Zobrazeno 1 - 7
of 7
pro vyhledávání: '"MESH: Splenomegaly"'
Autor:
Samia Menif, Amel Lakhal, Yosra Ben Youssef, Raihane Ben Lakhal, Manel Bedoui, Z. Manai, Mohamed Adnène Laatiri, Tarek Ben Othmen, Hela Ghedira, Neila Ben Romdhane, Abderrahmane Khélif, Hatem Bellaaj, F. Msadek, Balkis Meddeb, Moez Elloumi
Publikováno v:
Annals of Hematology
Annals of Hematology, Springer Verlag, 2018, 97 (4), pp.597--604. ⟨10.1007/s00277-017-3224-2⟩
Annals of Hematology, Springer Verlag, 2018, 97 (4), pp.597--604. ⟨10.1007/s00277-017-3224-2⟩
International audience; Data are limited in developing countries regarding the clinicopathologic features and response to therapy of chronic myeloid leukemia (CML) in the era of imatinib (IM). The objective of this study is to report on the clinicoep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66925fcc39af00c0fb63c3b0c040da14
https://hal.archives-ouvertes.fr/hal-01876259
https://hal.archives-ouvertes.fr/hal-01876259
Autor:
Xavier Sastre, Sandrine Oyegue, Violaine Arnaud, Odette Mariani, Anne-Marie Dombey, Sandrine Cabantous, Mathieu Sertorio, Martine Daujat-Chavanieu, Pablo Oliveira, Jun Li, Yuesheng Li, Xunya Hou, Hélia Dessein, Xin-Song Luo, Hongbin He, Audrey Romano, Alain Dessein
Publikováno v:
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases, Public Library of Science, 2016, 10 (1), pp.e0004306. ⟨10.1371/journal.pntd.0004306⟩
PLoS Neglected Tropical Diseases, Vol 10, Iss 1, p e0004306 (2016)
PLoS Neglected Tropical Diseases, 2016, 10 (1), pp.e0004306. ⟨10.1371/journal.pntd.0004306⟩
PLoS Neglected Tropical Diseases, Public Library of Science, 2016, 10 (1), pp.e0004306. ⟨10.1371/journal.pntd.0004306⟩
PLoS Neglected Tropical Diseases, Vol 10, Iss 1, p e0004306 (2016)
PLoS Neglected Tropical Diseases, 2016, 10 (1), pp.e0004306. ⟨10.1371/journal.pntd.0004306⟩
Schistosoma eggs cause chronic liver inflammation and a complex disease characterized by hepatic fibrosis (HF) and splenomegaly (SplM). FOXP3+ Tregs could regulate inflammation, but it is unclear where these cells are produced and what roles they pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa2fc9e628ed9d74dcf537daf60e5f44
https://hal.archives-ouvertes.fr/hal-01477135/document
https://hal.archives-ouvertes.fr/hal-01477135/document
Autor:
Béma, Coulibaly, Manuela, Delage-Corre, Sylvaine, Durand-Fontanier, Muriel, Mathonnet, François, Paraf, François, Labrousse
Publikováno v:
Annales de Pathologie
Annales de Pathologie, Elsevier Masson, 2013, 33 (6), pp.406-409. ⟨10.1016/j.annpat.2013.10.003⟩
Annales de Pathologie, Elsevier Masson, 2013, 33 (6), pp.406-409. ⟨10.1016/j.annpat.2013.10.003⟩
International audience; A 59-year-old male, was admitted to our hospital for a tumor of the pancreatic tail. Serum CEA and CA 19-9 levels were normal. Splenopancreasectomy found a desmoid tumour. A 69-year-old male was referred to our institution for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::0cd0d108bc46b2c632f951fe4fda65be
https://hal.archives-ouvertes.fr/hal-02437053
https://hal.archives-ouvertes.fr/hal-02437053
Autor:
Matt Kalaycio, Mukta Arora, Joseph H. Antin, Joerg Halter, Richard T. Maziarz, Wael Saber, Matthew Carabasi, Kwang Woo Ahn, Harry C. Schouten, Vikas Gupta, Ann E. Woolfrey, Mahmoud Aljurf, Brian J. Bolwell, David L. Porter, Ian D. Lewis, Xiaochun Zhu, H. Joachim Deeg, Jean-Yves Cahn, Mary M. Horowitz, Philip L. McCarthy, Gregory A. Hale, Bipin N. Savani, Biju George, Mehdi Hamadani, Steven Z. Pavletic, Jorge E. Cortes, Ed Copelan, Baldeep Wirk, Karen K. Ballen
Publikováno v:
Biology of Blood and Marrow Transplantation
Biology of Blood and Marrow Transplantation, Elsevier, 2012, 18 (9), pp.1446-54. ⟨10.1016/j.bbmt.2012.03.009⟩
Biology of Blood and Marrow Transplantation, 18(9), 1446-1454. Elsevier Science
Biology of Blood and Marrow Transplantation, Elsevier, 2012, 18 (9), pp.1446-54. ⟨10.1016/j.bbmt.2012.03.009⟩
Biology of Blood and Marrow Transplantation, 18(9), 1446-1454. Elsevier Science
Allogeneic hematopoietic cell transplantation (HCT) is curative for selected patients with advanced essential thrombocythemia (ET) or polycythemia vera (PV). From 1990 to 2007, 75 patients with ET (median age 49 years) and 42 patients with PV (median
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::623a77dea852f4a22050b6106c0c5a93
https://hal.archives-ouvertes.fr/hal-00849698
https://hal.archives-ouvertes.fr/hal-00849698
Publikováno v:
Annals of Hematology
Annals of Hematology, Springer Verlag, 2011, 90 (3), pp.349-51. ⟨10.1007/s00277-010-1003-4⟩
Annals of Hematology, Springer Verlag, 2011, 90 (3), pp.349-51. ⟨10.1007/s00277-010-1003-4⟩
Dear Editor, More than 900 hemoglobin (Hb) variants have been reported, and most variants are caused by mutations in the αor β-globin gene clusters [1]. Clinically, most of hemoglobin variants are asymptomatic, but some variants are unstable, with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6807f029fdd704f4bb8ff40f2496e895
https://hal-riip.archives-ouvertes.fr/pasteur-00750569/file/fulltext.pdf
https://hal-riip.archives-ouvertes.fr/pasteur-00750569/file/fulltext.pdf
Autor:
A S, Bourgault-Rouxel, T P, Loughran, R, Zambello, P K, Epling-Burnette, G, Semenzato, J, Donadieu, L, Amiot, T, Fest, T, Lamy
Publikováno v:
Leukemia Research
Leukemia Research, Elsevier, 2008, 32 (1), pp.45-8. ⟨10.1016/j.leukres.2007.04.011⟩
Leukemia Research, 2008, 32 (1), pp.45-8. ⟨10.1016/j.leukres.2007.04.011⟩
Leukemia Research, Elsevier, 2008, 32 (1), pp.45-8. ⟨10.1016/j.leukres.2007.04.011⟩
Leukemia Research, 2008, 32 (1), pp.45-8. ⟨10.1016/j.leukres.2007.04.011⟩
International audience; We report on the clinico-biological characteristics of 20 cases of gammadelta T cell large granular lymphocyte (LGL) leukemia. All the data were compared to that of 196 cases with alphabeta T cell subtype, which represents the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::31e05d5d5e164ed45448f0a09e1c3c21
https://hal.archives-ouvertes.fr/hal-00690765
https://hal.archives-ouvertes.fr/hal-00690765
Publikováno v:
Journal of Virology
Journal of Virology, 2008, 82 (6), pp.2661-72. ⟨10.1128/JVI.02308-07⟩
Journal of Virology, American Society for Microbiology, 2008, 82 (6), pp.2661-72. ⟨10.1128/JVI.02308-07⟩
Journal of Virology, 2008, 82 (6), pp.2661-72. ⟨10.1128/JVI.02308-07⟩
Journal of Virology, American Society for Microbiology, 2008, 82 (6), pp.2661-72. ⟨10.1128/JVI.02308-07⟩
Herpes simplex virus type 1 (HSV-1) mutants that fail to express the viral immediate-early protein ICP0 have a pronounced defect in viral gene expression and plaque formation in limited-passage human fibroblasts. ICP0 is a RING finger E3 ubiquitin li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76454ed2d66a522dcc6e6b68a162129c
https://europepmc.org/articles/PMC2258993/
https://europepmc.org/articles/PMC2258993/