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Differential
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abdominal muscle paralysis
acid maltase deficiency
acid maltase deficiency, adult
activities of daily living scale
adverse drug reaction
alpha glucosidase
aminoacidopathies
aneurysm
anterior horn cell disease
aspartate aminotransferase
asymptomatic
bright tongue sign
bulbar palsy
calf hypertrophy
cardiomegaly
cardiomyopathy
CAT scan, abnormal
children
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
compartment syndrome
complications
congenital myopathy
congestive heart failure
consanguinity
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
delay in diagnosis
developmental retardation
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
distal muscle atrophy
distal muscle weakness
dysarthria
dysphagia
dyspnea
efficacy
electrocardiogram, abnormal
electromyogram
electron microscopy
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme treatment
enzyme, defect
enzyme, muscle disease
exercise
exercise intolerance
exercise-related muscle strength increase
facial weakness
falling
familial
fatigue
fibrillations
floppy infant
gene
gene mutation
gene therapy
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glycogen debranching enzyme deficiency
glycogen storage disease
Gowers maneuver
hepatomegaly
heralding manifestation
hip flexor weakness
histochemistry of muscle
hypoglycemia
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
immunomodulation
immunosuppressive agents
inborn errors of metabolism, screening
ischemic exercise test
leg weakness, bilateral
leukocytes
limb-girdle weakness
lipid storage myopathy
low back pain
lysosomal storage disease
lysosomes, abnoral
McArdle's disease
McArdle's disease, adult onset
misdiagnosis
molecular genetics
monoclonal gammopathy
monoclonal gammopathy of uncertain significance
mortality
MRI
MRI, abnormal
MRI, muscle
mucopolysaccharidoses
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle strength, testing
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
myoglobinuria
myopathy
myopathy, acquired
myopathy, amyloid
myopathy, distal, vacuolar
myopathy, genetic
myopathy, glycogen storage
myopathy, metabolic
myopathy, necrotizing
myopathy, scleromyxedema
myopathy, vacuolar
myositis
myotonia congenita
myotonic discharges
neck weakness
nemaline rod myopathy
nemaline rod myopathy, adult onset
nerve biopsy
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neuropathy
newborn, evaluation of
next-generation sequencing
old age, neurology of
orthopnea
pain
pain, arm
pain, back
paraspinal muscle
paraspinal muscle weakness
PAS positive
patient in waiting
phosphorylase b kinase deficiency
polymerase chain reaction
Pompe's disease of glycogen storage
Pompe's disease, infantile
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
proximal muscle atrophy
pseudomyotonia
pulmonary function tests
pulmonary hypertension
renal failure
respiratory failure
respiratory tract infection
review article
RFLPs
screening
second wind phenomena
seizure
short stature
sphingolipodoses
spinal muscular atrophy
spinocerebellar degeneration
stem cell transplantation
storage disease of CNS
subarachnoid hemorrhage
systemic illness
tongue, enlarged
tongue, weakness
treatment of neurologic disorder
urine, dark
vital capacity
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
winging of scapula
workup
Showing articles 1000 to 1050 of 1146 << Previous Next >>

Alcoholic Myopathy in Heart & Skeletal Muscle
NEJM 301:28-33, Rubin,E., 1979

Alcoholic Myopathy
NEJM 301:1239, Rubenstein,A.E., 1979

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

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

Extraocular Muscle Biopsy in Chronic Progressive External Ophthalmoplegia
Ann Neurol 6:326-339, Ringel,S.P.,et al, 1979

Sciatic Nerve Entrapment by Pentazocine-Induced Muscle Fibrosis, A Case Report
Arch Neurol 36:723-724, Rousseau,J.J.,et al, 1979

Phenytoin Hypersensitivity:38 Cases
Neurol 29:1480-1485, Harunda,F., 1979

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Cytomegalovirus Infection of the Adult Nervous System
Ann Neurol 5:458-461, Duchowny,M.,et al, 1979

Dermatomyositis & Toxoplasmosis
Ann Neurol 5:393-395, Hendrickx,G.F.M.,et al, 1979

Epidemic Toxoplasmosis Associated With Infected Cats
NEJM 300:695-699, Teutsch,S.M.,et al, 1979

Prednisone Use in Concurrent Autoimmune Diseases
Arch Neurol 36:103-106, Harati,Y.,et al, 1979

Cranial Neuropathy, Myeloradiculopathy, & Myositis, Complications of Mycoplasma Pneumoniae Infection
Arch Neurol 36:476-477, Rothstein,T.L.,et al, 1979

Benign Acute Childhood Myositis
Neurol 29:1068-1071, Henly,J.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Eosinophilic Polymyositis
Arch Neurol 36:721-722, 1979, Stark,R.J., 1979

Reversibility of Human Myopathy Caused by Vitamin E Deficiency
Neurol 29:1182-1186, Tomasi,L.G., 1979

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

Quadriceps Myopathy in Two Brothers
Rhode Island Med J 62:125, Finelli,P.F., 1979

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Proximal Myopathy During Beta-blockade
BMJ 2:1331-1332, Forfar,J.C.,et al, 1979

Headache
In Clinical Neurology, Baker & Baker Editor. In Vol. II, Harper & Row, Publishers 1979, Chap. 13, p., 38-43. n,A.P., 1979

Retraction of the Lower Eyelid
Neurol 29:386-389, Cohen,M.M.,et al, 1979

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Malignant Hyperthermia & Central Core Disease in a Child with Congenital Dislocating Hips
Arch Neurol 35:189, Eng,G.D.,et al, 1978

HLA-B8 in Polymyositis
NEJM 298:1260, Behan,W.M.H.,et al, 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Inclusion Body Myositis:A Distinct Variety of Idiopathic Inflammatory Myopathy
Neurol 28:8, Carpenter,S.,et al, 1978

A Case of Schwartz-Jampel Syndrome with Unusual Muscle Biopsy Findings
Ann Neurol 3:93, Fariello,R.,et al, 1978

Juvenile Neuroaxonal Dystrophy:Clinical, Electrophysiological, & Neuropathological Features
Ann Neurol 3:419, Dorfman,L.J.,et al, 1978

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

Diagnostic Significance of Myeloperoxidase Assay in Neuronal Ceroidlipofuscinoses (Batten-Vogt Syndrome)
Neurol 28:924-927, Pilz,H.,et al, 1978

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

The Muscular Pain-fasciculation Syndrome
Neurol 28:1105-1109, Hudson,A.J.,et al, 1978

Quinine Sulfate for Pain in the Guillain-Barre Syndrome
Ann Neurol 4:386-387, Nixon,R.A., 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Weakness in Malignancy:Evidence for a Remote Effect of Tumor on Distal Axons
Ann Neurol 4:268-274, Barron,S.A.,et al, 1978

Isolated Trigeminal Sensory Neuropathy:Early Manifestation of Mixed Connective Tissue Disease
Neurol 28:1286-1289, Searles,R.P.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Pellagra
In Brain's Diseases of the Nervous System, 8th Ed. 1977, p 849-851, Oxford University Press., , 1977

Clinical Pathological Conference
Dermatomyositis, Case Record, 33-1977, NEJM 297:37877., , 1977

Alternating Proptosis
Arch Neurol 34:642, Keane,J.R., 1977

Neonatal Ophthalmoplegia with Microfibers:A Reversible Myopathy
Neurol 27:974, Hanson,P.A.,et al, 1977

Neurologic Manifestations in Sarcoidosis
Ann Int Med 87:336, Delaney,P., 1977



Showing articles 1000 to 1050 of 1146 << Previous Next >>