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Differential
(Click to cross reference)
abscess, intracerebral
acetazolamide
aciduria
acoustic nerve, vestibular division of
acoustic neurinoma
acquired immunodeficiency syndrome
acromicria
Adies pupil
adrenal mass
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
agitation
Alexanders disease
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, pathogenesis
Alzheimer's disease, risk factors in
Alzheimer's disease, treatment of
amimia
amniocentesis
amyloid
amyloid beta protein
amyloid plaques
amyotrophic lateral sclerosis
anaplastic large cell lymphoma
anchor bias
anemia
anemia, hemolytic
anesthesia, general
aneurysm
aneurysm, intracranial, screening for
Angelman syndrome
angiofibroma, facial
angiomyolipomas
animal exposure
ankle edema
anterior horn cell disease
anterior tibial muscle weakness
antibiotic prophylaxis
antibiotics
antibodies to voltage-gated calcium channels
anticonvulsants
anticonvulsants, selection of
antiviral agents
apolipoprotein E
APP
APP gene
arbovirus
areflexia
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
arteriovenous malformation, cerebral
arthralgia
arthritis
arthrogryposis multiplex
ascites
ash leaf spots
aspartocyclase
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
ATP1A3 gene
atrioventricular block
attention deficit disorder with hyperactivity
autism
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
automatic implantable cardioverter-defibrillator
autonomic dysfunction
azidodeoxythymidine
Babinski sign
bacterial infection
bacterial infection, CNS
baldness
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
beta-D-glucon
bias
biologic markers
biotinidase deficiency
bitemporal visual field defect
bladder dysfunction
blindness
brachial neuritis
brachial plexus
brachial plexus neuropathy
brachial plexus neuropathy, familial
bradycardia
brain biopsy
brain biopsy, negative
brainstem, atrophy
brainstem, lesion of
Brazil
bronchoscopy
bruising
bulbar palsy
burning paresthesia
cachexia
cafe au lait spots
CAG repeats
calcification, intracranial
calf hypertrophy
Canavan's disease
candida albicans
carbamazepine
carcinoma
carcinoma of pancreas
cardiomegaly
cardiomyopathy
caribbean
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, chest
CAT scan, false negative
CAT scan, muscle
cataracts
cavernous hemangioma
CD30
Central America
central core disease
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar lesion
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral edema, origin and treatment
cerebral edema, vasogenic
cerebral embolism
cerebral palsy
cerebral palsy, etiology
cerebral palsy, work up
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, beta-D-glucan
cerebrospinal fluid, biochemical markers of CNS tumors
cerebrospinal fluid, childhood
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, silent
cerebrovascular accident, young adult
cerebrovascular disease
ceruloplasmin, serum
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
cherry red spot-myoclonus syndrome
chest x-ray, abnormal
chewing, impaired
children
chloride channel dysfunction
cholecystitis
chorea
choreoathetosis
chromosomal abnormality
chromosome 1
chromosome 11
chromosome 12
chromosome 14
chromosome 15
chromosome 16
chromosome 17
chromosome 19
chromosome 21
chromosome 22
chromosome 3
chromosome 5
chromosome 9
chronic progressive external ophthalmoplegia
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clinical trials
clonus
clubbing of fingers
clubfoot as related to neurologic disease
cobalamin C deficiency
cognition
collagen vascular disease
coma
complications
compression neuropathy
compression neuropathy, recurrent
conduction block
confidentiality
confusion
congenital malformation
congenital myasthenic syndromes
congenital myopathy
congenital myopathy, inflammatory
congestive heart failure
conjunctival biopsy
conjunctivitis
consanguinity
contractures, joint
controversies in neurology
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cranial nerve enhancement
cranial nerve tumor
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cry, abnormal
cry, weak
cultured skin fibroblasts
deafness
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental abnormality of brain
developmental disability
developmental evaluation
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
dichlorphenamide
diet
differential diagnosis
difficulty going down stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
diurnal variation
DNA probes
DNA sequencing
dopa responsive dystonia
dopaminergic dysfunction
double-cortex syndrome
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, etiology of
dystonia, painful
dystroglycanopathies
dystrophin
dystrophin associated proteins
eating disorder
edema, pedal
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, inflammatory disease
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, diagnosis of
encephalitis, viral
encephalitis, viral-causes of
encephalopathy
encephalopathy, progressive
endolymphatic sac tumors
endovascular therapy
enzyme, defect
eosinophilia
ependymoma
epidemic
epidemiology of neurology
epistaxis
esophageal varices
ethambutol
ethics in neurology
evoked potentials
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
falling
false negative
familial
fatal familial insomnia
fatigue
feeding disorder
fever
fibrillations
fibroma, ungual
fine motor function, impaired
fingerprint bodies
fish
fistula, arterio-venous, pulmonary
flavivirus
floppy infant
foot deformity
foot drop
foot drop, bilateral
fourth ventricle, compression
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
fungal infection
fungal infection, CNS
gadolinium
gait disorder
gait, spastic
gait, waddling
GAMT gene
gangliosidosis GM1
gangliosidosis GM2
gastrointestinal bleeding
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
giant axonal neuropathy
glioblastoma multiforme(astrocytoma Gr.III)
glioma
glioma, low-grade
gliomatosis cerebri
globus pallidus, lesion of, bilateral
glucocerebrosidase
GLUT1 deficiency syndrome
glycogen storage disease
gram positive cocci
grimacing
growth hormone deficiency
growth retardation
Guillain Barre syndrome
gyrus, abnormal
hamartin
hamartoma
hammertoes
hand deformity
hand flapping
hand weakness
head lag
headache
headache, awakening with
headache, positional
headache, progressive
hearing loss
heart block
heart block, complete
heart murmur
helminthic infection of CNS
hemangioblastoma
hemiparesis, transient
hemoglobin abnormality, neurologic complications of
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
herniation syndromes, intracranial
herpes virus
heterotopia
hexosaminidase-A
high arched feet
high arched palate
histochemistry of muscle
history of neurology
human genome
human herpesvirus 6
huntingtin
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperactivity
hypercapnia
hyperhomocysteinemia
hyperkalemic periodic paralysis
hyperphagia
hyperreflexia
hypoalbuminemia
hypoglycorrhachia
hypogonadism
hypogonadism, hypogonadotropic
hypokalemic periodic paralysis
hypopigmentation of skin
hyporeflexia
hypotelorism
hypotonia
hypotonia, causes of
hypotonia, infants
imbalance
immunodeficiency
immunohistochemistry
immunosuppressive agents
in situ hybridization
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
inclusion body myositis
incoordination
India
infantile spasm
infection
intellectual deficit
intellectual deterioration
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial pressure, increased
intranasal medication
intrauterine infection
intrauterine infection, viral
intravenous drug abuse
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
Jewish
joint hypermobility
karyotyping
Kayser-Fleischer ring
Kearns-Sayre syndrome
Krabbe's disease
kuru
lactic acidemia
Lafora's disease
laminopathies
L-dopa
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg spasms
leg spasms, painful
leg weakness, bilateral
Legius syndrome
Leigh's disease
leptospirosis
Lesch-Nyhan syndrome
leukocytes
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
life expectancy
linear lesion
lissencephaly
liver disease
liver function enzymes
LMNA gene
lordosis
lung nodule
lung-brain syndromes
lymphadenopathy
lymphangiomyomatosis
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, screening for
malignant hyperpyrexia
marche a petits pas
McArdle's disease
medulloblastoma
megalencephaly
MELAS syndrome
memory, impairment of
meningeal enhancement
meningeal sarcomatosis
meningioma
meningitis
meningitis, basilar
meningitis, candida
meningitis, chronic
meningitis, fungal
meningitis, leptospira
meningitis, neutrophilic
meningoencephalitis
mental retardation
mental status, abnormal
merlin
MERRF syndrome
mestinon
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
methylmalonic acidemia
mexiletine
microcephaly
micrognathia
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
Miller-Dieker syndrome
mimics
mineralization
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
molecular genetics
molecular markers
mononeuropathy
mononeuropathy, recurrent
mortality
mosquito
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, angiography
MRI, blooming effect
MRI, contrast enhanced
MRI, diffusion weighted
MRI, fetal
MRI, mass effect on
MRI, muscle
MRI, negative
MRI, nodular enhancement
MRI, serial
MRI, spinal cord
MRI, spine
MRI, target sign
multiple sclerosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle phosphorylase deficiency
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelin protein zero gene
myelitis, longitudinal
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, distal Laing
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, mitochondrial
myopathy, proximal
myopathy, vacuolar
myostatin
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
nasal bridge, wide
nasal speech
nausea and vomiting
neck weakness
needle tracks
negative
nemaline rod myopathy
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, peripheral nerve
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplasm, primary of CNS-classification
neoplasm, primary of CNS-surgical treatment of
neoplasm, primary of CNS-survival
neoplasm, primary of CNS-treatment of
nephritis
nerve biopsy
nerve biopsy, indication
nerve conduction studies
nerve hypertrophy
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic practice
neurologic signs
neurologic testing
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal intranuclear inclusion disease
neuronal migration disorder
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
neuropathy, recurrent
neuropathy, work up for
neurotomy
newborn, evaluation of
next-generation sequencing
NF1 gene
night blindness
normal
NOTCH2NLC
numbness, extremity
nystagmus
obesity
obsessive-compulsive disorder
ocular motility, disorders of
oculogyric crisis
oculopharyngeal muscular dystrophy
oligodendroglioma
omphalocele
opened mouth
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
orthostatic hypotension
ovarian dysgenesis
overlap syndrome
owl's eye sign of spinal cord
pacemaker, cardiac-transvenous
pachygyria
pain
pancytopenia
papilledema
paragonimiasis
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegin
parasitic infection, CNS
paresthesias
Parkinson disease
Parkinson disease, etiology of
Parkinson disease, familial
Parkinson disease, pathogenesis of
Parkinson disease, treatment of
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
patient information and support
penicillamine
percussion induced muscle contraction
periodic paralysis
Perrault syndrome
personality change
pes cavus
phakomatoses
pheochromocytoma
phonophobia
photophobia
PICU
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pleural effusion
POLG1 gene
polyglucosan body disease
polymerase chain reaction
polymicrogyria
polyneuropathy, familial
pons, lesion of
positive sharp waves
posterior fossa, lesion of
postural abnormality
potassium channel dysfunction
practice guidelines
Prader-Labhart-Willi syndrome
precipitating factors
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prevention of neurologic disorders
prion disease
PRKN gene
progeria
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
Puerto Rico
pulmonary embolism
pupil
pupil, dilated and fixed, bilateral
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriplegia
quality of life
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
ragged-red fibers
rapidly fatal neurologic illness
rash
recombinant DNA
recurrent
renal cell carcinoma
renal cyst
renal stones
respirator
respiratory failure
respiratory tract infection
retina, abnormal
retinal hamartoma
retinal hemangioma
retinal lesion
retinitis pigmentosa
retinopathy
Rett's syndrome
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
rhabdomyoma, cardiac
rhabdomyosarcoma of heart
rigidity
risk factors
Romberg's sign
root lesion, nerve
Rosenthal fibers
saccadic eye movements, abnormal
salivation, excessive
sarcoglycan
schwannoma
scissors gait
scoliosis
scotoma
scotoma, central
screening
seizure
seizure, focal
seizure, paradoxical
seizure, treatment of
senile plaques
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
shagreen patch
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
sickle cell disease
sinemet
skin, biopsy
skin, darkening of
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
slit lamp examination
SMN1 gene
sodium channel dysfunction
South America
spartin
spastic ataxia
spastic paraplegia, type 7
spasticity
spastin
speech disorder
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinal cord, vascular malformation of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar degeneration
spirochete infection
splenomegaly
spongy degeneration of brain
SPRED1 mutation
squirrels
staggering
status epilepticus
steppage gait
steroid
strabismus
striatal encephalitis
strokelike episodes
subarachnoid hemorrhage
subependymal nodules
substantia nigra
suck, poor
sudden death
survival motor neuron gene
symmetric brain lesions
syncope
systemic illness
T cell lymphoma
tandem gait, ataxic
Tay-Sachs disease
telangiectases
temozolomide
temper tantrums
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thalamus, lesion of
thalamus, lesion of-bilateral
thalassemia
thalassemia/mental retardation syndrome
thiazide diuretic
thrombocytopenia
tinnitus
toe walking
tomaculous neuropathy
tongue, protrusion of
trauma
travel, foreign
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremulousness
trichopoliodystrophy
trientine dihydrochloride
trinucleotide repeats
tripping
trisomes
tuber, cortical
tuberin
tuberous sclerosis
tuberous sclerosis, screening for
twins
ultrasonography, head
ultrasonography, head, fetus-neonate
undiagnosed
Unverricht-Lundborg disease
upgaze, paralysis of
urinary catecholamines
urinary urgency
urine test for metabolic disorders
uveitis
vasculitides
vasculopathy
vegetarianism
viral infection
viral infection, CNS
vision loss, sequential
vision, blurred
vision, failure of in childhood
visual acuity, decreased
visual evoked response
visual field defect
visual impairment
visual loss
visual loss, progressive
visual loss, slow
visual loss, transient
visual obscurations, transient
vitamin E deficiency
Von Hippel Lindau
Von Hippel Lindau, carrier
Von Hippel Lindau, screening protocol for
walking, delayed
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
West disease
Western immunoblot test
wheelchair
Whipple's disease
white freckles
white matter disease
wide based gait
winging of scapula
Wood's light
workup
wound healing, poor
X-linked bulbospinal neuronopathy
x-linked intellectual deficit
x-linked mental retardation
Zika virus infection
zinc
Showing articles 650 to 700 of 1733 << Previous Next >>

Practice Parameter:Diagnostic Assessment of the Child with Cerebral Palsy
Neurol 62:851-863, Ashwal,S.,et al, 2004

Developmental Dyslexia
Lancet 363:1451-60, Demonet,J-F.,et al, 2004

Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004

Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
JNNP 75:1463-1466, Jin,K.,et al, 2004

CADASIL: Cerebral Autosomal Subcortical Infarcts and Leukoecephalopathy
, Chabriat, H., Joutel A., Vahedi, K., Tournier-Lasserve, &E., Bousser M.G., 2004

Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
Arch Neurol 61:106-113, Guis,S.,et al, 2004

Hyperhomocysteinemia in Cerebral Vein Thrombosis
Blood 102:1363-1366, Martinelli,I.,et al, 2003

Repeated Screening for Intracranial Aneurysms in Familial Subarachnoid Hemorrhage
Stroke 34:2788-2791, Wermer,M.J.H.,et al, 2003

Anticoagulation or Inferior Vena Cava Filter Placement for Patients with Primary Intracerebral Hemorrhage Developing Venous Thromboembolism?
Stroke 34:2999-3005, Kelly,J.,et al, 2003

The Clinicopathological Spectrum of Rosenthal Fibre Encephalopathy and Alexanders Disease: A Case Report and Review of the Literature
JNNP 74:807-810, Jacob,J.,et al, 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
Neurol 60:57-63,8, Vahedi,K.,et al, 2003

Treatment of Sporadic Hemiplegic Migraine with Calcium-Channel Blocker Verapamil
Neurol 60:120-121, Yu,W. &Horowitz,S.H., 2003

Primary Brain Tumours in Adults
Lancet 361:323-331, Behin,A.,et al, 2003

Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints
BMJ 326:331-333, Tassicker,R.,et al, 2003

Learning Disability
Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003

Clinical Features and Neuropathology of Autosomal Dominant Spinocerebellar Ataxia (SCA17)
Ann Neurol 43:367-375, Rolfs,A.,et al, 2003

Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003

Identification of New Presenilin Gene Mutations in Early-Onset Familial Alzheimer Disease
Arch Neurol 60:1541-1544,1521, Tedde,A.,et al, 2003

Kennedy Disease
Arch Neurol 60:893-894, Paparounas,K.,et al, 2003

Autosomal Dominant Acute Necrotizing Encephalopathy
Neurol 61:226-230, Neilson,D.E.,et al, 2003

Mental Retardation
Neurol 61:156-157, Patterson,M.C. &Zoghbi,H.Y., 2003

Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope
BMJ 326:1078-1079, Plunkett,A.,et al, 2003

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Association of Multidrug Resistance in Epilepsy with a Polymorphism in the Drug-Transporter Gene ABCB1
NEJM 348:1442-1448,1480, Siddiqui,A.,et al, 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Practice Paramenter: Neuroimaging of the Neonate
Neurol 58:1726-1738, Ment,L.R.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Low-Molecular-Weight Heparins or Heparinoids Versus Standard Unfarctionated Heparin for Acute Ischemic Stroke (Cochrane Review)
Stroke 33:1925-1926, Counsell,C. &Sandercock,P., 2002

Anticoagulants and Antiplatelet Agents in Acute Ischemic Stroke
Neurol 59:13-22, Coull,B.M.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Expression of p53 and Prognosis in Children With Malignant Gliomas
NEJM 346:420-427, Pollack,I.F.,et al, 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Friedreich Ataxia
Arch Neurol 59:743-747, Lynch,D.R.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

New Strategy for Prenatal Diagnosis of X-Linked Disorders
NEJM 346:1502, Costa,J.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002



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