Tchernia G - 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: tchernia g. 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. Among authors: tchernia g. 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: tchernia g. 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: tchernia g. 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: tchernia g. Blood. 2001 Jan 15;97(2):399-403. doi: 10.1182/blood.v97.2.399. Blood. 2001. PMID: 11154215 Free article.

6

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia.

Da Costa L, Mohandas N, Sorette M, Grange MJ, Tchernia G, Cynober T. Da Costa L, et al. Among authors: tchernia g. Blood. 2001 Nov 15;98(10):2894-9. doi: 10.1182/blood.v98.10.2894. Blood. 2001. PMID: 11698268 Free article.

7

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. Hematol J. 2000;1(3):146-52. doi: 10.1038/sj.thj.6200022. Hematol J. 2000. PMID: 11920183

8

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: tchernia g. Pediatr Hematol Oncol. 2006 Jul-Aug;23(5):387-97. doi: 10.1080/08880010600646662. Pediatr Hematol Oncol. 2006. PMID: 16728359

9

Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis.

Tchernia G, Gauthier F, Mielot F, Dommergues JP, Yvart J, Chasis JA, Mohandas N. Tchernia G, et al. Blood. 1993 Apr 15;81(8):2014-20. Blood. 1993. PMID: 8471763 Free article.

10

Myelodysplasia in childhood may be a polyclonal disease.

Tchernia G, Bader-Meunier B, Lavergne JM, Miélot F, Dommergues JP. Tchernia G, et al. Hematol Cell Ther. 1996 Aug;38(4):325-30. doi: 10.1007/s00282-996-0325-0. Hematol Cell Ther. 1996. PMID: 8891724 Review.

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