Zobrazeno 1 - 10
of 718
pro vyhledávání: '"H. Wajcman"'
Autor:
H. Wajcman, S. Pissard
Publikováno v:
Journal de Pédiatrie et de Puériculture. 34:244-250
Resume Le deficit en G6PD est une affection produisant une hypersensibilite au stress oxydant et qui se traduit par une hemolyse aigue, un ictere neonatal, une anemie chronique, ou aucun symptome tant le facteur declenchant essentiel est le stress ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ada4c293e2f7a284920b8ce9b877fb43
https://doi.org/10.1016/j.jpp.2021.04.001
https://doi.org/10.1016/j.jpp.2021.04.001
Publikováno v:
International journal of laboratory hematology. 39(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aef5f0a0a3e569eae472aa042466a221
https://pubmed.ncbi.nlm.nih.gov/27976500
https://pubmed.ncbi.nlm.nih.gov/27976500
Autor:
H. Wajcman
Publikováno v:
EMC - Hématologie. 3:1-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4530084f99260cb663d88b40f1deb821
https://doi.org/10.1016/s1155-1984(08)50911-3
https://doi.org/10.1016/s1155-1984(08)50911-3
Autor:
H. Wajcman
Publikováno v:
EMC - Hématologie. 1:1-9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1911dae38ea93fd1f3d114481776796
https://doi.org/10.1016/s1155-1984(06)43441-5
https://doi.org/10.1016/s1155-1984(06)43441-5
Autor:
H. Wajcman
Publikováno v:
EMC - Hématologie. 1:1-9
Resume Les hemoglobines humaines appartiennent a une tres ancienne famille de molecules dont l'origine remonte a plus de 1,8 milliard d'annees. Le caractere commun a toutes ces molecules, affirmant leur appartenance a la superfamille des globines, es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0374051b85a2c963daa46b7cab69f3f4
https://doi.org/10.1016/s1155-1984(05)41605-2
https://doi.org/10.1016/s1155-1984(05)41605-2
Autor:
H. Wajcman, Abdelhakim Ahmed-Belkacem, Bhisetti Govinda Rao, Douglas J. Bartels, Christophe Hézode, Yi Zhou, Nagraj Mani, Shelley George, Andrzej Ardzinski, Stéphane Chevaliez, Alexandre Soulier, Jean-Michel Pawlotsky, Laetitia Barbotte, Ann D. Kwong
Publikováno v:
Antimicrobial Agents and Chemotherapy. 54:2681-2683
We characterized a novel substitution conferring moderate resistance to telaprevir, a peptidomimetic inhibitor of hepatitis C virus protease. V36C conferred a 4.0-fold increase in the telaprevir 50% inhibitory concentration in an enzyme assay and a 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e36af380b4ba4711039a8c0df7d7c61
https://doi.org/10.1128/aac.01796-09
https://doi.org/10.1128/aac.01796-09
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:
P, Lacan, G, Souillet, M, Aubry, D, Promé, S, Richelme-David, J, Kister, H, Wajcman, A, Francina
Publikováno v:
American journal of hematology. 69(3)
Hemoglobin Lyon-Bron was found in two members of a family of German ascent presenting with a moderate normocytic anemia. In this alpha 2 globin variant, the N-terminal valine of the chain was replaced by an alanine. Electrospray mass spectrometry of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e485ec737b29030a8631554333b23d8
https://pubmed.ncbi.nlm.nih.gov/11891810
https://pubmed.ncbi.nlm.nih.gov/11891810
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:
H, Wajcman, F, Galacteros
Publikováno v:
Bulletin de la Societe de pathologie exotique (1990). 94(2)
The diagnosis of any sickle cell disease syndrome is based on the unambiguous identification of HbS. Electrophoretic tests are usually the first to be performed. A much better resolution is obtained with isoelectricfocusing than with the more convent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cde0efc871499c7108ae1dba148f2e35
https://pubmed.ncbi.nlm.nih.gov/11475032
https://pubmed.ncbi.nlm.nih.gov/11475032