Cynober T - Search Results

1

The GEN.S: a fortuitous finding of a routine screening test for hereditary spherocytosis.

Chiron M, Cynober T, Mielot F, Tchernia G, Croisille L. Chiron M, et al. Among authors: cynober t. Hematol Cell Ther. 1999 Jun;41(3):113-6. doi: 10.1007/s00282-999-0113-8. Hematol Cell Ther. 1999. PMID: 10456441

2

Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity.

Cynober T, Mohandas N, Tchernia G. Cynober T, et al. J Lab Clin Med. 1996 Sep;128(3):259-69. doi: 10.1016/s0022-2143(96)90027-x. J Lab Clin Med. 1996. PMID: 8783633

3

[Hereditary spherocytosis. Course and value of subtotal splenectomy].

Castillo B, Cynober T, Bader-Meunier B, Gauthier F, Miélot F, Tchernia G, Dommergues JP. Castillo B, et al. Among authors: cynober t. Arch Pediatr. 1997 Jun;4(6):515-20. doi: 10.1016/s0929-693x(97)87569-0. Arch Pediatr. 1997. PMID: 9239265 French.

4

Natural history of hereditary spherocytosis during the first year of life.

Delhommeau F, Cynober T, Schischmanoff PO, Rohrlich P, Delaunay J, Mohandas N, Tchernia G. Delhommeau F, et al. Among authors: cynober t. Blood. 2000 Jan 15;95(2):393-7. Blood. 2000. PMID: 10627440 Free article.

5

Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis.

Bader-Meunier B, Gauthier F, Archambaud F, Cynober T, Miélot F, Dommergues JP, Warszawski J, Mohandas N, Tchernia G. Bader-Meunier B, et al. Among authors: cynober t. Blood. 2001 Jan 15;97(2):399-403. doi: 10.1182/blood.v97.2.399. Blood. 2001. PMID: 11154215 Free article.

6

Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis.

Tchernia G, Delhommeau F, Perrotta S, Cynober T, Bader-Meunier B, Nobili B, Rohrlich P, Salomon JL, Sagot-Bevenot S, del Giudice EM, Delaunay J, DeMattia D, Schischmanoff PO, Mohandas N, Iolascon A; ESPHI working group on hemolytic anemias. Tchernia G, et al. Among authors: cynober t. Hematol J. 2000;1(3):146-52. doi: 10.1038/sj.thj.6200022. Hematol J. 2000. PMID: 11920183

7

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

8

Search for the candidate genes in dominant hereditary spherocytosis using linkage analysis.

Garbarz M, Bibas D, Cynober T, Galand C, Bournier O, Devaux I, Tchernia G, Dhermy D. Garbarz M, et al. Among authors: cynober t. C R Acad Sci III. 1996 Oct;319(10):913-9. C R Acad Sci III. 1996. PMID: 8977772

9

Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects.

Dhermy D, Galand C, Bournier O, Boulanger L, Cynober T, Schismanoff PO, Bursaux E, Tchernia G, Boivin P, Garbarz M. Dhermy D, et al. Among authors: cynober t. Br J Haematol. 1997 Jul;98(1):32-40. doi: 10.1046/j.1365-2141.1997.1893005.x. Br J Haematol. 1997. PMID: 9233560 Free article.

10

Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression.

Silveira P, Cynober T, Dhermy D, Mohandas N, Tchernia G. Silveira P, et al. Among authors: cynober t. Am J Clin Pathol. 1997 Oct;108(4):391-9. doi: 10.1093/ajcp/108.4.391. Am J Clin Pathol. 1997. PMID: 9322591

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