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abdominal distention
abdominal muscle paralysis
abiotrophy
acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
algorithm
allopurinol
alopecia
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, familial
amniocentesis
amyloidosis
amyotrophic lateral sclerosis
analgesic
anesthesia, general
anterior tibial muscle weakness
anxiety
apnea
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
ataxia
ataxia, hereditary
atrial fibrillation
atrial flutter
atrial paralysis
atrioventricular block
attention deficit disorder with hyperactivity
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
azathioprine
baldness
benign congenital hypotonia
bent spine syndrome
benzodiazepine
botulism
bradycardia
brainstem, lesion of
bulging of biceps
cachexia
calcium antagonist
calf atrophy
calf hypertrophy
calpain III deficiency
camptocormia
cancer of colon
carcinoma
carcinoma of ovary
carcinoma of pancreas
carcinoma of uterus
cardiac arrest
cardiac arrest and resuscitation
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomegaly
cardiomyopathy
cardiovascular disease
case studies
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, carotid origin
cerebral palsy
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, young adult
cervical spine injury
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 1
chromosome 17
chromosome 19
chromosome 3
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
coma
complications
compression fracture
concussion
conduction block
confidentiality
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
conversion reaction
cost
cost effectiveness
CPAP
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cry, weak
cyclosporine
defibrillator, implanted
degenerative diseases of CNS
delay in diagnosis
dementia
dermatomyositis
descending paralysis
developmental disability
developmental milestones
developmental retardation
diagnostic criteria
diaphragmatic paralysis
dieting
differential diagnosis
difficulty climbing stairs
diltiazem
disability, neurological
distal muscle atrophy
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dying
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dyspraxia
dystroglycanopathies
dystrophin
dystrophin associated proteins
echinocyte
echocardiogram
efficacy
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electrocardiogram, LVH
electromyogram
electron microscopy
ELISA
embolism
emerin
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy, carrier
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
ethics in neurology
euthanasia
evidence-based research
eye closure
Fabry's disease
facial appearance, abnormal
facial expression abnormality
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
family planning
fasciculation
fatigue
feeding disorder
fetal movements, reduced
fetus
fibrillations
fine motor function, impaired
floppy infant
fluorescein angiography
foot drop
fracture, long bone
fragile-X syndrome
Friedreich's ataxia
frontal balding
gait disorder
gait, waddling
gastric dilatation, acute
gastrocnemius muscle weakness
gastrointestinal motility
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glycogen storage disease
glycosyltransferase
Gowers maneuver
Guillain Barre syndrome
hammertoes
hand weakness
head circumference
head injury
headache
hearing loss
hearing problems in children
heart block
heart block, complete
heart murmur
high arched feet
high arched palate
hip pain
Hispanics
histochemistry
histochemistry of muscle
Holter monitoring
hospice
hunger
Huntington's chorea
hydrocephalus
hypercapnia
hypersomnia
hyperthyroidism
hypoglycemia
hypoglycemic coma
hyporeflexia
hypotonia
hypotonia, infants
idebenone
immunohistochemistry
immunosuppressive agents
implantable cardioverter defibrillator
inability to stand on tiptoes
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion body myositis
influenza
influenza immunization
intellectual deficit
intelligence quotient
intermittent positive pressure breathing
intestinal pseudoobstruction
iris, abnormal
joint hypermobility
Kearns-Sayre syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
kyphosis
lactic dehydrogenase(LDH)
laminopathies
learning disability
learning disability, in children
left ventricular dilatation
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
lid closure, weakness of
life expectancy
life sustaining treatment
lipid storage disorder of CNS
liver function enzymes
LMNA gene
locked-in syndrome
lordosis
low back pain
lymphocyte capping, diminished
machine learning
macrocephaly
malignancy screen
malignant hyperpyrexia
manic-depressive
medical-legal aspects of neurology
megalencephaly
Melkersson's syndrome
mental retardation
merosin
metachromatic leukodystrophy
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
molecular genetics
mononeuropathy
morphine
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, muscle
MRI, serial
MRS
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle relaxant
muscle stiffness
muscle swelling
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
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, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, neurogenic hypothesis of
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenic crisis
myoblast transfer
myocardial biopsy
myocarditis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, neurogenic hypothesis of
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonic discharges
neck weakness
nemaline rod myopathy
neonatal screening, genetic neurologic disorders
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neuritis, causes of
neurocardiology
neurofibromatosis 1
neurofibromatosis 2
neurogenic vs.myopathic atrophy
neurologic complications of, systemic disease
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal migration disorder
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, peripheral
next-generation sequencing
nucleotidase-5 activity
obesity
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
opened mouth
ophthalmoplegia
Oppenheim muscular dystrophy
orbicularis oculi muscle
ovarian tumor
oxygen therapy
pacemaker, cardiac-transvenous
pain, abdominal
palliative care
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
pathology
pediatric neurology
pediatric neurology, transition to adult care
percussion induced muscle contraction
periodic paralysis
phrenic nerve pacemaker
physical therapy
physician assisted suicide
poliomyelitis
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
polyneuropathy
porphyria
positive sharp waves
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
proximal myotonic myopathy
pseudohypertrophy
psychiatric disorder
psychological testing
psychological testing, children
ptosis
ptosis, bilateral
pulmonary embolism
pulmonary function tests
quadriceps atrophy
quadriceps weakness
quality of life
recombinant DNA
respirator
respiratory depression
respiratory failure
respiratory tract infection
retinal detachment
retinopathy
review article
RFLPs
rhabdomyolysis
right to die
rigid spine syndrome
rippling muscle disease
risk factors
safety
sarcoglycan
sarcoglycanopathy
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
sedation
seizure
sensorineural hearing loss
serum glutamic oxaloacetic transaminase
serum glutamic pyruvic transaminase
shoulder, pain in
shoulder-girdle wasting
skin, biopsy
sleep apnea
slit lamp examination
sloped shoulders
somnolence
speech disorder, childhood
speech, delayed development of
spinal cord, injury of
spinal cord, neoplasm
spinal fusion
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar degeneration
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
stooped posture
suck, poor
sudden death
symptomatic
syncope
syringomyelia
systemic illness
Tay-Sachs disease
telangiectases
telangiectases, retinal
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thrombus, mural
toe walking
torticollis
tracheostomy
transient ischemic attack
transverse smile
treatment of neurologic disorder
trinucleotide repeats
tripping
ultrasonography
urine, dark
vaccine
valium
ventricular tachycardia
vertebral fracture
viral infection, CNS
vision, failure of in childhood
visual loss
vital capacity
Walker-Warburg syndrome
walking frame
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
Showing articles 500 to 550 of 788 << Previous Next >>

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998

More on Reflex Sympathetic Dystrophy Syndrome Following Air-Bag Inflation
NEJM 338:334-335, Quarino,H.A., 1998

Flail Arm Syndrome: A Distinctive Variant of Amyotrophic Lateral Sclerosis
JNNP 65:950-951, Hu, M.T.M.,et al, 1998

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
Neurol 48:55-57, Juneja,T.,et al, 1997

ALS Standard of Care Consensus
Neurol 48 (Suppl 4) :S33-S37997., Miller,R.G.,et al, 1997

Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
Ann Int Med 127:450-453, Aboussouan,L.S.,et al, 1997

Practice Advisory on the Trtm of ALS with Riluzole
Quality Standards Subcommittee of the AAN, Neurol 49:657-6591997., , 1997

Motor Neuron Syndromes in Cancer Patients
Ann Neurol 41:722-730, 7031997., Forsyth,P.A.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
JNNP 62:88-91, Waragai,M.,et al, 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

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

Riluzole
Lancet 348:795-799, Wokke,J., 1996

Neurogenic Muscle Hypertrophy
Muscle & Nerve 19:811-818996., Gutmann,L., 1996

Brain and Spinal Cord MRI in Motor Neuron Disease
JNNP 61:314-317, Thorpe,J.W.,et al, 1996

Amyotrophic Lateral Sclerosis and Occupational History
Arch Neurol 53:730-733, Strickland,D.,et al, 1996

Avoiding False Positive Diagnoses of Motor Neuron Disease:Lessons from the Scottish Motor Neuron Disease Register
JNNP 60:147-151, Davenport,R.J.,et al, 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Motor Neuron Disease
BMJ 313:244, Shneerson,J.M., 1996

Motor Neuron Disease Presenting as Acute Respiratory Failure:A Clinical and Pathological Study
JNNP 60:455-458, Chen,R.,et al, 1996

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Development of General Weakness in a Patient with Amyotrophic Lateral Sclerosis after Focal Botulinum Toxin Injection
Neurol 46:845-846, Mezaki,T.,et al, 1996

Motor Neuron Disease with Parkinsonism
Arch Neurol 53:987-991, Qureshi,A.I.,et al, 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

MRI of White Matter Changes in the Sjogren-Larsson Syndrome
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Amyotrophic Lateral Sclerosis:Correlation of Clinical & MR Imaging Findings
Radiology 194:263-270, Cheung,G.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Pseudoneurogenic Thoracic Outlet Syndrome
Muscle & Nerve 17:242-244, Simpson,D.M., 1994

Detection of Cortical Neuron Loss in Motor Neuron Disease by Proton Magnetic Resonance Spectroscopic Imaging in Vivo
Neurol 44:1933-1938, Pioro,E.P.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

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

Growth Factors:Potential Therapeutic Applications in Neurology
JNNP 54:1445-1450, Drago,J.,et al, 1994

Amyotrophic Lateral Sclerosis Patient Antibodies Label CA2+Channel a1 Subunit
Ann Neurol 35:164-171, 1311994., Fumiharu,K.,et al, 1994

Clinical Significance of Hypointensity in the Motor Cortex on T2-Weighted Images
Neurol 44:1181, Iwasaki,Y.,et al, 1994

The Shoulder-Hand Syndrome after Stroke:A Prospective Clinical Trial
Ann Neurol 36:728-733, Braus,D.F.,et al, 1994

Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
Neurol 44:2006-2014, Jankovic,J., 1994

Intestinal Pseudo-Obstruction in Adult Spinal Muscular Atrophy
Muscle & Nerve 17:946-948994., Ionasescu,V.,et al, 1994

Location of the Corticospinal Tract in the Internal Capsule at MR Imaging
Radiology 191:455-460, Yagishita,A.,et al, 1994



Showing articles 500 to 550 of 788 << Previous Next >>