tetany
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
third nerve palsy, bilateral
thrombocytopenia
thrombocytosis
thrombosis, cerebral
thyroiditis
titubation
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
tongue, ulcer
tonic spasms
toxoplasmosis, acquired
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, resting
tremor, wing beating
tremor, writing
trientine dihydrochloride
trinucleotide repeats
tripping
Trousseau's sign
twins
twitching
upgaze
upgaze, paralysis of
uremia
uremic encephalopathy
uremic twitching
urinary incontinence
urine test for metabolic disorders
urine, dark
vasculopathy
vegetarianism
Venereal Disease Research Laboratory test
venous hypertension
venous ischemia
very long chain fatty acids
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual impairment
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
vitamin supplementation
vocal cord paralysis
voice, abnormality of
Waldenstrom's macroglobulinemia
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Wernicke's aphasia
Wernicke's encephalopathy
wheelchair
Whipple's disease
white matter disease
wide based gait
Wolfram syndrome
word-finding difficulty
work loss
workup
writing
zinc
Showing articles 0 to 50 of 3175 Next >>

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Rapidly Progressive Thalamic Dementia
Neurol 96:e809-e813, Rizzo, A.C.,et al, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

A 42-year-old Woman with Progressive Cognitive Difficulties and Gait Imbalance
Neurol 94:e1219-e1226, Slama, M.C.C.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

Wilson Disease
NIDDK Oct2018, , 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Clinicopathologic Conference, Poststroke Mania and the Frontal Lobe Syndrome
NEJM 379:182-189, Case 21-2018, 2018

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

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

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

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Aphasic Variant of Alzheimer Disease
Neurol 87:1337-1343, Rogalski, E.,et al, 2016

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

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

A 64-year-old Woman with Subacute Encephalopathy
Neurol 85:e64-e65, Bhai, S.,et al, 2015

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
Adams & Victors Principles of Neurology Chp 40, pg 1156, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Progressive Rubella Panencephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 766, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Parkinson Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1082, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Gertsmann-Straussler Schneinker Syndrome
Adams & Victors Principles of Neurology, Chp 33, pg 773, 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 Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

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

Limbic Encephalitis as the Presenting Feature of Sj�gren Syndrome
Neurol Clin Pract 3:165-167, Finelli, P. & Inoa, V., 2013

Folic Acid Supplements in Pregnancy and Severe Language Delay in Children
JAMA 36:1566-1573, Roth, C.,et al, 2011



Showing articles 0 to 50 of 3175 Next >>