Zobrazeno 1 - 10
of 1 008
pro vyhledávání: '"Tchernia, G."'
Publikováno v:
In Transfusion clinique et biologique 2010 17(3):112-119
Publikováno v:
In Transfusion clinique et biologique 2007 14(4):386-392
Autor:
Delhommeau, F., Cynober, T., Schischmanoff, P.O., Rohrlich, P., Delaunay, J., Mohandas, N., Tchernia, G.
Publikováno v:
In Blood 15 January 2000 95(2):393-397
Publikováno v:
Annals of Nutrition & Metabolism, 1983 Jan 01. 27(4), 320-327.
Externí odkaz:
https://www.jstor.org/stable/45099628
Autor:
GROOTENBOER S, SCHISCHMANOFF PO, LAURENDEAU I, CYNOBER T, TCHERNIA G, DOMMERGUES JP, DHERMY D, BOST M, VARET B, SNYDER M, BALLAS SK, GASPARINI, PAOLO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dris___01099::0928084b04e38822dd11cd77a6cfe6cb
https://hdl.handle.net/11368/1695526
https://hdl.handle.net/11368/1695526
Autor:
Beauchamp-Nicoud, A., Morle, L., Lutz, H. U., Stammler, P., Agulles, O., Petermann-Khder, R., Iolascon, A., Silverio Perrotta, Cynober, T., Tchernia, G., Delaunay, J., Baudin-Creuza, V.
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
A patient with hereditary spherocytosis (HS) was found not to have red cell membrane protein 4.2. This rare form of HS, or 4.2 (-) HS, stems from mutations within the ELB42 or the EPB3 genes. The patient had long suffered from a gastric ulcer and imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::99d53f73244e3029ad5ae30f2d69eb75
http://hdl.handle.net/11591/196244
http://hdl.handle.net/11591/196244
Autor:
TCHERNIA G, DELHOMMEAU F, PERROTTA, Silverio, CYNOBER T, BADER MEUNIER B, NOBILI, Bruno, ROHRLICH P, SALOMON JL, SAGOT BEVENOT S, DELAUNAY J, DEMATTIA D, SCHISCHMANOFF PO, MOHANDAS N, IOLASCON A., MIRAGLIA DEL GIUDICE, Emanuele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::f5a8defa4903a320c0e9d67aabd31bc2
http://hdl.handle.net/11591/203383
http://hdl.handle.net/11591/203383
Autor:
Grootenboer, S., Schischmanoff, P. -O, Laurendeau, I., Cynober, T., Tchernia, G., Dommergues, J. -P, Dhermy, D., Bost, M., Varet, B., Snyder, M., Ballas, S. K., Ducot, B., Babron, M. -C, Stewart, G. W., Paolo Gasparini, Iolascon, A., Delaunay, J.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c39d7359a6934452772015b4318b47e8
http://hdl.handle.net/11588/148706
http://hdl.handle.net/11588/148706
Autor:
Beauchamp Nicoud A, Schischmanoff PO, Alloisio N, Boivin P, Parsons SF, Mielot F, Tchernia G, Legrand A, Miraglia Del Giudice E, Gasparini P, Wickramasinghe SN, Delaunay J., IOLASCON, ACHILLE
Publikováno v:
British journal of haematology. 106(4)
The CDAN2 gene, responsible for congenital dyserythropoietic anaemia, type II (CDA II), was recently mapped to 20q11.2. We report data on an additional member of a previously studied CDA II family. This member had always been regarded as haematologic
Autor:
BEAUCHAMP NICOUD, A, Schischmanoff, Po, Alloisio, N, Boivin, P, Parsons, Sf, Mielot, F, Tchernia, G, Legrand, A, MIRAGLIA DEL GIUDICE, E, Gasparini, Paolo, Iolascon, A, Wickramasinghe, Sn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c9143fa041dc3300b60bc4cad4b9823b
https://hdl.handle.net/11368/1695520
https://hdl.handle.net/11368/1695520