Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acetylcholine receptor antibody
acetylcholinesterase
acetylcholinesterase deficiency
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anterior tibial muscle weakness
antibiotics
antibiotics, neurologic complications with
antibodies to voltage-gated calcium channels
areflexia
arm weakness
arthralgia
arthritis
arthrogryposis multiplex
asymptomatic
atypical
autoimmune disease
autonomic dysfunction
botulism
brachial plexus neuropathy
bulbar palsy
bulbar palsy, acute
calcification, intracranial
calf atrophy
cancer associated myopathy
carcinoma
carcinoma of lung
cardiomyopathy
cardiotoxicity
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, false negative
central core disease
cerebral cortical atrophy
cerebral venous thrombosis
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
Charcot-Marie-Tooth
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
collagen vascular disease
coma
complications
congenital myasthenic syndromes
congenital myopathy
consanguinity
constipation
contractures, joint
cranial neuropathy
creatine phosphokinase(CPK)elevated
dementia
dermatitis
dermatomyositis
developmental retardation
diarrhea
diarrhea, bloody
diplopia
distal muscle weakness
DYSF gene
dysferlin
dysferlinopathy
dysphagia
electromyogram
electromyogram, incremental response
encephalopathy
encephalopathy, progressive
exercise
exercise-related muscle strength increase
exome sequencing
facial nerve palsy
facial nerve palsy, recurrent
facial weakness
facioscapulohumeral syndrome
familial
fatigue
finger weakness
foot drop
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Guillain Barre syndrome
hand weakness
headache
hearing loss
heat intolerance
high arched palate
hot bath test
H-reflex testing
hyporeflexia
iatrogenic neurologic disorders
immune checkpoint inhibitors
immune-related adverse events
impotence
ipilimumab
klippel feil syndrome
lactic acidemia
leg weakness, bilateral
leg weakness, unilateral
lid closure, weakness of
lordosis
MELAS syndrome
Melkersson's syndrome
mental retardation
mestinon
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
mononeuritis multiplex
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, brachial plexus
MRI, muscle
multiple sclerosis
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle diseases, characteristics of
muscle pain
muscle strength, testing
muscle weakness
muscle weakness, proximal
muscle weakness, sudden onset of
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, diagnosis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, presenting manifestations
myasthenia gravis, treatment of
myasthenic crisis
myasthenic syndrome
myasthenic syndrome, treatment of
myelopathy
myelopathy, chronic progressive
myocarditis
myoclonus
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, mitochondrial
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myositis, ocular
myotonia dystrophica
nasal speech
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction
neuromuscular junction, abnormality of
neuroophthalmology
neuropathy
neuropathy, diabetic
nivolumab
normal
opened mouth
ophthalmoplegia
optic atrophy
optic neuritis
pain, abdominal
paresthesias
pembrolizumab
poliomyelitis
polymyositis
polyneuropathy
porphyria
prognosis
ptosis
ptosis, bilateral
ragged-red fibers
regional enteritis
remote effect of cancer on the nervous system
repetitive nerve stimulation
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
sarcoidosis
sedimentation rate, elevated
seizure
sensorineural hearing loss
short stature
single-fiber electromyography
spinal muscular atrophy
steroid
stiff man syndrome
strokelike episodes
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tensilon test, false positive
torticollis
transient ischemic attack
treatment of neurologic disorder
type 1 muscle fiber
ulcerative colitis
upgaze, paralysis of
viral infection
vision, blurred
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
xerostomia
Showing articles 150 to 200 of 1924 << Previous Next >>

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Myelitis Due to Coxsackievirus B Infection
Neurol 45:1626-1627, Jadoul,C.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Lambert-Eaton Myasthenic Syndrome (LEMS) in Association with Lymphoproliferative Disorders
Muscle & Nerve 18:715-719995., Argov,Z.,et al, 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Bilateral Distal Upper Limb Amyotrophy and Watershed Infarcts from Vertebral Dissection
Stroke 25:1870-1872, Pullicino,P., 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Osteomalacic Myopathy
Muscle & Nerve 17:578-580994., Russell,J.A., 1994

Myasthenia Gravis
NEJM 330:1797-1810, Drachman,D.B., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

Focal Weakness Following Herpes Zoster
JNNP 56:1001-1003, Cockerell,O.C.&Ormerod,I.E.C., 1993

Sudden Onset of Profound Weakness in a Toddler
J Pediatr 122:663-667, Carraccio,C.,et al, 1993

Neuromuscular Manifestations of Wegener's Granulomatosis:A Case Report
Neurol 43:617-618, Finkelman,R.,et al, 1993

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Pravastatin-Associated Inflammatory Myopathy
NEJM 327:649-650, Schalke,B.B.,et al, 1992

Thyrotoxic Periodic Paralysis in the US, Report of 7 Cases & Review of the Literature
Medicine 71:109-120, Ober,K.P., 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

Pseudoradicular Syndrome in Multiple Sclerosis. 4 Cases Diagnosed by Magnetic Resonance Imaging
Revue Neurologique 148:692-695, Uldry,P.A.&Regli,F., 1992

Prognosis in AZT Myopathy
Neurol 41:1181-1184, Chalmers,A.C.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Colchicine-Induced Myopathy and Neuropathy
Neurol 41:943, Younger,D.S.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

The Bruns-Garland Syndrome (Diabetic Amyotrophy) , Revisited 100 Years Later
Arch Neurol 48:1130-1135, Barohn,R.J.,et al, 1991

Neurological Paraneoplastic Syndromes in Patients with Small Cell Lung Cancer, A Prospective Survey of 150 Pts
JNNP 54:764-767, Elrington,G.M.,et al, 1991

Benign Plexus Neuropathy in Children
J Pediatr 116:276-278, Zeharia,A.,et al, 1990

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

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

Relapsing Bilateral Brachial Plexopathy During Pregnancy, Report of a Case
Arch Neurol 46:462-464, Redmond,J.M.T.,et al, 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,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

Man-In-The-Barrel Syndrome Caused by Cerebral Metastases
Neurol 39:1134-1135, Moore,A.P.&Humphrey,P.R.D., 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Myasthenia Gravis
In Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, 697, Penn,A.S.&Rowland,L.P., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

Early-Onset Benign Autosomal Dominant Limb-Girdle with Contractures (Bethlem Myopathy)
Neurol 38:573-580, Mohire,M.D.,et al, 1988

Human Immunodeficiency Virus-Associated Myopathy:Analysis of 11 Pts
Ann Neurol 24:79-84, Simpson,D.M.&Bender,A.N., 1988

Progressive Nemaline (Rod) Myopathy Associated with HIV Infection
NEJM 317:1602-1603, Dalakas,M.C.,et al, 1987

Man-In-The-Barrel Syndrome:First CT Images
Neuroradiology 29:501, Delavelle,J.,et al, 1987

Progressive Multifocal Leukoencephalopathy Associated with Human Immunodeficiency Virus Infection
Ann Int Med 107:78-87, Berger,J.R., 1987

Chloroquine Neuromyotoxicity, Clinical & Pathological Perspective
Am J Med 82:447-455, Estes,M.L.,et al, 1987



Showing articles 150 to 200 of 1924 << Previous Next >>