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Differential
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abscess, intracerebral
acetazolamide
acetylcholinesterase
acid maltase deficiency
acid maltase deficiency, adult
acoustic neurinoma
acoustic neurinoma, bilateral
acrocyanosis
acromicria
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
agenesis of corpus callosum
Aicardi-Goutieres syndrome
algorithm
alpha glucosidase
alpha-fetoprotein
alveolar hypoventilation
aminoacidurias
ammonia
amniocentesis
anemia
anencephaly
anesthesia, general
aneurysm
Angelman syndrome
angiofibroma, facial
angiography, spinal
angiokeratoma
ankle edema
anterior horn cell disease
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
anxiety
arbovirus
areflexia
arm weakness
arrhythmia, cardiac
arteriovenous malformation
arteriovenous malformation, pulmonary
arthralgia
arylsulfatase B
ascites
aspartate aminotransferase
aspartocyclase
aspiration
asymptomatic
ataxia
ataxia, hereditary
ataxia, paroxysmal
attention deficit disorder with hyperactivity
atypical
audiogram
auditory evoked brainstem potentials
autism
Babinski sign
baldness
basal ganglia, calcification of
behavior, combative
behavioral disorder
birth injury
bleeding disorder
body odor
bone marrow transplantation
brachial neuritis
brachial neuritis, acute
brachial neuritis, bilateral
brachial plexus neuropathy
brachial plexus neuropathy, bilateral
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brain atrophy
Brazil
breast feeding
bruit
cachexia
cafe au lait spots
CAG repeats
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamazepine
carcinoma
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, indications for
cataracts
cataracts, congenital
Central America
central nervous system, infection of
cerebellar ataxia, children
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral palsy
cerebral palsy, risk factors
cerebral palsy, work up
cerebro hepato renal syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, multiple
cerebrovascular accident, neonatal
cerebrovascular accident, recurrent
cerebrovascular disease
ceruloplasmin, serum
cesarean section
Charcot-Marie-Tooth
chilbran skin lesions
children
chorea
choroid plexus
choroid plexus, abnormality of
choroid plexus, cyst
chromosomal abnormality
chromosome 15
chromosome 19
chromosome 3
chromosome 5
chronic graft versus host disease
cleft lip
Clinical Pathologic Conference(C.P.C.)
clonazepam
clubbing of fingers
cocaine
Cockayne's syndrome
cognition
cold temperature
coma
complications
confidentiality
congenital birth defects
congenital heart disease
congenital infection, viral
congenital malformation
congenital malformation, dilantin therapy causing
congenital malformation, non CNS
congestive heart failure
consanguinity
constipation
contractures, joint
controversies in neurology
copper metabolism, abnormal
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum, atrophy of
counselling
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cultured skin fibroblasts
cyanosis
cyst, porencephalic
deafness
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dentate nuclei, lesion of
depression
developmental abnormality of brain
developmental disability
developmental evaluation
developmental milestones
developmental retardation
diagnostic criteria
diaphragmatic paralysis
diet
differential diagnosis
digits, abnormal
dilantin
dilantin, toxicity
disability, neurological
dissociated sensory loss
distal muscle weakness
diurnal variation
DNA probes
dopamine agonist
drooling
drug abuse
drug interactions
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmorphic
dysostosis multiplex
dysphagia
dysphasia
dyspnea
dyspraxia
dystonia
dystonia, children
dystrophin
ear, abnormal
eating disorder
echocardiogram
eczema
edema, pedal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, monitoring, continuous
electromyogram
electron microscopy
embolism, paradoxical
employment
encephalocele
encephalopathy
encephalopathy, neonatal
endovascular therapy
enzyme treatment
enzyme, defect
enzyme, induction
epidemic
epidemiology of neurology
epileptic encephalopathy
epistaxis
epistaxis, recurrent
epoxide hydrolase
esophageal varices
ethics in neurology
extracorporeal membrane oxygenation
Fabry's disease
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
familial
fasciculation
fatty acid, elevated plasma content
feeding disorder
fetus
fever
fibroma, ungual
fistula, arterio-venous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
flavivirus
flow study, carotid artery
folic acid
fragile-X syndrome
fragile-X syndrome, carrier
fucosidosis
gabapentin
gait disorder
galactocerebrosidase
gangliosidosis GM1
gangliosidosis GM2
gastrointestinal bleeding
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
granular osmiphilic material
gray matter
grimacing
growth hormone deficiency
growth retardation
Guillain Barre syndrome
hamartin
hamartoma
hand flapping
head lag
headache
health insurance
hearing loss
heart block
hemiparesis
hemiplegia
hemiplegia, congenital
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
hereditary hemorrhagic telangiectasia(HHT)
hexosaminidase-A
high arched palate
hormone replacement
human genome
human T-lymphotropic virus type I(HTLV-I)
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's chorea, presymptomatic detection of
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperactivity
hypercapnia
hyperphagia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypoalbuminemia
hypogonadism
hypokinesia
hypopigmentation of skin
hyporeflexia
hypotelorism
hypothermia
hypothyroidism
hypothyroidism, congenital
hypothyroxinemia
hypotonia
hypotonia, infants
hypoxia
hypoxic-ischemic leukoencephalopathy
imbalance
immunohistochemistry
in situ hybridization
inborn errors of metabolism
inborn errors of metabolism, screening
infant, evaluation of
infection
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
intelligence testing in children
interferon alpha
internet
intracranial hemorrhage
intrauterine
intrauterine growth retardation
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intraventricular hemorrhage
iris, abnormal
iron, brain
iron, serum
irritability
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lamotrigine
learning disability
learning disability, in children
leg weakness, bilateral
lens, dislocation of
leukodystrophy
leukoencephalopathy
leukopenia
levonorgestrel
lipid storage disorder of CNS
Lisch nodules
lissencephaly
liver disease
liver function enzymes
long bone lesion
Lorenzo's oil
low birth weight
lymphangiomyomatosis
lymphoma
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malformation, vascular, cerebral
medical-legal aspects of neurology
meningocele
mental retardation
mental retardation, familial
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
micrognathia
migraine
Miller-Dieker syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
molybdenum cofactor deficiency
mongolism
mortality
mosquito
motor dysfunction
motor neuron disease
mousy odor
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, fetal
MRI, indications for
MRI, intrauterine
mucopolysaccharidoses
multiple sclerosis, misdiagnosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myelomeningocele
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, distal
myopathy, metabolic
myopathy, vacuolar
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
nasal bridge, wide
nausea and vomiting
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neoplasm, primary of CNS
nerve conduction studies
nerve growth factor
neural tube defect
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic practice
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neurosis
newborn, evaluation of
Niemann-Pick disease
nose, abnormal
Notch3 gene
nusinersen
nystagmus, hereditary
nystagmus, periodic
obesity
obstetric neurologic injuries
oculopharyngeal muscular dystrophy
omphalocele
opiate
optic atrophy
oral contraceptives
ornithine transcarbamylase deficiency
orthopnea
pain
pain, severe
papilledema
paraparesis
paraparesis, spastic
parasitic infection, CNS
paresthesias
Parkinsonism syndrome
paroxysmal neurologic deficits
partruition
pathology
patient information and support
penicillamine
percussion induced muscle contraction
periventricular leukomalacia
peroxisomal disease
peroxisomes
personality change
phakomatoses
phenylketonuria
pheochromocytoma
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
post hemorrhagic hydrocephalus
postoperative neurologic complications
postpartum
postpartum coma
postural abnormality
practice guidelines
Prader-Labhart-Willi syndrome
pramipexole
precipitating factors
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
premature infant, problems in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pruritus
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
ptosis
puerperium
pyramidal tract dysfunction
quadriparesis
Rankin score
rash
recombinant DNA
recurrent
Refsum's disease
renal cyst
renal stones
respiratory failure
restless leg syndrome
retinal degeneration
retinal hamartoma
reversible neurologic disorder
review article
RFLPs
rhabdomyoma, cardiac
rigidity
risk factors
rubella syndrome
scoliosis
scoliosis, neurologic association with
screaming
screening
seizure
seizure, complications following
seizure, diagnosis of
seizure, etiology of
seizure, familial
seizure, intractable
seizure, neonatal
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
seizure, workup of
self-mutilation
shagreen patch
short stature
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
slit lamp examination
SMN1 gene
South America
Southern immunoblot test
speech disorder
speech disorder, childhood
sphingolipodoses
spina bifida
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, vascular malformation of
spinal muscular atrophy
spinal muscular atrophy, classification
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
subarachnoid fluid collection, benign
subarachnoid hemorrhage
subdural hematoma
subdural hematoma, neonates and infants
subependymal nodules
suck, poor
sudden infant death syndrome
suicide
Tay-Sachs disease
telangiectases
temper tantrums
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
teratogenesis
teratogenic drugs
term infant
testicular atrophy
testicular enlargement
thrombocytopenia
thyroxine
tissue plasminogen activator, intravenous
titinopathy
tongue, enlarged
tongue, fasciculations of
tongue, protrusion of
tongue, weakness
toxoplasmosis, CNS
toxoplasmosis, congenital
trauma
treatment of neurologic disorder
tremor
tremulousness
trichopoliodystrophy
trientine dihydrochloride
trinucleotide repeats
trisomes
trisomy 18
tuber, cortical
tuberin
tuberous sclerosis
tuberous sclerosis, screening for
twins
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
umbilical-cord blood transplantation
undiagnosed
urea-cycle enzymopathies
uric acid, low
urine test for metabolic disorders
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
visual loss
vital capacity
vitamin K
vitamin supplementation
walking, difficulty with
weakness
weakness, congenital
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white freckles
white matter disease
wide based gait
Wood's light
workup
x-linked hydrocephalus
x-linked mental retardation
Zika virus infection
zinc
Showing articles 950 to 1000 of 2198 << Previous Next >>

Recurrent Orbital Myositis,Report of a Familial Incidence
Arch Neurol 56:1407-1409, Maurer,I.&Zierz,S., 1999

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Progressive Multifocal Leukoencephalopathy:Unusual MRI Findings and Prolonged Survival in a Pregnant Woman
Neurol 522:657-659, Rosas,M.J.,et al, 1999

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Pregnant,Vomiting,and Going Blind
Lancet 352:1594, Tesfaye,S.,et al, 1998

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Stroke and Intracranial Venous Thrombosis During Pregnancy and Puerperium
Neurol 51:1622-1628, Lanska,D.J.&Kryscio,R.J., 1998

Sneddon's Syndrome:Neuro-Ophthalmologic Manifestations in a Possible Autosomal Recessive Pattern
Neurol 51:1185-1187, Rehany,U.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Localization of the Giant Axonal Neuropathy Gene to Chromosome 16q24
Ann Neurol 43:143-148, Flanigan,K.M.,et al, 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Chromosome 20 Ring:A Chromosomal Disorder Associated with a Particular Electroclinical Pattern
Epilepsia 39:942-951, Canevini,M.P.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Reduced Penetrance,Variable Expressivity,and Genetic Heterogeneity of Familial Atrial Septal Defects
Circulation 97:2043-2048, Benson,D.W.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Epilepsies in Twins:Genetics of the Major Epilepsy Syndromes
Ann Neurol 43:435-445, Berovic,S.F.,et al, 1998

Intravenous Immunoglobulin Treatment in Multiple Sclerosis, Effect on Relapses
Neurol 50:398-402, Achiron,A.,et al, 1998

The Genetics of Alzheimer Disease, Current Status and Future Prospects
Arch Neurol 55:294-296, Blacker,D.&Tanzi,R.E., 1998

Creutzfeldt-Jacob Disease in a Husband and Wife
Neurol 50:684-688, Brown,P.,et al, 1998

Proton Spectroscopy in Myotonic Dystrophy, Correlations with CTG Repeats
Arch Neurol 55:305-311, 2911998., Chang,L.,et al, 1998

Distal Hereditary Upper Limb Muscular Atrophy
JNNP 64:217-220, Gross,D.W.,et al, 1998

Management Issues for Women with Epilepsy,A Review of the Literature
Neurol 51:949-956, Zahn,C.A.,et al, 1998

Carbon Monoxide Poisoning
NEJM 339:1603-1608, Ernst,A. & Zibrak,J. D., 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Is There a Familial Carpal Tunnel Syndrome? An Evaluation and Literature Review
Muscle & Nerve 21:1533-1536, Gossett,J.G.&Change,P.F., 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Antepartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1549-1553,1537, Badawi,N.,et al, 1998

Intrapartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1554-1558,1537, Badawi,N.,et al, 1998

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura
Neurol 50:1157-1160, Kelly,P.J.,et al, 1998

Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998

Recurrent Intracranial Hemorrhage Due to Postpatrum Cerebral Angiopathy, Implications for Management
Stroke 29:1995-1998, Ursell,M.R.,et al, 1998

Postpartum Cerebral Angiopathy with Intracerebral Hemorrhage in a Patient Receiving Lisuride
Neurol 50:1152-1154, Roh,J.K.&Park,K.S., 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

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Rate of Pregnancy-Related Relapse in Multiple Sclerosis
NEJM 339:285-291, 3391998., Confavreux,C.,et al, 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998



Showing articles 950 to 1000 of 2198 << Previous Next >>