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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 500 to 550 of 1980 << Previous Next >>

Polyarteritis Nodosa Presenting as Rhabdomyolysis
J Korean Rheum Assoc Mar13(1):76-81, Bae,Y.D.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

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

Ruptured Cavernous Sinus Aneurysms Causing Carotid Cavernous Fistula: Incidence, Clinical Presentation, Treatment, and Outcome
AJNR 27:185-189, van Rooij, W.J.,et al, 2006

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Cerebral Embolism from Left Atrial Myxoma Leading to Cerebral and Retinal Aneurysms
AJNR 26:666-669, Herbst, M.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Aneurysmal Rupture Without Subarachnoid Hemorrhage: Case Series and Literature Review
Neurosurg 57:225-229, Thai,Q-A.,et al, 2005

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

Intracerebral Hemorrhage
The Neurologist 11:311-324, Badjatia,N. &Rosand,J., 2005

Rhabdomyolysis: An Evaluation of 475 Hospitalized Patients
Medicine 84:377-385, Melli,G.,et al, 2005

Early Posttraumatic Subarachnoid Hemorrhage Due to Dissecting Aneurysms in Three Children
Neurol 65:1663-1665, Kneyber,M.C.J.,et al, 2005

Mild Intraoperative Hypothermia During Surgery for Intracranial Aneurysm
NEJM 352:135-145, Todd,M.M.,et al, 2005

Ruptured Cerebral Aneurysms
NEJM 352:121-124, Ellegala,D.B. & Day,A.L., 2005

Discontinuing Prophylactic Transfusions Used to Preven Stroke in Sickle Cell Disease
NEJM 353:2769-2778,2743, The Optimizing Primary Stroke Prevention in Sickle Cell Anemia (STOP 2) Trial Investigators, 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Patients With Small, Asymptomatic, Unruptured Intracranial Aneurysms and No History of Subarachnoid Hemorrhage Should Generally Be treated Conservatively-For
Stroke 36:408-409, 407, Wiebers, D.O., 2005

Patients with Small, Asymptomatic, Unruptured Intracranial Aneurysms and No History of Subarachnoid Hemorrhage Should be Treated Conservatively - Against
Stroke 36:410-411, 407, Weir,W, 2005

Predictors and Impact of Aneurysm Rebleeding After Subarachnoid Hemorrhage
Arch Neurol 62:410-416, Naidech, A.M., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Increased Rate of Major Malformations in Offspring Exposed to Valproate Durng Pregnancy
Neurol 64:961-965, 938, Wyszynski,D.F., et al, 2005

Lamotrigine and the Risk of Malformations in Pregnancy
Neurol 64:955-960, 938, Cunnington, M. , et al, 2005

Clinicopath Conf, Human Granulocytic Ehrlichiosis
NEJM 352:1358-1364, Case 10-2005, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Comparison of Warfarin and Aspirin for Symptomatic Intracranial Arterial Stenosis
NEJM 352:1305-1316, 1368, Chimowitz,M.I.,et al, 2005

Maternal and Infant Characteristics Associated with Perinatal Arterial Stroke in the Infant
JAMA 293:723-729, Lee,J.,et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Antiepileptic Drug Use of Women with Epilepsy and Congenital Malformations in Offspring
Neurol 64:1874-1878, Artama,M.,et al, 2005

International Subarachnoid Aneurysm Trial (ISAT) of Neurosurgical Clipping Versus Endovascular Coiling in 2143 Patients with Ruptured Intracranial Aneurysms:A Randomised Comparison of Effects on Survival, Dependency, Seizures, Rebleeding, Subgroups, and Aneurysm Occlusion
Lancet 366:809-817,783, Molyneux,A.J.,et al, 2005

Aggregate Analysis of the Literature for Unruptured Intracranial Aneurysm Treatment
AJNR 26:1902-1908, Lee,T.,et al, 2005

In Utero Magnetic Resonance Imaging for Brain and Spinal Abnormalities in Fetuses
BMJ 331:562-565, Griffiths,P.D.,et al, 2005

Normal Intelligence in Children with Prenatal Exposure to Carbamazepine
Neurol 62:28-32,8, Gaily,E.,et al, 2004

Yield of Screening for New Aneurysms After Treatment for Subarachnoid Hemorrhage
Neurol 62:369-375,354, Wermer,M.J.H.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Ophthalmologic Features of Parkinson's Disease
Neurol 62:177-180, Biousse,V.,et al, 2004

The AED (Antiepileptic Drug) Pregnancy Registry
Arch Neurol 61:673-678, Holmes,L.B.,et al, 2004

Fibromuscular Dysplasia
NEJM 350:1862-1871, Slovut,D.P. &Olin,J.W., 2004

Reading Disorder
JAMA 291:2040, Torpy,J.M.,et al, 2004

Sex Differences in Developmental Reading Disability
JAMA 291:2007-2012, Rutter,M.,et al, 2004

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

Intravenous Immunoglobulin in Autoimmune Neuromuscular Diseases
JAMA 291:2367-2375, Dalakas,M.C., 2004

Magnetoencephalography (MEG) and Magnetic Source Imaging (MSI)
The Neurologist 10:138-153, Wheless,J.W.,et al, 2004

Multiple Cerebral Aneurysms in Factor VII Deficiency
AJNR 25:784-786, Schilling,A.M.,et al, 2004

Recurrent Meningitis of Unknown Aetiology
Lancet 363:1772, Ellerin,T.B.,et al, 2004

Fatal Myositis Due to the Microsporidian Brachiola algerae, a Mosquito Pathogen
NEJM 351:42-47, Coyle,C.M.,et al, 2004

Pediatric Stroke Belt
Stroke 35:1570-1573, Fullerton,H.J.,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

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Multi-Section CT Angiography for Detection of Cerebral Aneurysms
AJNR 25:1485-1492, Teksam,M.,et al, 2004



Showing articles 500 to 550 of 1980 << Previous Next >>