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acanthocytosis
acetazolamide
acid maltase deficiency
adrenoleukodystrophy
advances in neurology
adverse drug reaction
airway obstruction
alveolar hypoventilation
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anesthesia, general
anterior tibial muscle weakness
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticonvulsants
antihistamines
aqueduct of Sylvius, stenosis
aqueductal stenosis
arrhythmia, cardiac
arthrogryposis multiplex
ataxia
ataxia, cerebellar
ataxia, paroxysmal
autoimmune disease
automatic implantable cardioverter-defibrillator
baldness
Bassen-Kornzweig syndrome
benign congenital hypotonia
blindness
botulism
brainstem, lesion of
calcium antagonist
calcium channel dysfunction
carbamazepine
carcinoma
cardiac surgery, neurologic complications with
cardiac transplantation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar hypoplasia
cerebral cortical atrophy
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
chromosomal abnormality
chromosome 1
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
complications
conduction block
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
controversies in neurology
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
cry, weak
deafmute
deafness
degenerative diseases of CNS
developmental disability
developmental milestones
developmental retardation
differential diagnosis
dilantin
disability, neurological
distal muscle weakness
dropped head syndrome
drug induced neurologic disorders
dwarfism
dystroglycanopathies
dystrophin
dystrophin associated proteins
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
epidemiology of neurology
eye closure
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
familial
familial hemiplegic migraine
Fazio-Londe's disease
feeding disorder
fetal movements, reduced
fetus
floppy infant
foot drop
Friedreich's ataxia
frontal balding
gait disorder
gargoylism
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glaucoma
glycosyltransferase
Gowers maneuver
Hallgren's syndrome
heart block
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
Huntington's chorea
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperkalemic periodic paralysis
hypokalemia
hypokalemic periodic paralysis
hyporeflexia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
joint hypermobility
kaliuresis
Kearns-Sayre syndrome
keratoconus
Kugelberg-Welander syndrome
laminopathies
Laurence-Moon-Bardet-Biedl syndrome
leukodystrophy
lid closure, weakness of
life expectancy
lissencephaly
LMNA gene
lordosis
macrocephaly
malformation, CNS, congenital
malignant hyperpyrexia
Melkersson's syndrome
mental retardation
merosin
metabolic acidosis
mexiletine
micrognathia
micropthalmia
migraine
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, muscle
MRI, serial
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
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, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopia
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia, treatment of
neck weakness
nemaline rod myopathy
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neuritis
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathology, brain
neuropathy
newborn, evaluation of
nifedipine
obesity
ocular myopathy
oculopharyngeal muscular dystrophy
opened mouth
ophthalmoplegia
Oppenheim muscular dystrophy
orbicularis oculi muscle
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
poison, mercury
poison, neurologic problems with
polydactyly
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymicrogyria
polymyositis
polymyositis, infantile
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
procainamide
progeria
prognosis
progressive muscular dystrophy
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
ptosis
quality of life
respirator
respiratory failure
retinal detachment
retinal dysplasia
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
rigid spine syndrome
schizophrenia
scoliosis
seizure
skin, biopsy
sloped shoulders
sodium channel dysfunction
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
steroid
suck, poor
sudden death
syncope
systemic illness
temporalis muscle wasting
term infant
tocainide
transverse smile
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
ultrasonography
Usher's syndrome
viral infection, CNS
visual field defect
visual fields, constricted
vital capacity
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, progressive
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
wide based gait
winging of scapula
workup
x-linked hydrocephalus
x-linked mental retardation
Showing articles 300 to 350 of 1797 << Previous Next >>

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

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Congenital Myotonic Dystrophy
Arch Neurol 37:693-696, Argov,Z.,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

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Emery-Dreifuss Muscular Dystrophy
Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

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

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Allopurinol Not Effective In Muscular Dystrophy
NEJM 301:785, Bakouche,P.,et al, 1979

5'-Nucleotidase Activity in Duchenne Muscular Dystrophy
NEJM 301:726, Scholte,H.R.,et al, 1979

Carrier Detection in Duchenne Muscular Dystrophy
Neurol 29:1423-1425, Tagliavini,J.,et al, 1979

Cholestasis & Myotonic Dystrophy
(letter) NEJM 301:329-330979., Theodore,Ch.,et al, 1979

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

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

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

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

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

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Deformed Erythrocytes in Muscular Dystrophies
Neurol 28:842-844, Grassi,E.,et al, 1978

Erythrocyte Metabolism in Muscular Dystrophy
Arch Neurol 35:592-595, Danon,M.J.,et al, 1978

Alteration in Erythrocyte Membrane Structure in Duchenne Muscular Dystrophy
Ann Neurol 4:253-256, Wakayama,Y.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Clinical Symposia, Scoliosis
CIBA, 30:21978., Keim,H.A., 1978

Myasthenia Gravis & Myotonic Dystrophy in a 13-year-old Girl
Neurol 27:546, Schoen,R.T., 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

The Spectrum of Mild X-Linked Recessive Muscular Dystrophy
Arch Neurol 34:408, Ringer,S.P.,et al, 1977

Prenatal Diagnosis of Duchenne's Muscular Dystrophy
NEJM 297:968, Mahoney,M.J.,et al, 1977

X-linked Muscular Dystrophy
Ann Neurol 2:414, Furukawa,T.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

Neurological Complications of Infections of the Head & Neck
Otolaryng Clin North Am 9:729, Kaplan,R.J., 1976

Carrier Detection in Duchenne Muscular Dystrophy
NEJM 294:193, Roses,A.D.,et al, 1976

Cardiac Features of Unusual X-linked Humeroperoneal Neuromuscular Disease
et al NEJM 293:1017, Waters,D.D., 1975

Polymyositis & Dermatomyositis
NEJM 292:344, 1975, 292:403975., Bohan,A.,et al, 1975

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Quadriceps Myopathy-Entity or Syndrome
Arch Neurol 31:60, Boddie,H.,et al, 1974

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Possible Neurogenic Factor in Muscular Dystrophy:Its Similarity to Denervation Atrophy
JNNP 36:399-410, Dastur,D.K.,et al, 1973

Thalmic Neuronal Inclusion Disease
Neurol 22, 3961972., Segarra,J., 1972

The Geography of Neurology
BMJ 2:506, Spillane,J.D., 1972

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972



Showing articles 300 to 350 of 1797 << Previous Next >>