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Differential
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abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
aciduria
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, heralded by neurologic invol
acrocyanosis
acute disseminated encephalomyelitis
acyclovir
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
Adies pupil
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
affect, inappropriate
agenesis of corpus callosum
Aicardi-Goutieres syndrome
akinetic mute
albendazole
Alexanders disease
Alexanders disease, adult onset
algorithm
alpha glucosidase
altered states of consciousness
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, treatment of
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloidoma
amyloid-related imaging abnormalities
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
ANA
anemia
anesthesia, general
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, cerebral, false negative
angiography, cerebral, negative
animal exposure
ankylosing spondylitis
anorexia
anterior horn cell disease
anterior tibial muscle weakness
antibodies to measles
antiphospholipid antibodies
antiviral agents
anxiety
aphasia
aphasia, global
apnea
apraxia
arachnoiditis
areflexia
arm atrophy
arm weakness
arrhythmia, cardiac
arthralgia
arylsulfatase A
ascending paralysis
aspartate aminotransferase
aspartocyclase
aspiration
aspirin
astrocytoma
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, sensory
ataxic gait
attention deficit disorder with hyperactivity
atypical
audiogram
auditory evoked brainstem potentials
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
autonomic neuropathy
axonal spheroid
B 12 deficiency
Babinski sign
bacterial infection
baldness
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basement membrane
basement membrane thickening
baylisascariasis
behavioral disorder
behavioral disorder, acute
Behcet's syndrome
biologic markers
BiPAP
bladder dysfunction
blindness
bone marrow biopsy
bone marrow infarction
bone marrow necrosis
bone marrow transplantation
bone pain
bone scanning
bradycardia
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brain biopsy, false negative
brain purpura
brainstem, atrophy
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
bulbar palsy, progressive
burning skin
cachexia
CAG repeats
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
carbon monoxide poisoning, chronic
carboxyhemoglobin
carcinoma
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
CAT scan, spine
cataracts
cataracts, congenital
catatonia
cauda equina, enhancement
CD4 counts
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellum
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral vasculature
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, women
cervical spine
Charcot-Marie-Tooth
chasing the dragon
chemotherapy, CNS treatment and complications with
chilbran skin lesions
children
chills
chorea
choreoathetosis
chorioretinitis
chromosome 12
chromosome 19
chromosome 3
chromosome 5
Clinical Pathologic Conference(C.P.C.)
cocaine
cognition
cognitive delay
collapsin response mediator protein 5 IgG
coma
complications
confusion
congestive heart failure
consanguinity
contractures, joint
copper deficiency
corona radiata
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cortical blindness, transient
cortical infarction
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
critical care unit
cry, abnormal
crying, pathologic
cultured skin fibroblasts
cyanosis
cyclophosphamide
cyst
cyst, parenchymal
DARS
deafness
deafness, bilateral
deafness, sudden
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delayed dentition
dementia
dementia, childhood
dementia, frontotemporal
dementia, rapidly progressive
demyelinating disease
denervation of muscle
denervation potentials
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
diffuse idiopathic skeletal hyperostosis
diplopia
diplopia, transient
disability, neurological
distal muscle weakness
disulfiram
DPPX, antibodies, encephalitis
drooling
dropped head syndrome
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
drug abuse, toxic screen In
dural sinus thrombosis
dying
dysarthria
dysdiadochokinesia
DYSF gene
dysferlinopathy
dyskinesia
dyskinesia, facial
dysmetria
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, diffuse slowing
electroencephalogram, periodic complexes
electromyogram
electron microscopy
embolism
embolism, fat
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, focal
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, acute
encephalopathy, anoxic
encephalopathy, delayed
encephalopathy, metabolic
encephalopathy, post anoxic
encephalopathy, progressive
enzyme treatment
enzyme, defect
enzyme, muscle disease
eosinophilia
epidemiology of neurology
episodic neurologic deficits
euphoria
evoked potentials
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
facial appearance, abnormal
facial nerve palsy
facial weakness
facial weakness, bilateral
faciobrachial dystonic seizure
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fever
fibrillations
flail arm syndrome
fluctuate
fluorescein angiography
foot deformity
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, atrophy
frontal lobe, pathologic signs of
fundus, abnormality of
funduscopic exam
gait disorder
gait, spastic
gamma amino butyric acid receptor antibody
gangliosidosis GM2
gastric partitioning
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy, vertical
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
genu of corpus callosum
GFAP gene
glabellar sign
glioma
gliomatosis cerebri
globoid cells
globus pallidus, hemorrhage
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycogen storage disease
GM1 ganglioside antibodies
gray hair
gray matter
Griscelli syndrome
growth retardation
Guillain Barre syndrome, differential diagnosis of
hair analysis
hallucination
hallucination, olfactory
hallucination, visual
hand weakness
hands, fisted
handwriting
head bobbing
head circumference
head lag
headache
headache, positional
headache, recurrent
hearing loss
hearing loss, bilateral
hearing loss, sudden, bilateral
heart block
helminthic infection of CNS
hemiparesis
hemiparesis, transient
hemiplegia
hemiplegia, progressive
hemoglobin abnormality, neurologic complications of
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes simplex encephalitis
herpes simplex virus
herpes virus
herpes virus infection
hexosaminidase-A
high arched feet
high arched palate
highly active antiretroviral therapy
hoarseness
hospice
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydroxyglutaric aciduria
hyperactivity
hyperbaric oxygen
hypercapnia
hyperekplexia
hyperhomocysteinemia
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertensive encephalopathy
hypertonia
hypodontia
hypoglycorrhachia
hypomyelination
hyponatremia
hyporeflexia
hypotension, systemic
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunosuppressive agents
immunotherapy
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
incontinence, fecal
incoordination
infection
infectious mononucleosis
infectious mononucleosis, neurologic findings with
insomnia
insular cortex
intellectual deficit
intellectual deterioration
interferon alpha
internal capsule
intestinal pseudoobstruction
intracerebral hemorrhage
intrauterine
intrinsic hand muscles, wasting of
irritability
Jakob-Creutzfeldt disease
Japan
Jewish
joint hypermobility
Kernig's sign
Krabbe's disease
lactate
lactic dehydrogenase(LDH)
laminar necrosis, cortical
laughing, pathologic
leg weakness, bilateral
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy with calcification and cysts
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
leukoencephalopathy, toxic
levamisole
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
life expectancy
life support, withdrawal of
limbic encephalitis
lipid storage disorder of CNS
lobar atrophy
lymphohistiocytosis
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malabsorption
Marinesco-Sjogren syndrome
masked facies
masseter muscle wasting
meconium staining
medulla oblongata, lesion of
megalencephaly
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningeal gliomatosis
meningismus
meningitis
meningitis, aseptic
meningitis, eosinophilic
meningitis, melanomatous
meningitis, Mollaret's
meningitis, recurrent
meningitis, treatment of
meningoencephalitis
mental retardation
mental status, abnormal
merosin
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylene tetrahydrofolate reductase
methylenetetrahydrofolate reductase deficiency
methylglutaconic aciduria
microaneurysm, retinal
microangiopathy, brain
microangiopathy, retina
microcephaly
microhemorrhage, intracerebral
microinfarcts
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
Middle east
migraine
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoclonal antibodies
monoclonal gammopathy
monoparesis
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, cortical enhancement
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, gray matter enhancement
MRI, high signal foci on
MRI, hypointense signal foci on
MRI, negative
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
MRS
multiple organ failure
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle pain
muscle spasm
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, limb-girdle
mutism
myelination of nervous system
myelitis, transverse, recurrent
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, acute
myopathy, critically ill
myopathy, drug-induced
myopathy, steroid induced
myopia
myotonia
myotonia dystrophica
nasal speech
nausea and vomiting
neck weakness
neoplasm, primary of CNS
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
nerve root enhancement
neurexin-3 alpha antibodies
neuroaxonal leukodystrophy
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic examination, focal
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal cell surface antigen
neuronal degeneration
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
neuroprotective agents
neurotoxic
neurotoxicity, acute
neurotoxin
next-generation sequencing
NMDA antagonists
nutritional deficiency
nystagmus
obesity
occipital lobe, lesion of
old age, neurology of
ophthalmoplegia
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve, enlarged
optic nerve, hypoplasia of
optic neuropathy
orthostatic hypotension
oxygen therapy
pain
pain, abdominal
pain, foot
pain, total body
papilledema
paralysis
paralysis, recurrent
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paresthesias
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, tremor, absence of
Parkinsonism syndrome
PAS positive material in the brain
pathology
patient information and support
pediatric neurology
percussion induced muscle contraction
peroxisomal disease
persistent vegetative state
personality change
pes cavus
phenylketonuria
pleocytosis of cerebrospinal fluid
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, critically ill
polyneuropathy, critically ill, children
polyradiculoneuropathy
Pompe's disease of glycogen storage
pons, atrophy
pons, lesion of
posterior column disease
posterior leukoencephalopathy syndrome
posterior longitudinal ligament, ossification of
precipitating factors
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive multifocal leucoencephalopathy
progressive myoclonic epilepsy
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychotic behavior
ptosis
pupil, abnormality in neurologic disorders
pupil, dilated, bilateral
pupil, dilated, episodic
pupil, tonic
pyramidal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
raccoon
radiation therapy, CNS treatment and complications with
ragged-red fibers
rapidly progressing neurologic illness
rash
reading disorder, acquired
recurrent
release phenomena
remternetug
respirator
respiratory failure
respiratory tract infection
retina, abnormal
retinal artery occlusion
retinal branch artery occlusion
retinal infarction
retinal lesion
retinal microvascular disease
retinopathy
retrovirus
reversible neurologic disorder
review article
rhabdomyolysis
rigidity
riluzole
risk factors
rituximab
Rosenthal fibers
roundworm
rubeola virus
saccadic eye movements, abnormal
sarcoidosis
sarcoidosis, CNS
Schilder's disease
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
sensorineural hearing loss
sensory loss
septicemia
serologic testing
serologic testing, false negative
sicca syndrome
sickle cell disease
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skew deviation
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
slit lamp examination
slow virus infection of CNS
small vessel disease
small-bowel resection
SMN1 gene
somatosensory evoked potentials
somnolence
spasticity
speech disorder, childhood
spinal cord
spinal cord degeneration
spinal cord, cervical
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinal stenosis
spinal stenosis, cervical canal
splenium of corpus callosum
spondylosis
spongy degeneration of brain
spontaneous remission
staggering
standing difficulty
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
stimulant drugs
striatal encephalitis
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
subdural hematoma
suicide
superior sagittal sinus thrombosis
sural nerve
survival motor neuron gene
Susac's syndrome
sweating
symmetric brain lesions
systemic illness
tandem gait, ataxic
Tay-Sachs disease
teeth, abnormal
teeth, number of in infants
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
teratoma
teratoma, ovarian
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thymoma
tinnitus
titubation
toe walking
tone, muscle, increased
tongue, atrophy
tongue, biting
tongue, enlarged
tongue, fasciculations of
tongue, weakness
tonic cerebellar fits
toxic encephalopathy
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, jaw
tremor, resting
tremulousness
trichopoliodystrophy
trigeminal neuralgia
trinucleotide repeats
tripping
unconsciousness
unconsciousness, transient
urinary incontinence
urine test for metabolic disorders
urine test in toxic screen
vasculitides
vasculopathy
vein of Galen
vertebral infarction
vertigo
very long chain fatty acids
vibratory sensation, abnormal
viral infection
viral infection, CNS
virus, slow
vision, blurred
visual acuity, decreased
visual loss
visual tracking
visuospatial disturbance
vitamin D
vitamin deficiency
vitamin E deficiency
Waldenstrom's macroglobulinemia
Walker-Warburg syndrome
walking, delayed
walking, difficulty with
weakness
weakness, acute
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
weight loss
wheelchair
Whipple's disease
white matter disease
white matter disease, periventricular
white matter disease, subcortical
wide based gait
winging of scapula
word-finding difficulty
workup
writing
xerophthalmia
xerostomia
X-linked neuropathy
Showing articles 0 to 50 of 3363 Next >>

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Severe Amyloid-Related Imaging Abnormalities After Anti-B-Amyloid Monoclonal Antibody Treatment
Neurol 101:1079-1080, Bonami,S.,et al, 2023

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

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

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

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
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Young Adult with Dysphagia and Severe Weight Loss
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Antibody-Mediated Encephalitis
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Fulminant Encephalopathy with Unusual Brain Imaging in Disulfiram Toxicity
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A 42-year-old man with unilateral leg weakness
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A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

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

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

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

A Case of Fulminant Encephalopathy in a 69-year-old Woman
Neurol 89:e109-e114, Lamotte, G. and Williams, C, 2017

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

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

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

DARS-Associated Leukoencephalopathy can Mimic a Steroid-Responsive Neuroinflammatory Disorder
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Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Adult Polyglycosan Body Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1081, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Cocaine
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Neuroimaging and Clinical Features in Type II (late-onset) Alexander Disease
Neurol 82:49-56, Graff-Radford, J.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Griscelli Syndrome and CNS Lymphohistiocytosis
Neurol 82:e122-e123, Saini, A.G.,et al, 2014

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

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

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 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

Primary Sjogren Syndrome
BMJ 344:e3821, Ramos-Casals, M.,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

Clinicopathologic Conference, Susacs Syndrome (retinocochleocerebral vasculopathy)
NEJM 365:549-559, Case 24-2011, 2011

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

3-Methylglutaconic Aciduria Type I Redefined: A Syndrome With Late-Onset Leukoencephalopathy
Neurol 75:1079-1083, Wortmann,S.B.,et al, 2010

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

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

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

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

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

Carbon Monoxide Poisoning
NEJM 360:1217-1225, Weaver,L.K., 2009

A 54-Year-Old Woman with Progressive Gait Disturbance and MRI Abnormalities
Neurol 73:466-474, Hochberg,F.H.,et al, 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

Diagnosis and Management of Motor Neurone Disease
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Spinal Muscular Atrophy
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