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Werner’s Syndrome and Astrocytoma
Dermatologica, 2009Werner’s syndrome, a relatively rare and autosomal recessive disorder, is well known to be characterized by a high frequency of malignant neoplasms. Werner’s syndrome has not infrequently been associated with meningiomas. We report a case of Werner’s syndrome and temporal astrocytoma in a 49-year-old male.
F J, Laso +4 more
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Werner's syndrome as “Hyaluronuria”
Clinica Chimica Acta, 1975Abstract Although excretion of acid glycosaminoglycans into urine of five patients with Werner's syndrome were within normal limits, the quantity of hyaluronic acid increased in this disease. To this novel finding, a term “Hyaluronuria” was proposed.
M, Tokunaga +4 more
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Pathology of the Werner Syndrome
1985Anatomic-pathological observation remains one of the fundamental approaches to the understanding of multiple system disease of unknown etiology. In this paper, we review the results of such anatomic investigations of necropsies of subjects with the Werner syndrome, including five cases (all Japanese subjects) that we have personally autopsied, one of ...
T, Ishii +5 more
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Dermatologica, 2009
The symptoms of Werner’s Syndrome are reported by means of 2 cases. The importance of an endocrinological and ophthalmological examination of patients with ‘systemic sclerosis’ is demonstrated.
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The symptoms of Werner’s Syndrome are reported by means of 2 cases. The importance of an endocrinological and ophthalmological examination of patients with ‘systemic sclerosis’ is demonstrated.
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Archives of Ophthalmology, 1974
To the Editor. —In the July issue of theArchives(90:53-56, 1973), Drs. Bullock and Howard reported a case of Werner syndrome. I find the diagnosis unconvincing because of the number of atypical features, which are as follows: Age of presentation. Cataract is commonly present by the age of 20, and by the age of 30 causes severe visual impairment.
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To the Editor. —In the July issue of theArchives(90:53-56, 1973), Drs. Bullock and Howard reported a case of Werner syndrome. I find the diagnosis unconvincing because of the number of atypical features, which are as follows: Age of presentation. Cataract is commonly present by the age of 20, and by the age of 30 causes severe visual impairment.
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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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New England Journal of Medicine, 1997
Figure 1. A 37-year-old man was admitted to the hospital because of hoarseness and progressive difficulty in walking. The patient's face had the characteristic beak-like appearance of Werner's syndrome (left panel). Examination disclosed juvenile cataracts, scleroderma-like skin changes, hair loss, deficiency of adipose tissue, and sensory neuropathy ...
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Figure 1. A 37-year-old man was admitted to the hospital because of hoarseness and progressive difficulty in walking. The patient's face had the characteristic beak-like appearance of Werner's syndrome (left panel). Examination disclosed juvenile cataracts, scleroderma-like skin changes, hair loss, deficiency of adipose tissue, and sensory neuropathy ...
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Neuropathology of the Werner Syndrome
1985In his original report, Werner (1) described four siblings who had in common shortness of stature, senile appearance, early graying of the hair and appearance of cataracts, skin changes and early cessation of menstruation. Subsequent authors added premature balding, tendency to diabetes mellitus and calcification of blood vessels to this picture ...
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Functional role of the Werner syndrome RecQ helicase in human fibroblasts
Aging Cell, 2007Julia Sidorova +2 more
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