Cynober T - Search Results

1

An extreme consequence of splenectomy in dehydrated hereditary stomatocytosis: gradual thrombo-embolic pulmonary hypertension and lung-heart transplantation.

Jaïs X, Till SJ, Cynober T, Ioos V, Garcia G, Tchernia G, Dartevelle P, Simonneau G, Delaunay J, Humbert M. Jaïs X, et al. Among authors: cynober t. Hemoglobin. 2003 Aug;27(3):139-47. doi: 10.1081/hem-120023377. Hemoglobin. 2003. PMID: 12908798

2

Sub-lethal hydrops as a manifestation of dehydrated hereditary stomatocytosis in two consecutive pregnancies.

Grootenboer-Mignot S, Crétien A, Laurendeau I, Poissonnier MH, Doireau V, Brossard Y, Tchernia G, Cynober T, Delaunay J. Grootenboer-Mignot S, et al. Among authors: cynober t. Prenat Diagn. 2003 May;23(5):380-4. doi: 10.1002/pd.598. Prenat Diagn. 2003. PMID: 12749034

3

A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema.

Grootenboer S, Schischmanoff PO, Cynober T, Rodrigue JC, Delaunay J, Tchernia G, Dommergues JP. Grootenboer S, et al. Among authors: cynober t. Br J Haematol. 1998 Nov;103(2):383-6. doi: 10.1046/j.1365-2141.1998.00992.x. Br J Haematol. 1998. PMID: 9827909 Free article.

4

Dehydrated hereditary stomatocytosis: a cause of prenatal ascites.

Grootenboer S, Barro C, Cynober T, Olivier Schischmanoff P, Ayoubi JM, Tchernia G, Delaunay J, Pons JC. Grootenboer S, et al. Among authors: cynober t. Prenat Diagn. 2001 Dec;21(13):1114-8. Prenat Diagn. 2001. PMID: 11787034

5

Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis.

Syfuss PY, Ciupea A, Brahimi S, Cynober T, Stewart GW, Grandchamp B, Beaumont C, Tchernia G, Delaunay J, Wagner JC. Syfuss PY, et al. Among authors: cynober t. Clin Lab Haematol. 2006 Aug;28(4):270-4. doi: 10.1111/j.1365-2257.2006.00774.x. Clin Lab Haematol. 2006. PMID: 16898969

6

Dehydrated hereditary stomatocytosis mimicking familial hyperkalaemic hypertension: clinical and genetic investigation.

Beaurain G, Mathieu F, Grootenboer S, Fiquet B, Cynober T, Tchernia G, Delaunay J, Jeunemaitre X. Beaurain G, et al. Among authors: cynober t. Eur J Haematol. 2007 Mar;78(3):253-9. doi: 10.1111/j.1600-0609.2006.00811.x. Epub 2007 Jan 23. Eur J Haematol. 2007. PMID: 17253968

7

Southeast Asian ovalocytosis in White persons.

Schischmanoff PO, Cynober T, Miélot F, Leclerc L, Vasseur-Godbillon C, Baudin-Creuza V, Magowan C, Yeung J, Mohandas N, Tchernia G, Delaunay J. Schischmanoff PO, et al. Among authors: cynober t. Hemoglobin. 1999 Feb;23(1):47-56. doi: 10.3109/03630269908996147. Hemoglobin. 1999. PMID: 10081985

8

[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: cynober t. 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.

9

Clinical and laboratory manifestations of congenital dyserythropoietic anemia type I in a cohort of French children.

Bader-Meunier B, Leverger G, Tchernia G, Schischmanoff O, Cynober T, Bernaudin F, Leblanc T, Munzer M, Roda L, Soler C, Thuret I, Delaunay J. Bader-Meunier B, et al. Among authors: cynober t. J Pediatr Hematol Oncol. 2005 Aug;27(8):416-9. doi: 10.1097/01.mph.0000175406.42427.c9. J Pediatr Hematol Oncol. 2005. PMID: 16096522

10

Incidence of hereditary spherocytosis in a population of jaundiced neonates.

Saada V, Cynober T, Brossard Y, Schischmanoff PO, Sender A, Cohen H, Delaunay J, Tchernia G. Saada V, et al. Among authors: cynober t. Pediatr Hematol Oncol. 2006 Jul-Aug;23(5):387-97. doi: 10.1080/08880010600646662. Pediatr Hematol Oncol. 2006. PMID: 16728359

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