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Frequency of thrombocytopenia and large platelets correlates neither with conotruncal cardiac anomalies nor immunological features in the chromosome 22q11.2 deletion syndrome.
Latger-Cannard V, Bensoussan D, Grégoire MJ, Marcon F, Cloez JL, Leheup B, Jonveaux P, Lecompte T, Bordigoni P. Latger-Cannard V, et al. Among authors: bensoussan d. Eur J Pediatr. 2004 Jun;163(6):327-8. doi: 10.1007/s00431-004-1426-9. Eur J Pediatr. 2004. PMID: 15346916 No abstract available.
WHIM syndromes with different genetic anomalies are accounted for by impaired CXCR4 desensitization to CXCL12.
Balabanian K, Lagane B, Pablos JL, Laurent L, Planchenault T, Verola O, Lebbe C, Kerob D, Dupuy A, Hermine O, Nicolas JF, Latger-Cannard V, Bensoussan D, Bordigoni P, Baleux F, Le Deist F, Virelizier JL, Arenzana-Seisdedos F, Bachelerie F. Balabanian K, et al. Among authors: bensoussan d. Blood. 2005 Mar 15;105(6):2449-57. doi: 10.1182/blood-2004-06-2289. Epub 2004 Nov 9. Blood. 2005. PMID: 15536153 Free article.
The WHIM syndrome shows a peculiar dysgranulopoiesis: myelokathexis.
Latger-Cannard V, Bensoussan D, Bordigoni P. Latger-Cannard V, et al. Among authors: bensoussan d. Br J Haematol. 2006 Mar;132(6):669. doi: 10.1111/j.1365-2141.2005.05908.x. Br J Haematol. 2006. PMID: 16487166 Free article. No abstract available.
Natural-killer cell amplification for adoptive leukemia relapse immunotherapy: comparison of three cytokines, IL-2, IL-15, or IL-7 and impact on NKG2D, KIR2DL1, and KIR2DL2 expression.
Decot V, Voillard L, Latger-Cannard V, Aissi-Rothé L, Perrier P, Stoltz JF, Bensoussan D. Decot V, et al. Among authors: bensoussan d. Exp Hematol. 2010 May;38(5):351-62. doi: 10.1016/j.exphem.2010.02.006. Epub 2010 Feb 19. Exp Hematol. 2010. PMID: 20172016 Free article.
103 results