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Differential
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amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
ANA
areflexia
arrhythmia, cardiac
atrioventricular block
autoantibodies
autoimmune disease
bradycardia
bulbar palsy
camptocormia
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
central core disease
cerebral embolism
cerebrovascular accident
children
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
congestive heart failure
contractures, joint
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
delay in diagnosis
dermatomyositis
developmental retardation
differential diagnosis
dislocated hip, congenital
distal muscle weakness
dysarthria
dysphagia
dyspraxia
dystrophic calcification
electromyogram
Emery-Dreifuss muscular dystrophy
enzyme, muscle disease
epidemiology of neurology
facial weakness
falling
familial
fasciculation
fatigue
fibrillations
finger flexor weakness
finger weakness
foot drop
gender
gene
gene mutation
genetic neurologic disorders
hand pain
hand weakness
heart block
heart block, complete
heart murmur
hemiparesis
heralding manifestation
hyperreflexia
hypoparathyroidism
hyporeflexia
hypotonia
hypotonia, infants
immunosuppressive agents
inclusion body myositis
intrinsic hand muscles, wasting of
jaw jerk, abnormal
kyphoscoliosis, neurologic causes of
lactic dehydrogenase(LDH)
leg weakness, bilateral
life expectancy
lordosis
malignant hyperpyrexia
mental retardation
Mills syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
motor neuron disease
MRI, abnormal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, distal, Miyoshi
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myocarditis
myopathy
myopathy, autoimmune
myopathy, distal
myopathy, distal, vacuolar
myopathy, hypocalcemic
myopathy, inclusion body
myopathy, quadriceps
myopathy, vacuolar
myositis
neck weakness
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuropathology
overlap syndrome
pacemaker, cardiac-transvenous
paraparesis, spastic
paresthesias
paresthesias, feet
paresthesias, hands
polymyositis
positive sharp waves
prognosis
progressive neurologic disorder
proximal muscle atrophy
pyramidal tract dysfunction
quadriceps atrophy
quadriceps weakness
repetitive nerve stimulation
review article
rigid spine syndrome
scoliosis
scoliosis, neurologic association with
sedimentation rate, elevated
steroid
stiff joints
sudden death
toe walking
treatment of neurologic disorder
type 1 muscle fiber
type 2 muscle fiber
weakness
weakness, generalized
weakness, progressive
winging of scapula
Showing articles 0 to 50 of 355 Next >>

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

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

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

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

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

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

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

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

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Rigid Spine Syndrome:A Type I Fiber Myopathy
Arch Neurol 34:119, Seay,A.R.,et al, 1977

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

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

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

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

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

A Teenager with Shortness of Breath and Difficulty Walking
Neurol 96:e2346-e2350, Liu, S.C.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Acetylcholine Receptor-Antibody-Positive Myasthenia Gravis Presenting with Early Atrophy and Nonfluctuating Weakness of Proximal Limb Muscles
J Clin Neurol 16:714-716, Pancheri, E.,et al, 2020

Progressive Proximal Weakness in a 61-Year-Old Man
Neurol 98:122-127, Yu, M.,et al, 2020

Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020

A 59-year-old Woman with Multiple Myeloma and Lower Extremity Weakness and Numbness
Neurol 94:794-800, Gadot, R.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

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

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
Neurol 92:663-674, Johansen, A.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018



Showing articles 0 to 50 of 355 Next >>