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Year Number of Results
1963 2
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1979 1
1980 1
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2002 2
2003 1
2004 2
2005 3
2006 2
2007 2
2008 6
2009 7
2010 5
2011 5
2012 4
2013 3
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106 results

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Page 1
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. Iolascon A, et al. Among authors: garcon l. Haematologica. 2017 Aug;102(8):1304-1313. doi: 10.3324/haematol.2016.161166. Epub 2017 May 26. Haematologica. 2017. PMID: 28550188 Free PMC article.
PIEZO1, sensing the touch during erythropoiesis.
Caulier A, Garçon L. Caulier A, et al. Among authors: garcon l. Curr Opin Hematol. 2022 May 1;29(3):112-118. doi: 10.1097/MOH.0000000000000706. Epub 2022 Feb 7. Curr Opin Hematol. 2022. PMID: 35441597 Review.
Recent advances in the pathophysiology of PIEZO1-related hereditary xerocytosis.
Jankovsky N, Caulier A, Demagny J, Guitton C, Djordjevic S, Lebon D, Ouled-Haddou H, Picard V, Garçon L. Jankovsky N, et al. Among authors: garcon l. Am J Hematol. 2021 Aug 1;96(8):1017-1026. doi: 10.1002/ajh.26192. Epub 2021 May 3. Am J Hematol. 2021. PMID: 33848364 Free article. Review.
Primary red cell hydration disorders: Pathogenesis and diagnosis.
Caulier A, Rapetti-Mauss R, Guizouarn H, Picard V, Garçon L, Badens C. Caulier A, et al. Among authors: garcon l. Int J Lab Hematol. 2018 May;40 Suppl 1:68-73. doi: 10.1111/ijlh.12820. Int J Lab Hematol. 2018. PMID: 29741259 Review.
Systematic analysis of SCN5A variants associated with inherited cardiac diseases.
Hermida A, Jedraszak G, Ader F, Denjoy I, Fressart V, Maury P, Beyls C, Bloch A, Clerici G, Daire E, Defaye P, Dupin-Deguine D, Garçon L, Klug D, Ginglinger E, Hermida JS, Jesel L, Khraiche D, Kubala M, Lacotte J, Laredo M, Leenhardt A, Le Guillou X, Lesaffre F, Maltret A, Magnin-Poull I, Marijon E, Nambot S, Neyroud N, Ninni S, Palmyre A, Pasquie JL, Proukhnitzky J, Reant P, Richard P, Rollin A, Rooryck C, Sacher F, Schaefer E, Vernier A, Winum PF, Wahbi K, Waintraub X, Waldmann V, Weber S, Zouaghi A, Charron P, Extramiana F, Gandjbakhch E. Hermida A, et al. Among authors: garcon l. Heart Rhythm. 2024 Aug 10:S1547-5271(24)03136-9. doi: 10.1016/j.hrthm.2024.08.018. Online ahead of print. Heart Rhythm. 2024. PMID: 39134129
Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases.
Jedraszak G, Jobic F, Receveur A, Bilan F, Gilbert-Dussardier B, Tiffany B, Missirian C, Willems M, Odent S, Lucas J, Dubourg C, Schaefer E, Scheidecker S, Lespinasse J, Goldenberg A, Guerrot AM, Joly-Helas G, Chambon P, Le Caignec C, David A, Coutton C, Satre V, Vieville G, Amblard F, Harbuz R, Sanlaville D, Till M, Vincent-Delorme C, Colson C, Andrieux J, Naudion S, Toutain J, Rooryck C, de Fréminville B, Prieur F, Daire VC, Amram D, Kleinfinger P, Raabe-Meyer G, Courage C, Lemke J, Stefanou EG, Loretta T, Emmanouil M, Tzeli SK, Sodowska H, Anderson J, Nandini A, Copin H, Garçon L, Liehr T, Morin G. Jedraszak G, et al. Among authors: garcon l. Am J Med Genet A. 2024 Apr;194(4):e63476. doi: 10.1002/ajmg.a.63476. Epub 2023 Nov 16. Am J Med Genet A. 2024. PMID: 37974505
Role of the mechanotransductor PIEZO1 in megakaryocyte differentiation.
Demagny J, Poirault-Chassac S, Ilsaint DN, Marchelli A, Gomila C, Ouled-Haddou H, Collet L, Le Guyader M, Gaussem P, Garçon L, Bachelot-Loza C. Demagny J, et al. Among authors: garcon l. J Cell Mol Med. 2024 Sep;28(18):e70055. doi: 10.1111/jcmm.70055. J Cell Mol Med. 2024. PMID: 39304946 Free PMC article.
106 results