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Differential
(Click to cross reference)
abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
anterior tibial muscle weakness
areflexia
arm weakness
atrioventricular block
axillary nerve
brachial neuritis
brachial plexus neuropathy
brachial plexus neuropathy, familial
brachial plexus neuropathy, recurrent
brachial plexus, lesion of
bradycardia
calf atrophy
calf hypertrophy
cardiomegaly
cardiomyopathy
case studies
CAT scan, abnormal
central core disease
cerebral embolism
cerebrospinal fluid, elevated protein of
cerebrovascular accident
children
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
compression neuropathy
congenital myopathy
contractures, joint
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
descending paralysis
differential diagnosis
diplegia, brachial
diplopia
distal muscle weakness
DYSF gene
dysferlinopathy
dysphonia
dyspnea
dyspraxia
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
entrapment neuropathy
enzyme, defect
exophthalmus
exophthalmus, unilateral
eye closure
face, elongated
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
fibrillations
fine motor function, impaired
foot drop
gait disorder
gait, waddling
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hammertoes
hand weakness
heart block
heart block, complete
heart murmur
herniated disc, cervical
high arched feet
hip pain
histochemistry of muscle
hoarseness
immunohistochemistry
jugular foramen syndrome
leg weakness, bilateral
lid closure, weakness of
long thoracic nerve
lordosis
lymphoma
lymphoma involving CNS
mimics
misdiagnosis
molecular genetics
mononeuropathy
motor neuron disease
MRI, abnormal
MRI, brachial plexus
multicore myopathy
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, vacuolar
myotonic discharges
neck pain
neck weakness
nemaline rod myopathy
nerve conduction studies
nerve grafting
neurofibroma
neurologic complications of, surgery
neurologic disease, diagnoses of
neuropathy
neuropathy, hereditary peripheral
next-generation sequencing
numbness, extremity
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
orbit, lesions of
orbit, neoplasms of
pacemaker, cardiac-transvenous
pain
pain, arm
pain, scapula
pain, sensation
pain, severe
palate, paralysis-unilateral
paraspinal muscle
paraspinal muscle weakness
pneumonia
polymyositis
positive sharp waves
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proptosis, unilateral
proximal muscle atrophy
pseudomyotonia
ptosis
ptosis, bilateral
radial nerve
radial nerve, palsy of
radiculopathy
recruitment
recruitment, reduced
recurrent
respiratory failure
reticulum cell sarcoma
reversible neurologic disorder
review article
rhabdomyolysis
schwannoma
scoliosis
serratus anterior muscle, weakness
serum sickness
shoulder, pain in
shoulder-girdle wasting
sloped shoulders
spinal accessory nerve
spinal accessory nerve palsy
spinal cord, compression of
spinal muscular atrophy
standing difficulty
sudden death
suprascapular neuropathy
toe walking
tomaculous neuropathy
tongue, enlarged
tongue, weakness
transverse smile
trapezius weakness
trauma
treatment of neurologic disorder
urine, dark
vocal cord paralysis
weakness
weakness, generalized
weakness, progressive
weakness, proximal
whistle, inability to
winging of scapula
wrist drop
Showing articles 0 to 19 of 19

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,et al, 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

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

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

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

The Limbic-Girdle Muscular Dystrophies
Neuro Clin 32:729-749, Wicklund, M.P. and Kissel, J.T., 2014

A 52-year-old Woman with Progressive Proximal Weakness
Neurol 83:e106-e109, Enduri, S.,et al, 2014

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

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

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Facioscapulohumeral Dystrophy, in Myology, Basic & Clinical
McGraw-Hill Book Co, NY, p1251986., Munsat,T.L., 1986

C7 Radiculopathy:Importance of Scapular Winging in Clinical Diagnosis
JNNP 49:640-644, Makin,G.J.V.,et al, 1986

Clinicopath. Conference
Malignant Lymphoma, Diffuse Small Cleaved-Cell Type, of Spinal Epidural Space ( & Orbit) , Case 47-1, 86, NEJM1-1409,1986., 1986

Familial Long Thoracic Nerve Palsy:A Manifestation of Brachial Plexus Neuropathy
Neurol 36:1251-1253, Phillips,L.H., 1986

Accessory Nerve Palsy
JNNP 40:1113, Olarte,M.,et al, 1977

Neuralgic Amyotrophy
Handbook of Clinical Neurology 8:77, 1970 Ed by Vinken & Bruyn Chp 4., Gathier,J.,et al, 1970

Shoulder-Girdle Neuritis-Brain-Textbook of Neurology p. 808
775-776., , 1850



Showing articles 0 to 19 of 19