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Differential
(Click to cross reference)
abdominal distention
abducens nerve paralysis
acanthocytosis
acoustic nerve
acoustic nerve, vestibular division of
acral sensory symptoms
Addison's disease
Adies pupil
adrenal biopsy
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcohol
alcohol intolerance
alcohol intoxication
alcohol, blood level of
alcohol, neurologic complications with
alcoholic blackout
alcoholic coma
alcoholic dementia
alcoholic polyneuropathy
alcoholic withdrawal states, DT's, convulsions, etc.
alcoholism
algorithm
alkylating agents
alpha-fetoprotein
altered states of consciousness
alternating rapid movement
aminoacidopathies
amitriptyline
amnesia
amyloid
amyloid angiopathy, cerebral
amyloidosis
amyloidosis, oculoleptomeningeal, familial
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anemia
ankle reflex, absent
anosmia
anterior interosseous neuropathy
anterior tibial muscle weakness
antimetabolite
aphasia
apraxia of eye movements
areflexia
arm atrophy
arm weakness
Arnold Chiari malformation
arrhythmia, cardiac
arteritis, temporal
arthralgia
arthrogryposis multiplex
arthropathy
arthropathy, neuropathic
arylsulfatase A
asparginase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxin
ataxin-2
atherosclerosis, premature
atonic bladder
auditory evoked brainstem potentials
automatic implantable cardioverter-defibrillator
autonomic dysfunction
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
azospermia
B 12 deficiency
Babinski sign
bacterial infection
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
Bassen-Kornzweig syndrome
behavioral disorder
benign essential tremor
bicaudate index
biologic markers
blacks
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial neuritis, prognosis of
brachial plexus
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brainstem
brainstem, dysfunction
brainstem, lesion of
Brown-Vialetto-Van Laere syndrome
burning feet
burning paresthesia
cachexia
CAG repeats
calcification, intracranial
caloric testing
carcinoembryonic antigen
carcinoma
cardiomyopathy
carotid angiogram
carpal tunnel syndrome
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, metrizamide
CAT scan, myelogram with
cataracts
cataracts, congenital
cauda equina
cauda equina, enhancement
cauda equina, lesion of
caudate nucleus
caudate nucleus, atrophy
cavernous sinus
cavernous sinus, lesion of
central core disease
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral edema
cerebral infarction, subcortical
cerebral palsy
cerebritis
cerebro hepato renal syndrome
cerebrospinal fluid, abnormal
cerebrospinal fluid, culture of, viral
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, pressure low
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
children
choking
cholestanol
cholesterol
cholesterol, HDL
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 16
chromosome 17
chromosome 22
chromosome 9
chronic progressive external ophthalmoplegia
cirrhosis
cirrhosis, infancy
claudication, intermittent of cauda equina
cleft palate
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
cold temperature
coloboma
coma
compression neuropathy
compression neuropathy, recurrent
conduction block
congestive heart failure
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corneal dystrophy
corpus callosum, lesion of
corpus callosum, thinning
cough
cranial nerve enhancement
cranial nerve enlargement
cranial nerve palsies
cranial nerve palsies, familial
cranial nerve tumor
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
crying
Cuba
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
deep tendon reflexes
degenerative diseases of CNS
Dejerine-Sottas syndrome
dementia
dementia, childhood
dementia, rapidly progressive
demyelinating disease
denervation of muscle
dermatitis
dermatomyositis
developmental milestones, loss of
diabetes mellitus
diarrhea
differential diagnosis
diplegia, brachial
diplopia
diplopia, transient
disability, neurological
dissociated sensory loss
distal muscle atrophy
distal muscle weakness
DNA probes
dopamine agonist
drooling
drug abuse, inhalation
drug induced neurologic disorders
dysarthria
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dyspnea
dyspraxia
dystonia
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, inflammatory disease
electromyogram
electron microscopy
electronystagmography
electroretinograph
emergencies, neurologic
Emery-Dreifuss muscular dystrophy
encephalopathy
endarterectomy, carotid
enophthalmous
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
ependymoma
epidemiology of neurology
episodic neurologic deficits
equinovarus
erythromelalgia
evoked potentials
exercise intolerance
exome sequencing
extraocular muscle lesion
eye movement, disorders of
Fabry's disease
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve palsy, familial
facial nerve palsy, recurrent
facial pain
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
family planning
fasciculation
fatigue
fatty acid, elevated plasma content
Fazio-Londe's disease
fetal alcohol syndrome
fever
fibrillations
fine motor function, impaired
finger nose finger test
fluorouracil
flush syndrome
foot deformity
foot drop
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
frataxin
Friedreich's ataxia
frontal lobe, pathologic signs of
fundus, abnormality of
F-wave response
gadolinium
gait disorder
gait, spastic
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gender
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
giant axonal neuropathy
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucose tolerance test, abnormal
granulomatosis with polyangiitis
granulomatous disease
growth retardation
Guillain Barre syndrome
hair analysis
Hallervorden Spatz disease
hallucination
hammertoes
hand deformity
hand numbness
hand weakness
handwriting
head injury
head lag
headache
hearing loss
hearing problems in children
heart block
heavy metal intoxication
heel-knee-shin test
hemianopia
hemiparesis
hemiparesis, transient
hemiplegia
hemochromatosis
hemochromatosis, primary
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatic encephalopathy
hepatic failure
hepatitis C virus
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
Hicks disease
high arched feet
hoarseness
Horner's syndrome
H-reflex testing
human genome
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hyperinsulinism
hyperostosis
hyperostosis cranialis interna
hyperreflexia
hypertonia
hypertriglyceridemia
hypofibrinogenemia
hypoglossal nerve paralysis
hypogonadism
hyponatremia
hyporeflexia
hyposmia
hypotelorism
hypotonia
idiopathic polyneuropathy
ileus, paralytic
imbalance
imbalance, postural
immunodeficiency
immunologic disease
immunosuppression
impotence
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
incoordination
infection
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracranial pressure, increased
intrinsic hand muscles, wasting of
iron, brain
irritability
Isaacs syndrome
isoniazid
jaw pain
Jewish
Kearns-Sayre syndrome
keratitis
klippel feil syndrome
Korsakoff's psychosis
Krabbe's disease
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lacunar infarction
laminectomy, cervical
laminectomy, lumbar
laminopathies
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's congenital amaurosis
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
leprosy
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
leukopenia
Lhermitte's sign
light-near dissociation, causes of
lip, biting
lipid storage disorder of CNS
lipomatosis
lipomatosis, multiple symmetrical
liver disease
liver transplantation
LMNA gene
long thoracic nerve
lumbosacral plexopathy
lumbosacral plexus
lymphadenopathy
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
macular degeneration
magnetic stimulation
magnetic stimulation, brain
Marinesco-Sjogren syndrome
masked facies
McLeod syndrome
median neuropathy
MELAS syndrome
memory, impairment of
meningioma
meningismus
meningoencephalopathy
mental retardation
MERRF syndrome
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
methotrexate
methylhydrazine derivatives
microcephaly
microhemorrhage, intracerebral
midbrain, atrophy
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoamine oxidase inhibitors
mononeuropathy
mononeuropathy multiplex
mononeuropathy, children
mononeuropathy, recurrent
monoparesis
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, brachial plexus
MRI, contrast enhanced
MRI, cranial nerves
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, functional
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple system atrophy
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle culture
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle tenderness
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myelin protein zero gene
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloradiculopathy
myoclonus
myokymia
myopathy
myopathy, alcoholic
myopathy, carcinomatous
myopathy, distal
myopathy, distal, Welander's
myopathy, mitochondrial
myopathy, thyroid disease causing
myopia
myositis
myotonia dystrophica
nausea and vomiting
neck pain
neoplasm, peripheral nerve
neoplasm, primary of CNS
nerve biopsy
nerve biopsy, indication
nerve conduction studies
nerve conduction studies, motor
nerve conduction studies, sensory
nerve culture
nerve growth factor
nerve growth stimulating activity
nerve hypertrophy
nerve root enhancement
nerve root hypertrophy
neuraminidase deficiency
neuritis, causes of
neuroblastoma
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurogenic bladder
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromyotonia
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronopathy
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, classification of
neuropathy, demyelinating
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor
neuropathy, onion bulb
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, recurrent
neuropathy, sensory
neuropathy, sensory, hereditary
neuropathy, vasculitic, systemic
neuropathy, work up for
neurotoxin
neurotrophin-3
neutropenia
next-generation sequencing
night blindness
nitrogen mustard
nitrous oxide
NOTCH2NLC
numbness, extremity
nutritional deficiency
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, vertical
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic atrophy
optic atrophy, hereditary
optic nerve
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
optical coherence tomography
orthostatic hypotension
orthostatic hypotension, idiopathic
osteosclerosis, autosomal dominant
pacemaker, cardiac-transvenous
pain
pain, abdominal
pain, arm
pain, foot
pain, severe
pain, wrist
pancytopenia
papilledema
paralysis
paralysis, recurrent
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
paresthesias
paresthesias, feet
paresthesias, lower extremity
Parkinson disease
Parkinson disease, classification
Parkinson disease, etiology of
Parkinson disease, heterogeneity of
Parkinson disease, pathogenesis of
Parkinson disease, subtypes
Parkinsonism syndrome
past pointing
pathology
patient information and support
peroneal muscle atrophy, causes of
peroneal nerve
peroneal nerve, lesion of
peroxisomal disease
pes cavus
pheochromocytoma
phlebotomy
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pneumonia
poison, mercury
poison, neurologic problems with
POLG1 gene
poliomyelitis
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
pons, lesion of
porphyria
positional head-hanging test
positive sharp waves
post polio syndrome
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prisoners of war, neurologic complications in
procarbazine
progeria
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
puerperium
pulmonary function tests
pulmonary infiltrates
pupil
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, scalloped
pyramidal
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
quality of life
radial nerve, palsy of
radiation hypersensitivity
radiculopathy
ragged-red fibers
rash
reading disorder, acquired
recombinant DNA
recruitment
recruitment, reduced
recurrent
recurrent laryngeal nerve paralysis
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
renal tubular acidosis
respiratory depression
respiratory failure
restless leg syndrome
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retrovirus
reversible neurologic disorder
review article
RFLPs
riboflavin transporter deficiency
rigidity
Riley-Day syndrome
risk factors
Romberg's sign
root lesion, nerve
Roussy Levy syndrome
saccadic eye movements, abnormal
sarcoidosis
schwannoma
scoliosis
screening
seizure
self-mutilation
sensorineural hearing loss
sensory ganglia
sensory ganglia, abnormal
sensory loss
sensory loss, truncal
sensory nerve action potentials
sensory polyneuropathy
serratus anterior muscle, weakness
short stature
shoulder, numbness
shoulder, pain in
Shy-Drager syndrome
single photon emission computed tomography
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep
small vessel disease
somatosensory evoked potentials
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinal cord, pathologic exam of
spinal muscular atrophy
spinal stenosis
spinal stenosis, familial
spinocerebellar ataxia
spinocerebellar ataxia type 2
spinocerebellar ataxia type 7
spinocerebellar degeneration
splenium of corpus callosum
splenomegaly
spontaneous muscle activity
spontaneous remission
steppage gait
steroid therapy, CNS treatment and complications with
stiff man syndrome
striatum, lesion of
strokelike episodes
subarachnoid hemorrhage
subdural hematoma
substantia nigra
sudden death
suprascapular neuropathy
sural nerve
symmetric brain lesions
syncope
systemic illness
tandem gait, ataxic
Tangier's disease
tapetoretinal degeneration
tauopathy
telangiectases
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thrombocytopenia
thyrotoxicosis
tic
tinnitus
titubation
toe walking
tomaculous neuropathy
tongue, biting
tongue, enlarged
tonic spasms
torticollis
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, orthostatic
tremor, physiologic
tremor, post traumatic
tremor, postural
tremor, psychogenic
tremor, resting
tremor, treatment of
tremor, voice
tremor, writing
trichopoliodystrophy
tricresylphosphate
trigeminal nerve
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
tyrosine
tyrosinemia
ulnar neuropathy
ultrasonography, nerve
upgaze, paralysis of
urinary incontinence
Usher's syndrome
vertigo
vestibular function, tests of
vestibulopathy
vibratory sensation, abnormal
vinblastine
vincristine neurotoxicity
viral infection
viral infection, CNS
viral isolation
visceral neuropathy
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
visual loss, congenital
vitamin deficiency
vitamin E
vitamin E deficiency
vitreous opacities
vocal cord paralysis
voice, abnormality of
Von Hippel Lindau
walking frame
walking, difficulty with
war
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Werdnig-Hoffman disease
Werner's syndrome
Wernicke's encephalopathy
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
winging of scapula
wrist drop
xeroderma pigmentosa
X-linked neuropathy
x-ray, spine
Showing articles 0 to 50 of 5139 Next >>

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

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

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

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

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

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

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

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

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

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

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

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

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

Neuronal Intranuclear Inclusion Disease Cases with Leukoencephalopathy Diagnosed via Skin Biopsy
JNNP 85:354-356, Sone, J.,et al, 2014

Chronic and Slowly Progressive Weakness of the Legs and Hands
BMJ 348:g459, Nightingale, H.,et al, 2014

Parkinson Disease Subtypes
JAMA 71:499-504, Thenganatt, M. & Jankovic, J., 2014

Inherited Metabolic Diseases of the Nervous System, Globoid Cell Leukodystrophy (Krabbe Disease, Galactocerebrosidase)
Adams & Victors Principles of Neurology, Chp 37, pg 959, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Fabry Disease
Adams & Victors Principles of Neurology, Chp 37, pg 991, Ropper, A.H.,et al, 2014

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

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

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

Clinical Reasoning: A 34-Year-Old Woman with Recurrent Bouts of Acral Paresthesias
Neurol 74:775-778, Karam,C. &Scelsa,S., 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Neurofibromatosis Type 2
Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

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

Fragile X-Associated Tremor/Ataxia Syndrome: An Aging Face of the Fragile X Gene
Arch Neurol 65:19-25, Amiri,K.,et al, 2008

Clinicopath Conf, Charcot-Marie-Tooth Disease Type 2, with Aides Pupil and a Mutation in MPZ Gene
NEJM 354:2584-2592, Case 18-2006, 2006

Finding the Causes of Inherited Neuropathies
Arch Neurol 63:812-816, Scherer,S.S., 2006

CNS Involvement in Hereditary Neuropathy With Pressure Palsies (HNPP)
Neurol 67:2250-2252, Tackenberg,B.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

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

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
Neurol 65:681-689, 662, Sahenk,Z.,et al, 2005

Quality of Life in Patients with Charcot-Marie-Tooth Disease
Neurol 65:922-924, Vinci,P.,et al, 2005

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Hypoglossal Neuropathy in Hereditary Neuropathy with Liability to Pressure Palsy
Neurol 61:1154-1155, Winter,W.C. &Juel,V.C., 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Hereditary Neuropathy With Liability to Pressure Palsies Mimicking Hypoglossal Nerve Injuries
Neurol 61:1457-1458, Corwin,H.M. &Girardet,R.E., 2003



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