Results 241 to 250 of about 35,494 (256)
Some of the next articles are maybe not open access.
Marfan's syndrome (arachnodactyly)
The American Journal of Medicine, 1951Abstract 1.1. A review of the literature concerning Marfan's syndrome is given and a case presenting the classical characteristics is discussed. 2.2. An attempt to find aberrations in the endocrine system was unsuccessful. 3.3. Nitrogen balance studies are presented which demonstrate the ability of tissue protoplasm to respond to growth stimuli.
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Annual Review of Medicine, 2000
▪ Abstract The Marfan syndrome (MFS), initially described just over 100 years ago, was among the first conditions classified as a heritable disorder of connective tissue. MFS lies at one end of a phenotypic continuum, with people in the general population who have one or another of the features of MFS at the other end, and those with a variety of ...
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▪ Abstract The Marfan syndrome (MFS), initially described just over 100 years ago, was among the first conditions classified as a heritable disorder of connective tissue. MFS lies at one end of a phenotypic continuum, with people in the general population who have one or another of the features of MFS at the other end, and those with a variety of ...
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Nursing
Abstract: This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. The Ghent II Nosology of MFS criteria are crucial in MFS diagnosis, guiding clinicians in identifying high-risk patients.
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Abstract: This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. The Ghent II Nosology of MFS criteria are crucial in MFS diagnosis, guiding clinicians in identifying high-risk patients.
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AORN Journal, 1986
Marfan's patients share the same problems as anyone with a lifelong, progressive, hereditary condition. The more knowledgeable an individual is about his disease and the more willing he is to accept the responsibility for his own well-being, the more control he has over his life. Medical and life insurance is not a luxury, but an absolute must.
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Marfan's patients share the same problems as anyone with a lifelong, progressive, hereditary condition. The more knowledgeable an individual is about his disease and the more willing he is to accept the responsibility for his own well-being, the more control he has over his life. Medical and life insurance is not a luxury, but an absolute must.
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Marfan-Syndrom — Marfan-Erkrankung
1994Dem Marfan-Syndrom liegt eine Storung des fur die Fibrillin-bildung verantwortlichen Gens auf dem langen Arm von Chromosom 15 zugrunde. Damit ist aus dem Marfan-Syndrom eine abgrenzbare Marfan-Erkrankung geworden. Weil die Krankheit dominant vererbt wird, ist an eine Gentherapie nicht zu denken.
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