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PIEZO1 activation delays erythroid differentiation of normal and Hereditary Xerocytosis-derived human progenitors.

Caulier A, Jankovsky N, Demont Y, Ouled-Haddou H, Demagny J, Guitton C, Merlusca L, Lebon D, Vong P, Aubry A, Lahary A, Rose C, Gréaume S, Cardon E, Platon J, Ouadid-Ahidouch H, Rochette J, Marolleau JP, Picard V, Garçon L.

Haematologica. 2019 Aug 14. pii: haematol.2019.218503. doi: 10.3324/haematol.2019.218503. [Epub ahead of print]


Hodgkin lymphoma infiltration with associated haemophagocytosis in bone marrow films.

Demagny J, Guiheneuf E, Joris M, Garçon L, Harrivel V.

Br J Haematol. 2019 Jul 29. doi: 10.1111/bjh.16108. [Epub ahead of print] No abstract available.


Clinical and biological features in PIEZO1-hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients.

Picard V, Guitton C, Thuret I, Rose C, Bendelac L, Ghazal K, Aguilar-Martinez P, Badens C, Barro C, Bénéteau C, Berger C, Cathébras P, Deconinck E, Delaunay J, Durand JM, Firah N, Galactéros F, Godeau B, Jaïs X, de Jaureguiberry JP, Le Stradic C, Lifermann F, Maffre R, Morin G, Perrin J, Proulle V, Ruivard M, Toutain F, Lahary A, Garçon L.

Haematologica. 2019 Aug;104(8):1554-1564. doi: 10.3324/haematol.2018.205328. Epub 2019 Jan 17.


Subtotal and total splenectomy for hereditary pyropoikilocytosis: Benefits and outcomes.

Pincez T, Guitton C, Landman-Parker J, Brousse V, Gauthier F, Da Costa L, Ghazal K, Dufillot D, Tchernia G, Picard V, Garçon L.

Am J Hematol. 2018 Oct;93(10):E340-E342. doi: 10.1002/ajh.25223. Epub 2018 Sep 26. No abstract available.


Primary red cell hydration disorders: Pathogenesis and diagnosis.

Caulier A, Rapetti-Mauss R, Guizouarn H, Picard V, Garçon L, Badens C.

Int J Lab Hematol. 2018 May;40 Suppl 1:68-73. doi: 10.1111/ijlh.12820. Review.


[Multidisciplinary oncopalliative meeting: Aims and pratical recommendations].

Goldwasser F, Nisenbaum N, Vinant P, Balladur E, Dauchy S, Farota-Romejko I, Colombet I, Alby ML, Giroux J, Larrouy A, Destaintot E, Garcon L, Legrand D, Marin I; groupe soins palliatifs en cancérologie de l’ARS d’Île-de-France.

Bull Cancer. 2018 May;105(5):458-464. doi: 10.1016/j.bulcan.2018.01.017. Epub 2018 Mar 19. French.


Impact of MICA and NKG2D polymorphisms in HLA-fully matched related and unrelated hematopoietic stem cell transplantation.

Apithy MJ, Charbonnier A, Desoutter J, Diouf M, Morel P, Garçon L, Marolleau JP, Guillaume N.

Bone Marrow Transplant. 2018 Jul;53(7):918-922. doi: 10.1038/s41409-017-0083-3. Epub 2018 Jan 29. No abstract available.


DHEA prevents ribavirin-induced anemia via inhibition of glucose-6-phosphate dehydrogenase.

Handala L, Domange B, Ouled-Haddou H, Garçon L, Nguyen-Khac E, Helle F, Bodeau S, Duverlie G, Brochot E.

Antiviral Res. 2017 Oct;146:153-160. doi: 10.1016/j.antiviral.2017.09.002. Epub 2017 Sep 8.


[Immortalization of erythroid progenitors for in vitro large-scale red cell production].

Caulier A, Guyonneau Harmand L, Garçon L.

Transfus Clin Biol. 2017 Sep;24(3):263-267. doi: 10.1016/j.tracli.2017.06.030. Epub 2017 Jul 21. Review. French.


Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.

Rapetti-Mauss R, Picard V, Guitton C, Ghazal K, Proulle V, Badens C, Soriani O, Garçon L, Guizouarn H.

Haematologica. 2017 Oct;102(10):e415-e418. doi: 10.3324/haematol.2017.171389. Epub 2017 Jun 15. No abstract available.


Recommendations regarding splenectomy in hereditary hemolytic anemias.

Iolascon A, Andolfo I, Barcellini W, Corcione F, Garçon L, De Franceschi L, Pignata C, Graziadei G, Pospisilova D, Rees DC, de Montalembert M, Rivella S, Gambale A, Russo R, Ribeiro L, Vives-Corrons J, Martinez PA, Kattamis A, Gulbis B, Cappellini MD, Roberts I, Tamary H; Working Study Group on Red Cells and Iron of the EHA.

Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26.


A Versatile Electronic Tongue Based on Surface Plasmon Resonance Imaging and Cross-Reactive Sensor Arrays-A Mini-Review.

Garçon LA, Genua M, Hou Y, Buhot A, Calemczuk R, Livache T, Billon M, Le Narvor C, Bonnaffé D, Lortat-Jacob H, Hou Y.

Sensors (Basel). 2017 May 6;17(5). pii: E1046. doi: 10.3390/s17051046. Review.


A somatic mosaicism in the G6PD gene inducing a late onset chronic non-spherocytic hemolytic anemia.

Couronné L, Tertian G, Boutron A, Picard V, Ouled-Haddou H, Hughes P, Hermine O, Préhu C, Tchernia G, Garçon L.

Am J Hematol. 2017 Aug;92(8):E153-E155. doi: 10.1002/ajh.24760. Epub 2017 Jun 1. No abstract available.


Medical and Assistive Health Technology: Meeting the Needs of Aging Populations.

Garçon L, Khasnabis C, Walker L, Nakatani Y, Lapitan J, Borg J, Ross A, Velazquez Berumen A.

Gerontologist. 2016 Apr;56 Suppl 2:S293-302. doi: 10.1093/geront/gnw005. Review.


Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study.

Pincez T, Guitton C, Gauthier F, de Lambert G, Picard V, Fénéant-Thibault M, Turhan A, Mohandas N, Tchernia G, Garçon L.

Blood. 2016 Mar 24;127(12):1616-8. doi: 10.1182/blood-2015-11-679357. Epub 2016 Jan 15. No abstract available.


Dysregulation of the Transforming Growth Factor β Pathway in Induced Pluripotent Stem Cells Generated from Patients with Diamond Blackfan Anemia.

Ge J, Apicella M, Mills JA, Garçon L, French DL, Weiss MJ, Bessler M, Mason PJ.

PLoS One. 2015 Aug 10;10(8):e0134878. doi: 10.1371/journal.pone.0134878. eCollection 2015.


Industry Speed Bumps on Local Tobacco Control in Japan? The Case of Hyogo.

Yamada K, Mori N, Kashiwabara M, Yasuda S, Horie R, Yamato H, Garçon L, Armada F.

J Epidemiol. 2015;25(7):496-504. doi: 10.2188/jea.JE20150001.


ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

King MJ, Garçon L, Hoyer JD, Iolascon A, Picard V, Stewart G, Bianchi P, Lee SH, Zanella A; International Council for Standardization in Haematology.

Int J Lab Hematol. 2015 Jun;37(3):304-25. doi: 10.1111/ijlh.12335. Epub 2015 Mar 18.


Microfabrication, characterization and in vivo MRI compatibility of diamond microelectrodes array for neural interfacing.

Hébert C, Warnking J, Depaulis A, Garçon LA, Mermoux M, Eon D, Mailley P, Omnès F.

Mater Sci Eng C Mater Biol Appl. 2015 Jan;46:25-31. doi: 10.1016/j.msec.2014.10.018. Epub 2014 Oct 5.


Electronic tongue generating continuous recognition patterns for protein analysis.

Hou Y, Genua M, Garçon LA, Buhot A, Calemczuk R, Bonnaffé D, Lortat-Jacob H, Livache T.

J Vis Exp. 2014 Sep 16;(91):51901. doi: 10.3791/51901.


SPR imaging based electronic tongue via landscape images for complex mixture analysis.

Genua M, Garçon LA, Mounier V, Wehry H, Buhot A, Billon M, Calemczuk R, Bonnaffé D, Hou Y, Livache T.

Talanta. 2014 Dec;130:49-54. doi: 10.1016/j.talanta.2014.06.038. Epub 2014 Jul 3.


Genetic background-dependent thrombotic microangiopathy is related to vascular endothelial growth factor receptor 2 signaling during anti-glomerular basement membrane glomerulonephritis in mice.

Mesnard L, Cathelin D, Vandermeersch S, Rafat C, Luque Y, Sohier J, Nochy D, Garcon L, Callard P, Jouanneau C, Verpont MC, Tharaux PL, Hertig A, Rondeau E.

Am J Pathol. 2014 Sep;184(9):2438-49. doi: 10.1016/j.ajpath.2014.05.020. Epub 2014 Jul 6.


A double red cells population in a woman with a microcytic anemia.

Garçon L, Kannengiesser C.

Blood. 2014 Feb 6;123(6):808. No abstract available.


Designated smoking areas in streets where outdoor smoking is banned.

Yamato H, Mori N, Horie R, Garcon L, Taniguchi M, Armada F.

Kobe J Med Sci. 2013 Jun 17;59(3):E93-105.


Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.

Garçon L, Ge J, Manjunath SH, Mills JA, Apicella M, Parikh S, Sullivan LM, Podsakoff GM, Gadue P, French DL, Mason PJ, Bessler M, Weiss MJ.

Blood. 2013 Aug 8;122(6):912-21. doi: 10.1182/blood-2013-01-478321. Epub 2013 Jun 6.


Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.

Albuisson J, Murthy SE, Bandell M, Coste B, Louis-Dit-Picard H, Mathur J, Fénéant-Thibault M, Tertian G, de Jaureguiberry JP, Syfuss PY, Cahalan S, Garçon L, Toutain F, Simon Rohrlich P, Delaunay J, Picard V, Jeunemaitre X, Patapoutian A.

Nat Commun. 2013;4:1884. doi: 10.1038/ncomms2899. Erratum in: Nat Commun. 2013;4:2440.


Transfusion medicine illustrated. Red blood cell anomalies in the context of hereditary pyropoikilocytosis.

Bock I, Perrin J, Braun F, Garçon L, Lesesve JF.

Transfusion. 2012 Aug;52(8):1646. doi: 10.1111/j.1537-2995.2012.03563.x. No abstract available.


[A case of hereditary pyropoikilocytosis with mild expression and delayed onset].

Bock I, Perrin J, Braun F, Garçon L, Lesesve JF.

Ann Biol Clin (Paris). 2012 Jul-Aug;70(4):483-8. French.


Red cells exchanges in sickle cells disease lead to a selective reduction of erythrocytes-derived blood microparticles.

Mahfoudhi E, Lecluse Y, Driss F, Abbes S, Flaujac C, Garçon L.

Br J Haematol. 2012 Feb;156(4):545-7. doi: 10.1111/j.1365-2141.2011.08897.x. Epub 2011 Oct 11. No abstract available.


p52 Activation in monomorphic B-cell posttransplant lymphoproliferative disorder/diffuse large B-cell lymphoma without BAFF-R expression.

Proust A, Rincé P, Creidy R, Lazure T, Joab I, Garçon L, Fabre M, Guettier C, Raphael M.

Am J Pathol. 2011 Oct;179(4):1630-7. doi: 10.1016/j.ajpath.2011.07.003. Epub 2011 Aug 24.


Finding knizocytes in a peripheral blood smear.

Lesesve JF, Garçon L, Lecompte T.

Am J Hematol. 2012 Jan;87(1):105-6. doi: 10.1002/ajh.22007. Epub 2011 Apr 20. No abstract available.


Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations.

Ducamp S, Kannengiesser C, Touati M, Garçon L, Guerci-Bresler A, Guichard JF, Vermylen C, Dochir J, Poirel HA, Fouyssac F, Mansuy L, Leroux G, Tertian G, Girot R, Heimpel H, Matthes T, Talbi N, Deybach JC, Beaumont C, Puy H, Grandchamp B.

Hum Mutat. 2011 Jun;32(6):590-7. doi: 10.1002/humu.21455. Epub 2011 Feb 24.


[Hemolytic anemia in adults: Main causes and diagnostic procedure].

Loustau V, Guillaud C, Garcon L, Godeau B, Michel M.

Presse Med. 2011 May;40(5):470-85. doi: 10.1016/j.lpm.2010.11.013. Epub 2011 Feb 4. Review. French.


A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain.

Garçon L, Iolascon A, Pissard S, Esposito MR, Russo R, Fenneteau O, Fénéant-Thibault M, Heimpel H, Delaunay J.

Hemoglobin. 2010;34(6):576-81. doi: 10.3109/03630269.2010.526922.


Frequency of congenital dyserythropoietic anemias in Europe.

Heimpel H, Matuschek A, Ahmed M, Bader-Meunier B, Colita A, Delaunay J, Garcon L, Gilsanz F, Goede J, Högel J, Kohne E, Leichtle R, Munoz J, Perrotta S, Piscopo C, Renella R, Schwarz K, Smolenska-Sym G, Wickramasinghe S, Zanella A, Iolascon A.

Eur J Haematol. 2010 Jul;85(1):20-5.


Aurora B is dispensable for megakaryocyte polyploidization, but contributes to the endomitotic process.

Lordier L, Chang Y, Jalil A, Aurade F, Garçon L, Lécluse Y, Larbret F, Kawashima T, Kitamura T, Larghero J, Debili N, Vainchenker W.

Blood. 2010 Sep 30;116(13):2345-55. doi: 10.1182/blood-2010-01-265785. Epub 2010 Jun 14.


Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

Iolascon A, Russo R, Esposito MR, Asci R, Piscopo C, Perrotta S, Fénéant-Thibault M, Garçon L, Delaunay J.

Haematologica. 2010 May;95(5):708-15. doi: 10.3324/haematol.2009.014985. Epub 2009 Dec 16.


Southeast Asian ovalocytosis and a sickle cell trait in a young patient with sudden retinal stroke: a fortuitous association?

Favale F, Gardembas M, Pajot O, Saada V, Fénéant-Thibault M, Delaunay J, Garçon L.

Hemoglobin. 2009;33(6):475-9. doi: 10.3109/03630260903344440.


First-trimester nuchal abnormalities secondary to dehydrated hereditary stomatocytosis.

Ami O, Picone O, Garçon L, Castel C, Guitton C, Delaunay J, Frydman R, Senat MV.

Prenat Diagn. 2009 Nov;29(11):1071-4. doi: 10.1002/pd.2342. No abstract available.


Transient red-blood-cell morphological anomalies after acute liver dysfunction.

Lesesve JF, Garçon L, Lecompte T.

Eur J Haematol. 2010 Jan 1;84(1):92-3. doi: 10.1111/j.1600-0609.2009.01323.x. Epub 2009 Jul 18. No abstract available.


[Hereditary spherocytosis: guidelines for the diagnosis and management in children].

Guitton C, Garçon L, Cynober T, Gauthier F, Tchernia G, Delaunay J, Leblanc T, Thuret I, Bader-Meunier B.

Arch Pediatr. 2009 Jun;16(6):556-8. doi: 10.1016/S0929-693X(09)74065-5. French. No abstract available.


[Biological diagnosis of red cell membrane disorders].

Garçon L.

Arch Pediatr. 2009 Jun;16(6):553-5. doi: 10.1016/S0929-693X(09)74064-3. French. No abstract available.


Reconstitution inflammatory syndrome related to histoplasmosis, with a hemophagocytic syndrome in HIV infection.

De Lavaissière M, Manceron V, Bourée P, Garçon L, Bisaro F, Delfraissy JF, Lambotte O, Goujard C.

J Infect. 2009 Mar;58(3):245-7. doi: 10.1016/j.jinf.2008.11.010. Epub 2008 Dec 17.


[Hereditary spherocytosis: guidelines for the diagnosis and management in children].

Guitton C, Garçon L, Cynober T, Gauthier F, Tchernia G, Delaunay J, Leblanc T, Thuret I, Bader-Meunier B.

Arch Pediatr. 2008 Sep;15(9):1464-73. doi: 10.1016/j.arcped.2008.04.023. Epub 2008 Jun 16. French.


Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis.

Medejel N, Garçon L, Guitton C, Cynober T, Bader-Meunier B.

Br J Haematol. 2008 Jun;142(2):315-7. doi: 10.1111/j.1365-2141.2008.07140.x. Epub 2008 May 19. No abstract available.


The human spleen is a major reservoir for long-lived vaccinia virus-specific memory B cells.

Mamani-Matsuda M, Cosma A, Weller S, Faili A, Staib C, Garçon L, Hermine O, Beyne-Rauzy O, Fieschi C, Pers JO, Arakelyan N, Varet B, Sauvanet A, Berger A, Paye F, Andrieu JM, Michel M, Godeau B, Buffet P, Reynaud CA, Weill JC.

Blood. 2008 May 1;111(9):4653-9. doi: 10.1182/blood-2007-11-123844. Epub 2008 Mar 3.


Usefulness of the eosin-5'-maleimide cytometric method as a first-line screening test for the diagnosis of hereditary spherocytosis: comparison with ektacytometry and protein electrophoresis.

Girodon F, Garçon L, Bergoin E, Largier M, Delaunay J, Fénéant-Thibault M, Maynadié M, Couillaud G, Moreira S, Cynober T.

Br J Haematol. 2008 Feb;140(4):468-70. Epub 2007 Dec 19. No abstract available.


Association between myeloid malignancies and acquired deficit in protein 4.1R: a retrospective analysis of six patients.

Alanio-Bréchot C, Schischmanoff PO, Fénéant-Thibault M, Cynober T, Tchernia G, Delaunay J, Garçon L.

Am J Hematol. 2008 Apr;83(4):275-8.


Use of hematopoietic progenitor cell count on the Sysmex XE-2100 for peripheral blood stem cell harvest monitoring.

Letestu R, Marzac C, Audat F, Belhocine R, Tondeur S, Baccini V, Garçon L, Cortivo LD, Perrot JY, Lefrère F, Valensi F, Ajchenbaum-Cymbalista F.

Leuk Lymphoma. 2007 Jan;48(1):89-96.


Constitutive activation of STAT5 and Bcl-xL overexpression can induce endogenous erythroid colony formation in human primary cells.

Garçon L, Rivat C, James C, Lacout C, Camara-Clayette V, Ugo V, Lecluse Y, Bennaceur-Griscelli A, Vainchenker W.

Blood. 2006 Sep 1;108(5):1551-4. Epub 2006 May 9.

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