Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acid maltase deficiency
advances in neurology
alveolar hypoventilation
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
analgesic
anesthesia, general
anterior interosseous neuropathy
anterior tibial muscle weakness
anxiety
apnea
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
asymptomatic
atrioventricular block
axonopathy, distal
baldness
benign congenital hypotonia
benzodiazepine
brachial neuritis
bulging of biceps
cachexia
CAG repeats
calf atrophy
carcinoma
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebrovascular accident
cervical spine injury
Charcot-Marie-Tooth
children
chromosome 19
chronic polyneuritis, children
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
complications
compression neuropathy
concussion
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
cost
cost effectiveness
CPAP
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
dermatomyositis
diaphragmatic paralysis
differential diagnosis
distal muscle atrophy
distal muscle weakness
dying
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspnea
dystrophic calcification
dystrophin
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
ethics in neurology
euthanasia
evidence-based research
exercise
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
Fazio-Londe's disease
fibrillations
floppy infant
foot drop
fragile-X syndrome
gastrocnemius muscle weakness
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Guillain Barre syndrome
Guyon's canal
hand weakness
head injury
headache
heart block
heavy metal intoxication
hepatomegaly
high arched palate
hospice
hunger
huntingtin
Huntington's chorea
hypercapnia
hypoglycemia
hypoglycemic coma
hypotonia
hypotonia, infants
hypoxic encephalopathy
immunohistochemistry
immunologic disease
immunosuppressive agents
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intermittent positive pressure breathing
intrinsic hand muscles, wasting of
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
lid closure, weakness of
life sustaining treatment
locked-in syndrome
lordosis
median neuropathy
medical-legal aspects of neurology
mental retardation
methotrexate
misdiagnosis
molecular genetics
mononeuropathy
morphine
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, muscle
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 strength, testing
muscle swelling
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenic crisis
myocarditis
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, mitochondrial
myopathy, necrotizing
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia congenita
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
neuritis, causes of
neurofibrillary degeneration
neurogenic vs.myopathic atrophy
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neuromuscular blockade
neuromuscular junction, abnormality of
neuronal migration disorder
neuropathy
neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
next-generation sequencing
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
Oppenheim muscular dystrophy
oxygen therapy
palliative care
Parkinson disease
percussion induced muscle contraction
phosphorylase b kinase deficiency
phrenic nerve pacemaker
physician assisted suicide
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
posterior interosseous neuropathy
practice guidelines
pregnancy, neurologic complications in
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proximal muscle atrophy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
rash
respirator
respiratory depression
respiratory failure
review article
RFLPs
right to die
sarcoidosis
sedation
seizure
short stature
sleep apnea
slit lamp examination
spinal cord, injury of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinocerebellar ataxia type 1
spinocerebellar degeneration
standing difficulty
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
thoracic outlet syndromes
torticollis
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
ulnar neuropathy
valium
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 400 to 450 of 1368 << Previous Next >>

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
Lancet 336:651-653, Wijmenga,C.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989

Duchenne Muscular Dystrophy Carrieris
Neuroradiology 31:373-376, Matsumura,K., 1989

Mosaic Expression of Dystrophic in Symptomatic Carriers of Duchenne's Muscular Dystrophy
NEJM 320:138-142, Arahata,K.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Distinction of Becker from Limb-Girdle Muscular Dystrophy by Means of Dystrophin cDNA Probes
Lancet 1:466-468, Norman,A.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Randomized, Double-Blind Six-Month Trial of Prednisone in Duchenne's Muscular Dystrophy
NEJM 320:1592-1597, 1621-16231989., Mendell,J.R.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

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

Magnetic Resonance Imaging and Clinical Correlates of Intellectual Impairment in Myotonic Dystrophy
Arch Neurol 46:536-540, Huber,S.J.,et al, 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

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

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

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

Hydrops and Pleural Effusions in Congenital Myotonic Dystrophy
J Pediatr 113:555-557, Curry,C.J.R.,et al, 1988

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

Magnetic Resonance Imaging in Amyotrophic Lateral Sclerosis
Ann Neurol 23:418-420, Goodin,D.S.,et al, 1988

A Double-Blind Study of the Effectiveness of Cyclosporine in Amyotrophic Lateral Sclerosis
Arch Neurol 45:381-386, Appel,S.H.,et al, 1988

Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,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

Hearing Loss in Myotonic Dystrophy
Ann Neurol 23:202-203, Wright,R.B.,et al, 1988

Central Nervous System Magnetic Resonance Imaging Findings in Myotonic Dystrophy
Arch Neurol 45:36-37, Glantz,R.H.,et al, 1988

Amyotrophic Lateral Sclerosis, Recent Advances in Pathogenesis & Therapeutic Trials
Arch Neurol 45:189-202, Mitsumoto,H.,et al, 1988

The Natural History of Motoneuron Loss in Amyotrophic Lateral Sclerosis
Neurol 38:409-413, Munsat,T.L.,et al, 1988



Showing articles 400 to 450 of 1368 << Previous Next >>