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Differential
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advances in neurology
adverse drug reaction
amyloidosis
amyotrophic lateral sclerosis
anesthesia, general
anterior tibial muscle weakness
arrhythmia, cardiac
arthrogryposis multiplex
asymptomatic
automatic implantable cardioverter-defibrillator
bradycardia
bulging of biceps
calf atrophy
calf hypertrophy
calpain III deficiency
cardiomegaly
cardiomyopathy
cardiovascular disease
case studies
central core disease
Charcot-Marie-Tooth
children
complications
conduction block
congenital myopathy
congestive heart failure
contractures, joint
creatine phosphokinase(CPK)elevated
dermatomyositis
diamond on quadriceps
differential diagnosis
distal muscle atrophy
distal muscle weakness
DNA probes
DYSF gene
dysferlin
dysferlinopathy
dystroglycanopathies
dystrophin
dystrophin associated proteins
echocardiogram
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
Emery-Dreifuss muscular dystrophy
epidemiology of neurology
erythrocyte
exercise
facial weakness
facioscapulohumeral syndrome
familial
fibrillations
foot drop
gait disorder
gait, waddling
gastrocnemius muscle weakness
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gowers maneuver
Guillain Barre syndrome
hand weakness
heart block
histochemistry of muscle
immunohistochemistry
inability to stand on tiptoes
klippel feil syndrome
Kugelberg-Welander syndrome
laminopathies
leg weakness, bilateral
lid closure, weakness of
life expectancy
limb-girdle weakness
LMNA gene
lordosis
lymphocyte capping, diminished
misdiagnosis
molecular genetics
mononeuropathy
motor neuron disease
MRI
MRI, abnormal
MRI, muscle
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle diseases, characteristics of
muscle hypertrophy
muscle pain
muscle stiffness
muscle swelling
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, differential diagnosis of
muscular dystrophy, distal, Miyoshi
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, pattern of muscle involvement
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenic crisis
myoglobinuria
myopathy
myopathy, carcinomatous
myopathy, centronuclear
myopathy, distal
myopathy, distal, vacuolar
myopathy, mitochondrial
myopathy, quadriceps
myopathy, thyroid disease causing
myopathy, vacuolar
myositis
myotonia dystrophica
neck weakness
nemaline rod myopathy
neuritis, causes of
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neuropathy
neuropathy, diabetic
next-generation sequencing
oculopharyngeal muscular dystrophy
old age, neurology of
pacemaker, cardiac-transvenous
poliomyelitis
polymerase chain reaction
polymyositis
polyneuropathy
porphyria
pregnancy, neurologic complications in
progeria
prognosis
progressive neurologic disorder
proximal muscle atrophy
pseudohypertrophy
quadriceps atrophy
quadriceps weakness
quality of life
respirator
respiratory failure
review article
RFLPs
rhabdomyolysis
rippling muscle disease
sarcoglycan
sarcoglycanopathy
sarcoidosis
scoliosis
spinal muscular atrophy
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
sudden death
syncope
systemic illness
toe walking
torticollis
treatment of neurologic disorder
urine, dark
walking frame
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
Werdnig-Hoffman disease
wheelchair
whistle, inability to
winging of scapula
workup
Showing articles 800 to 850 of 1006 << Previous Next >>

Tubular Aggregates, Their Association with Neuromuscular Diseases, Including the Syndrome of Myalgias/Cramps
Arch Neurol 42:973-976, Rosenberg,N.L.,et al, 1985

The Frequency of Malignant Neoplasms in Patients with Polymyositis-Dermatomyositis, A Controlled Study
Arch Int Med 145:1835-1839, Manchul,L.A.,et al, 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Graves'Disease Presenting with Bilateral Acute Painful Proptosis, Ptosis, Ophthalmoplegia, & Visual Loss
Lancet 2:431-433, Leonard,T.J.K.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Clin. Path. Conference
Coproporphyria with Polyneuropathy, Case Record 39-1984, NEJM 311:839-847984., , 1984

Nemaline Myopathy Appearing in Adults as Cardio-myopathy
Arch Neurol 41:443-445, Meier,C.,et al, 1984

Unilateral Myopathy:An Unusual Presentation of Thyrotoxicosis
BMJ 288:1124, Gimlette,T.,et al, 1984

Pentazocine Abuse Masquerading as Familial Myopathy
Neurol 34:524-527, Choucair,A.K.,et al, 1984

Polymyositis Associated with Monoclonal Gammopathy
Lancet 2:1183-1186, Kiprov,D.D.,et al, 1984

Penicillamine-Induced Myositis
Am J Med 77:719-722, Halla,J.T.,et al, 1984

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Fibrous Myopathy in Association with Pentazocine
Arch Int Med 143:2203-2204, Adams,F.M.,et al, 1983

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Idiopathic Recurrent Myoglobinuria & Persistent Weakness
Neurol 33:1613-1615, Bermils,C.,et al, 1983

Endocrine Myopathies
BMJ 287:705-708, Kendall-Taylor,P.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Childhood-Type Myositis & Linear Scleroderma
Neurol 33:928-930, Miike,T.,et al, 1983

Isolated Ocular Myopathy & Celiac Disease in Childhood
Neurol 33:792, Sandyk,R.,et al, 1983

Carpal Tunnel Syndrome, Complication of Toxic Shock Syndrome
Arch Neurol 40:414-415, Sahs,A.L.,et al, 1983

Implications of Diagnostic Delay in Duchenne Muscular Dystrophy
BMJ 287:1106-1107, Zellweger,H., 1983

Recognising & Preventing Duchenne Muscular Dystrophy
BMJ 287:1083-1084, Firth,M.A.,et al, 1983

Nemaline Myopathy in the Neonate
Neurol 33:351-356, Norton,P.,et al, 1983

Nemaline Myopathy Presenting as Cardiomyopathy
NEJM 308:1536-1537, Meier,C.,et al, 1983

Proximal Myopathy Due to Discrete Carcinomatous Metastases in Muscle
JNNP 46:358-360, Doshi,R.,et al, 1983

Investigative Strategies for Muscle Pain
J Neurol Sci 58:73-88, Mills,K.R.,et al, 1983

An Unusual Cause of Hypokalemic Muscle Weakness
Neurol 33:1242-1243, Valeriano,J.,et al, 1983

Myositis of Chronic Graft Versus Host Disease
Neurol 33:1222-1224, Reyes,M.G.,et al, 1983

Acute Myopathy Associated with Gasoline Sniffing
Neurol 33:629-631, Kovanen,J.,et al, 1983

Chronic Progressive External Ophthalmoplegia (CPEO) :Clinical, Morphologic, & Biochemical Studies
Neurol 33:452-461, Mitsumoto,H.,et al, 1983

Myopathy & Hypersensitivity to Phenytoin
Neurol 33:790-791, Harney,J.,et al, 1983

Presentation, Treatment, & Prognosis of Idiopathic Inflammatory Muscle Disease in a Rural Hospital
Am J Med 75:433-438, Hoffman,G.S.,et al, 1983

Childhood Dermatomyositis:Factors Predicting Functional Outcome and Development of Dystrophic Calcification
Pediatrics 103:882-888, Bowyer,L.S.,et al, 1983

Necrotizing Myopathy Associated with Steroid Therapy, Report of Two Cases
Pathology 14:435-438, Ojeda,V.J., 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Transient Myopathy Apparently Due to Tetracycline
NEJM 307:821-822, Sinclair,D.,et al, 1982

Myopathy Due to Mercaptopropionyl Glycine
BMJ 285:939, Hales,D.S.M.,et al, 1982

Inflammatory Facioscapulohumeral Muscular Dystrophy & Coats Syndrome
Ann Neurol 12:398-401, Wulff,J.D.,et al, 1982

External Carotid-Cavernous Sinus Fistula Simulating Unilateral Graves Ophthalmopathy
J Comput Assist Tomogr 6:1006-1009, Merlis,A.L.,et al, 1982

Clinical Use Of Nuclear Magnetic Resonance In The Investigation Of Myopathy
Lancet 1:725-730, Edwards,R.H.T.,et al, 1982

Inclusion Body Myositis Associated With Sjogren's Syndrome
Arch Neurol 39:186-188, Chad,D.,et al, 1982

Sjogren's Syndrome & Polymyositis or Dermatomyositis
Arch Neurol 39:157-163, Ringel,S.P.,et al, 1982

Ipecac-induced Myopathy Simulating Dermatomyositis
Neurol 32:91-94, Bennett,H.S.,et al, 1982

Trigeminal Neuropathy in Progressive Systemic Sclerosis
Am J Med 73:57-62, Farrell,D.A.,et al, 1982

Multifocal Interstitial Myositis Associated With Localized Lipoatrophy
Arch Neurol 39:722-724, Palliyath,S.,et al, 1982

Remission From Polymyositis After Total Body Irradiation
BMJ 284:1915-1916, Hubbard,W.N.,et al, 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982



Showing articles 800 to 850 of 1006 << Previous Next >>