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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 150 to 200 of 788 << Previous Next >>

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

Effect of Chronic Treatment with the Calcium Antagonist Diltiazem in Duchenne Muscular Dystrophy
Neurol 38:609-613, Bertorini,T.E.,et al, 1988

Characterization of Dystrophin in Muscle-Biopsy Spec from Pts with Duchenne's or Becker's Muscular Dystrophy
NEJM 318:1363-1368, 13921988., Hoffman,E.P.,et al, 1988

Dystrophin
Editorial, Lancet 2:429-4301988., , 1988

Gastric Hypomotility in Duchenne's Muscular Dystrophy
NEJM 319:15-18, Barohn,R.J.,et al, 1988

Peripheral Neuropathy in Myotonic Dystrophy:A Nerve Biopsy Study
Ann Neurol 23:470-476, Cros,D.,et al, 1988

Life Spans of Duchenne Muscular Dystrophy Patients in the Hospital Care Program in Japan
J Neurol Sci 81:155-158, Mukoyama,M.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Prednisone Treatment in Duchenne Muscular Dystrophy, Long-Term Benefit
Arch Neurol 44:818-822, DeSilva,S.,et al, 1987

Practical Problems in the Respiratory Care of Patients with Muscular Dystrophy
NEJM 316:1197-1205, Smith,P.E.M.,et al, 1987

Frequency of Cerebral Infarction in Patients with Inherited Neuromuscular Disease
Stroke 18:805-807, Biller,J.,et al, 1987

Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

Abnormalities of Eyelid Closure
In Walsh & Hoyt's Clinical Neuro-ophthalmology, Williams & Wilkins, Baltimore, 2:967, Miller,M.R., 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985

Increased Head Circumference in Patients with Duchenne Muscular Dystrophy
Ann Neurol 17:620-621, Schmidt,B.,et al, 1985

Facioscapulohumeral Dystrophy Presenting in Infancy with Facial Diplegia & Sensorineural Deafness
Ann Neurol 17:513-516, Korf,B.R.,et al, 1985

Cardiac Involvement in Myotonic Muscular Dystrophy
Medicine 64:371-387, Moorman,J.R.,et al, 1985

Computed Tomographic Patterns of Muscles in Neuromuscular Diseases
Arch Neurol 41:383-387, Hawley,R.J.,et al, 1984

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Duchenne Muscular Dystrophy:Carrier Detection by Ultrasound & Computerised Tomography
Lancet 2:1199-1200, Rott,H., 1983

Implications of Diagnostic Delay in Duchenne Muscular Dystrophy
BMJ 287:1106-1107, Zellweger,H., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

The Female Carrier of Duchenne Muscular Dystrophy
BMJ 284:1423-1424, Dubowitz,V., 1982

Progressive Muscle Disease in a Young Woman With Family History of Duchenne's Muscular Dystrophy
Arch Neurol 39:378-380, Olson,B.J.,et al, 1982

Serial Two-dimensional Echocardiography in Duchenne Muscular Dystrophy
Neurol 32:1101-1105, Goldberg,S.J.,et al, 1982

An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982

Facioscapulohumeral Dystrophy Associated with Hearing Loss & Coats Syndrome
Ann Neurol 12:395-398, Taylor,D.A.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

Myotonic Dystrophy, Mitral Valve Prolapse, and Cerebral Embolism
Stroke 13:93-94, Morris,L.K.,et al, 1982

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Hypersomnia Associated with Alveolar Hypoventilation in Myotonic Dystrophy
Neurol 31:1336-1337, Hansotia,P.,et al, 1981

Electrocardiogram Abnormalities in Carriers of Duchenne Muscular Dystrophy
Neurol 30:497-501, Lane,R.J.M.,et al, 1980

Echocardiographic Evaluation of Cardiac Abnormalities in Duchenne's Dystrophy & Myotonic Muscular Dystrophy
Arch Neurol 37:273-277, Reeves,W.C.,et al, 1980

Myotonic Dystrophy
In Harrison's Principles of Internal Medicine, 9th Ed, McGraw-Hill Book Co, NY 206180., Adams,R.D.,et al, 1980

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Lymphocyte Capping in Muscular Dystrophy
Neurol 29:1419-1421, Hauser,S.L.,et al, 1979

Muscular Dystrophy in Six Young Girls
Neurol 29:1486-1491, Hazama,R.,et al, 1979



Showing articles 150 to 200 of 788 << Previous Next >>