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acetazolamide
acid maltase deficiency
advances in neurology
adverse drug reaction
airway obstruction
alopecia
alveolar hypoventilation
Alzheimer's disease
Alzheimer's disease, familial
amniocentesis
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
anasarca
anesthesia, general
anterior interosseous neuropathy
antiarrhythmic drugs
antibodies to voltage-gated calcium channels
anticoagulant, treatment
anticoagulant, treatment in CVD
anticonvulsants
anticonvulsants, untoward effects of
antihistamines
arrhythmia, cardiac
arthrogryposis multiplex
aspiration
aspirin
asymptomatic
ataxia
ataxia, paroxysmal
atelectasis
atrioventricular block
audiogram
auditory evoked brainstem potentials
autoimmune disease
automatic implantable cardioverter-defibrillator
axonopathy, distal
baldness
basal ganglia, calcification of
botulism
brachial neuritis
bradycardia
brainstem, lesion of
cachexia
CAG repeats
calcification, intracranial
calcium antagonist
calcium channel dysfunction
cancer of colon
carbamazepine
carbamazepine, toxicity
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
carotid angiogram
CAT scan
CAT scan, abnormal
CAT scan, muscle
cataracts
central core disease
central nervous system, infection of
cerebral blood flow
cerebral embolism
cerebral embolism, cardiac origin
cerebral ischemia
cerebrovascular accident
cerebrovascular accident, young adult
Charcot-Marie-Tooth
chewing, impaired
children
chloride channel dysfunction
cholestasis
chromosomal abnormality
chromosome 19
chromosome 3
chronic progressive external ophthalmoplegia
clubfoot as related to neurologic disease
complications
compression neuropathy
conduction block
confidentiality
congenital birth defects
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
corneal dystrophy
corpus callosum
corpus callosum, thinning
coumarin
creatine phosphokinase(CPK)elevated
defibrillator, implanted
degenerative diseases of CNS
dementia, thalamic
dentatorubral-pallidoluysian atrophy
dermatomyositis
diabetes mellitus
diaphragmatic paralysis
differential diagnosis
dilantin
dilantin, toxicity
diplopia
distal muscle weakness
DNA probes
dropped head syndrome
drug induced neurologic disorders
dysphagia
echocardiogram
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
electronystagmography
electronystagmography, abnormal
electrophoretic pattern, serum
electroretinograph
embolism
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
epidemiology of neurology
erythrocyte
evoked potentials
exercise
exercise electrocardiography
eye closure
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
falling
false negative
familial
familial hemiplegic migraine
Fazio-Londe's disease
floppy infant
fluorescein angiography
fragile-X syndrome
Friedreich's ataxia
frontal balding
F-wave response
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
glucose tolerance test, abnormal
gray matter
Guillain Barre syndrome
Guyon's canal
hand weakness
hearing loss
heart block
heart block, complete
heavy metal intoxication
high arched feet
high arched palate
histochemistry
histochemistry of muscle
H-reflex testing
huntingtin
Huntington's chorea
hydrocephalus
hydrops fetalis
hypercapnia
hyperinsulinism
hyperkalemic periodic paralysis
hyperostosis
hyperparathyroidism
hypersomnia
hypokalemia
hypokalemic periodic paralysis
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion body myositis
intellectual deficit
intelligence quotient
iris, abnormal
kaliuresis
Kearns-Sayre syndrome
klippel feil syndrome
Kugelberg-Welander syndrome
lid abnormalities
lid closure, weakness of
lid retraction, lower
life expectancy
lordosis
malignancy screen
malignant hyperpyrexia
manic-depressive
median neuropathy
Melkersson's syndrome
mental retardation
metabolic acidosis
mexiletine
microcephaly
micrognathia
migraine
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve prolapse
modafinil
molecular genetics
mononeuropathy
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, functional
MRI, muscle
MRS
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myasthenic syndrome
myocarditis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, distal
myopathy, drug-induced
myopathy, mitochondrial
myopathy, proximal
myopathy, thyroid disease causing
myositis
myotonia
myotonia congenita
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myotonia, causes of
myotonia, treatment of
neck weakness
neoplasm, metastatic to CNS
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
neuritis, causes of
neurofibrillary degeneration
neurofibromatosis 1
neurofibromatosis 2
neurogenic vs.myopathic atrophy
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuromuscular disease, electrodiagnosis of
neuronal migration disorder
neuropathy
neuropathy, amyloid
neuropathy, diabetic
neuropathy, motor, multifocal
neuropathy, peripheral
newborn, evaluation of
nifedipine
ocular myopathy
oculovestibular reflex
ophthalmoplegia
optic atrophy
orbicularis oculi muscle
orbit, lesions of
ovarian tumor
pacemaker, cardiac-transvenous
paramyotonia congenita
paresthesias
paroxysmal neurologic deficits
percussion induced muscle contraction
periodic paralysis
physical activity
platelet inhibiting drugs
pleural effusion
pneumonia
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
polymyositis
polyneuropathy
porphyria
posterior interosseous neuropathy
postoperative neurologic complications
potassium channel antibodies
potassium channel dysfunction
pregnancy, neurologic complications in
prevention of neurologic disorders
procainamide
prognosis
proptosis
proximal myotonic myopathy
psychological testing
ptosis
ptosis, bilateral
pulmonary function tests
radionuclide angiocardiography
recombinant DNA
respiratory failure
review article
RFLPs
rhabdomyolysis
risk factors
saccadic eye movements
saccadic eye movements, abnormal
safety
sarcoidosis
screening
seizure
sensorineural hearing loss
single photon emission computed tomography
sleep apnea
slit lamp examination
sodium channel dysfunction
somnolence
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 6
spinocerebellar degeneration
stiff man syndrome
sudden death
taurine
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
term infant
testicular atrophy
thoracic outlet syndromes
thyrotoxicosis
tocainide
torticollis
transient ischemic attack
treatment of neurologic disorder
tricresylphosphate
trinucleotide repeats
tubular aggregates, muscle
twins
ulnar neuropathy
ultrasonography
ventricular tachycardia
viral infection, CNS
visual evoked response
weakness
weaning from respirator, failure to
Werdnig-Hoffman disease
wheelchair
white matter disease
white matter disease, periventricular
workup
X-linked bulbospinal neuronopathy
Showing articles 500 to 550 of 797 << Previous Next >>

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998

Magnetic Resonance Imaging of Muscle in Amyotrophic Lateral Sclerosis
Neurol 51:110-113, Bryan,W.W.,et al, 1998

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

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

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

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

Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
Neurol 48:33-37, Hund,E.,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

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 & 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

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

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

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

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

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

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

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



Showing articles 500 to 550 of 797 << Previous Next >>