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Page 1
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: bordigoni p. 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: bordigoni p. 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.
Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.
Beaussant Cohen S, Fenneteau O, Plouvier E, Rohrlich PS, Daltroff G, Plantier I, Dupuy A, Kerob D, Beaupain B, Bordigoni P, Fouyssac F, Delezoide AL, Devouassoux G, Nicolas JF, Bensaid P, Bertrand Y, Balabanian K, Chantelot CB, Bachelerie F, Donadieu J. Beaussant Cohen S, et al. Among authors: bordigoni p. Orphanet J Rare Dis. 2012 Sep 25;7:71. doi: 10.1186/1750-1172-7-71. Orphanet J Rare Dis. 2012. PMID: 23009155 Free PMC article.
Complete recovery from Cryptosporidium parvum infection with gastroenteritis and sclerosing cholangitis after successful bone marrow transplantation in two brothers with X-linked hyper-IgM syndrome.
Dimicoli S, Bensoussan D, Latger-Cannard V, Straczek J, Antunes L, Mainard L, Dao A, Barbe F, Araujo C, Clément L, Feugier P, Lecompte T, Stoltz JF, Bordigoni P. Dimicoli S, et al. Among authors: bordigoni p. Bone Marrow Transplant. 2003 Oct;32(7):733-7. doi: 10.1038/sj.bmt.1704211. Bone Marrow Transplant. 2003. PMID: 13130323
T-cell immune constitution after peripheral blood mononuclear cell transplantation in complete DiGeorge syndrome.
Bensoussan D, Le Deist F, Latger-Cannard V, Grégoire MJ, Avinens O, Feugier P, Bourdon V, André-Botté C, Schmitt C, Jonveaux P, Eliaou JF, Stoltz JF, Bordigoni P. Bensoussan D, et al. Among authors: bordigoni p. Br J Haematol. 2002 Jun;117(4):899-906. doi: 10.1046/j.1365-2141.2002.03496.x. Br J Haematol. 2002. PMID: 12060129 Free article.
Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).
Pachlopnik Schmid J, Canioni D, Moshous D, Touzot F, Mahlaoui N, Hauck F, Kanegane H, Lopez-Granados E, Mejstrikova E, Pellier I, Galicier L, Galambrun C, Barlogis V, Bordigoni P, Fourmaintraux A, Hamidou M, Dabadie A, Le Deist F, Haerynck F, Ouachée-Chardin M, Rohrlich P, Stephan JL, Lenoir C, Rigaud S, Lambert N, Milili M, Schiff C, Chapel H, Picard C, de Saint Basile G, Blanche S, Fischer A, Latour S. Pachlopnik Schmid J, et al. Among authors: bordigoni p. Blood. 2011 Feb 3;117(5):1522-9. doi: 10.1182/blood-2010-07-298372. Epub 2010 Nov 30. Blood. 2011. PMID: 21119115 Free article.
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: bordigoni p. 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.
247 results