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Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia.
Terre C, Eclache V, Rousselot P, Imbert M, Charrin C, Gervais C, Mozziconacci MJ, Maarek O, Mossafa H, Auger N, Dastugue N, Talmant P, Van den Akker J, Leonard C, N'Guyen Khac F, Mugneret F, Viguié F, Lafage-Pochitaloff M, Bastie JN, Roux GL, Nicolini F, Maloisel F, Vey N, Laurent G, Recher C, Vigier M, Yacouben Y, Giraudier S, Vernant JP, Salles B, Roussi J, Castaigne S, Leymarie V, Flandrin G, Lessard M; France Intergroupe pour la Leucemie Myeloide Chronique. Terre C, et al. Leukemia. 2004 Aug;18(8):1340-6. doi: 10.1038/sj.leu.2403399. Leukemia. 2004. PMID: 15190256
[Accreditation strategy for rare somatic molecular abnormalities detected or quantified by polymerase chain reaction: GBMHM recommendations].
Sujobert P, Dulucq S, Alary AS, Etancelin P, Bouvier A, Boureau L, Chauveau A, Kosmider O, Flandrin P; Pour l’ensemble des auteurs de la session « Posters » sélectionnés pour le Challenge 180 secondes. Sujobert P, et al. Ann Biol Clin (Paris). 2019 Dec 1;77(6):681-684. doi: 10.1684/abc.2019.1498. Ann Biol Clin (Paris). 2019. PMID: 31859645 Free article. French.
A case of chronic neutrophilic leukemia with deletion (11)(q23).
Terré C, Garcia I, Bastie JN, Mayeur D, Decombe L, Gruyer P, Berger R, Castaigne S. Terré C, et al. Cancer Genet Cytogenet. 1999 Apr;110(1):70-1. doi: 10.1016/s0165-4608(98)00177-0. Cancer Genet Cytogenet. 1999. PMID: 10198627
Cytogenetic, interphase, and multicolor fluorescence in situ hybridization analyses in primary plasma cell leukemia: a study of 40 patients at diagnosis, on behalf of the Intergroupe Francophone du Myélome and the Groupe Français de Cytogénétique Hématologique.
Avet-Loiseau H, Daviet A, Brigaudeau C, Callet-Bauchu E, Terré C, Lafage-Pochitaloff M, Désangles F, Ramond S, Talmant P, Bataille R. Avet-Loiseau H, et al. Among authors: terre c. Blood. 2001 Feb 1;97(3):822-5. doi: 10.1182/blood.v97.3.822. Blood. 2001. PMID: 11157506 Free article.
Long-term complete haematological and molecular remission after allogeneic bone marrow transplantation in a patient with a stem cell myeloproliferative disorder associated with t(8;13)(p12;q12).
Suzan F, Guasch G, Terre C, Garcia I, Bastie JN, Maarek O, Ribaud P, Gluckman E, Daniel MT, Pébusque MJ, Castaigne S. Suzan F, et al. Among authors: terre c. Br J Haematol. 2003 Apr;121(2):312-4. doi: 10.1046/j.1365-2141.2003.04269.x. Br J Haematol. 2003. PMID: 12694254 Free article.
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.
Romana SP, Radford-Weiss I, Ben Abdelali R, Schluth C, Petit A, Dastugue N, Talmant P, Bilhou-Nabera C, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Andrieu J, Lai JL, Terre C, Rack K, Cornillet-Lefebvre P, Luquet I, Nadal N, Nguyen-Khac F, Perot C, Van den Akker J, Fert-Ferrer S, Cabrol C, Charrin C, Tigaud I, Poirel H, Vekemans M, Bernard OA, Berger R; Groupe Francophone de Cytogénétique Hématologique. Romana SP, et al. Among authors: terre c. Leukemia. 2006 Apr;20(4):696-706. doi: 10.1038/sj.leu.2404130. Leukemia. 2006. PMID: 16467868
Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Français de Cytogénétique Hématologique.
Jeandidier E, Dastugue N, Mugneret F, Lafage-Pochitaloff M, Mozziconacci MJ, Herens C, Michaux L, Verellen-Dumoulin C, Talmant P, Cornillet-Lefebvre P, Luquet I, Charrin C, Barin C, Collonge-Rame MA, Pérot C, Van den Akker J, Grégoire MJ, Jonveaux P, Baranger L, Eclache-Saudreau V, Pagès MP, Cabrol C, Terré C, Berger R; Groupe Français de Cytogénétique Hématologique (GFCH). Jeandidier E, et al. Among authors: terre c. Cancer Genet Cytogenet. 2006 Apr 1;166(1):1-11. doi: 10.1016/j.cancergencyto.2005.08.005. Cancer Genet Cytogenet. 2006. PMID: 16616106
93 results