Results 151 to 160 of about 2,140 (193)
Some of the next articles are maybe not open access.
American Journal of Clinical Pathology, 1979
A patient who had masses in the breasts clinically suggestive of neoplasia had fibrous mastopathy and striking deposition of ochronotic pigment within the soft tissue of the breast. The gross appearance and light microscopic features are illustrated. The histochemical features of ochronotic pigment and the difficulty in differentiating it from melanin ...
L G, Lefer, R P, Rosier
openaire +2 more sources
A patient who had masses in the breasts clinically suggestive of neoplasia had fibrous mastopathy and striking deposition of ochronotic pigment within the soft tissue of the breast. The gross appearance and light microscopic features are illustrated. The histochemical features of ochronotic pigment and the difficulty in differentiating it from melanin ...
L G, Lefer, R P, Rosier
openaire +2 more sources
Orthopedics, 2014
Alkaptonuria, with its sequel, ochronosis, is a rare disease, with an incidence of 1:125,000 to 1:1 million worldwide. Reported cases of ochronotic arthropathy and other orthopedic manifestations are mostly limited to a single family tree, and few cases have been reported.
Mukand, Lal +2 more
openaire +2 more sources
Alkaptonuria, with its sequel, ochronosis, is a rare disease, with an incidence of 1:125,000 to 1:1 million worldwide. Reported cases of ochronotic arthropathy and other orthopedic manifestations are mostly limited to a single family tree, and few cases have been reported.
Mukand, Lal +2 more
openaire +2 more sources
Urology, 2017
Alkaptonuria is a rare autosomal recessive disorder of tyrosine metabolism. Deficiency of homogentisate 1,2 dioxygenase results in accumulation of oxidized homogentisic acid in the connective tissues of the skin, eyes and ears, musculoskeletal system, and cardiac valves, and in urolithiasis. Excretion of excessive homogentisic acid in urine causes dark-
Onkar, Singh +2 more
openaire +2 more sources
Alkaptonuria is a rare autosomal recessive disorder of tyrosine metabolism. Deficiency of homogentisate 1,2 dioxygenase results in accumulation of oxidized homogentisic acid in the connective tissues of the skin, eyes and ears, musculoskeletal system, and cardiac valves, and in urolithiasis. Excretion of excessive homogentisic acid in urine causes dark-
Onkar, Singh +2 more
openaire +2 more sources
Archives of Internal Medicine, 1929
Up to the present time there have been few reports in the English literature on the subject of ochronosis. The term ochronosis (Greek, pale yellow) was applied by Virchow,1in 1866, to the pigmentation of cartilages and cartilage-like tissues found at autopsy in a man, aged 67, who died of an aneurysm of the ascending aorta.
openaire +1 more source
Up to the present time there have been few reports in the English literature on the subject of ochronosis. The term ochronosis (Greek, pale yellow) was applied by Virchow,1in 1866, to the pigmentation of cartilages and cartilage-like tissues found at autopsy in a man, aged 67, who died of an aneurysm of the ascending aorta.
openaire +1 more source
Journal of the American Academy of Dermatology, 1993
R L, Snider, B H, Thiers
openaire +2 more sources
R L, Snider, B H, Thiers
openaire +2 more sources