Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nadia Zidani"'
Autor:
Mohamed Amine Bekadja, Pierre Fenaux, Sabrina Akrouf, Redhouane Ahmed-Nacer, Rose-marie Hamladji, Amina Bouchakour, Souad Taoussi, Mohand Tahar Abad, Mohamed Bradai, Brahim Benzineb, Naima Mesli, M Cheritti, Z Zouaoui, Mohamed Benlazar, Soraya Bougherira, Fatiha Grifi, Hocine Ait-Ali, Malika allouda, Malika Djillali, Khadija Djouadi, Fatima Kherbache, Selma Hamdi, Hakim Hamouda, Imene Boumeida, Meriem Belhani, Nadia Boudjerra, Fatima Zohra Kaci, Soufi Osmani, Nabil Yafour, Soumia Barkat, Fatma Soltani, Razika Nacib, Mahdia Saidi, Laid Touati, Noureddine Lakhdari, Samira Zouani, Hadj Touhami, Djamel Saidi, Lamia Cherif Louazani, Mohamed Ramaoun, Cherifa Akkal, Nemra Mehalhal, Amina Krim, Noureddine Sidimansour, Zohra Ouchenane, Nadia Zidani, Salim Nekkal, Samia Barkat, Y Ouarlent, Mohamed Aberkane, Salah Eddine Belakehal, Aissa Bachiri, Samir Baghdad
Publikováno v:
Asian Pacific Journal of Cancer Biology, Vol 8, Iss 1, Pp 21-29 (2023)
Introduction: Myelodysplastic syndromes (MDS) are a group of haematological disorders, whose diagnosis is based mainly on cytological studies of blood and marrow cells and cytogenetic analysis. Moreover, national epidemiological data on MDS are very
Externí odkaz:
https://doaj.org/article/5a0d9fca78854b11a57eac59027b46af
Autor:
Samir Baghdad, Aissa Bachiri, Salah Eddine Belakehal, Mohamed Aberkane, Y Ouarlent, Samia Barkat, Salim Nekkal, Nadia Zidani, Zohra Ouchenane, Noureddine Sidimansour, Amina Krim, Nemra Mehalhal, Cherifa Akkal, Mohamed Ramaoun, Lamia Cherif Louazani, Djamel Saidi, Hadj Touhami, Samira Zouani, Noureddine Lakhdari, Laid Touati, Mahdia Saidi, Razika Nacib, Fatma Soltani, Soumia Barkat, Nabil Yafour, Soufi Osmani, Fatima Zohra Kaci, Nadia Boudjerra, Meriem Belhani, Imene Boumeida, Hakim Hamouda, Selma Hamdi, Fatima Kherbache, Khadija Djouadi, Malika Djillali, Malika Allouda, Hocine Ait-Ali, Fatiha Grifi, Soraya Bougherira, Mohamed Benlazar, Z Zouaoui, M Cheritti, Naima Mesli, Brahim Benzineb, Mohamed Bradai, Mohand Tahar Abad, Souad Taoussi, Amina Bouchakour, Rose-marie Hamladji, Redhouane Ahmed-Nacer, Sabrina Akrouf, Pierre Fenaux, Mohamed Amine Bekadja
Publikováno v:
Asian Pacific Journal of Cancer Biology. 8:21-29
Introduction: Myelodysplastic syndromes (MDS) are a group of haematological disorders, whose diagnosis is based mainly on cytological studies of blood and marrow cells and cytogenetic analysis. Moreover, national epidemiological data on MDS are very
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::173facbc66bf607cb0fafbb64dacf1a5
https://doi.org/10.31557/apjcb.2023.8.1.21-29
https://doi.org/10.31557/apjcb.2023.8.1.21-29
Autor:
Nassima Boudrahem-Addour, Nadia Zidani, Bahia Djerdjouri, Nassima Nadjem, Malika Izem-Meziane, Meriem Belhani, Khadidja Bouguerra
Publikováno v:
Hemoglobin. 39:36-41
β-Thalassemia (β-thal) is a genetic disorder, representing a major health problem in Algeria. It is associated with altered lipid levels and a state of oxidative stress that can lead to cardiac complications and premature death. We examined the pla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be412ce5c5df3347a3cdfff9d360a365
https://doi.org/10.3109/03630269.2014.979997
https://doi.org/10.3109/03630269.2014.979997
Autor:
Nathalie Carion, Meriem Belhani, Nassima Boudrahem-Addour, Nadia Zidani, Dominique Labie, Cherif Beldjord
Publikováno v:
Hemoglobin. 33:24-36
This study concerns the molecular characterization of beta-thalassemia (beta-thal) alleles in 210 chromosomes. In the studied population, mutations were detected in 98% of the beta-thalassemic chromosomes. Twenty-one molecular defects have been found
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd98d003476cd6ff0a4b6a8ea7dba490
https://doi.org/10.1080/03630260802626061
https://doi.org/10.1080/03630260802626061
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