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Myelodysplastic Syndrome in a Patient with Werner’s Syndrome
Acta Haematologica, 1994Werner's syndrome is a relatively rare autosomal recessive disorder characterized by several features generally associated with aging. This syndrome is classified in the group of chromosome instability syndromes and there is an increased incidence of neoplasia. Hematologic malignancies associated with this syndrome are, however, unusual.
Mustafa Artvinli+3 more
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Bladder carcinoma with werner syndrome
Urology, 1987Werner syndrome is a rapid premature aging disease and is considered chromosomal instability syndrome, occasionally associated with malignancy. Urologic malignancy associated with this syndrome is unusual. Herein we report a case of Werner syndrome with urinary bladder carcinoma.
Shun Kondo+5 more
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Insulin resistance in werner's syndrome
Mechanisms of Ageing and Development, 1992Insulin resistance in Werner's syndrome (WS) was studied using the glucose clamp technique, and compared with physiologically aged and young subjects. Fasting immuno-reactive insulin (IRI) was increased in patients with Werner's syndrome compared with aged and young subjects. Metabolic clearance rate (MCR) of glucose was decreased in the aged and WS. A
Masashi Kubota+12 more
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Radiology, 1948
THE PAST generation has witnessed a revolutionary change in our conception of bone function. Considered originally an inert framework for the anchorage or support of viscera, or a part of the blood-forming system, the skeleton is now known to be a functioning organ of vital importance in the metabolism of the body.
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THE PAST generation has witnessed a revolutionary change in our conception of bone function. Considered originally an inert framework for the anchorage or support of viscera, or a part of the blood-forming system, the skeleton is now known to be a functioning organ of vital importance in the metabolism of the body.
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The Werner syndrome protein: an update
BioEssays, 2000Progeria and progeroid syndromes are characterized by the earlier onset of complex senescent phenotypes. WRN was originally identified as a gene responsible for Werner syndrome (WS; "Progeria of Adults"). The WRN gene product has RecQ-type helicase domains in the central region of the protein.
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British Journal of Dermatology, 1953
R. N. Tattersall, R. H. Seville, R. Reed
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R. N. Tattersall, R. H. Seville, R. Reed
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Management guideline for Werner syndrome 2020. 2. Sarcopenia associated with Werner syndrome
Geriatrics and Gerontology International, 2021Akira Taniguchi+2 more
exaly
A comparative analysis testing Werner's theory of complex life cycles
Functional Ecology, 2022Emily L Richardson+2 more
exaly