Garçon L - Search Results

1

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. Ami O, et al. Among authors: garcon l. Prenat Diagn. 2009 Nov;29(11):1071-4. doi: 10.1002/pd.2342. Prenat Diagn. 2009. PMID: 19655317 No abstract available.

2

Infantile pyknocytosis: a cause of haemolytic anaemia of the newborn.

Eyssette-Guerreau S, Bader-Meunier B, Garcon L, Guitton C, Cynober T. Eyssette-Guerreau S, et al. Among authors: garcon l. Br J Haematol. 2006 May;133(4):439-42. doi: 10.1111/j.1365-2141.2006.06033.x. Br J Haematol. 2006. PMID: 16643454 Free article.

3

[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. Guitton C, et al. Among authors: garcon l. Arch Pediatr. 2008 Sep;15(9):1464-73. doi: 10.1016/j.arcped.2008.04.023. Epub 2008 Jun 16. Arch Pediatr. 2008. PMID: 18556182 French.

4

[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. Guitton C, et al. Among authors: garcon l. Arch Pediatr. 2009 Jun;16(6):556-8. doi: 10.1016/S0929-693X(09)74065-5. Arch Pediatr. 2009. PMID: 19541083 French. No abstract available.

5

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. Favale F, et al. Among authors: garcon l. Hemoglobin. 2009;33(6):475-9. doi: 10.3109/03630260903344440. Hemoglobin. 2009. PMID: 19958192

6

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. Garçon L, et al. Hemoglobin. 2010;34(6):576-81. doi: 10.3109/03630269.2010.526922. Hemoglobin. 2010. PMID: 21077766

7

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. Albuisson J, et al. Among authors: garcon l. Nat Commun. 2013;4:1884. doi: 10.1038/ncomms2899. Nat Commun. 2013. PMID: 23695678 Free PMC article.

8

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. Pincez T, et al. Among authors: garcon l. Blood. 2016 Mar 24;127(12):1616-8. doi: 10.1182/blood-2015-11-679357. Epub 2016 Jan 15. Blood. 2016. PMID: 26773041 Free PMC article. No abstract available.

9

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. Rapetti-Mauss R, et al. Among authors: garcon l. Haematologica. 2017 Oct;102(10):e415-e418. doi: 10.3324/haematol.2017.171389. Epub 2017 Jun 15. Haematologica. 2017. PMID: 28619848 Free PMC article. No abstract available.

10

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. Picard V, et al. Among authors: garcon l. Haematologica. 2019 Aug;104(8):1554-1564. doi: 10.3324/haematol.2018.205328. Epub 2019 Jan 17. Haematologica. 2019. PMID: 30655378 Free PMC article.

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