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abdominal distention
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
ataxia
atrioventricular block
automatic implantable cardioverter-defibrillator
blepharophimosis
blepharospasm
bradycardia
bulging of biceps
cachexia
calcification, intracranial
calf atrophy
calf hypertrophy
calpain III deficiency
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
coma
complications
conduction block
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
creatine kinase
creatine phosphokinase(CPK)elevated
deafness
dementia
dermatomyositis
descending paralysis
developmental retardation
diamond on quadriceps
diarrhea
differential diagnosis
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspraxia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
exercise
exercise intolerance
extraocular muscle lesion
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fatigue
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
hammertoes
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
high arched feet
hip dysplasia
hip flexor weakness
hip pain
histochemistry of muscle
hyperthyroidism
hypoglycemia
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunohistochemistry
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
insulin
intestinal pseudoobstruction
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lactic dehydrogenase(LDH)
laminopathies
leg weakness, bilateral
leukodystrophy
lid closure, weakness of
life expectancy
limb-girdle weakness
LMNA gene
lordosis
lymphocyte capping, diminished
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
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, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, pattern of muscle involvement
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hypokalemic
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia
myotonia dystrophica
myotonic discharges
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuroophthalmology
neuropathy
neuropathy, diabetic
next-generation sequencing
normal
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
pacemaker, cardiac-transvenous
pain, abdominal
pain, leg
pinched face
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
positive sharp waves
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
ragged-red fibers
recurrent
respirator
respiratory failure
retina, abnormal
retinal lesion
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
Schwartz-Jampel syndrome
scoliosis
seizure
sensorineural hearing loss
short stature
shoulder, pain in
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
syncope
systemic illness
toe walking
torticollis
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
workup
Showing articles 1700 to 1750 of 2171 << Previous Next >>

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

Bilateral Infarction of the Medullary Pyramids in Humans
Neurol 39:21-24, Jagiella,W.M.&Sung,J.H., 1989

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Cauda Equina Syndrome Secondary to Disseminated Zygomycosis
JAMA 260:3638-3640, Rozich,J.,et al, 1988

Clinicopath Conf
Lyme Disease, Case Record 51-1988, NEJM 319:1654-1662988., , 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,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

The Minor Symptoms of Increased Intracranial Pressure:101 Pts with Benign Intracranial Hypertension
Neurol 38:1461-1464, Round,R.&Keane,J.R., 1988

Acute Paralysis from Inhaled Barium Carbonate
Arch Neurol 45:579-580, Shankle,R.&Keane,J.R., 1988

Bilateral Neuralgic Amyotrophy Induced by Interferon Treatment
Arch Neurol 45:449-451, Bernsen,P.L.J.A.,et al, 1988

Brachial Plexus Neuropathy Associated with Human Parvovirus Infection
BMJ 296:896, Walsh,K.J.,et al, 1988

Overuse Syndrome:A Muscle Biopsy Study
Lancet 1:905-908, Dennett,X.&Fry,H.J.H., 1988

Weakness of the Lower Extremity in Carotid Occlusive Disease
Arch Neurol 45:297-301, Yanagihara,T.,et al, 1988

Severe Polymyositis-Like Syndrome Associated with Zidovudine Therapy of AIDS & ARC
NEJM 318:708, Bessen,L.J.,et al, 1988

Vertebral Osteomyelitis Presenting as Spinal Compression Fracture, Six Pts with Underlying Osteoporosis
Arch Int Med 148:417-423, McHenry,M.C.,et al, 1988

Lyme Disease & Its Neurologic Complications
Arch Neurol 45:99-104, Finkel,M.F., 1988

Detection of HTLV-I DNA & Antigen in Spinal Fluid & Blood of Pts with Chronic Progressive Myelopathy
NEJM 318:1141-1147, 11951988., Bhagavati,S.,et al, 1988

Limb Pain in Migraine & Cluster Headache
JNNP 51:1022-1031, Guiloff,R.J.&Fruns,M., 1988

Mycobacterial Meningomyelitis Associated with Human Immunodeficiency Virus Infection
Arch Neurol 45:691-693, Woolsey,R.M.,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

Use of Composite Scores (Megascores) to Measure Deficit in Amyotrophic Lateral Sclerosis
Neurol 38:405-408, Andres,P.L.,et al, 1988

Dialysis Myelopathy:Quardiparesis Due to Extradural Amyloid of B2 Microglobulin Origin
BMJ 296:752-753, Allain,T.J.,et al, 1988

Back Pain & Sciatica
NEJM 318:291-300, Frymoyer,J.W., 1988

Partial Epilepsy Presenting as Focal Paroxysmal Pain
Neurol 38:329-330, Trevathan,E.&Cascino,G.D., 1988

Clinicopath Conf
Adenocarcinoma of Lung, with Metastasis to Meninges of Brain, Spinal Cord & Optic Nerves, Case Recor, 14-1EJM 318:903-915,1988., 1988

Aortic Dissection Presenting with Neurologic Signs
NEJM 318:1070, Garcia-Diaz,J.D.,et al, 1988

Acute Paraplegia:A Presenting Manifestation of Aortic Dissection
Am J Med 84:765-770, Zull,D.N.&Cydulka,R., 1988

'Convulsions'in Basilar Artery Occlusion
Neurol 38:1500-1501, Ropper,A.H., 1988

Postmarketing Surveillance for Neurologic Adverse Events after Hepatitis B Vaccination, Exp of the First 3 Yrs
Am J Epidemiol 127:337-352, Shaw,F.E.,et al, 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Paraplegia and Quadriplegia after Intrathecal Chemotherapy
Arch Phys Med Rehabil 69:1054-1056, Werner,R.A., 1988

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

Hysterical Conversion Reactions Mimicking Neurological Disease
Am J Dis Child 142:1203-1206, Bangash,I.H.,et al, 1988

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

Hyperthyroidism Presenting as Pyramidal Tract Disease
BMJ 297:1395-1396, Shaw,P.J.,et al, 1988

Dysphagia in Inclusion Body Myositis
JNNP 51:1542-1545, Wintzen,A.R.,et al, 1988

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

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

The Prevention of Injuries of the Brachial Plexus Secondary to Malpostition of the Patient During Surgery
ClinOrhop 288:33-41, Cooper,D.E.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988



Showing articles 1700 to 1750 of 2171 << Previous Next >>