Výsledky vyhledávání - "C, San Román"

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Akademický článek

Penetrancia familiar del gen HFE: los cuatro hermanos de una familia afectados por hemocromatosis hereditaria Familiar penetrancy of HFE gene: four brothers of the same family affected by hereditary haemochromatosis

Autor: M. Vázquez Romero, D. Boixeda de Miquel, C. Martín de Argila de Prados, I. Vallcorba Gómez del Valle, P. Cabello Albendea, A. López San Román, C. San Román Cos-Gayón

Publikováno v: Revista Espanola de Enfermedades Digestivas, Vol 97, Iss 8, Pp 608-609 (2005)

Externí odkaz: https://doaj.org/article/4b5e148ca551493189877522cb305865

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Occurrence of BCR-ABL rearrangement in a Philadelphia chromosome-negative patient with 5q and 13q deletions and myeloproliferative syndrome

Autor: Villegas A, C. San Román, González Fa, Eduardo Anguita, M.T. Ferro

Publikováno v: Cancer Genetics and Cytogenetics. 100:1-4

We report the case of a patient with a myeloproliferative syndrome and traits of myelodysplasia and myelofibrosis whose karyotype showed 5q and 13q deletions, as well as Philadelphia chromosome negativity. A molecular biology study performed by South

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0d76241cf502393b4e3c42bc9b25ba0
https://doi.org/10.1016/s0165-4608(97)00003-4

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Chromosomal disorder and neoplastic diseases in a family with inherited fragile 16

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

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Burkitt lymphoma with a duplication of der(8)t(2;8)

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

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Chronic obstructive pulmonary disease. Are the times changing?

Autor: P, Almagro, A, Sangil, J, Custardoy, C, San Román Terán, J C, Martín Escudero, J, Díez-Manglano

Publikováno v: Revista clinica espanola. 213(3)

Chronic obstructive pulmonary disease (COPD) is one of the most prevalent diseases and a major cause of morbidity and mortality in Spain. Currently, COPD is considered a treatable disease with an inflammatory origin that is frequently associated with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::076b4902eeeaadb074ad1317d35fa1ab
https://pubmed.ncbi.nlm.nih.gov/22404992

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Multiple sclerosis prevalence in Malaga, Southern Spain estimated by the capture-recapture method

Autor: Miguel Guerrero, F. Romero, J. A. Tamayo, E de Ramón, M Romero, Jose Carlos López-Madrona, Oscar Fernandez, Victoria Fernández, G Sanchís, A. Alonso, M. Bravo, M Papais-Alvarenga, R. Bustamante, Leandro García, América de León, C. San Román, G. Luque

Publikováno v: Multiple sclerosis (Houndmills, Basingstoke, England). 18(3)

Background: Although not definitively proven, there is commonly accepted to be a latitudinal gradient in the distribution of multiple sclerosis (MS), which is more frequent in temperate zones. The European Mediterranean countries are situated in a zo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0251e997d7abcbf0a7037aea4fb9887b
https://pubmed.ncbi.nlm.nih.gov/21878452

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Unusual translocations and other changes in acute leukemia

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

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