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2021
Muscular dystrophies (MDs) are a genetically heterogeneous group of degenerative muscle disorders with protein defects characterized by progressive muscle weakness and wasting of variable distribution and severity. Recent advances made in genetic medicine have highlighted the diversity of this group of disorders.
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Muscular dystrophies (MDs) are a genetically heterogeneous group of degenerative muscle disorders with protein defects characterized by progressive muscle weakness and wasting of variable distribution and severity. Recent advances made in genetic medicine have highlighted the diversity of this group of disorders.
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Duchenne Muscular Dystrophy (or Meryon's Disease)
The Lancet, 2001Abstract This disease is eponymously associated with the name Duchenne because this French physician described the condition in detail in the 1860s (Duchenne 1861; 1868). His contributions were concerned with the clinical description of the condition and the muscle histology findings.
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Neurologic and Muscular Disease
2006An understanding of the basic pathophysiology of these neurologic conditions is essential for appropriate anesthetic care. Often, planned elective anesthetic consultation well in advance of delivery will ensure that all members of the team are knowledgeable and all issues regarding the particular condition are addressed.
Angela M. Bader, David Acker
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[Muscular diseases: epidemiology of progressive muscular dystrophies].
Minerva medica, 1981Epidemiology of muscular dystrophies has been important in the prevention of these diseases. In fact the genetic counselling, after a preliminary epidemiological investigation, reduced the incidence rate of Duchenne muscular dystrophy in the Veneto Region. Furthermore the new biochemical data on dismetabolic muscular diseases revealed a future strategy
E, Schergna, M, Armani
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Abberrant Muscular Insertions in Crouzon's Disease
Journal of Pediatric Ophthalmology & Strabismus, 1980Herein we present a case of Crouzon's disease with anomalous medial rectus formation and horizontal recti insertions. This adds a feature of the disease to the literature and reminds us to approach strabismus in orbital anomalies cautiously via a limbal peritomy.
A R, Captuo, R W, Lingua
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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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Duchenne muscular dystrophy—Meryon's disease
Neuromuscular Disorders, 1993In a communication to the Royal Medical and Chirurgical Society of London in December 1851, which was published in the Transactions of the Society the following year, Edward Meryon, an English physician, described, in considerable detail, eight boys in three families with a disease later referred to as Duchenne muscular dystrophy.
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