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Annals of Internal Medicine, 1965
Excerpt In his classic review on Werner's syndrome published in the ANNALS in 1945, Thannhauser (1) was the first to define clearly the essential features of the syndrome and to distinguish it from...
T R, RILEY +3 more
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Excerpt In his classic review on Werner's syndrome published in the ANNALS in 1945, Thannhauser (1) was the first to define clearly the essential features of the syndrome and to distinguish it from...
T R, RILEY +3 more
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The American Journal of Medicine, 1973
Abstract This is a report of a new case of Werner's syndrome. The clinical picture consisted of short stature, premature aging of the skin, bilateral cataracts, high-pitched voice, generalized subcutaneous and muscle atrophy, scleroderma-like plaques, gangrene, Monckeberg sclerosis and organic brain syndrome. Plasma lipids and lipoprotein pattern were
R, Fleischmajer, A, Nedwich
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Abstract This is a report of a new case of Werner's syndrome. The clinical picture consisted of short stature, premature aging of the skin, bilateral cataracts, high-pitched voice, generalized subcutaneous and muscle atrophy, scleroderma-like plaques, gangrene, Monckeberg sclerosis and organic brain syndrome. Plasma lipids and lipoprotein pattern were
R, Fleischmajer, A, Nedwich
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Archives of Internal Medicine, 1952
ORIGINALLY believed to be an excessively rare heredofamilial disorder, Werner's syndrome has been recognized with increasing frequency in recent years. The syndrome is featured by the unique combination of physical immaturity, early senescence, premature cataracts, scleroderma-like skin changes, and a tendency toward development of diabetes mellitus ...
H, BOATWRIGHT, C E, WHEELER, E P, CAWLEY
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ORIGINALLY believed to be an excessively rare heredofamilial disorder, Werner's syndrome has been recognized with increasing frequency in recent years. The syndrome is featured by the unique combination of physical immaturity, early senescence, premature cataracts, scleroderma-like skin changes, and a tendency toward development of diabetes mellitus ...
H, BOATWRIGHT, C E, WHEELER, E P, CAWLEY
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Australian and New Zealand Journal of Medicine, 1977
A case of Werner syndrome is reported. The patient was prematurely old, had skin atrophy, characteristic posterior subcapsular cataracts and prepubertal primary hypogonadism. Additional ocular features compatible with premature ageing included presbyopia, arcus seniles and diminished tear flow.
S K, Samantray +3 more
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A case of Werner syndrome is reported. The patient was prematurely old, had skin atrophy, characteristic posterior subcapsular cataracts and prepubertal primary hypogonadism. Additional ocular features compatible with premature ageing included presbyopia, arcus seniles and diminished tear flow.
S K, Samantray +3 more
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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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Dermatology, 1971
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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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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[Kango gijutsu] : [Nursing technique], 1985
• Werner's syndrome is a rare condition of autosomalrecessive inheritance, showing some features of accelerated aging. We describe the clinical findings and laboratory studies in a 29-year-old man with this disorder, who presented because of a leg ulcer. Skin fibroblasts from our patient were difficult to culture and proliferated more slowly than those
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• Werner's syndrome is a rare condition of autosomalrecessive inheritance, showing some features of accelerated aging. We describe the clinical findings and laboratory studies in a 29-year-old man with this disorder, who presented because of a leg ulcer. Skin fibroblasts from our patient were difficult to culture and proliferated more slowly than those
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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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