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Autor:
B. Dupriez, J.-L. Demory, M.-C. Le Bousse-Kerdiles, S. Giraudier, C. Bilhou-Nabera, J.-F. Abgrall, J. Rey
Publikováno v:
EMC - Hématologie. 3:1-14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75adffceaf77e5aa505f9501fd6235bd
https://doi.org/10.1016/s1155-1984(08)49958-2
https://doi.org/10.1016/s1155-1984(08)49958-2
Autor:
Jeanne-Marie Libouton, Guy Cornu, Christine Verellen-Dumoulin, Véronique Deneys, C Bilhou-Nabera, Caroline Jacquy, Michel Stul, Lucienne Michaux, A. Zenebergh, Anne Hagemeijer, Philippe Martiat, Jean-Luc Vaerman, G Ameye
Publikováno v:
Annals of Hematology. 79:259-268
Translocation t(12;21)(p13;q22) is the most frequent cytogenetic abnormality in childhood acute lymphoblastic leukemia (ALL) and is generally associated with favorable prognosis. In this report, we assessed the value of dual-color interphase fluoresc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b7a2ba9c21b39414a62b3169b605c8d
https://doi.org/10.1007/s002770050590
https://doi.org/10.1007/s002770050590
Autor:
Sandrine Javorschi, S Dief, M.J. Lerebeller, C Bilhou-Nabera, M.R. Boisseau, Sylvie Labrouche, Geneviève Freyburger
Publikováno v:
Thrombosis and Haemostasis. 75:460-465
SummaryPoor anticoagulant response to APC is conveniently screened by a commercially available functional test (Coatest® APC Resistance) allowing identification of APC-resistant patients. These patients may then be genotyped with respect to factor V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3638737147237388e4b04f34f1c8dcf3
https://doi.org/10.1055/s-0038-1650297
https://doi.org/10.1055/s-0038-1650297
Autor:
C Bilhou-Nabera
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Note: An isochromosome 17 results in a loss of the short arm (17p) and duplication of the long arm (17q) leading to a single copy of 17p and three copies of 17q. An i(17q), usually observed in a complex karyotype, has been reported in solid tumors an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82d5dec07033c64e0941d5fcae3a9c80
https://doi.org/10.4267/2042/37589
https://doi.org/10.4267/2042/37589
Autor:
C Bilhou-Nabera
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on CDKN1B (cyclin-dependent kinase inhibitor 1 B ), with data on DNA, on the protein encoded, and where the gene is implicated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e32b40e39f669ba130b28012e38fcd9e
https://doi.org/10.4267/2042/37450
https://doi.org/10.4267/2042/37450
Autor:
C Bilhou-Nabera
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on RBTN2 (rhombotin-2), with data on DNA, on the protein encoded, and where the gene is implicated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6140557446be9a94e634fec6edb0d48
https://doi.org/10.4267/2042/37451
https://doi.org/10.4267/2042/37451
Autor:
C Bilhou-Nabera
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
The breakpoint on chromosome 20 is not constant; 20qis frequently associated with other cytogenetic abnormalities as del(5q), trisomy 8, trisomy 21, deletions or translocations involving the long arm of chromosome 13; a newly described translocation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75ef40f33b3dbc800fde002acfbbf068
https://doi.org/10.4267/2042/37701
https://doi.org/10.4267/2042/37701
Autor:
C Bilhou-Nabera
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on t(8;14)(q24;q32) - t(2;8)(p12;q24) - t(8;22)(q24;q11), with data on clinics, and the genes involved.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e76131d9b8ff642869e20b850659955a
https://doi.org/10.4267/2042/37512
https://doi.org/10.4267/2042/37512
Autor:
K. Abbed, C. Bilhou-Nabera, Gérard Tertian, David Adams, P. Lozeron, Thierry Lazure, Vincent Ribrag, C. Denier, Catherine Lacroix
Publikováno v:
Journal of the neurological sciences. 277(1-2)
Symptomatic nervous system leukemic infiltration is rarely observed in CLL. Various clinical manifestations including headache, confusion, cranial nerve palsies, focal central deficits and peripheral neuropathies have been seldom reported, occurring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0881595825984155c81748fc46b19adf
https://pubmed.ncbi.nlm.nih.gov/19100998
https://pubmed.ncbi.nlm.nih.gov/19100998