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achilles tendon, enlarged
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adult polyglucosan body disease
advances in neurology
affect, inappropriate
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
Angelman syndrome
antidepressant
antitoxin
apnea
applause sign
arm weakness
aspiration
asymmetric crying facies
ataxia
autonomic dysfunction
axonal degeneration
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
BiPAP
bladder dysfunction
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, infarction of
brainstem, lesion of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
calcification, intracranial
caries
CAT scan, abnormal
CAT scan, emission, abnormal
cataracts
cerebral dominance
cerebrovascular accident
cerebrovascular accident, bilateral
children
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
congenital birth defects
congenital heart disease
congenital malformation
constipation
contractures, joint
conversion reaction
cortical blindness
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cystatin C mutation
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, frontotemporal
depression
developmental disability
developmental retardation
differential diagnosis
disability rating scale, neurological
disability, neurological
distal muscle weakness
drooling
dying
dysarthria
dysdiadochokinesia
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
eating disorder
echocardiogram
efficacy
electroencephalogram, abnormalities of
electromyogram
emotional lability
epidemiology of neurology
Erdheim-Chester disease
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial asymmetry
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
fasciculation
fatigue
feeding disorder
fibrillations
flail arm syndrome
floppy infant
fluoxetine
foam cells
food poisoning
food-borne infection
foot drop
gait disorder
gait, spastic
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen storage disease
growth hormone deficiency
growth retardation
hand flapping
head bobbing
hearing loss
heel swelling
hemiparesis
heralding manifestation
histiocytosis
honey
hospice
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertension
hypogonadism
hypometric saccades
hypopigmentation of skin
hyporeflexia
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
inappropriate antidiuretic(A.D.H.)hormone
inclusion bodies
infant, evaluation of
intellectual deficit
intellectual deterioration
internal capsule
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
intubation
irritability
irritable baby
jaw jerk, abnormal
Jewish
laughing
laughing, pathologic
leg weakness, unilateral
lethargy
leukodystrophy
leukoencephalopathy
life expectancy
locked-in syndrome
masked facies
memory, defect of recent
memory, impairment of
mental retardation
merosin
middle cerebellar peduncle, lesion
mimics
misdiagnosis
molecular genetics
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, mouse ears
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle wasting, diffuse
muscular dystrophy
muscular dystrophy, congenital
mutism
myelomalacia
myeloneuropathy
neck weakness
neurogenic bladder
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathy
neuroprotective agents
neurotoxin
next-generation sequencing
obesity
ocular bobbing
opened mouth
ophthalmoplegia
optic neuropathy
palliative care
paraparesis, spastic
Parkinsonism syndrome
pathologic reflex
peroxisomal disease
personality change
photosensitivity, skin
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymicrogyria
pons, infarction of
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychomotor retardation
ptosis
ptosis, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
rash
release phenomena
respirator
respiratory arrest
respiratory failure
retinopathy
review article
riluzole
risk factors
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
sertraline
short stature
skew deviation
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
spasticity
speech disorder
speech, loss of
stooped posture
strabismus
suck, poor
symmetric brain lesions
systemic illness
tachycardia
temper tantrums
term infant
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
toxins, nervous system
tracheostomy
trauma
treatment of neurologic disorder
tremulousness
tripping
ultrasonography
urinary incontinence
very long chain fatty acids
walking, difficulty with
weakness
weakness, generalized
weakness, infant
weakness, progressive
wheelchair
white matter disease
wide based gait
Showing articles 1100 to 1150 of 2560 << Previous Next >>

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997

The Therapeutic Dilemma of Inclusion Body Myositis
Neurol 48:567-568, Barohn,R.J., 1997

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Three Get Ready
Arch Neurol 53:1222-1223, Goldblatt,D., 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Lambert-Eaton Myasthenic Syndrome Presenting with Severe Respiratory Failure
Muscle & Nerve 19:1328-1333996., Nicolle,M.W.,et al, 1996

Inclusion Body Myositis:Clinical and Pathological Boundaries
Ann Neurol 40:581-586, Amato,A.A.,et al, 1996

Human T-Cell Lymphotrophic Virus Type II-Associated Myelopathy:Clinical and Immunologic Profiles
Ann Neurol 40:714-723, Lenky,T.J.,et al, 1996

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Clinicopath Conf
Varicella-Zoster Leukoencephalitis with Hemorrhage and Large-Vessel Vasculopathy, AIDS, Case 36-1996, NE335:1587-1595,1996., 1996

Stimulus-Evoked Sinus Arrest in Severe Guillain-Barre Syndrome:A Case Report
Neurol 47:1239-1242, Minahan,R.E.,et al, 1996

Taste Loss as an Initial Symptom of Guillain-Barre Syndrome
Neurol 47:1604-1605, Combarros,O.,et al, 1996

Total Alopecia, Diabetes Mellitus, and Falls
Lancet 348:1420, Mueller-Schoop,J.W., 1996

Acute Lumbosacral Polyradiculopathy Due to Cytomegalovirus in Advanced HIV Disease:CSF Findings in 17 Patients
JNNP 61:456-460, Miller,R.F.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Cranial Neuropathies and Liver Failure Due to Hepatitis A
Neurol 46:1774-1775, Varona,L.,et al, 1996

Twelfth-Nerve Palsy:Analysis of 100 Cases
Arch Neurol 53:561-566, Keane,J.R., 1996

Multifocal Motor Neuropathy
JNNP 60:599-603, Nobile-Orazio,E., 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

Startle Provoked Epileptic Seizures:Features in 19 Patients
JNNP 61:151-156, Manford,M.R.A.,et al, 1996

Ataxic Hemiparesis and Hemiageusia from an Isolated Post-Traumatic Midbrain Lesion
Neurol 47:1348-1349, Johnson,T.M., 1996

Cognitive and Brain Magnetic Resonance Imaging Findings in Adrenomyeloneuropathy
Ann Neurol 40:675-678, Edwin,D.,et al, 1996

Medial Medullary Infarction:Analysis of Eleven Patients
Neurol 47:1141-1147, Toyoda,K.,et al, 1996

Another Kind of Knapsack Palsy
Neurol 46:585-586, Pringle,C.E.,et al, 1996

A 64-Year-Old Man with Diabetes and Ascending Paraplegia
Lancet 347:516, Gliemroth,J.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

The Stroke Syndrome of Cortical Vein Thrombosis
Neurol 47:376-382, Jacobs,K.,et al, 1996

Internal Carotid Artery Dissection:MR Imaging Features and Clinical-Radiologic Correlation
Radiology 199:191-198, Ozdoba,C.,et al, 1996

The Syndrome of Posterior Choroidal Artery Territory Infarction
Ann Neurol 39:779-788, Neau,J.&Bogousslavsky,J., 1996

Mechanical Ventilation in Stroke Patients-Is It Worthwhile
Neurol 47:657-659, El-Ad,B.,et al, 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Progressive Deterioration of Intellect and Motor Function Occurring Several Decades after Cranial Irradiation
ARch Neurol 53:814-818, Duffey,P.,et al, 1996

Human T-Cell Lymphotropic Virus Type 1-Associated Myelopathy, Sjogren Syndrome, and Lymphocytic Pneumonitis
Arch Neurol 53:940-942, Kompoliti,A.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

Delayed Radiation-Induced Bulbar Palsy
Neurol 46:1604-1606, Shapiro,B.E.,et al, 1996

Cost-Effectiveness Analysis:What Is It and How Will It Influence Neurology
Ann Neurol 39:818-823, Holloway,R.G., 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Cytomegalovirus Infection and Guillain-Barre Syndrome:The Clinical, Electrophysiologic, and Prognostic Features
Neurol 47:668-673, Visser,L.H.,et al, 1996

Prospective Evaluation of MRI Lumbosacral Nerve Root Enhancement in Acute Guillain-Barre Syndrome
Neurol 47:813-817, Gorson,K.C.,et al, 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Lyme Radiculoneuritis Treated with Intravenous Immunoglobin
Neurol 46:1174-1175, Crisp,D.&Ashby,P., 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Inclusion Body Myositis
JNNP 60:251-255, Garlepp,M.J.&Mastaglia,F.L., 1996

Muscle is Electrically Inexcitable in Acute Quadriplegic Myopathy
Neurol 46:731-736, 6001996., Rich,M.M.,et al, 1996

Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
Neurol 46:815-818, Kobayashi,O.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996



Showing articles 1100 to 1150 of 2560 << Previous Next >>