Zobrazeno 1 - 10
of 354
pro vyhledávání: '"I, Elomaa"'
Autor:
I. Elomaa, T. Kylmälä, T. Tammela, J. Viitanen, J. Ottelin, M. Ruutu, K. Jauhiainen, M. Ala-Opas, L. Roos, J. Seppänen, O. Alfthan
Publikováno v:
International Urology and Nephrology. 24:159-166
Although osteosclerotic metastases are characteristic of prostatic carcinoma, bone resorption is also accelerated. Since clodronate inhibits bone resorption and relieves bone pain, we have given it to patients with painful bone disease from prostatic
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 117(18)
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 117(10)
Autor:
I, Elomaa
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 116(6)
Autor:
M, Tarkkanen, T A, Wiklund, M J, Virolainen, M L, Larramendy, N, Mandahl, F, Mertens, C P, Blomqvist, E J, Tukiainen, M M, Miettinen, A I, Elomaa, Y S, Knuutila
Publikováno v:
Cancer. 92(7)
Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes.Twen
Among numerous DNA copy number changes, losses of chromosome 13 are highly recurrent in plasmacytoma
Publikováno v:
Genes, chromosomescancer. 25(2)
Chromosomal imbalances were studied by comparative genomic hybridization (CGH) on 27 specimens from 24 patients with plasmacytoma. All the specimens exhibited DNA copy number changes (mean, 7.7 aberrations/tumor; range, 2-15). The most recurrent chan
Autor:
J, Szymanska, M, Serra, B, Skytting, O, Larsson, M, Virolainen, M, Akerman, M, Tarkkanen, R, Huuhtanen, P, Picci, P, Bacchini, S, Asko-Seljavaara, I, Elomaa, S, Knuutila
Publikováno v:
Genes, chromosomescancer. 23(3)
We used comparative genomic hybridization (CGH) to evaluate DNA sequence copy number changes in 67 synovial sarcomas of both monophasic and biphasic histological subtypes. Changes (mean among aberrant cases: 4.7 aberrations/tumor; range: 1-17), affec
Publikováno v:
Genes, chromosomescancer. 23(2)
DNA sequence copy number changes were studied by comparative genomic hybridization (CGH) in 28 desmoid tumors. Changes were detected in 12 tumors (43%) with a mean of 1.4 changes per sample (range: 1 to 7). Out of 12 tumors associated with pregnancy
Autor:
M, Tarkkanen, T, Böhling, G, Gamberi, P, Ragazzini, M S, Benassi, A, Kivioja, P, Kallio, I, Elomaa, P, Picci, S, Knuutila
Publikováno v:
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 11(5)
Very little is known concerning the cytogenetic and molecular genetic changes of low-grade central osteosarcoma, a rare form of osteosarcoma. In the present study, we used comparative genomic hybridization (CGH) to screen for DNA sequence copy number
Autor:
M L, Larramendy, M, Tarkkanen, J, Valle, A H, Kivioja, H, Ervasti, E, Karaharju, T, Salmivalli, I, Elomaa, S, Knuutila
Publikováno v:
The American journal of pathology. 150(2)
Comparative genomic hybridization was used to search for previously unknown gains and losses of DNA sequences along all chromosome arms in 29 chondrosarcoma specimens obtained from 23 patients. Extensive genetic aberrations, with a mean of 6 changes