Results 191 to 200 of about 21,295 (232)
WRN loss accelerates abnormal adipocyte metabolism in Werner syndrome. [PDF]
Cell BiosciTian Y +5 more
europepmc +1 more source
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion, 1969 M, García Viveros +3 more
openaire +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Annals of Internal Medicine, 1965
Excerpt Otto Werner (1), as a medical student at the Ophthalmology Clinic in Kiel, studied four siblings with cataracts and scleroderma whom he described in 1904 in his doctoral dissertation.
T R, RILEY +3 more
openaire +4 more sources
Excerpt Otto Werner (1), as a medical student at the Ophthalmology Clinic in Kiel, studied four siblings with cataracts and scleroderma whom he described in 1904 in his doctoral dissertation.
T R, RILEY +3 more
openaire +4 more sources
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
openaire +4 more sources
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
openaire +4 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources
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
openaire +2 more sources