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pro vyhledávání: '"N Mehalhal"'
Akademický článek
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Autor:
Azzam Alzoebie, Fati Hamzy, S Hamdi, Hadj Touhami, Hossam Saad, Tarek Owaidah, N Mehalhal, Nouredine Sidi Mansour, Abdulkareem Al-Momen, Naima Mesli, F Grifi, Yasser Wali, Meriem Bensadok, Soraya Benchikh El Fegoun
Publikováno v:
Blood Coagulation & Fibrinolysis
Supplemental Digital Content is available in the text
Home therapy for uncomplicated mild/moderate bleeding can decrease healthcare burden, promote self-esteem, reduce complications, and provide near-normal quality of life. To evaluate recombina
Home therapy for uncomplicated mild/moderate bleeding can decrease healthcare burden, promote self-esteem, reduce complications, and provide near-normal quality of life. To evaluate recombina
Autor:
N Boudjerra, Nourredine Lakhdari, Ryma Tiaiba, Hossam A Saad, Sarah Lakehal, M Saidi, N Mehalhal, Mohamed Bradai, Hocine Ait Ali, Mohamed Amine Bekadja, F Grifi, Naima Mesli, S Hamdi, Noureddine Sidimansour, Z Zouaoui, Djamel Saidi
Publikováno v:
Blood. 136:3-4
Background: Immune thrombocytopenia (ITP), is an acquired immune mediated disease characterized by a platelet count of Methods: This non-interventional, longitudinal, nationwide estimation study investigated the epidemiology and care of ITP pts treat
Autor:
Nadia Merad Boudia, Badra Antar Soltan, Samia Dorgham, Lotfi Louhibi, N Mehalhal, Hadj Touhami, Meriem Aberkane, Noureddine Sidimansour, Wefa Boughrara, Abdallah Boudjema
Publikováno v:
Bulletin du Cancer. 101:803-807
Resume MTHFR est une enzyme cle du metabolisme des folates. Peu d’etudes ont ete rapportees a propos de sa correlation avec le risque de leucemie myeloide chronique (LMC). Dans le but de rechercher l’association entre les polymorphismes C677T et
Autor:
Nouri Midoun, N Mehalhal, MT Abad, F Grifi, Noureddine Sidimansour, M Belhani, Hocine Ait-Ali, Fatima Zohra Ardjoun, S Hamdi, Mohamed Amine Bekadja, Rose Marie Hamladji, R. Bouhass, Hadj Touhami, Naima Mesli, Yousuf Mohamed Said, Z Zouaoui, M Saidi, A Bachiri
Publikováno v:
Hematology/Oncology and Stem Cell Therapy, Vol 4, Iss 4, Pp 161-166 (2011)
BACKGROUND AND OBJECTIVES In Algeria, the incidence of hematologic malignancies has been difficult to estimate for many years. Today, many hematological centers, including 14 university hospitals, have been developed in the entire north and have usef
Autor:
Benkhira Nadjia, Zouaoui Zahia, Chekkaf Ismahane, Brahim Benzineb, Hadj Touhami, Othman Ibraheem, A Bachiri, Djamel Saidi, Asma Hadjeb, Mohamed Aberkane, Mohammed Amine Bekadja, Bendahmane Ahmed Fouad, Amina Krim, Mesli Naima, Samira Zouani, N Mehalhal, Faiza Bensmail
Publikováno v:
Blood. 132:5189-5189
Introduction: Death during induction therapy remains a problem in the management of acute myeloid leukemia (AML). An estimated 6.1% in adult patients and between 19.3% and 27% in subjects of all ages have died of AML during induction therapy. The pur
Autor:
S Boughrira, Mohamed Amine Bekadja, S Nekkal, A Bensenouci, MT Abad, F Bendahmane, N Cherif, F Mehdid, Z Zouaoui, M Belhani, S Hamdi, Rose-Marie Hamladji, M Achir, N Rekkab, Y Ouarlhent, Hadj Touhami, F Serradj, N Sidi Mansour, L Touati, N Hendel, Djamel Saidi, Naima Mesli, R Ahmed Nacer, SE Belakehal, S Oukid, Malek Benakli, H Boudiaf, B Gareh, H Ait Ali, S Benaichou, N Boudjerra, N Bensmaine, F Boukhemia, N Lakhdari, N Benmoufek, F Grifi, Mohamed Bradai, Z Kaci, M Benhalilou, M Allouda, L Sahraoui, F Arbaoui, A Bachiri, N Ferroudj, M Kehal, Fz Ardjoun, A Fafa, S Hadji, N Mehalhal, S Ladj, W Hadji, M Saidi, S Chichoune
Publikováno v:
Blood. 132:5109-5109
Introduction: The aim of this work is to establish an epidemiological approach of aplastic anemia (AA) in Algeria, to identify the different therapeutic strategy and the patients outcomes. Material and methods: This is a retrospective multi-center ep
Autor:
N Boudjerra, N Houti, Y Ghassoul, F Tensaout, R Fenghour, H Mansour, N Bouterfa, H Bouaricha, A Aribi, Djamel Saidi, A Bekache, Mohamed Amine Bekadja, R Nacib, Rose-Marie Hamladji, N Lakhdari, Z Ouchenane, MT Abad, M Belhani, N Sidi Mansour, S Bougherira, Y Ouarlhent, M Saidi, Naima Mesli, R Dridi, N Bouchair, A Graine, Fz Ardjoun, Z Zouaoui, A Benallal, L Touati, Hadj Touhami, M Djilali, N Hamani, F Grifi, N Mehalhal, SE Belakehal, N Ait amer, Malek Benakli, H Ait Ali, C Aboura, Fz Benhassine, A Djenouni, C Boucherit, W Sfaoui, S Chichoune, A Bouacha, M Allouda, S Nekkal, S Hamdi, S Zatout, R Ahmed Nacer, N Zidani
Publikováno v:
Blood. 132:4902-4902
Introduction : Among genetic diseases in hematology, β Thalassemia ranks second after sickle cell disorders in Algeria. Given the seriousness and cost of the care that arises, a national action plan is needed. As a starting point, a national survey
Autor:
N Mehalhal, M Talbi, A Bachiri, M Michallet, Z Zouaoui, Hadj Touhami, Mohamed Amine Bekadja, Badra Entasoltan, Naima Mesli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017062-e2017062 (2017)
Mediterranean Journal of Hematology and Infectious Diseases
Mediterranean Journal of Hematology and Infectious Diseases
Introduction: In a developing country like Algeria, such expensive therapy is not available. Alternative approaches are needed to help these adult. In Algeria ‘imatib’ (CIPLA-India) was introduced in 2006; but no study has been published yet in t
Autor:
Amine Ma Bekadja, Naima Mesli, Hadj Touhami, Fatiha Mekkous-Touhami, Z Zouaoui, A Bachiri, Asma Hadjeb, Nadia Houti, Tamim Alsuliman, R. Bouhass, Abdessamed Arabi, N Mehalhal
Publikováno v:
Journal of Blood & Lymph.
Introduction: The principal object of this study is to represent - in maximum accuracy- the real status of Hodgkin’s lymphoma in west of Algeria, we think also it serves as an adequate indicator for the epidemiological characteristics of HL patient