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Differential
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abdominal protrusion
acanthocytosis
acetazolamide
acid maltase deficiency
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome, infants and children
acquired immunodeficiency syndrome, medical precautions with
acquired immunodeficiency syndrome-related complex
acyl CoA dehydrogenase deficiency
adducted thumb
advances in neurology
adverse drug reaction
agenesis of corpus callosum
airway obstruction
alpha-fetoprotein
alveolar hypoventilation
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
aneurysm, intracranial
ankle clonous
ankle, swelling of
anterior horn cell disease
anterior tibial muscle weakness
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
anticonvulsants, absorption
anticonvulsants, bioavailability
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, subtherapeutic
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
antihistamines
arbovirus
areflexia
arrhythmia, cardiac
arthralgia
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, paroxysmal
autoimmune disease
automatic implantable cardioverter-defibrillator
azidodeoxythymidine
bacterial infection
baldness
basal ganglia, calcification of
basal ganglia, infarction
Bassen-Kornzweig syndrome
benign congenital hypotonia
blindness
blindness, sudden
botulism
brainstem, lesion of
Brazil
breast feeding
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcium antagonist
calcium channel dysfunction
camptocormia
carbamazepine
carcinoma
cardiac arrest
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cataracts, congenital
Central America
central core disease
central nervous system, infection of
central nuclei, muscle
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
cholelithiasis
chromosomal abnormality
chromosome 1
chromosome 5
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
complications
conduction block
congenital birth defects
congenital deformities
congenital heart disease
congenital heart disease, CNS complications with
congenital malformation
congenital myasthenic syndromes
congenital myopathy
congenital myopathy, inflammatory
congestive heart failure
consanguinity
contractures, joint
cornea, abnormal
corpus callosum
corpus callosum, thinning
cortical blindness
counselling
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
deafmute
deafness
degenerative diseases of CNS
delivery, complicated
dementia
developmental abnormality of brain
developmental disability
developmental milestones
developmental retardation
differential diagnosis
difficulty climbing stairs
digits, abnormal
dilantin
disability, neurological
dislocated hip, congenital
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dwarfism
dysmorphic
dysphagia
dyspnea
dystroglycanopathies
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, induction
epidemic
epidemiology of neurology
episodic disorders
episodic neurologic deficits
exome sequencing
exostosis
eye closure
face, elongated
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
false negative
familial
familial hemiplegic migraine
fasciculation
fatigue
Fazio-Londe's disease
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
flavivirus
floppy infant
folic acid
foot drop
Friedreich's ataxia
frontal balding
gait disorder
gait, waddling
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
glycosyltransferase
gonadal dysgenesis
Gowers maneuver
Guillain Barre syndrome
hair, loss
Hallgren's syndrome
head circumference
headache
hearing loss
heart block
heavy metal intoxication
hemiparesis
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
high arched feet
high arched palate
highly active antiretroviral therapy
histochemistry
histochemistry of muscle
human immunodeficiency virus type 1
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperkalemic periodic paralysis
hyperreflexia
hypertelorism
hypertrophic cardiomyopathy
hypokalemia
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
infection
intellectual deficit
intrauterine
intrauterine infection
intrauterine infection, viral
jaundice
joint hypermobility
kaliuresis
karyotyping
Kearns-Sayre syndrome
keratoconus
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lactic acidemia
laminopathies
lamotrigine
Laurence-Moon-Bardet-Biedl syndrome
leg weakness, bilateral
lenticular nucleus, lesion of, bilateral
leukodystrophy
levonorgestrel
lid closure, weakness of
life expectancy
lissencephaly
liver function enzymes
LMNA gene
lordosis
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
MELAS syndrome
Melkersson's syndrome
melphalan
mental retardation
merosin
mestinon
metabolic acidosis
mexiletine
microcephaly
microdactyly
micrognathia
migraine
migraine, hemiplegic
Miller-Dieker syndrome
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mortality
mosquito
motor neuron disease
MRI
MRI, abnormal
MRI, fetal
MRI, intrauterine
MRI, muscle
mucopolysaccharidoses
multicore myopathy
multiminicore disease
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
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, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, limb-girdle
myasthenia gravis, neuromuscular junction in
myasthenia gravis, treatment of
myasthenic syndrome
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, focal
myopathy, metabolic
myopathy, mitochondrial
myopathy, monomelic
myopia
myositis
myositis ossificans, progressive
myositis, bacterial
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
myotubularin
nasal bridge, wide
nasal speech
nausea and vomiting
neck extension
neck weakness
neck, webbed
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, metastatic to CNS
neoplasm, primary of CNS
nerve conduction studies
neuritis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuronal migration disorder
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, painful
neuropathy, peripheral
newborn, evaluation of
nifedipine
Noonan Syndrome
nusinersen
obesity
obstetric neurologic injuries
occipital lobe, infarction
occipital lobe, lesion of
ocular myopathy
oculopharyngeal muscular dystrophy
opened mouth
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
Oppenheim muscular dystrophy
opportunistic infection
oral contraceptives
orbicularis oculi muscle
pacemaker, cardiac-transvenous
paramyotonia congenita
paraparesis
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
paroxysmal neurologic deficits
patient information and support
pectus excavatum
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polydactyly
polyhydramnios
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
polyneuropathy, chronic inflammatory demyelinating
positive sharp waves
potassium channel antibodies
potassium channel dysfunction
practice guidelines
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
procainamide
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudohypertrophy
pseudoretinitis pigmentosa
psychiatric disorder
ptosis
ptosis, bilateral
pulmonary stenosis
pyloric stenosis
pyomyositis
quadriparesis
quadriparesis, progressive
quadriplegia, transient
quality of life
ragged-red fibers
rash
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
riboflavin
rigid spine syndrome
schizophrenia
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, injury following
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
serum alanine aminotransferase
short stature
short thumb
skin, biopsy
skin, lesions in neurologic disorders
sloped shoulders
SMN1 gene
sodium channel dysfunction
South America
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinal muscular atrophy, classification
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
steroid
stooped posture
suck, poor
sudden death
syncope
systemic illness
temporalis muscle wasting
term infant
tocainide
tongue, fasciculations of
transverse smile
trauma
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
type 1 muscle fiber
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
Usher's syndrome
valvulopathy
viral infection
viral infection, CNS
viral myopathy
visual field defect
visual fields, constricted
visual impairment
vital capacity
vitamin K
vitamin supplementation
vomiting, recurrent
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, episodic
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
xerostomia
x-linked hydrocephalus
X-linked myopathy
Zika virus infection
Showing articles 600 to 650 of 1980 << Previous Next >>

Prospective Assessment of Risk Factors for Recurrent Stroke During Childhood--A 5-year Follow-up Study
Lancet 360:1540-1545,1526, Strater,R.,et al, 2002

Posterior Circulation Stroke in Childhood
Neurol 59:1552-1556, Ganesan,V.,et al, 2002

The Evaluation of Isolated Third Nerve Palsy Revisited: An Update on the Evolving Role of Magnetic Resonance, Computed Tomography, and Catheter Angiography
Surv Ophthalmol 47:137-157, Lee,A.G.,et al, 2002

Cause and Prognosis of Nontraumatic Sixth Nerve Palsies in Young Adults
Ophthalmology 109:1925-1928, Peters III,G.B.,et al, 2002

Paresis Acquired in the Intensive Care Unit
JAMA 288:2859-2867, De Jonghe,B.,et al, 2002

Is Coagulopathic Liver Disease a Factor in Spontaneous Cerebral Hemorrhage?
J Comput Assist Tomogr 26:69-72, Lee,H. &Hinrichs,C.R., 2002

Quality of Life, Anxiety, and Depression in Patients With an Untreated Intracranial Aneurysm or Arteriovenous Malformation
Stroke 33:440-443, van der Schaaf,I.C.,et al, 2002

Women With Pregnancy-related Polymyotis and High Serum CK Levels in the Newborn
Neurol 58:482-484, Messina,S.,et al, 2002

Intravenous Immunoglobulin for Dysphagia of Inclusion Body Myositis
Neurol 58:326-327, Cherin,P.,et al, 2002

Clinicopath Conf, Infection with Loa loa
NEJM 346:115-122, Case 1-2002, 2002

Thunderclap Headache
JNNP 72:6-11, Dodick,D.W., 2002

A Novel, Blood-Based Diagnostic Assay for Limb Girdle Muscular Dystrophy 2B and Miyoshi Myopathy
Ann Neurol 51:129-133, Ho,M.,et al, 2002

Central Nervous System Infection in Congenital Syphilis
NEJM 346:1792-1798, Michelow,I.C.,et al, 2002

A Forearm Exercise Screening Test for Mitochondrial Myopathy
Neurol 58:1533-1538, Jensen,T.D.,et al, 2002

Hemodynamic Studies in Early Ischemic Stroke
Stroke 33:1274-1279, Akopov,S. &Whitman,G.T., 2002

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

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

Neonatal Cerebral Infarction Diagnosed by Diffusion-Weighted MRI
Stroke 33:1142-1145, Mader,I.,et al, 2002

Demonstration of Acute Ischemic Lesions in the Fetal Brain by Diffusion Magnetic Resonance Imaging
Ann Neurol 52:243-246, Baldoli,C.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Safety of HMG-CoA Reductase Inhibitors: Focus on Atorvastatin
Cardiovasc Drugs Ther 15:211-218, Bernini,F.,et al, 2001

Endovascular Treatment of Unruptured Aneurysms
Stroke 32:1998-2004, Roy,D.,et al, 2001

Arterial Dissection and Stroke in Children
Neurol 57:1155-1160, Fullerton,H.J.,et al, 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

The Neurologic Complications of Scleromyxedema
Medicine 80:313-319, Berger,J.R.,et al, 2001

Neurology of Ciguatera
JNNP 70:4-8, Pearn,J., 2001

Changes in Intervention and Outcome in Elderly Patients With Subarachnoid Hemorrhage
Stroke 32:2845-2849, Johansson,M.,et al, 2001

Silent Infarcts in Children With Sickle Cell Anemia and Abnormal Cerebral Artery Velocity
Arch Neurol 58:2017-2021, Pegelow,C.H.,et al, 2001

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

Acute Compartment Syndrome After Forearm Ischemic Work Test in a Patient with McArdle's Disease
Neurol 56:1779-1780, Lindner,A.,et al, 2001

Impact of Folic Acid Fortification of the US Food Supply on the Occurrence of Neural Tube Defects
JAMA 285:2981-2986,3022, Honein,M.A.,et al, 2001

Focal Myopathy Mimicking Posterior Interosseous Nerve Syndrome
Muscle Nerve 24:969-972, Erdem,S.,et al, 2001

Is Carbamazepine Teratogenic? A Prospective Controlled Study of 210 Pregnancies
Neurol 57:321-324, Diav-Citrin,O.,et al, 2001

Two Controlled Trials of Antibiotic Treatment in Patients with Persistent Symptoms and a History of Lyme Disease
NEJM 345:85-92, Klempner,M.S.,et al, 2001

Cerebral Sinovenous Thrombosis in Children
NEJM 345:417-423, DeVeber,G.,et al, 2001

Inclusiong Body Myositis Mimicking Motor Neuron Disease
Arch Neurol 58:1253-1256, Dabby,R.,et al, 2001

MR Diagnosis of Myxomatous Aneurysms: Report of Two Cases
AJNR 22:1349-1352, Nucifora,P.G.P .&Dillon,W.P., 2001

Clinicopath Conf,Systemic Sclerosis with Scleroderma Renal Crisis
NEJM 345:596-605, Case 26-2001, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

A Controlled Study of Intravenous Immunoglobulin Combined with Prednisone in the Treatment of IBM
Neurol 56:323-327, Dalakas,M.C.,et al, 2001

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Treatment of Unruptured Cerebral Aneurysms in California
Stroke 32:597-605, Claibrone Johnston,S.,et al, 2001

Relative Pupil-Sparing Third Nerve Palsy:Etiology and Clinical Variables Predictive of a Mass
Neurol 56:797-798, Jacobson,D.M., 2001

A Blind Panic
Lancet 357:1262, Ayuk,J.,et al, 2001

The Diagnosis of Brain Death
NEJM 344:1215-1221, 1244, Wijdicks,E.F.M., 2001

Guglielmi Detachable Coiling for Intracranial Aneurysms
Arch Neurol 58:559-564, Dovey,Z.,et al, 2001

Stroke Prevention and Treatment in Sickle Cell Disease
Arch Neurol 58:565-568, Adams,R.J., 2001

The Teratogenicity of Anticonvulsant Drugs
NEJM 344:1132-1138, Holmes,L.B.,et al, 2001

Malpractice Claims: Outcome Evidence to Guide Neurologic Education?
Neurol 56:1099-1100,991, Glick,T.H., 2001

Intracranial Aneurysms: CT Angiography and MR Angiography for Detection-Prospective Blinded Comparison in a Large Patient Cohort
Radiology 219:739-749, White,P.M.,et al, 2001



Showing articles 600 to 650 of 1980 << Previous Next >>