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Differential
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abortion, spontaneous
absence
acanthocytosis
acetazolamide
acetylcholine
acetylcholine receptor
acetylcholine receptor antibody
acetylcholinesterase
acetylcholinesterase deficiency
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
adolescent medicine
adoption
advances in neurology
adverse drug reaction
affective disorders
airway obstruction
alcohol
alcohol intolerance
algorithm
alopecia
alpha-fetoprotein
Alzheimer's disease
Alzheimer's disease, familial
amantadine
amnesia
amyloid angiopathy, cerebral
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
analgesic overuse
anemia
anesthesia, general
anesthesia, local
anterior horn cell disease
antibiotics
antibiotics, neurologic complications with
anticholinergic drugs
anticonvulsants, cognitive function with
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, effectiveness
anticonvulsants, untoward effects of
antimetabolite
anxiety
apomorphine
apraxia
apraxia of eyelid opening
areflexia
arm atrophy
arm weakness
arthralgia
arthritis
arthrogryposis multiplex
arylsulfatase A
aspartate aminotransferase
asthma
asthma, poliomyelitis-like syndrome with
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
athetosis
athetosis, causes of
atidarsagene autotemcel
atlanto axial dislocation, congenital
atypical lymphocytes
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
automobile accidents
autonomic dysfunction
axonal spheroid
azathioprine
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
bicaudate index
biologic markers
biopterin deficiency
biotin
biotin deficiency
biotin deficiency, juvenile form
biotin-responsive basal ganglia disease
blacks
body mass index
bone marrow transplantation
botulism
bradykinesia
brain atrophy
brain biopsy
brain transplantation
breast feeding
Brueghel's syndrome
bulbar palsy
bulbar palsy, acute
bulbar palsy, juvenile
bulbar palsy, progressive
CAG repeats
calf amyotrophy
calf atrophy
captopril
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
cavernous sinus, syndrome
central nervous system, infection of
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral blood flow
cerebral cortex
cerebral cortical atrophy
cerebral death
cerebral glucose metabolism
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gamma amino butyric acid
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, risk factors in
cervical collar
cesarean section
children
chorea
chorea, causes of
chorea, senile
chorea, treatment of
choreoathetosis
chromosomal abnormality
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
clonazepam
clozapine
clubbing of fingers
cognition
cogwheel rigidty
cold temperature
collagen vascular disease
comorbidities
complications
congenital birth defects
congenital infection, CNS
congenital malformation
congenital myasthenic syndromes
congenital paresis
conjunctivitis
consanguinity
controversies in neurology
corpus callosum, lesion of
cortical muscular atrophy
cough
crawl regression
cryopyrin-associated periodic syndrome
D-dimer
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delivery, complicated
dementia
dementia, childhood
dementia, frontotemporal
dementia, presenile
dementia, subcortical
dentatorubral-pallidoluysian atrophy
depression
dermatitis
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
donepezil
dopa responsive dystonia
dopamine
dopamine agonist
driving
driving test
dropped head syndrome
drug abuse
drug abuse, adolescent
drug addiction
drug induced neurologic disorders
drug overdose
dying
dysarthria
dyskinesia
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphasia
dysphonia
dyspnea
dystonia
dystonia musculorum deformens
dystonia, painful
dystonia, treatment of
edema, periorbital
efficacy
electrical sensation
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electromyogram, decremental response
electron microscopy
employment
empty sella
encephalitis
encephalitis, viral
encephalocele
encephalopathy
encephalopathy, neonatal
ephedrine
epidemiology of neurology
episodic neurologic deficits
Epstein-Barr virus
equinovarus
erythrocyte
ethics in neurology
evoked potentials
excitotoxin
exercise
exercise-induced neurologic dysfunction
extrapyramidal
extremity, cold
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fetal tissue
fetus
fever
fibrillations
flaccid paralysis
floppy infant
fluctuate
fragile-X syndrome
Friedreich's ataxia
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gammaglobulin therapy, intravenous
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
Gilles de la Tourette syndrome
glioma
glutamic acid
grimacing
gyrus, abnormal
Hallervorden Spatz disease
haloperidol
hand weakness
head injury
headache
headache, children
headache, chronic
headache, drug induced
headache, icepick
headache, severe
headache, treatment of
headache, unilateral
health insurance
hemangioma
hemiplegia
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus
hiccoughs
HLA
hoarseness
homovanillic acid
human parechovirus
huntingtin
Huntington's chorea
Huntington's chorea, age at onset
Huntington's chorea, akinetic-rigid form
Huntington's chorea, differential diagnosis
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
hydroxyindole acetic acid 5(5HIAA)
hyperhidrosis
hyperreflexia
hyperthyroidism
hyporeflexia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
imbalance
immunologic disease
immunosuppression
immunosuppressive agents
inclusion bodies, intranuclear
India
indomethacin
infantile tremor syndrome
infectious mononucleosis
infectious mononucleosis, neurologic findings with
intellectual deficit
intellectual deterioration
internet
intracranial hypertension, benign
intranasal medication
intrauterine infection
intrauterine infection, viral of CNS
intrinsic hand muscles, wasting of
irritability
isoniazid
Jakob-Creutzfeldt disease
juvenile distal and segmental muscular atrophy
juvenile idiopathic inflammatory myopathy
juvenile myoclonus epilepsy
juvenile paresis
keratoconjunctivitis
Kluver-Bucy syndrome
Kugelberg-Welander syndrome
labor, complicated
L-dopa
lecithin
leg atrophy
leg weakness, unilateral
leukocytosis
leukodystrophy
leukoencephalopathy
Lewy body disease, diffuse
Lhermitte's sign
lipoma of CNS
liver disease
liver function enzymes
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lymphocyte capping, diminished
lysosomal storage disease
magnesium sulfate
malaise
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
manic-depressive
Mary Walker phenomenon
masked facies
medical-legal aspects of neurology
memory, impairment of
meningitis, aseptic
meningitis, chronic
meningoencephalitis
mental retardation
mestinon
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
migraine
migraine, children
migraine, seizures in
migraine, treatment of
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monomelic amyotrophy
monoparesis
mortality
motor neuron disease
motor neuron disease, juvenile form
motor signs
movement disorder
movement disorder, extrapyramidal
movement disorder, extrapyramidal-treatment of
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, functional
MRI, muscle
MRI, serial
MRI, spinal cord
MRI, spine
MRI, sunburst pattern
MRI, volumetry
MRS
multiple sclerosis
multiple system atrophy
muscimol
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Duchenne
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, congenital
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, ocular
myasthenia gravis, passive transfer of
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, receptor site in
myasthenia gravis, remission of
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic crisis
myasthenic syndrome
mycophenolate
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy
myopathy inflammatory, classification
myopathy, inflammatory
myopathy, inflammatory, classification
myositis
myositis specific autoantibody
myositis, juvenile
myotonia dystrophica
nasal speech
nasal spray
neck flexion
neck weakness
neoplasm, intracranial
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neuroleptic
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic history
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuronal intranuclear inclusion disease
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
neurosyphilis
neurotoxin
neurotransmitter
newborn, evaluation of
next-generation sequencing
NMDA receptors
nursing home
obesity
obesity, childhood
old age, neurology of
ophthalmoplegia
ophthalmoplegia, painful
optic atrophy
optic atrophy, bilateral
pain
pain, elbow
palpebral erythema
pancytopenia
paraparesis, spastic
parechovirus encephalitis
paresthesias
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinson disease, drug induced
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, treatment of
Parkinsonism syndrome
peptides, brain
periodic paralysis
periodic paralysis, thyrotoxic
persistent vegetative state
personality change
personality disorder
pes cavus
photophobia
photosensitivity, skin
Pick's disease
piracetam
plasmapheresis
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
poliomyelitis-like illness
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
postpartum
postural abnormality
practice guidelines
preclinical
pregnancy, neurologic complications in
prevention of neurologic disorders
PRKN gene
procyclidine
prognosis
progressive neurologic disorder
progressive supranuclear palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, acute
ptosis
ptosis, bilateral
putamen, lesion of
putamen, lesion of, bilateral
quadriparesis
quality of life
rash
reaction time
recombinant DNA
remission
renal stones
repetitive nerve stimulation
respiratory depression
respiratory failure
reverse split hand sign
review article
RFLPs
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
rigidity
riluzole
risk factors
rituximab
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
running
saccadic eye movements
saccadic eye movements, abnormal
safety
Saudi Arabia
schizophrenia
screening
sedimentation rate, elevated
seizure
seizure, classification of
seizure, diagnosis of
seizure, differential diagnosis of
seizure, familial
seizure, focal
seizure, neonatal
seizure, paradoxical
seizure, prognosis in adults
seizure, stimulus sensitive
seizure, treatment of
septicemia
serologic testing
serologic testing, false negative
seronegative
serositis
serotonin
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sneeze
sodium valproate
somatostatin
sore throat
spasticity
speech disorder
speech disorder, childhood
spina bifida
spinal cord, cervical
spinal cord, compression of
spinal cord, enlargement
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenium of corpus callosum
splenomegaly
sports medicine, neurology of
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stiff joints
stillbirth
striatum, lesion of
striatum, lesion of, bilateral
stridor
stuttering
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
substance P
suicide
sumatriptan
sural nerve
symmetric brain lesions
syphilis, congenital
syphilis, neurologic complications with
systemic illness
systemic juvenile idiopathic arthritis
systemic lupus erythematosus
systemic lupus erythematosus, neonatal
systemic lupus erythematosus, neurologic complications with
tardive dyskinesia
tardive dyskinesia, treatment of
tardive dystonia
Tay-Sachs disease
temporal lobe, lesion
temporal lobe, lesion, bilateral
tensilon test, false negative
term infant
tetrabenazine
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
thymectomy
thymus and neuromuscular function
titubation
toe walking
Tolosa Hunt syndrome
tongue, atrophy
tongue, fasciculations of
tongue, weakness
tonic foot response
topiramate
torticollis
transplacental virus infections
trauma
treatment of neurologic disorder
tremor
tremor, postural
trigeminal autonomic cephalgia
trinucleotide repeats
varicella zoster virus
varicella zoster virus, encephalitis
viral infection
viral infection, CNS
viral isolation
visual evoked response
visual loss
visual loss, progressive
visuospatial disturbance
vocal cord paralysis
walking
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weaning from respirator, failure to
weight loss
West Nile fever
wheelchair
white matter disease
whites
workup
writers cramp
xerostomia
X-linked bulbospinal neuronopathy
Showing articles 50 to 100 of 237 << Previous Next >>

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

Predictors of Nursing Home Placement in Huntington Disease
Neurol 60:998-1001, Wheelock,V.L.,et al, 2003

Benign Calf Amyotrophy
Arch Neurol 60:1415-1420, Felice,K.J.,et al, 2003

Myasthenia Gravis
Neurol 61:1362-1366, Hoff,J.M.,et al, 2003

Intoxication with Riluzole in Huntington's Diease
Neurol 57:1141-1143, Bodner,Th.,et al, 2001

Family History and DNA Analysis in Patients With Suspected Huntington's Disease
JNNP 69:54-59, Siesling,S. et al, 2000

A Randomized, Double-Blind, Placebo-Controlled Study of Sumatriptan Nasal Spray in the Treatment of Acute Migraine in Adolescents
Pediatrics 106:989-997, Winner,P.,et al, 2000

Predictive Testing for Huntington's Disease: the Calm After the Storm
Lancet 356:1944-1945, Hayden,M.R., 2000

Motor and Cognitive Improvements in Patients with Huntington's Disease after Neurol Trasnplantation
Lancet 356:1975-1979,1945, Bachoud-Levi,A.,et al, 2000

Course and Treatment of Myasthenia Gravis During Pregnancy
Neurol 52:447-452, Batocchi,A.P.,et al, 1999

Topiramate in Clinical Practice:First Year's Postlicensing Experience in a Specialist Epilepsy Clinic
JNNP 66:759-763, Kellett,M.W.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Long-Term Stabilization After Bone Marrow Transplantation in Juvenile Metachromatic Leukodystrophy
Arch Neurol 55:98-99, Kidd,D.,et al, 1998

iH NMR Spectroscopy Studies of Huntington's Disease, Correlations with CAG Repeat Numbers
Neurol 50:1357-1365, Jenkins,B.G.,et al, 1998

Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998

Recovery From Myasthenic Crisis After Use of IVIG Therapy
Indian Pediatrics 35:901-903, Jain,K.,et al, 1998

Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
Lancet 349:4, Bundey,S., 1997

Longitudinal Change in Basal Ganglia Volume in Patients with Huntington's Disease
Neurol 48:394-399, Aylward,E.H.,et al, 1997

CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
Ann Neurol 41:689-692, Penney,J.B.,et al, 1997

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
Ann Neurol 39:132-136, Furtado,S.,et al, 1996

Late Juvenile Metachromatic Leukodystrophy Treated with Bone Marrow Transplantation:A 4-Year Follow-up Study
Neurol 46:254-256, Navarro,C.,et al, 1996

Assessment of Brain SPECT:Report of the Therapeutics and Technology Assessment Subcommittee of the AAN
Neurol 46:278-285, , 1996

Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
Neurol 46:527-531, Brandt,J.,et al, 1996

Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
Arch Neurol 53:493-497, Zappacosta,B.,et al, 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996

Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

Correlations Between Triplet Repeat Expansion and Clinical Features in Huntington's Disease
Arch Neurol 113:749-753, Claes,S.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Juvenile Huntington Disease:CT and MR Features
AJNR 16:1405-1412, Ho,V.B.,et al, 1995

Cortical Myoclonus in Huntington's Disease
Movement Disorders 9:633-641, Thompson,P.D.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Serial MR After Bone Marrow Transplantation in Two Patients with Metachromatic Leukodystrophy
AJNR 15:1929-1932, Stillman,A.E.,et al, 1994

Characteristics of the Dementia in Late-Onset Metachromatic Leukodystrophy
Neurol 44:662-665, Shapiro,E.G.,et al, 1994

The Neurogenetic Genie:Testing for Huntington's Disease Mutation
Neurol 44:1369-1373, 1533-15361994., Hersch,S.,et al, 1994

CAG Repeat Size and Clinical Presentation in Huntington's Disease
Neurol 44:1137-1143, Ashizawa,T.,et al, 1994

A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994

Clozapine in Huntington's Chorea
Neurol 44:821-823, Bonuccelli,U.,et al, 1994

Congenital Myasthenic Syndromes
In:Neurologic Clinics, 12:401-4371994., Engel,A.G., 1994

Race, Sex, and Puberty Influence Onset, Severity, and Outcome in Juvenile Myasthenia Gravis
Neurol 44:1208-1214, Andrews,P.I.,et al, 1994

Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

Mutation Analysis in Patients with Possible but Apparently Sporadic Huntington's Disease
Lancet 344:714-717, Davis,M.B.,et al, 1994

Clinical and Magnetic Resonance Features of the Classic & Akinetic-Rigid Variants of Huntington's Dis
Arch Neurol 50:17-19, Oliva,D.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Acetylcholine Receptor Antibodies in Juvenile Myasthenia Gravis
Neurol 43:977-982, Andrews,P.I.,et al, 1993

Juvenile Myoclonic Epilepsy
Arch Neurol 50:594-598, Grunewald,R.A.&Panayiotopoulos,C.P., 1993



Showing articles 50 to 100 of 237 << Previous Next >>