Florensa L - Search Results

1

Pentasomy 21 with two isochromosomes 21 in a case of acute myeloid leukemia without maturation.

Salido M, Solé F, Espinet B, Fernández C, Zamora L, Woessner S, Florensa L. Salido M, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2002 Jan 1;132(1):71-3. doi: 10.1016/s0165-4608(01)00529-5. Cancer Genet Cytogenet. 2002. PMID: 11801314

2

Contribution of cytogenetics and in situ hybridization to the study of monoclonal gammopathies of undetermined significance.

Lloveras E, Solé F, Florensa L, Besses C, Espinet B, Gil M, Pérez-Vila ME, Pedro C, Abella E, Sans-Sabrafen J, Woessner S. Lloveras E, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2002 Jan 1;132(1):25-9. doi: 10.1016/s0165-4608(01)00511-8. Cancer Genet Cytogenet. 2002. PMID: 11801304

3

Translocation (5;17)(q13;q21) in a case with precursor T-lymphoblastic lymphoma/leukemia.

Zamora L, Espinet B, Solé F, Salido M, Rodon N, Florensa L, Woessner S. Zamora L, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2002 Jan 1;132(1):81-2. doi: 10.1016/s0165-4608(01)00523-4. Cancer Genet Cytogenet. 2002. PMID: 11801318 No abstract available.

4

A new case of acute nonlymphocytic leukemia (French-American-British subtype M1) with double minutes and c-MYC amplification.

Rodon N, Solé F, Espinet B, Salido M, Zamora L, Cigudosa JC, Woessner S, Florensa L. Rodon N, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2002 Jan 15;132(2):161-4. doi: 10.1016/s0165-4608(01)00557-x. Cancer Genet Cytogenet. 2002. PMID: 11850082

5

Monosomy 15 in chronic myelomonocytic leukemia. description of a case and review of the literature.

Zamora L, Espinet B, Salido M, Florensa L, Woessner S, Pedro C, Serrtano S, Solé F. Zamora L, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2002 Apr 15;134(2):165-7. doi: 10.1016/s0165-4608(01)00629-x. Cancer Genet Cytogenet. 2002. PMID: 12034533 Review.

6

Genetic characterization of the paraimmunoblastic variant of small lymphocytic lymphoma/chronic lymphocytic leukemia: A case report and review of the literature.

Espinet B, Larriba I, Salido M, Florensa L, Woessner S, Sans-Sabrafen J, Barranco C, Serrano S, Solé F. Espinet B, et al. Among authors: florensa l. Hum Pathol. 2002 Nov;33(11):1145-8. doi: 10.1053/hupa.2002.129209. Hum Pathol. 2002. PMID: 12454822

7

Cytogenetic and fluorescence in situ hybridization studies in 60 patients with multiple myeloma and plasma cell leukemia.

Lloveras E, Granada I, Zamora L, Espinet B, Florensa L, Besses C, Xandri M, Pérez-Vila ME, Millà F, Woessner S, Solé F. Lloveras E, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2004 Jan 1;148(1):71-6. doi: 10.1016/s0165-4608(03)00233-4. Cancer Genet Cytogenet. 2004. PMID: 14697644

8

Is fluorescence in situ hybridization a useful method in diagnosis of polycythemia vera patients?

Zamora L, Espinet B, Florensa L, Besses C, Woessner S, Serrano S, Solé F. Zamora L, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2004 Jun;151(2):139-45. doi: 10.1016/j.cancergencyto.2003.09.011. Cancer Genet Cytogenet. 2004. PMID: 15172751

9

Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia.

Puigdecanet E, Espinet B, Villa O, Florensa L, Besses C, Serrano S, Solé F. Puigdecanet E, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2006 May;167(1):39-42. doi: 10.1016/j.cancergencyto.2005.08.016. Cancer Genet Cytogenet. 2006. PMID: 16682284

10

Gain of multiple copies of the CBFB gene: a new genetic aberration in a case of granulocytic sarcoma.

Mallo M, Espinet B, Salido M, Ferrer A, Pedro C, Besses C, Pérez-Vila E, Serrano S, Florensa L, Solé F. Mallo M, et al. Among authors: florensa l. Cancer Genet Cytogenet. 2007 Nov;179(1):62-5. doi: 10.1016/j.cancergencyto.2007.07.018. Cancer Genet Cytogenet. 2007. PMID: 17981216

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