Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Nada Assaf"'
Autor:
Nada Assaf, Christine Lefebvre, Victoria Raggueneau, Geoffroy Guignedoux, Alice Marceau-Renaut, Simon Chevalier, Sylvie Tondeur, Dominique Bories, Riad Benramdane, Philippe Rousselot, Christine Terré
Publikováno v:
Hematology, Vol 27, Iss 1, Pp 636-641 (2022)
Objectives Acute myeloid leukemia (AML) with inv(16)/t(16;16) is among the most frequent AML subtypes. It is recognized by the detection of the CBFB-MYH11 fusion which confers a favorable prognosis, irrespective of the presence of secondary cytogenet
Externí odkaz:
https://doaj.org/article/4dd069fddb6846608d1dbcb4e7d4a46f
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e15515- (2023)
Objective: To report the case of a young woman with repeated conception failure, whose karyotype showed an unbalanced complex chromosomal rearrangement involving a large duplication harboring >115 genes and overlapping the 8p23.1 duplication syndrome
Externí odkaz:
https://doaj.org/article/89a88ad5b9cc4d2da2198749c3365bb4
Autor:
Abdul K. El Karaaoui, Nada Assaf
Publikováno v:
African Journal of Laboratory Medicine, Vol 12, Iss 1, Pp e1-e8 (2023)
Background: The Stepwise Laboratory Improvement Process Towards Accreditation (SLIPTA) helps prepare laboratories in low- and middle-income countries to achieve international accreditation aligned with the ISO 15189:2012 standards. Accreditation by t
Externí odkaz:
https://doaj.org/article/5a28f7c9654646aaa43945f53ba4521b
Autor:
Nada Assaf, Zaher Chakhachiro
Publikováno v:
eJHaem, Vol 4, Iss 3, Pp 857-858 (2023)
Externí odkaz:
https://doaj.org/article/1d96cbed2b5042f6959688f7159706d3
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100062- (2023)
Externí odkaz:
https://doaj.org/article/28f059230ad34240ae2ef0bb890854bc
Publikováno v:
HeartRhythm Case Reports. 9:171-177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::959f66a84e4c356f3f3457c4de17da08
https://doi.org/10.1016/j.hrcr.2022.12.013
https://doi.org/10.1016/j.hrcr.2022.12.013
Autor:
Nagi El Saghir, Nadine Safi, Ahmad Masri, Firas Kreidieh, Deborah Mukherji, Nada Assaf, Rami Mahfouz, Hiba Moukadem
Publikováno v:
Cancer Research. 83:P6-02
Background: The prevalence of pathogenic BRCA mutations in high hereditary risk breast cancer patients (pts) in ethnic Lebanese Arab women was 5.6% in a study published in 2015 (El Saghir, et al. The Oncologist). In this study, we look at real world
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d48b285fd5a1d3ddfc8836446756bd30
https://doi.org/10.1158/1538-7445.sabcs22-p6-02-17
https://doi.org/10.1158/1538-7445.sabcs22-p6-02-17
Autor:
Noor Hanania, Elie Najem, Hani Tamim, Nada Assaf, Ghaidaa Majari, Wael Younes, Fatmeh Abbas, Ghina Berjawi, Rami Mahfouz
Publikováno v:
Human Gene. 35:201150
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::391e653b6611d459fcf5eada2d7441bd
https://doi.org/10.1016/j.humgen.2023.201150
https://doi.org/10.1016/j.humgen.2023.201150
Autor:
Ali Bazarbachi, Nada Assaf, Chantal Farra, Jean El-Cheikh, Samer Nassif, Ziad Salem, Zaher Chakhachiro, Ghazi Zaatari, Rami Mahfouz
Publikováno v:
Molecular Biology Reports. 46:2003-2011
Recurrent genetic abnormalities confer distinct morphologic features and play a role in determining the clinical behavior, prognosis and adequate treatment of acute leukemia. In the MENA region, only one study targets the frequency of genetic modific
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc505dbb560b7004e2f5aae92842defd
https://doi.org/10.1007/s11033-019-04649-2
https://doi.org/10.1007/s11033-019-04649-2
Autor:
Mariella D'Angiò, Victoria Raggueneau, Christine Terré, Nada Assaf, Claus Meyer, Rolf Marschalek, Jenifer Osman, Raphael Liévin, Patrizia Larghero, Fatiha Merabet, Francine Garnache, Rathana Kim, Philippe Rousselot
Publikováno v:
Molecular biology reports. 48(10)
The detection of KMT2A gene rearrangements have an important impact on the prognosis and management of acute leukemias. These alterations most commonly involve reciprocal translocations at specific breakpoint regions within KMT2A. To date, more than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cabac3ad68ebfb675fc4f8d2c74c7d1a
https://pubmed.ncbi.nlm.nih.gov/34383244
https://pubmed.ncbi.nlm.nih.gov/34383244