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Differential
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abdominal muscle paralysis
abducens nerve paralysis
abducens nerve paralysis, bilateral
abscess, intracerebral
acanthocytosis
acetylcholine receptor antibody
acid maltase deficiency
acid maltase deficiency, adult
acyl CoA dehydrogenase deficiency
adverse drug reaction
alopecia
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, misdiagnosis
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ankle clonous
anterior horn cell disease
anterocollis
anti Hu antibody
antibodies to voltage-gated calcium channels
anticholinergic drugs
anticoagulant, complications of
anticoagulant, treatment
anticoagulant, treatment in CVD
aphasia
areflexia
arm weakness
arrhythmia, cardiac
artane
aspiration
ataxia
ataxia, truncal
atrioventricular block
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial infection, CNS
baldness
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
blacks
blepharospasm
bone marrow biopsy
Borrelia burgdorferi infection
botulinum toxin
botulinum toxin, complications of
botulism
botulism immune globulin
botulism, infant
Brueghel's syndrome
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
camptocormia
campylobacter infection
carcinoma
carcinoma of lung
cardiomyopathy
cardiovascular disease
carnitine deficiency
carnitine deficiency myopathy
CAT scan, chest
cataracts
cauda equina, enhancement
central core disease
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, flow cytometry
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, prognosis in
chemotherapy, CNS treatment and complications with
children
choking
chorea
chromosomal abnormality
chromosome 1
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
complications
conduction block
confusion
congenital heart disease
congenital myopathy
congestive heart failure
constipation
contractures, joint
coumarin
cranial nerve enhancement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine kinase
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
critical care unit
cry, abnormal
cry, weak
cyclic vomiting
decompressive spinal cord surgery
degenerative diseases of CNS
delay in diagnosis
dementia
denervation of muscle
denervation potentials
dermatomyositis
descending paralysis
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplegia, brachial
diplopia
distal muscle atrophy
distal muscle weakness
drooling
dropped head syndrome
drug induced neurologic disorders
drug withdrawal
duvalumab
dysarthria
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dysphonia
dyspnea
dystonia
dystonia, cervical
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, post traumatic
dystonia, treatment of
dystrophic calcification
efficacy
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electromyogram, incremental response
electron microscopy
ELISA
emergencies, neurologic
emergencies, neurosurgical
Emery-Dreifuss muscular dystrophy
encephalitis, brainstem
encephalomyelitis
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exercise-related muscle strength increase
eye closure
face, elongated
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
familial
fasciculation
fatigue
fever
fibrillations
floppy infant
fluctuate
foot drop
foot drop, bilateral
frontal balding
gait disorder
gammaglobulin therapy, intravenous
ganglionitis
gangliosidosis GM2
gastric dilatation, acute
gastrocnemius muscle weakness
gaze deviation
gemfibrozil
gene
gene mutation
genetic neurologic disorders
genetic testing
GM1 ganglioside antibodies
Gowers maneuver
Guillain Barre syndrome
Guillain Barre syndrome, pharyngeal-cervical-brachial variant
Guillain Barre syndrome, variant forms of
hand weakness
headache
heart block
heat intolerance
hematoma, epidural-spinal
hemifacial spasm
hemiparesis
hepatomegaly
heralding manifestation
hexosaminidase-A
high arched palate
highly active antiretroviral therapy
hip flexor weakness
histochemistry of muscle
HMGcoA reductase inhibitors
hoarseness
horse bite
hot bath test
H-reflex testing
human immunodeficiency virus type 1
Huntington's chorea
hydroxychloroquine
hypercapnia
hyperreflexia
hypoglycemia
hypomyelination
hyporeflexia
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immune checkpoint inhibitors
immune-related adverse events
immunosuppression
immunosuppressive agents
immunotherapy
impotence
inability to stand on tiptoes
inborn errors of metabolism
inclusion bodies
inclusion body myositis
infant, evaluation of
INR values
insecticides
interstitial pulmonary fibrosis
intestinal biopsy
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
ipecac
ipilimumab
jaw jerk, abnormal
Jewish
lactic acidemia
laterocollis
leg weakness, bilateral
Leigh's disease
lid closure, weakness of
limb-girdle weakness
limbic encephalitis
lipid lowering agent
lipid storage disorder of CNS
lipid storage myopathy
liver transplantation
lovastatin
Lyme disease
lymphoma
lymphoma involving CNS
lysosomal storage disease
macrocephaly
masseter muscle wasting
mediastinum, mass of
mediastinum, widening
MEK inhibitor
melanoma, malignant
meningeal enhancement
meningitis
meningitis, bacterial
meningitis, pneumococcal
metabolic acidosis
Mills syndrome
misdiagnosis
mixed connective tissue disease
molecular genetics
monoclonal antibodies
monoclonal gammopathy
monomelic myositis
mortality
motor neuron disease
motor neuron disease, spontaneous recovery
movement disorder
movement disorder, drug induced
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, emergent
MRI, hypointense signal foci on
MRI, muscle
MRI, perfusion
MRI, ring sign
MRI, spine
multicore myopathy
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle twitching
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, facioscapulohumeral
muscular dystrophy, LAMA2
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, drug induced
myasthenia gravis, limb-girdle
myasthenia gravis, paraneoplastic
myasthenia gravis, presenting manifestations
myasthenic syndrome
myocarditis
myoclonus
myoclonus, epilepsy
myoneuropathy
myopathy
myopathy, acute
myopathy, axial
myopathy, centronuclear
myopathy, critically ill
myopathy, distal
myopathy, distal Laing
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, focal
myopathy, genetic
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, necrotizing, immune-mediated
myopathy, proximal
myopathy, radiation-induced
myopathy, steroid induced
myopathy, toxic
myopathy, vacuolar
myositis
myositis, bacterial
myositis, eosinophilic
myositis, focal
myositis, fungal
myositis, granulomatous
myositis, ocular
myositis, parasitic
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myxedema, neurologic manifestations of
nasal speech
nausea and vomiting
neck extension
neck flexion
neck pain
neck stiffness
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, metastatic to CNS
neoplasm, primary of CNS-intraventricular
nerve biopsy
nerve conduction studies
nerve root enhancement
neurologic complications of, chronic pulmonary disease
neurologic disease, diagnoses of
neurological intensive care
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronopathy
neuronopathy, sensory
neuropathology
neuropathy
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, toxic
neurotoxic
neurotoxin
next-generation sequencing
nivolumab
nystagmus
nystagmus, rotary
ocular motility, disorders of
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
opened mouth
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
organ transplantation
oropharyngeal weakness
pain
pain, abdominal
pain, back
pain, interscapular
pain, severe
paraneoplastic ganglionopathy
paraparesis, spastic
paraplegia
paraplegia, progressive
paraspinal muscle
paraspinal muscle weakness
paresthesias
Parkinson disease
pediatric neurology
pembrolizumab
pleocytosis of cerebrospinal fluid
pneumonia
poison, neurologic problems with
poison, organophosphate
polymerase chain reaction
polymyositis
polyneuropathy
polyneuropathy, chronic inflammatory demyelinating
positive sharp waves
precipitating factors
prognosis
progressive neurologic disorder
proximal muscle atrophy
proximal myotonic myopathy
pseudomyotonia
ptosis
ptosis, bilateral
ptosis, unilateral
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
radiculopathy
ragged-red fibers
remote effect of cancer on the nervous system
repetitive nerve stimulation
respiratory failure
retrocollis
reversible neurologic disorder
review article
rhabdomyolysis
rheumatoid arthritis
riboflavin
rigid spine syndrome
rigidity
risk factors
saddle anesthesia
sarcoidosis
scleroderma
scoliosis
seizure
seizure, children
selumetinib
sensory level
sensory symptoms
serologic testing
serologic testing of cerebrospinal fluid
single-fiber electromyography
Sjogren's syndrome
spastic dysphonia
spasticity
speech, loss of
spinal cord, compression of
standing difficulty
startle reaction
statin therapy
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatonigral degeneration
striatonigral degeneration, infantile
suck, poor
suicide
systemic lupus erythematosus, neurologic complications with
tachycardia
Tay-Sachs disease
temporalis muscle wasting
tensilon test, false positive
testicular atrophy
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thymoma
tick bite
titubation
tone, muscle, increased
tongue, atrophy
tongue, enlarged
tongue, fasciculations of
tongue, weakness
torticollis
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
urinary incontinence
valsalva maneuver
vecuronium
viral infection
viral myopathy
vision, blurred
Waldenstrom's macroglobulinemia
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
weight loss
Western immunoblot test
wheelchair
white matter disease
wide based gait
winging of scapula
xerostomia
zoonoses
Showing articles 0 to 50 of 1114 Next >>

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
Ther Adv Neurol Disord 12:1-15, Angelini, C.,et al, 2019

Subacute Paresis in a 28-year-old man with HIV
Neurol 90:432-435, Harada, Y.,et al, 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Immune Checkpoint Inhibitor-Related Myositis and Myocarditis in Patients with Cancer
Neurol 91:e985-e994, Touat, M.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

Pembrolizumab-Induced Myasthenia Gravis
Neurol 91:e1365-e1367, Algaeed, M.,et al, 2018

A 30-year-old Man with Progressive Weakness and Atrophy
Neurol 87:e227-e230, Quinn, C.,et al, 2016

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,et al, 2016

Clinical Laboratory and Findings of 21 Patients with Radiation-Induced Myopathy
JNNP 86:152-158, Ghosh, P.S. & Milone M., 2015

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Pharyngeal-Cervical-Brachial Variant of Guillain-Barr� Syndrome
JNNP 85:339-344, Wakerley, B.R. & Yuki, N., 2014

Head Drop in Huntington Disease: Insights into the Pathophysiology
Neurol 81:769-770, Morgante, F.,et al, 2013

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Dropped Head Syndrome: Report of Three Cases During Treatment with a Mek Inhibitor
Neurol 79:1929-1932, Chen, X.,et al, 2012

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Myasthenia Gravis as a Cause of Head Drop in Parkinson Disease
The Neurologist 17:144-146, Uludag, I.F.,et al, 2011

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

A 49-Year-Old Man with Contractures, Weakness, and Cardiac Arrhythmia
Neurol 72:2036-2043, Kissel,J.T.,et al, 2009

Admission International Normalized Ratio and Acute Infarct Volume in Ischemic Stroke
Ann Neurol 64:499-506, Ay,H.,et al, 2008

Clinicopath Conf,Lyme Disease of the Nervous System
NEJM 356:1561-1570, Case Record 11-2007, 2007

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Isolated Dropped Head Due to Adult-Onset Nemaline Myopathy Treated by Posterior Fusion
Neurol 65:1504-1505, Katirji,B.,et al, 2005

Axial Myopathy in Myasthenia: A Misleading Cause of Dropped Head
Muscle Nerve 29:329-330, Rodolico,C.,et al, 2004

The Dropped Head Sign: An Unusual Presenting Feature of Myasthenia Gravis
Neuromuscul Disord 14:378-379, Puruckherr,M.,et al, 2004

Early or Late Appearance of "Dropped Head Syndrome" in Amyotropic Lateral Sclerosis
JNNP 74:683-686, Gourie-Devi,M.,et al, 2003

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

Dilated Stomach and Weak Muscles
Lancet 356:1898, Rigby,S.P.,et al, 2000

Treatable Dropped Head Syndrome in Hypothyroidism
Neurol 55:896-897, Askmark,H. et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

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

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

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

Weak at the Knees
Lancet 354:1696, Webster,G.&Beynon,H., 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Dropped Head Synd & Bent Spine Synd:Two Separate Clin Entities or Different Manifest of Axial Myopathy
JNNP 65:258-259, Oerlemans,W.G.H.&Visser,M., 1998

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
Muscle & Nerve 20:347-351997., Pringle,C.E.,et al, 1997

Isolated Neck Extensor Myopathy:A Common Cause of Dropped Head Syndrome
Neurol 46:917-921, Katz,J.S.,et al, 1996

Motor Neuron Disease:A Paraneoplastic Process Associated with Anti-Hu Antibody and Small-Cell Lung Carcinoma
Ann Neurol 40:112-116, Verma,A.,et al, 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

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

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995



Showing articles 0 to 50 of 1114 Next >>