Garçon L - Search Results

1

[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.

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

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. Alanio-Bréchot C, et al. Among authors: garcon l. Am J Hematol. 2008 Apr;83(4):275-8. doi: 10.1002/ajh.21088. Am J Hematol. 2008. PMID: 17994571 Free article.

4

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. Girodon F, et al. Among authors: garcon l. Br J Haematol. 2008 Feb;140(4):468-70. doi: 10.1111/j.1365-2141.2007.06944.x. Epub 2007 Dec 19. Br J Haematol. 2008. PMID: 18162119 Free article. No abstract available.

5

Effect of subtotal splenectomy for management of hereditary pyropoikilocytosis.

Medejel N, Garçon L, Guitton C, Cynober T, Bader-Meunier B. Medejel N, et al. Among authors: garcon l. Br J Haematol. 2008 Jun;142(2):315-7. doi: 10.1111/j.1365-2141.2008.07140.x. Epub 2008 May 19. Br J Haematol. 2008. PMID: 18492110 Free article. No abstract available.

6

[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.

7

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.

8

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

9

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.

10

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.

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