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Differential
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acquired immunodeficiency syndrome
acyl CoA dehydrogenase deficiency
adult polyglucosan body disease
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
aldolase
aminoacidurias
amniocentesis
arrhythmia, cardiac
atrioventricular block
Babinski sign
bladder dysfunction
blood dyscrasias, neurologic findings with
bone age
bulimia
bulimia nervosa
calf hypertrophy
carcinoma
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
cathartic
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
clofibrate
coenzyme Q10 deficiency
complications
congestive heart failure
contractures, joint
creatine kinase
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
delay in diagnosis
dermatomyositis
developmental retardation
diagnostic criteria
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
DNA probes
drug induced neurologic disorders
dysphagia
dystrophic calcification
dystrophin
eating disorder
electrocardiogram, abnormal
electromyogram
ELISA
encephalitis
encephalopathy
enzyme, defect
enzyme, muscle disease
enzyme, serum
exercise
exercise intolerance
Fabry's disease
falling
familial
fatigue
femoral neuropathy
fever
fine motor function, impaired
gait disorder
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
growth retardation
heart block
hemophilia
hepatomegaly
hip flexor weakness
human immunodeficiency virus type 1
hypocalcemia
hypoglycemia
hypokalemia
hypoparathyroidism, idiopathic
hyporeflexia
imbalance
immunologic disease
immunosuppressive agents
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion body myositis
insulin
ischemic exercise test
Jewish
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
lactic dehydrogenase(LDH)
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
lipid lowering agent
lipid storage disorder of CNS
liver function enzymes
Lowe's syndrome
MELAS syndrome
MERRF syndrome
metachromatic leukodystrophy
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
mononeuropathy
mortality
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle strength, testing
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, insidious onset of
muscle weakness, intermediate onset of
muscle weakness, proximal
muscle weakness, sudden onset of
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
myelomalacia
myeloneuropathy
myelopathy
myocarditis
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, distal, vacuolar
myopathy, drug-induced
myopathy, hypokalemic
myopathy, inflammatory
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myositis
neck weakness
neonatal screening, genetic neurologic disorders
nerve biopsy
nerve conduction studies
neurogenic bladder
neurologic complications of, surgery
neurologic disease, diagnoses of
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, sensory
oculopharyngeal muscular dystrophy
ophthalmoplegia, progressive external
pain
pain, foot
pain, leg
paraparesis
paraparesis, spastic
phosphorylase b kinase deficiency
polyglucosan body
polyglucosan body disease
polymyositis
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proteinuria
quinidine
rash
recurrent
renal failure
review article
rhabdomyolysis
sensory loss
serum glutamic oxaloacetic transaminase
serum glutamic pyruvic transaminase
short stature
skin, lesions in neurologic disorders
spasticity
speech disorder, childhood
speech, delayed development of
spinal muscular atrophy
spinal muscular atrophy, adult onset
standing difficulty
statin therapy
steroid
systemic illness
Tay-Sachs disease
toxoplasma gondii
toxoplasmosis, muscle
treatment of neurologic disorder
tripping
type 2 muscle fiber
urinary incontinence
urine, dark
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
wheelchair
white matter disease
Showing articles 0 to 50 of 1204 Next >>

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017

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

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Outcome of Neonatal Screening for Medium-Chain acyl-CoA Dehydrogenase Deficiency in Australia: A Cohort Study
Lancet 369:37-42,5, Wilcken,B.,et al, 2007

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

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

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

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

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

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

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

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

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

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

Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988

Diagnostic Delay in Duchenne's Muscular Dystrophy
JAMA 247:478-480, Crisp,D.E.,et al, 1982

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Peripheral Source of MB Band of Creatine Kinase in Alcoholic Rhabdomyolysis
JAMA 244:580-582, Siegel,A.J., 1980

Haemophilic Neuromyopathy
JNNP 42:600-605, Defaria,C.R.,et al, 1979

Insulin-Induced Weakness in Hypokalemic Myopathy
Ann Neurol 6:139-140, Ruff,R.L., 1979

Creatine Phosphokinase MB Band In Oculopharyngeal Muscular Dystrophy
(Letter) NEJM 301:270979., Diskin,C.J., 1979

Elevated Skeletal-Muscle Enzymes During Quinidine Therapy
NEJM 300:1218, Weiss,M.,et al, 1979

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Prenatal Genetic Diagnosis in 3000 Amniocenteses
NEJM 300:157-163, Golbus,M.S.,et al, 1979

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

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

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

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

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

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

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

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

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

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

"Boule Du Biceps" in Dysferlinopathy
Neurol 94:83-84, El Sherif, R.,et al, 2020

Accuracy of a Machine Learning Muscle MRI - Based Tool for the Diagnosis of Muscular Dystrophies
Neurol 94:e1094-e1102, Verdu-Diaz, J.,et al, 2020

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

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

Long-term Effects of Glucocorticoids on Function, Quality of Life, and Survival in Patients with Duchenne Muscular Dystrophy: A Prospective Cohort Study
Lancet 391:451-461, McDonald, C.M.,et al, 2018

Cerebral Mitochondrial Microangiopathy Leads to Leukoencephalopathy in Mitochondrial Neurogastrointestinal Encephalopathy
AJNR 39:427-434, Gramegna, L.L.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

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



Showing articles 0 to 50 of 1204 Next >>