Two groups of chronic myelomonocytic leukaemia: myelodysplastic and myeloproliferative. Prognostic implications in a series of a single center

Autor: González-Medina, I, Bueno, J, Torrequebrada, A, López, A, Vallespı́, T, Massagué, I

Publikováno v: In Leukemia Research 2002 26(9):821-824

P030 Prognostic impact on survival of an unsuccessful conventional cytogenetic study in patients with myelodysplastic syndromes (MDS)

Autor: Cervera, J., Solé, F., Haase, D., Luño, E., Such, E., Nomdedeu, B., Costa, D., Bernal, T., Vallespí, T., Bueno, J., Pedro, C., Mallo, M., Ardanaz, M.T., Calasanz, M.J., del Cañizo, C., Hernández-Rivas, J.M., Schanz, J., Steidl, C., Hildebrandt, B., Carbonell, F., Orero, M., Ramos, F., Marco, V., Tormo, M., Gomez, V., Andreu, R., Xicoy, B., Amigo, M.L., Muñoz, J.A., Bonanad, S., Arrizabalaga, B., Senent, M.L., Germing, U., Sanz, G.F.

Publikováno v: In Leukemia Research 2009 33 Supplement 1:S75-S76

Complex, not monosomal, karyotype is the cytogenetic marker of poorest prognosis in patients with primary myelodysplastic syndrome

Autor: Valcárcel D, Ademà V, Solé F, Ortega M, Nomdedeu B, Sanz G, Luño E, Cañizo C, de la Serna J, Ardanaz M, Marco V, Collado R, Grau J, Montoro J, Mallo M, Vallespí T

Publikováno v: JOURNAL OF CLINICAL ONCOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname

Complex karyotype (CK) is the poorest risk factor in patients with myelodysplastic syndrome (MDS). It has recently been reported that monosomal karyotype (MK) worsens the prognosis of patients with CK. PATIENTS AND METHODS; We analyzed 1,054 adult pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::eb9f9401739f21bbbcfa0c87bf6839b5
https://fundanet.iislafe.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1276

Persistent polyclonal B-cell lymphocytosis: study of 35 cases

Autor: Florensa L, Navarro JT, Pérez Vila ME, Domingo A, De la Banda E, Rozman M, Camós-Guijosa M, Millá F, Perea G, Alonso E, Ayats R, Aventín A, Cabezudo E, Espinet B, Merino A, Romero P, Sánchez C, Tuset E, Solé F, Feliu E, Fernández C, Gallart M, Vallespí T, Woessner S

Publikováno v: MEDICINA CLINICA
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname

Background and objectives: Persistent polyclonal B-cell lymphocytosis (PPBL) is a rare entity, presenting especially in adult smoker women. It is characterized by an increase of serum IgM, DR7-HLA haplotype, cytogenetic abnormalities and multiple IgH

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3f86e8a33694f8dc6f0291ed945333a7
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=8783

[Cytogenetic abnormalities in seven patients with the Sezary syndrome]

Autor: Solé F, Woessner S, Vallespí T, Domingo A, Pérez Losada A, Lourdes Florensa, Irriguible D, Espinet B, Sans-Sabrafén J

Publikováno v: Europe PubMed Central

The cytogenetic studies performed on 7 patients diagnosed of Sezary's syndrome are reported. The chromosomal study was made after 72 hours of culture of phytohaemagglutinin-stimulated peripheral blood. The 7 patients had abnormal karyotypes, the nume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e65c6786bb654282d49cbf74571e0a1f
https://pubmed.ncbi.nlm.nih.gov/8553180