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pro vyhledávání: '"B, Luria"'
Autor:
לוריא, בן-ציון, B., LURIA
Publikováno v:
Proceedings of the World Congress of Jewish Studies / דברי הקונגרס העולמי למדעי היהדות, 1973 Jan 01. ו, 125-131.
Externí odkaz:
https://www.jstor.org/stable/23515535
Autor:
Rebecca B. Luria, Jeanmarie B. Rey
Publikováno v:
Journal of the American Academy of Dermatology. 60:1037-1041
Scleromyxedema is a rare disease characterized by extensive mucin deposition with fibrosis, and is associated with a monoclonal gammopathy. Currently there is no consensus on optimal treatment of this potentially fatal disease because of the lack of
Publikováno v:
Revista mexicana de tuberculosis y enfermedades del aparato respiratorio. 14(69)
Autor:
Rebecca B, Luria, Theresa, Conologue
Publikováno v:
Cutis. 83(2)
Atrophoderma vermiculatum (AV) is a rare follicular disorder primarily affecting children with reticular or honeycomb atrophy of the cheeks and forehead. Along with keratosis pilaris atrophicans faciei (KPAF) and keratosis follicularis spinulosa deca
Publikováno v:
Clinical nephrology. 44(2)
In recent years, adenocarcinoma of the colon mucosa has become a recognized complication of ureterosigmoidostomy and in most cases the tumor arises at the site of ureterocolonic anastomosis. We report a case of a 29-year-old renal transplant recipien
Publikováno v:
Archives of andrology. 35(1)
Interferon alpha IIb was injected to adult male rats at doses ranging from 10,000 to 200,000 units. Animals were dissected at intervals of 12 h, 24 h, and 5 days. The activity of the enzyme sialyltransferase in testis homogenates was estimated. In th
Publikováno v:
Harefuah. 124(5)
Autor:
I, Yron, Y, Kalechman, A, Langer, I, Lidor, B, Luria, H, Luria, J, Ovadia, Y, Pardo, L, Shohat
Publikováno v:
Journal of clinicallaboratory immunology. 33(3)
In a previous study we showed that endometrial carcinoma (EC) patients have a T cell deficiency manifested in a reduced ability to be stimulated in vitro by PHA and to produce IL-2. In an attempt to understand the mechanism responsible for this alter
Publikováno v:
The American journal of gastroenterology. 85(1)
We report on a 30-yr-old man with Budd-Chiari syndrome due to right hepatic vein membranous obstruction. The patient's older brother also suffered from Budd-Chiari syndrome, and died after emergent portocaval shunt operation. To the best of our knowl
Publikováno v:
Cancer. 22:581-586