Zobrazeno 1 - 10
of 104
pro vyhledávání: '"T Henni"'
Publikováno v:
European Journal of Haematology. 47:42-47
In a survey of more than 12,000 persons referred to a hematological outpatient clinic in Algiers, we estimated that the incidence of hereditary spherocytosis (HS) is 1/1000. Another 9 cases were found in nine of the corresponding families. Anemia was
Akademický článek
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Autor:
T. Henni, S. Champion, D. Drouet, M. C. Jaffar-Bandjee, S. Djourhi, N. Lugagne-Delpon, Guillaume Bossard, David Vandroux, E. Braunberger, Bernard-Alex Gaüzère
Publikováno v:
Bulletin de la Société de pathologie exotique. 104:105-107
Une jeune femme âgee de 19 ans, porteuse d’une maladie de Hodgkin et hospitalisee dans le service d’oncologie pour une autogreffe, a developpe, au 20e jour, un tableau de detresse respiratoire avec defaillance multiviscerale fatale, secondaire a
Publikováno v:
ICNSC
In this paper, we present a fuzzy logic based vector control for a permanent magnet synchronous machine (PMSM). Two schemes of fuzzy controllers are used, a fuzzy PI controller and a fuzzy parameters PI controller with adaptive parameters (FPPIC). Th
Autor:
D, Vandroux, N, Lugagne-Delpon, G, Bossard, D, Drouet, S, Djourhi, M C, Jaffar-Bandjee, T, Henni, E, Braunberger, S, Champion, B-A, Gaüzere
Publikováno v:
Bulletin de la Societe de pathologie exotique (1990). 104(2)
A 19-year-old patient admitted in an oncology unit for an autograft (Hodgkin disease), developed on day 20 a fatal acute respiratory failure and multiple organ failure due to an infection of the A(H1N1)v2009 virus, which was acquired in the hospital,
Autor:
M. F. Gourdin, L. Desforges, Michel Goossens, Felix Reyes, Jean-Pierre Farcet, P. Gaulard, M. Duc Dodon, Marine Divine, T Henni, Corinne Haioun
Publikováno v:
Journal of Clinical Immunology. 10:282-286
HTLV-I seronegative patients in nonendemic areas have been described with T-cell proliferations the DNA of which contains specific HTLV-I viral sequences. We have looked for the presence of HTLV-I DNA sequences in 27 HTLV-I seronegative patients with
Publikováno v:
Clinical Lymphoma and Myeloma. 9:S91-S92
Autor:
B, Bouadjar, F, Aït-Belkacem, L, Daya-Grosjean, A, Sarasin, S L, Larbaoui, R, Ferhat, M C, Cherid, A, Bendissari, A, Chouiter, K, Bouzid, T, Henni, A, Hafiz, A, Allouache, M, Ysmail-Dahlouk
Publikováno v:
Annales de dermatologie et de venereologie. 123(5)
Xeroderma pigmentosum (XP) is a rate autosomal recessive disorder related to DNA repair defects. Recently, modifications of oncogenes and mutations of the p53 suppressor gene have been reported in skin tumors of XP patients. The purpose is to study,
Publikováno v:
Archives of pathologylaboratory medicine. 119(2)
Patients with cutaneous lymphoid infiltrates that appear reactive histologically and immunophenotypically may develop clinically overt cutaneous lymphoma, suggesting the possibility of misdiagnosis by classical methods. We investigated DNA rearrangem