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Differential
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acetylcholine receptor antibody
adverse drug reaction
amyotrophic lateral sclerosis, differential diagnosis
anterior tibial muscle weakness
antistriational muscle antibody
areflexia
arrhythmia, cardiac
Bell's phenomenon
botulism
brainstem, lesion of
bulbar palsy
calf atrophy
canned food
cardiac arrest
cardiac arrest and resuscitation
cataracts
central core disease
chewing, impaired
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Collier's sign
congenital myopathy
creatine phosphokinase(CPK)elevated
descending paralysis
diplopia
distal muscle weakness
dysarthria
dysphagia
dyspnea
electromyogram
electromyogram, decremental response
eye closure
face, elongated
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fatigable chewing
fatigue
fibrillations
food poisoning
foot drop
gag reflex, depressed
gait disorder
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
hand weakness
histochemistry of muscle
hypophonia
hypotonia
immunohistochemistry
immunosuppressive agents
inclusion body myositis
internuclear ophthalmoplegia
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
leg weakness, bilateral
lid abnormalities
lid closure, weakness of
lid twitch
lordosis
mediastinum, mass of
Melkersson's syndrome
mestinon
misdiagnosis
mitochondrial disease
motor neuron disease
multicore myopathy
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, presenting manifestations
myasthenia gravis, prognosis of
myasthenia gravis, remission of
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myasthenic sneer
myopathy
myopathy, centronuclear
myopathy, inflammatory
myopathy, mitochondrial
myotonia
myotonia dystrophica
nasal regurgitation
nasal speech
nausea and vomiting
neck weakness
nemaline rod myopathy
nerve conduction studies
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuroophthalmology
neurotoxin
nystagmus
ocular motility, disorders of
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
orbicularis oculi muscle
oropharyngeal weakness
overlap syndrome
penicillamine
percussion induced muscle contraction
plasmapheresis
polymyositis
positive sharp waves
prognosis
progressive neurologic disorder
pseudointernuclear ophthalmoplegia
ptosis
ptosis, alternating
ptosis, bilateral
quadriparesis, acute
quinine
ragged-red fibers
rapidly progressing neurologic illness
repetitive nerve stimulation
respiratory failure
review article
saccadic eye movements
saccadic eye movements, abnormal
scoliosis
seronegative
shoulder-girdle wasting
single-fiber electromyography
sleep
sloped shoulders
spinal muscular atrophy
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
temporalis muscle wasting
tensilon
tensilon test, false negative
tensilon test, false positive
tensilon test, paradoxical
thymectomy
thymoma
tongue, weakness
toxins, nervous system
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
voice, abnormality of
walking, difficulty with
weakness
weakness, acute
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weaning from respirator, failure to
weight loss
wheelchair
whistle, inability to
winging of scapula
Showing articles 1150 to 1200 of 3180 << Previous Next >>

Linkage of Proximal Myotonic Myopathy to Chromosome 3q
Neurol 52:170-171,12, Ricker,K.,et al, 1999

Medical Complications in Long-Term Survivors with X-Linked Myotubular Myopathy
J Pediatr 134:206-214, Herman,G.E.,et al,, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Electromyography and Magnetic Resonance Imaging in the Evaluation of Radiculopathy
Muscle & Nerve 22:151-155,149, Nardin,R.A.,et al,, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Churg-Strauss Syndrome, Clinical Study and Long-Term Follow-Up of 96 Patients
Medicine 78:26-37, Guillevin,L.,et al, 1999

Ischemic Stroke,Impact of a Recent Myocardial Infarction
Stroke 30:997-1001, Mooe,T.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Neurology and the Skin
JNNP 66:417-430, Hurko,O.&Provost,T.T., 1999

Myocardial Injury and Left Ventricular Performance After Subarachnoid Hemorrhage
Stroke 30:780-786, Mayer,S.A.,et al, 1999

Outcome in Severe Pediatric Guillain-Barre Syndrome after Immunotherapy or Supportive Care
Neurol 52:1494-1497, Graf,W.D.,et al, 1999

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Chronic Cryptogenic Sensory Polyneuropathy,Clinical and Laboratory Characteristics
Arch Neurol 56:540-547, 519, Wolfe,G.I.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Pain and the Guillain-Barre Syndrome in Children Under 6 Years
J Pediatr 134:773-776, Nguyen,D.K.,et al, 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

Focal, Steroid Responsive Myositis Causing Dropped Head Syndrome
Muscle & Nerve 22:769-771, Biran,I.,et al, 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

Generalised Muscular Weakness after Botulinum Toxin Injections for Dystonia:A Report of Three Cases
JNNP 67:90-93, Bhatia,K.P.,et al, 1999

What is Carpal Tunnell Syndrome?
JAMA 282:186-187,153, Franzblau,A.&Werner,R.A., 1999

Intravenous Immunoglobulin Treatment in Neurologic Disorders
Arch Neurol 56:1025-1027,1032, Sorensen,P.S., 1999

Is the Routine Use of Intravenous Immunoglobulin Treatment in Neurologic Disorders Justified?
Arch Neurol 56:1028-1032, Karussis,D.&Abramsky,O., 1999

Tracheostomy, In Guillain- Barre Syndrome
Muscle & Nerve 22:1058-1062, Lawn,N.D.&Wijdicks,E.F.M., 1999

Prognostic Factors of Guillain-Barre Syndrome After Intravenous Immunoglobulin or Plasma Exchange?
Neurol 53:598-604, Visser,L.H.,et al, 1999

Amyloid Myopathy:An Underdiagnosed Entity
Ann Neurol 43:719-728, Spuler,S.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Medical Complications Associated with Carotid Endarterectomy
Stroke 30:1759-1763, Paciaroni,M.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Neurologic Complications Associated with Hepatitis C Virus Infection
Neurol 53:861-864, Tembl,J.I.,et al, 1999

Adult-Onset "Infant" Botulism:An Unusual Cause of Weakness in the Intensive Care Unit
Neurol 53:891, Li,L.Y.J.,et al, 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Brachial Amyotrophic Diplegia, A Slowly Progressive Motor Neuron Disorder
Neurol 53:1071-1076, Katz,J.S.,et al, 1999

Optimality Score for the Neurologic Examination of the Infant at 12 and 18 Months of Age
J Pediatr 135:153-161,140, Haataja,L.,et al, 1999

Neurologic Manifestations of Compressive Radiculopathy of the First Thoracic Root
Neurol 53:1149-1151, Levin,K.H., 1999

A Sartorial Challenge
Lancet 354:996, Reading,P.J.,et al, 1999

The Stiff-Person Syndrome:An Autoimmune Disorder Affecting Neurotransmission of y-Aminobutyric Acid
Ann Int Med 131:522-530, Levy,L.M.,et al, 1999

Microscopic Polyangiitis: Clinical and Laboratory Findings in Eighty-five Patients
Arthritis Rheum 42:421--430, Guillevin, L.,et al, 1999

Suprascapular Neuropathy
J Am Acad Orthop Surg 7:358-367, Romeo, A.A.,et al, 1999

Leukoencephalopathy and Raised Brain Lactate from Heroin Vapor Inhalation ("Chasing the Dragon")
Neurol 53:589-1048, Kriegstein,A.R., et al, 1999

Delayed Movement Disorders After Carbon Monoxide Poisoning
Eur Neurol 42:141-144, Choi,I.S. &Cheon,H.Y., 1999

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998



Showing articles 1150 to 1200 of 3180 << Previous Next >>