Results 311 to 320 of about 433,578 (358)
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Is Camptocormia a Primary Muscular Disease?
Spine, 1995This study analyzed computed tomographic scans, magnetic resonance images, and biopsies of the paravertebral muscles of patients with camptocormia and age-matched patients with lumbar interapophyseal osteoarthritis or lumbar vertebral stenosis.To define the muscular lesions and clarify their nature in this particular disorder.Progressive lumbar ...
M, Laroche +4 more
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The muscular variant of Pompe's disease
The Journal of Pediatrics, 1967A patient with the muscular variant of Pompe's disease is presented. Premortem studies showed normal leukocyte α-1, 4 glucosidase activity. Muscle and liver α-1, 4 glucosidase activity was absent. A review of the literature on this variant is presented, and a therapeutic approach is discussed.
J C, Roth, H E, Williams
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Neurogenic muscular atrophy in Behcet's disease
Clinical Rheumatology, 1985A child is reported with Behcet's disease who presented with skin and joint manifestations, oral ulcers, brainstem syndrome and neurogenic muscular atrophy. The neurogenic muscular atrophy was confirmed by electrophysiologic, histologic and histochemical studies. Electron microscopy of muscle showed a vasculopathy.
R A, Frayha +4 more
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Journal of the American College of Surgeons, 2003
Miguel M, Echenique Elizondo +1 more
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Miguel M, Echenique Elizondo +1 more
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Chemical Laboratory Studies in Muscular Disease
Postgraduate Medicine, 1967Although studies have been made of the relationship of numerous enzymes to diagnosis of muscular disease, only those concerning aldolase, glutamic-oxalacetic transaminase, lactic dehydrogenase and creatine phosphokinase have been of real value. Because the increase in serum activity of these enzymes fluctuates, it is necessary to study them on several ...
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[Muscular diseases in hyperthyroidism].
Acta medica portuguesa, 1995Hyperthyroidism may present various muscular diseases, namely thyrotoxic chronic myopathy, myasthenia gravis, disthyroid ophthalmopathy and thyrotoxic periodic paralysis. Although infrequent, it is possible to find some of these clinical situations in a medical ward of a general hospital.
F, Pissarra +5 more
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[Diagnosis of muscular disease].
Ugeskrift for laeger, 2000Diagnostic evaluation of muscle disease has gained considerably from the expanding development in molecular science in the last decade. This paper gives an overview of current diagnostic procedures in the evaluation of patients with muscle disease.
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