Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal muscle paralysis
acetylcholine receptor antibody
acid maltase deficiency
acid maltase deficiency, adult
Addison's disease
advances in neurology
algorithm
alveolar hypoventilation
amyloid
amyloidosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, treatment of
amyotrophic lateral sclerosis-like syndrome
anemia
anesthesia, general
anosmia
anterior horn cell disease
anterior interosseous neuropathy
anterior tibial muscle weakness
aphonia
apnea
areflexia
arrhythmia, cardiac
arsenic
arthrogryposis multiplex
ascending paralysis
aspiration
asymptomatic
ataxia, cerebellar
ataxia, sensory
ataxic gait
atrioventricular block
autoantibodies
autoimmune disease
azathioprine
BAL
baldness
basal ganglia, infarction
basophilic stippling of red blood cells
benign congenital hypotonia
bitemporal visual field defect
bone marrow suppression
brachial neuritis
bulbar palsy
bulbar palsy, acute
bulging of biceps
burning feet
burning paresthesia
cachexia
CAG repeats
calcification, intracranial
calf atrophy
calf hypertrophy
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carpo-pedal spasm
cataracts
central core disease
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
Charcot-Marie-Tooth
chewing, impaired
children
chromosomal abnormality
chromosome 17
chromosome 19
chromosome 5
chromosome 9
chronic polyneuritis, children
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
collagen vascular disease
coma
complications
compression neuropathy
concussion
conduction block
congenital heart disease
congenital myopathy
congestive heart failure
contractures, joint
controversies in neurology
coronavirus
cortical hand knob
cost
cost effectiveness
COVID-19
coxsackievirus
coxsackievirus, myopathy with
CPAP
craniopharyngioma
creatine phosphokinase(CPK)elevated
critical illness
Cushing's syndrome
cystinosis
degenerative diseases of CNS
delay in diagnosis
dementia
dermatitis
dermatomyositis
desmin
developmental retardation
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diaphragmatic paralysis
diarrhea
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dropped head syndrome
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dysphonia
dyspnea
dystrophic calcification
dystrophin
edema, pedal
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
encephalitis, brainstem
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
entrapment neuropathy
enzyme, defect
enzyme, muscle disease
eosinophilia
epidemiology of neurology
erythrocyte
evidence-based research
evoked potentials
exercise
exophthalmus
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
failure to thrive
falling
familial
fasciculation
fatigable chewing
fatigue
Fazio-Londe's disease
fibrillations
fine motor function, impaired
finger drop
finger flexor weakness
finger weakness
fingernails, abnormal
floppy infant
foot deformity
foot drop
foot drop, bilateral
fracture, long bone
fragile-X syndrome
gag reflex, depressed
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gastrocnemius muscle weakness
gastroenteritis
gender
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
Guillain Barre syndrome, differential diagnosis of
Guyon's canal
gynecomastia
hallucination
hallucination, auditory
hammertoes
hand deformity
hand weakness
Hand-Schuller-Christian disease
head injury
headache
heart block
heart block, complete
heavy metal intoxication
hemidiaphragm, paralysis of
hemoglobinuria
hepatitis
hepatomegaly
heralding manifestation
hereditary myopathy with early respiratory failure
high arched feet
high arched palate
histochemistry
histochemistry of muscle
hoarseness
Huntington's chorea
hyperadrenalism
hyperamylasemia
hypercalcemia
hypercapnia
hyperinsulinism
hyperkalemia
hyperkeratosis
hyperparathyroidism
hyperreflexia
hypertension
hyperthyroidism
hypoglycemia
hypokalemic periodic paralysis
hypoparathyroidism
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypotonia
hypotonia, infants
hypoxic encephalopathy
imbalance
immunohistochemistry
immunologic disease
immunosuppressive agents
inability to sit up
inability to stand on tiptoes
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion body myositis
intermittent positive pressure breathing
intrinsic hand muscles, wasting of
islet cell tumor
klippel feil syndrome
Kugelberg-Welander syndrome
leg weakness, bilateral
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukopenia
level of consciousness, decreased
lid closure, weakness of
life expectancy
liver disease
liver function enzymes
lordosis
median neuropathy
Mees lines
MELAS syndrome
mental retardation
methotrexate
middle cerebral artery, occlusion of
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mononeuritis multiplex
mononeuropathy
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, muscle
multiple myeloma
multiple sclerosis
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
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, causes of
muscle weakness, insidious onset of
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, diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, treatment of
myasthenic crisis
myocarditis
myoedema
myopathy
myopathy, amyloid
myopathy, autoimmune
myopathy, carcinomatous
myopathy, centronuclear
myopathy, desmin
myopathy, distal
myopathy, distal Laing
myopathy, distal, vacuolar
myopathy, distal, Welander's
myopathy, hereditary
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, necrotizing
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia
myotonia congenita
myotonia dystrophica
myxedema coma
myxedema, neurologic manifestations of
nasal speech
nausea and vomiting
neck extension
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, pituitary
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
nerve hypertrophy
neuritis, causes of
neuritis, heavy metals causing
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal migration disorder
neuronopathy
neuropathy
neuropathy, diabetic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, motor, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, toxic
newborn, evaluation of
next-generation sequencing
nusinersen
occipital lobe, infarction
occipital lobe, lesion of
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, total
Oppenheim muscular dystrophy
orthopnea
osteomalacia
pain
pancreatitis
pancytopenia
pandemic
papilledema
paranoia
paraparesis
paraspinal muscle
paraspinal muscle weakness
parathyroid adenoma
paresthesias, feet
paresthesias, hands
percussion induced muscle contraction
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
pes cavus
pheochromocytoma
phosphorylase b kinase deficiency
phrenic nerve pacemaker
plasmapheresis
pleural effusion
poison, mercury
poison, neurologic problems with
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic inflammatory demyelinating, variant form
polyneuropathy, chronic inflammatory demyelinating-pure motor syn
polyneuropathy, chronic inflammatory demyelinating-sens atax var
polyneuropathy, chronic inflammatory demyelinating-variant forms
polyneuropathy, familial
porphyria
position sensation, abnormal
positive sharp waves
post polio syndrome
posterior interosseous neuropathy
pregnancy, neurologic complications in
primary aldosteronism
prognosis
progressive muscular dystrophy
progressive neurologic disorder
progressive spinal muscular atrophy
proprioception, abnormal
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
psychosis
ptosis
quadriceps atrophy
quadriceps weakness
quadriparesis
quadriplegia
quality of life
rash
renal stones
repetitive nerve stimulation
respirator
respiratory depression
respiratory failure
review article
RFLPs
rheumatoid arthritis
Romberg's sign
sarcoidosis
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, treatment of
serologic testing
severe acute respiratory syndrome
short stature
skin, lesions in neurologic disorders
sleep apnea
slit lamp examination
SMN1 gene
spinal cord, injury of
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar degeneration
standing difficulty
steppage gait
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
survival motor neuron gene
sweating, abnormality of
syringomyelia
tandem gait, ataxic
teleconsulting
telemedicine
teleneurology
telestroke
temporalis muscle wasting
temporalis muscle weakness
temporomandibular joint, dislocation
tetany
thoracic outlet syndromes
thrombocytopenia
thyrotoxicosis
titinopathy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
treatment of neurologic disorder
tremor
tremor, postural
tricresylphosphate
trigger finger
trinucleotide repeats
Trousseau's sign
ulnar neuropathy
uremia
urine test in toxic screen
vasculitides
viral infection
viral infection, CNS
visual evoked response
vital capacity
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
X-linked bulbospinal neuronopathy
Showing articles 1200 to 1250 of 1838 << Previous Next >>

Treatment of Dermatomyositis with Intravenous Gammaglobulin
Am J Med 91:169-172, Lang,B.A.,et al, 1991

Efficacy of Intravenous Gammaglobulin Therapy in Chronic Refactory Polymyositis & Dermatomyositis:20 Adult Patients
Am J Med 91:162-168, Cherin,P.,et al, 1991

The Idiopathic Inflammatory Myopathies and Their Treatment
JNNP 54:285-287, Walton,J., 1991

Magnetic Resonance Imaging Shows Specific Abnormalities in the MELAS Syndrome
Neurol 41:1043-1046, Matthews,P.M., 1991

Mitochondril Encephalopathies:Molecular Genetic Diagnosis from Blood Samples
Lancet 337:1311-1313, Hammans,S.R.,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

Steroid-Induced Weakness in Patients with Primary Brain Tumors
Neurol 41:1235-1239, Dropcho,E.J.&Soong,S., 1991

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Polymyositis Mediated by T Lymphocytes that Express the y/8 Receptor
NEJM 324:877-881, Hohlfeld,R.,et al, 1991

Cyclosporin in the Management of Polymyositis and Dermatomyositis
JNNP 54:1007-1008, Lueck,C.J.,et al, 1991

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

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

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

Adult Reye's Syndrome:A Review with New Evidence for a Generalized Defect in Intramitochondrial Enzyme Processing
Neurol 41:1815-1821, VanCoster,R.N.,et al, 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Necrotizing Myopathy with Pipestem Capillaries, Microvasc Depos
Neurol 41:936-939, Emslie-Smith,A.M.&Engel,A.G., 1991

Traumatic Pseudoaneurysm of the Cervical Carotid Artery:The Value of Arteriography
Neurosurgery 26:312-315, Applegate,L.J.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Neurologic Sequelae of Domoic Acid Intoxication Due to the Ingestion of Contaminated Mussels
NEJM 322:1781-1787, Teitelbaum,J.S.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Hemiplegia in Posterior Cerebral Artery Occlusion
Neurol 40:1496-1499, Hommel,M.,et al, 1990

Diagnosis of Cerebrovascular Disease in Sickle Cell Anemia by Magnetic Resonance Angiography
J Pediatr 117:551-555, Wiznitzer,M.,et al, 1990

Noninvasive Detection of Occlusive Disease of the Carotid Siphon & Middle Cerebral Artery
Ann Neurol 28:640-647, Ley-Pozo,J.&Ringelstein,E.B., 1990

The Large Striatocapsular Infarct, A Clinical and Pathophysiological Entity
Arch Neurol 47:1085-1091, Weiller,C.,et al, 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,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

Stroke in Young Adults
Stroke 21:382-386, Bevan,H.,et al, 1990

Anterior Cerebral Artery Territory Infarction in the Lausanne Stroke Registry
Arch Neurol 47:144-150, Bogousslavsky,J.&Regli,F., 1990

Carotid Plaque Morphology and Risk for Stroke
Stroke 21:148-151, Gomez,C.G., 1990



Showing articles 1200 to 1250 of 1838 << Previous Next >>