Zobrazeno 1 - 10
of 69
pro vyhledávání: '"J Bardakdjian-Michau"'
Autor:
J. Bardakdjian-Michau
Publikováno v:
EMC - Biologie médicale. 2:1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6856177fe436475f03dda835d3191e7
https://doi.org/10.1016/s2211-9698(07)71389-4
https://doi.org/10.1016/s2211-9698(07)71389-4
Autor:
J. Bardakdjian-Michau
Publikováno v:
Archives de Pédiatrie. 15:738-740
Accepted 3 October 2008 ABSTRACT Background: As a result of population growth in AfricanCaribbean regions of overseas France, and now immigration essentially from North and sub-Saharan Africa to mainland France, neonatal screening for sickle cell dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caf10bafac597fbd29e2a3f1a9636b6f
https://doi.org/10.1016/s0929-693x(08)71894-3
https://doi.org/10.1016/s0929-693x(08)71894-3
Autor:
F Galactéros, J Bardakdjian-Michau, J.L Dhondt, J.P Farriaux, E Paux, D Ducrocq, J Elion, J Feingold, R Girot, M Maier-Redolsperger, D Lena Russo, F Giraud, M.L North, M.L Briard, J Rey
Publikováno v:
Archives de Pédiatrie. 3:1026-1031
Resume Un programme experimental de detection neonatale de la drepanocytose a ete initie en France metropolitaire en 1990. Apres les depistages mis en place en Guadeloupe et Martinique et differentes experiences regionales, sa strategie a ete affinee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d780bef61567420d1f0c4e513542c17b
https://doi.org/10.1016/0929-693x(96)81727-1
https://doi.org/10.1016/0929-693x(96)81727-1
Autor:
J, Bardakdjian-Michau, M, Bahuau, D, Hurtrel, C, Godart, J, Riou, M, Mathis, M, Goossens, C, Badens, R, Ducrocq, J, Elion, J M, Perini
Publikováno v:
Journal of clinical pathology. 62(1)
Background: As a result of population growth in African-Caribbean regions of overseas France, and now immigration essentially from North and sub-Saharan Africa to mainland France, neonatal screening for sickle cell disease (SCD) has been performed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c7be90629366876ae029ade2cc8acb
https://pubmed.ncbi.nlm.nih.gov/19103855
https://pubmed.ncbi.nlm.nih.gov/19103855
Autor:
J, Bardakdjian-Michau
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 15(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7df0180fcc8d732d18e5141430cced5
https://pubmed.ncbi.nlm.nih.gov/18582733
https://pubmed.ncbi.nlm.nih.gov/18582733
Autor:
J, Bardakdjian-Michau
Publikováno v:
Journal de gynecologie, obstetrique et biologie de la reproduction. 32
An experimental program for neonatal detection of sickle cell disease (SCD) was performed in France in 1990. Our data indicated a high prevalence of SCD, one patient in 1,250 newborns tested. The French national program for neonatal screening for SCD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8ca298d2324cc641b3c391c20db3795
https://pubmed.ncbi.nlm.nih.gov/12592166
https://pubmed.ncbi.nlm.nih.gov/12592166
Autor:
J, Bardakdjian-Michau, J-L, Dhondt, R, Ducrocq, F, Galactéros, A, Guyard, F-X, Huchet, A, Lahary, D, Lena-Russo, P, Maboudou, M-L, North, C, Prehu, A-M, Soummer, M, Verschelde, H, Wajcman
Publikováno v:
Annales de biologie clinique. 61(4)
Hemoglobinopathies have become a significant national health problem in France. The biologists have a pivotal role in the genetic diagnoses. Although sickle cell disease (SCD) is the most frequent abnormality found: not less than 200 new cases are ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4540445e3bb9f0f5197d1cb5ba10f281
https://pubmed.ncbi.nlm.nih.gov/12915349
https://pubmed.ncbi.nlm.nih.gov/12915349
Autor:
H, Wajcman, A P, Yapo, J, Riou, D, Promé, S, Richelme-David, D, Hurtrel, J, Bardakdjian-Michau
Publikováno v:
Hemoglobin. 25(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c797268b12f1fb024e2fd8f70fe30b82
https://pubmed.ncbi.nlm.nih.gov/11791877
https://pubmed.ncbi.nlm.nih.gov/11791877
Autor:
M, Cohen-Solal, C, Préhu, H, Wajcman, C, Poyart, J, Bardakdjian-Michau, J, Kister, D, Promé, C, Valentin, D, Bachir, F, Galactéros
Publikováno v:
British journal of haematology. 103(4)
A Guinean woman, heterozygous for haemoglobin (Hb) S, was studied because of episodes of marked anaemia, repeated typical metaphyseal painful crises and haemosiderosis. Her sickling syndrome resulted from the association of Hb S trait with a severe p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b440ccc8292e924b338ce368e338032f
https://pubmed.ncbi.nlm.nih.gov/9886305
https://pubmed.ncbi.nlm.nih.gov/9886305
Autor:
A Y, Segbena, C, Prehu, H, Wajcman, J, Bardakdjian-Michau, K, Messie, L, Feteke, A, Vovor, M, David, J, Feingold, F, Galacteros
Publikováno v:
American journal of hematology. 59(3)
The gene frequency of the most important hemoglobin (Hb) abnormalities is reported in a population of 171 Togolese newborns. Hb phenotypes, hematological parameters, and the more frequently described alpha-gene deletions were analyzed. Structural abn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::23c3efeed712ff0b8bf39ecb9dad34d5
https://pubmed.ncbi.nlm.nih.gov/9798658
https://pubmed.ncbi.nlm.nih.gov/9798658