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Differential
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abdominal distention
abulia
aciduria
acrocyanosis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
affect, inappropriate
Aicardi-Goutieres syndrome
akinetic mute
Alexanders disease
Alexanders disease, adult onset
algorithm
alopecia
aminoacidurias
ammonia
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
anti MAG antibodies
anxiety
aphasia
apraxia
areflexia
arteriopathy
arylsulfatase A
aspartocyclase
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal spheroid
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Binswanger disease
biologic markers
bladder dysfunction
blindness
body odor
bone marrow transplantation
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
cachexia
CAG repeats
calcification, intracranial
calcification, intracranial, rim
calcifications, intracranial, punctate
Canavan's disease
caries
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, serial
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
Charcot-Marie-Tooth
chilbran skin lesions
children
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 17
chromosome 19
chromosome 3
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cognition
complications
compression neuropathy
confusion
consanguinity
contractures, joint
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, weak
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cyst
cyst, parenchymal
cystic infarction
DARS
deafness
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delayed dentition
dementia
dementia, cerebrovascular disease causing
dementia, childhood
dementia, familial
dementia, frontal lobe type
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
diet
differential diagnosis
diplopia
diplopia, transient
DNA probes
dysarthria
dysarthria-clumsy hand syndrome
dyscalculia
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia, children
dystroglycanopathies
eczema
electromyogram
electron microscopy
emotional lability
encephalopathy
enzyme, defect
enzyme, muscle disease
epicanthal folds
episodic neurologic deficits
evoked potentials
exome sequencing
extraocular muscle lesion
eye movement, disorders of
eye, pain in
eyes, sunken
Fabry's disease
facial appearance, abnormal
failure to thrive
falling
familial
fatigue
fatty acid dehydrogenase deficiency
feeding disorder
fever
flow study, carotid artery
foot deformity
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, lesion of
frontal lobe, pathologic signs of
gadolinium
gait disorder
gait, spastic
galactocerebrosidase
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
globus pallidus, lesion of, bilateral
glycosyltransferase
gram negative rod
granular osmiphilic material
grasp reflex
growth retardation
gyrus, abnormal
handwriting
head lag
headache
hearing loss
hemiparesis
hemiparesis, transient
hemophagocytic lymphohistiocytosis
hemophagocytic lymphohistiocytosis, cerebromeningeal
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
hiccoughs
hormone replacement
HTRA1 gene
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hyperactivity
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypodontia
hypogonadism
hypomyelination
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
imbalance
immunodeficiency
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incontinentia pigmenti
incoordination
intellectual deficit
intellectual deterioration
intelligence quotient
interferon alpha
intestinal pseudoobstruction
intracerebral hemorrhage
intrauterine
irritability
Jewish
Kearns-Sayre syndrome
Krabbe's disease
lactate
lacunar infarction
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukodystrophy, pigmented orthochromatic
leukoencephalopathy
leukoencephalopathy with calcification and cysts
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
life expectancy
Lorenzo's oil
low back pain
lysosomes, abnoral
macrocephaly
mania
manic-depressive
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
memory, impairment of
meningeal enhancement
meningitis, brucellosis
mental retardation
metabolic acidosis
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
methylmalonic aciduria
microangiopathy, brain
microcephaly
microdontia
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine with aura
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
mousy odor
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, black holes on
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, gradient-echo
MRI, high signal foci on
MRI, negative
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
myelination of nervous system
myelitis, longitudinal
myelitis, transverse
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonus
myopathy
myopia
myotonia
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve root enhancement
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neurogenic bladder
neuroichthyosis
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neuromuscular disease, electrodiagnosis of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
next-generation sequencing
NOTCH2NLC
Notch3 gene
nystagmus, rotary
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
optic atrophy
optic neuritis
optic neuritis, bilateral
optic neuropathy
overlap syndrome
owl's eye sign of spinal cord
pain
pain, abdominal
pain, back
pain, foot
palatal myoclonus
palmoplantar keratoderma
paralysis
paralysis, recurrent
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraparesis, spastic, tropical
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
phenylketonuria
photosensitivity, skin
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
pons, lesion of
posterior fossa, lesion of
posterior leukoencephalopathy syndrome
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
propionic aciduria
proximal myotonic myopathy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
psychotic behavior
ptosis
pupil, dilated, bilateral
pupil, dilated, episodic
putamen, lesion of, bilateral
pyramidal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
ragged-red fibers
rash
recurrent
Red flags
retina, abnormal
retinal degeneration
retinal lesion
retinopathy
retrovirus
reversible neurologic disorder
review article
RFLPs
rigidity
Rosenthal fibers
saccadic eye movements, abnormal
sarpropterin
Saudi Arabia
Schilder's disease
schizophrenia
screening
seizure
seizure, drug resistance
self-mutilation
sensorineural hearing loss
sensory loss
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
small vessel disease
somatosensory evoked potentials
spastic diplegia
spasticity
speech disorder, childhood
spinal cord, lesion of
spinocerebellar ataxia
splenium of corpus callosum
spondylolysis
spondylosis
spongy degeneration of brain
spontaneous remission
staggering
startle reaction
stem cell transplantation
steroid therapy, CNS treatment and complications with
stooped posture
striatum, lesion of
strokelike episodes
subarachnoid hemorrhage
subcortical U fibers
subdural hematoma
substantia nigra
succinate dehydrogenase deficiency
sural nerve
symmetric brain lesions
syndactyly
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
temporal lobe, lesion, bilateral
testicular biopsy
thalamus, lesion of
thalamus, lesion of-bilateral
titubation
tomaculous neuropathy
tongue, biting
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
treatment resistant
tremor
tremor, cerebellar
tremor, intention
trichopoliodystrophy
trinucleotide repeats
umbilical-cord blood transplantation
unconsciousness
unconsciousness, transient
urea-cycle enzymopathies
urinary incontinence
urine test for metabolic disorders
vanishing white matter
vasculitides
vasculopathy
very long chain fatty acids
vibratory sensation, abnormal
visceral neuropathy
vision loss, sequential
visual acuity, decreased
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden
vitamin E deficiency
walking, difficulty with
water channel antibodies
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
wheelchair
white matter disease
white matter disease, location
white matter disease, pattern
white matter disease, subcortical
white matter disease, unilateral
workup
writing
X-linked neuropathy
Showing articles 0 to 50 of 2901 Next >>

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Ann Neurol 91:889-890, Gollion, C.,et al, 2022

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

A 25-year-old Woman with Recurrent Episodes of Collapse and Loss of Consciousness
Neurol 94:994-999, Wildman, J.,et al, 2020

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Cerebral White Matter Abnormalities in Patients with Charcot-Marie-Tooth Disease
Ann Neurol 81:147-151, Lee, M.,et al, 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Bipolar II Disorder as the Initial Presentation of CADASIL:An Underdiagnosed Manifestation
Neuropsych Dis Treat 13:2175-2179, Wang,J.,et al, 2017

Neuroradiologic Patterns and Novel Imaging Findings in Aicardi-Goutieres Syndrome
Neurol 86:28-35, La Piana, R.,et al, 2016

Neuromyelitis Optica Spectrum Disorders
UpToDate, May, Glisson,C.C., 2016

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
Neurol 84:226-230,218, Wolf, N.I.,et al, 2015

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,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

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis
Neurol 78:1150-1156, Deiva,K.,et al, 2012

Restricted Diffusion in Vanishing White Matter
Arch Neurol 69:723-727, Van de Lei, H.D.W.,et al, 2012

The Ever-Expanding Spectrum of Congenital Muscular Dystrophies
Ann Neurol 72:9-17, Mercuri, E. & Muntoni, F., 2012

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Clinical Reasoning: A Young Man with Reversible Paralysis, Cerebral White Matter Lesions, and Peripheral Neuropathy
Neurol 79: e70-e72, Zhong, L.,et al, 2012

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

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

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Nearly Completely Reversible Brain Abnormalities in a Patient With Incontinentia Pigmenti
AJNR 29:431-433, Lou,H.,et al, 2008

Insights into the Dynamics of Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids
Neurol 71:925-929, Van Gerpen,J.A.,et al, 2008

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Phenylketonuria
eMedicine (December), Arnold,G.L., 2007

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
AJNR 27:1037-1039, Mascalchi,M.,et al, 2006

Fragile X Premutation With Atypical Symptoms at Onset
Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006

Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies
Arch Neurol 62:1911-1914, Sanahuja,J.,et al, 2005



Showing articles 0 to 50 of 2901 Next >>