Zobrazeno 1 - 10
of 46
pro vyhledávání: '"M, Resino"'
Autor:
E. Del Potro, Espinós D, J. Mediavilla, J.M. García-Sagredo, M. Resino, Villegas A, M.T. Ferro, C. San Román
Publikováno v:
Cancer Genetics and Cytogenetics. 78:160-164
We describe a family with an inherited fragile chromosome 16 with the concurrence of a constitutional chromosome abnormality, together with neoplastic pathology within the family. The following findings should be pointed out: in relation to the const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::527eb4b5112b6e18acff3548dcc78d14
https://doi.org/10.1016/0165-4608(94)90084-1
https://doi.org/10.1016/0165-4608(94)90084-1
Autor:
M. Mayayo, Y Vázquez-Mazariego, I Vallcorba, M.T. Ferro, I. Pérez, P. Cabello, M. Resino, R. Muñoz, J.M. García-Sagredo, A. López-Yarto, C. San Román
Publikováno v:
Cancer Genetics and Cytogenetics. 76:136-139
A 51-year-old male patient was diagnosed with Burkitt lymphoma 3 months after cardiac transplantation. The bone marrow karyotype was very complex, and to better define the complex karyotype we used the in situ suppression hybridization technique. Pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7aefc0f266fab075d97e021cf0c98ec4
https://doi.org/10.1016/0165-4608(94)90464-2
https://doi.org/10.1016/0165-4608(94)90464-2
Autor:
M.T. Ferro, J.M. Fernández-Rañada, J.M. García-Sagredo, E. Del Potro, M. Resino, Villegas A, C. San-Román, Isabel Krsnik
Publikováno v:
Cancer Genetics and Cytogenetics. 54:163-171
We report three cases of ANLL and one case of ALL in which we found chromosome abnormalities not previously described. The first patient had a (9;11;16)(p22;q23;p13) translocation in the relapse after bone marrow transplantation. In the second case,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a9186d739758a741a8e9408545e33b6
https://doi.org/10.1016/0165-4608(91)90204-8
https://doi.org/10.1016/0165-4608(91)90204-8
Autor:
M. Resino, P. Cabello, Y Vázquez-Mazariego, I Vallcorba, M.T. Ferro, A. López-Yarto, C. San Román, R. Muñoz, J.M. García-Sagredo, M. Mayayo
Publikováno v:
Cancer Genetics and Cytogenetics. 92:79-81
We describe the cytogenetic study of a neuroendocrine tumor of Merkel cells which appeared in a patient following a heart transplant. An abnormal karyotype was observed in a metastatic lymph node. The abnormality includes two markers derived from the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f394242d1007fdaf953bd27e665724
https://doi.org/10.1016/0165-4608(94)00189-8
https://doi.org/10.1016/0165-4608(94)00189-8
Publikováno v:
Environmental Health Perspectives
We exposed human peripheral lymphocytes in vitro to 0.3 and 1 Gy of 60Co gamma rays to evaluate whether the ability and sensitivity to detect chromosomal aberrations by chromosome painting is independent or not to the specific paint probes. To detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::254a44b472e1944bd88f023fc3ea44bf
http://europepmc.org/articles/PMC1469613
http://europepmc.org/articles/PMC1469613
Autor:
J L, Steegmann, M J, Requena, L F, Casado, M, Pico, M J, Peñarrubia, M T, Ferro, M, Resino, J M, Fernandez-Rañada
Publikováno v:
American journal of hematology. 53(3)
Cytogenetic analysis is the gold standard for the follow-up of CML patients. The sensitivity of cytogenetics is fairly similar to that of Southern detection of M-BCR rearrangement (5%); this last technique has the potential advantage of being indepen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fe23949f95ed1afd821c1475a829f33
https://pubmed.ncbi.nlm.nih.gov/8895687
https://pubmed.ncbi.nlm.nih.gov/8895687
Publikováno v:
Cancer genetics and cytogenetics. 80(2)
A patient with a myelodysplastic syndrome and a 12q deletion was studied and followed-up. After 10 years and several cytogenetic studies, it is suggested that this abnormality can be the sole chromosomal change in myelodysplastic syndromes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb0cd7702450c4f83e352d4c25f4e664
https://pubmed.ncbi.nlm.nih.gov/7736435
https://pubmed.ncbi.nlm.nih.gov/7736435
Autor:
M T, Ferro, J M, García-Sagredo, M, Resino, E, del Potro, A, Villegas, J, Mediavilla, D, Espinós, C, San Román
Publikováno v:
Cancer genetics and cytogenetics. 78(2)
We describe a family with an inherited fragile chromosome 16 with the concurrence of a constitutional chromosome abnormality, together with neoplastic pathology within the family. The following findings should be pointed out: in relation to the const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc9d46859571838b7369807104046214
https://pubmed.ncbi.nlm.nih.gov/7828147
https://pubmed.ncbi.nlm.nih.gov/7828147
Autor:
M, Resino, M T, Ferro, J, García-Laraña, J M, García-Sagredo, P, Cabello, A, López-Yarto, C, San Román
Publikováno v:
Sangre. 39(6)
We report a patient with chronic myelocytic leukaemia (CML) in blastic crisis with a del (7) (p11 p15) in addition to the Philadelphia chromosome. A potential relationship between the presence of this deletion and the therapy in chronic phase is sugg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f918bd98cd0ca5b9c969e279ecf4120f
https://pubmed.ncbi.nlm.nih.gov/7855700
https://pubmed.ncbi.nlm.nih.gov/7855700
Autor:
Y, Vázquez-Mazariego, P, Cabello, J M, García-Sagredo, A, López-Yarto, I, Vallcorba, M, Resino, R, Muñoz, I, Pérez, M, Mayayo, M T, Ferro
Publikováno v:
Cancer genetics and cytogenetics. 76(2)
A 51-year-old male patient was diagnosed with Burkitt lymphoma 3 months after cardiac transplantation. The bone marrow karyotype was very complex, and to better define the complex karyotype we used the in situ suppression hybridization technique. Pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e9c8fd8e8dcef7b7d3e5e40460bd7cdc
https://pubmed.ncbi.nlm.nih.gov/7923063
https://pubmed.ncbi.nlm.nih.gov/7923063