Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
ataxia
atrioventricular block
automatic implantable cardioverter-defibrillator
blepharophimosis
blepharospasm
bradycardia
bulging of biceps
cachexia
calcification, intracranial
calf atrophy
calf hypertrophy
calpain III deficiency
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
central core disease
cerebellar atrophy, secondary
cerebellar degeneration
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
coma
complications
conduction block
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
creatine kinase
creatine phosphokinase(CPK)elevated
deafness
dementia
dermatomyositis
descending paralysis
developmental retardation
diarrhea
differential diagnosis
diplopia
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
DYSF gene
dysferlin
dysferlinopathy
dysphagia
dyspraxia
dystroglycanopathies
dystrophic calcification
dystrophin
dystrophin associated proteins
ear, abnormal
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electron microscopy
Emery-Dreifuss muscular dystrophy
encephalopathy
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
enzyme, serum
epidemiology of neurology
erythrocyte
exercise
exercise intolerance
extraocular muscle lesion
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fatigue
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
Guillain Barre syndrome
hammertoes
headache
hearing loss
heart block
heart block, complete
heart murmur
hepatomegaly
heralding manifestation
high arched feet
hip dysplasia
hip flexor weakness
hip pain
histochemistry of muscle
hyperthyroidism
hypoglycemia
hypokalemia
hyporeflexia
hypotonia
hypotonia, infants
imbalance
immunohistochemistry
immunosuppressive agents
inability to stand on tiptoes
inclusion body myositis
insulin
intestinal pseudoobstruction
klippel feil syndrome
Kugelberg-Welander syndrome
lactic acidemia
lactic dehydrogenase(LDH)
laminopathies
leg weakness, bilateral
leukodystrophy
lid closure, weakness of
life expectancy
LMNA gene
lordosis
lymphocyte capping, diminished
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
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, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenic crisis
myocarditis
myoclonus
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hypokalemic
myopathy, metabolic
myopathy, mitochondrial
myopathy, myofibrillar
myopathy, proximal
myopathy, quadriceps
myopathy, steroid induced
myopathy, thyroid disease causing
myositis
myotonia
myotonia dystrophica
myotonic discharges
neck weakness
negative
nemaline rod myopathy
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuroophthalmology
neuropathy
neuropathy, diabetic
next-generation sequencing
normal
ocular myopathy
oculopharyngeal muscular dystrophy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
pacemaker, cardiac-transvenous
pain, abdominal
pain, leg
pinched face
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
positive sharp waves
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proteinuria
proximal muscle atrophy
proximal myotonic myopathy
pseudohypertrophy
ptosis
quadriceps atrophy
quadriceps weakness
quality of life
ragged-red fibers
recurrent
respirator
respiratory failure
retina, abnormal
retinal lesion
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
Schwartz-Jampel syndrome
scoliosis
seizure
sensorineural hearing loss
short stature
shoulder, pain in
shoulder-girdle wasting
sloped shoulders
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
sudden death
syncope
systemic illness
toe walking
torticollis
transverse smile
treatment of neurologic disorder
trinucleotide repeats
upgaze, paralysis of
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
white matter disease
winging of scapula
Showing articles 50 to 100 of 2144 << Previous Next >>

Chronic Spinal Muscular Atrophy in Adults
J Neurol Sci 9:527, Meadows,J.C.,et al, 1969

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

The Muscular Dystrophies
NEJM 273:537, 5961965., Zundel,W.,et al, 1965

Muscular Dystrophy
Am J Med 35:632, Pearson,C.M., 1963

Five Types of Dystrophy
Together with Other Conditions Producing Insidious Muscle Weakness-Table 1-Hospital Med p. 60., , 1850

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

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

Bilateral Ptosis, Dysphagia, and Progresive Weakness in a Patient of French-Canadian Background
Neurol 95:933-938, Paul,P.,et al, 2020

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

A 42-year-old man with unilateral leg weakness
Neurol 90:e1085-e1090, Schneider, R.,et al, 2018

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

Degenerative Diseases of the Nervous System, Kugelberg-Welander Syndrome SMAIII
Adams & Victors Principles of Neurology, Chp 39, pg 1118, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Kennedy Syndrome (X-Linked Bulbospinal Muscular Atrophy)
Adams & Victors Principles of Neurology, Chp 39, pg 1119, 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

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

Polymyositis and Dermatomyositis
Lancet 362:971-982, Dalakas,M.C.&Hohlfeld,R., 2003

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

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

Muscle Pain after Exercise
Lancet 353:1062, Nielen,C.&Mazzone,P., 1999

Signs and Symptoms of Duchenne Muscular Dystrophny and Becker Muscular Dystrophy Among Carriers in the Netherlands: A Cohort Study
Lancet 353:2116-2119, Hoogerwaard,E.M.,et al, 1999

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
Neurol 46:810-814, Connolly,A.M.,et al, 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

The Nondystrophic Myotonias
In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994

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

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Duchenne Muscular Dystrophy Manifesting Carriers
Arch Neurol 46:673-675, Barkhaus,P.E.&Gilchrist,J.M., 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988

Respiratory Muscle Function and Ventilatory Control in Patients with Myotonic Dystrophy
Q J Med 202:205-226, Serisier,D.E.,et al, 1982

Neuromuscular Disease in Primary Hyperparathyroidism
Ann Int Med 80:182, Patten,B.M.,et al, 1974

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

Complains of Muscle Weakness
Patient Care Clinical Concepts, 21, 1970 Jan., , 1970

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

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

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

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



Showing articles 50 to 100 of 2144 << Previous Next >>