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acanthocytosis
acetylcholine receptor antibody
acyl CoA dehydrogenase deficiency
adverse drug reaction
amyotrophic chorea-acanthocytosis
amyotrophic lateral sclerosis
anterocollis
anticholinergic drugs
anticoagulant, treatment
anticoagulant, treatment in CVD
arrhythmia, cardiac
artane
aspiration
Babinski sign
baldness
basal ganglia, lesion of
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
botulinum toxin
camptocormia
carcinoma
cardiomyopathy
cataracts
cerebrovascular accident
cerebrovascular accident, prognosis in
chemotherapy, CNS treatment and complications with
children
choking
chorea
Clinical Pathologic Conference(C.P.C.)
complications
congenital heart disease
coumarin
creatine phosphokinase(CPK)elevated
cyclic vomiting
delay in diagnosis
developmental milestones, loss of
developmental retardation
difficulty climbing stairs
drooling
dropped head syndrome
drug induced neurologic disorders
drug withdrawal
duvalumab
dysphagia
dysphonia
dyspnea
dystonia
dystonia, cervical
dystonia, drug induced
dystonia, face
dystonia, focal
dystonia, post traumatic
dystonia, treatment of
electrocardiogram, abnormal
electromyogram
electromyogram, decremental response
electron microscopy
encephalitis, brainstem
enzyme, defect
exercise intolerance
facial appearance, abnormal
facial weakness
false negative
familial
fatigue
frontal balding
gait disorder
gangliosidosis GM2
gene mutation
genetic neurologic disorders
genetic testing
heralding manifestation
hexosaminidase-A
high arched palate
hoarseness
Huntington's chorea
hypercapnia
hypomyelination
hypothyroidism
iatrogenic neurologic disorders
immune checkpoint inhibitors
immune-related adverse events
immunosuppression
immunosuppressive agents
INR values
ipilimumab
Jewish
laterocollis
limb-girdle weakness
lipid storage disorder of CNS
lysosomal storage disease
mediastinum, mass of
mediastinum, widening
MEK inhibitor
misdiagnosis
monoclonal gammopathy
movement disorder
movement disorder, drug induced
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, muscle
MRI, perfusion
muscle atrophy, focal
muscle biopsy
muscle pain
muscle spasm
muscular dystrophy
myasthenia gravis
myasthenia gravis, paraneoplastic
myasthenia gravis, presenting manifestations
myocarditis
myopathy
myopathy, axial
myopathy, focal
myopathy, genetic
myopathy, inflammatory
myopathy, metabolic
myopathy, necrotizing
myopathy, necrotizing, immune-mediated
myopathy, radiation-induced
myopathy, vacuolar
myositis
myositis, focal
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myxedema, neurologic manifestations of
nausea and vomiting
neck extension
neck flexion
neck pain
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
neoplasm, metastatic to CNS
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
nivolumab
ocular motility, disorders of
old age, neurology of
pain
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
pediatric neurology
pembrolizumab
pneumonia
polymyositis
polyneuropathy, chronic inflammatory demyelinating
prognosis
progressive neurologic disorder
ptosis
ptosis, unilateral
radiation therapy, CNS treatment and complications with
radiculopathy
remote effect of cancer on the nervous system
repetitive nerve stimulation
respiratory failure
retrocollis
reversible neurologic disorder
review article
riboflavin
rigidity
scoliosis
seizure
selumetinib
single-fiber electromyography
spasticity
startle reaction
steroid
steroid therapy, CNS treatment and complications with
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thymoma
tone, muscle, increased
torticollis
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
weakness
weakness, progressive
weakness, proximal
weight loss
white matter disease
wide based gait
Showing articles 0 to 50 of 2705 Next >>

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

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

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

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

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

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

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

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

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

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

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

The Dropped Head Syndrome with Chronic Inflammatory Demyelinating Polyneuropathy
Muscle & Nerve 17:808-810994., Hoffman,D.&Gutmann,L., 1994

The Dropped Head Syndrome
Neurol 42:1625-1627, Suarez,G.A.&Kelly,J.J., 1992

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

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

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

Giant-Cell Arteritis and Polymyalgia Rheumatica
NEJM 371:50-57, Weyand, C.M. & Goronzy J.J., 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

Polymyalgia Rheumatica
Lancet 381:63-72, Kermani, T. & Washington, K., 2013

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

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

Polymyalgia Rheumatica
BMJ 336:765-769, Michet,C.J. &Matteson,E.L., 2008

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

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

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

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

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

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

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,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

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

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

Clinicopath Conf
Small Cell CA (of lung) with Lambert-Eaton Myasthenic Syndr, Case 32-1994, NEJM 331:528-5354., , 1994

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

Neuropathic Findings in Oculopharyngeal Muscular Dystrophy, Seven Cases & Review of Literature
Arch Neurol 50:481-488, Hardiman,O.,et al, 1993



Showing articles 0 to 50 of 2705 Next >>