Zobrazeno 1 - 10
of 119
pro vyhledávání: '"H Ben Abid"'
Publikováno v:
European Psychiatry, Vol 64, Pp S215-S215 (2021)
Introduction Many children with autism spectrum disorder (ASD) experience high levels of anxiety. However, inconsistencies between parent and child reports may complicate the assessment of anxiety in this population. Objectives The aim of this stud
Externí odkaz:
https://doaj.org/article/587a22c504744343ba3c2828bf41ea8c
Akademický článek
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Autor:
Sonia Abdelhak, Ahlem Amouri, Lamia Aissaoui, Koussay Dellagi, Mounir Frikha, Hatem Bellaaj, Hatem Elghezal, H Ben Abid, S Hammemi, Lamia Torjemane, le Groupe d’étude tunisien de l’anémie de Fanconi Getaf, Mohamed Bejaoui, Y Ben Youssef, Mongia Hachicha, S. Hadiji Mseddi, Monia Ouederni, F Telmoudi, T Ben Othmen, Lobna Kammoun, Y. Ben Abdennebi
Publikováno v:
Archives de Pédiatrie. 19:467-475
Resume Introduction L’anemie de Fanconi (AF) est une maladie hereditaire caracterisee par une heterogeneite genetique et phenotypique. De nombreux groupes ont mis en place des registres propres a leur pays. En Tunisie, le groupe tunisien d’etude
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3da2f65142df715c4eaa3fe3c45edc10
https://doi.org/10.1016/j.arcped.2012.02.017
https://doi.org/10.1016/j.arcped.2012.02.017
Autor:
Hafsia A, Ramzi Jeddi, T. Ben Othman, R. Ben Lakhal, Balkis Meddeb, H. Ben Abid, Koussay Dellagi, Raouf Hafsia, Z. Bel Haj Ali, Emna Gouider, S. Guermazi
Publikováno v:
Pathologie Biologie. 49:232-236
We report two cases of atypical defibrination syndromes in patients with respectively acute monoblastic leukemia (chronic myeloid leukemia initially) and acute lymphoblastic leukemia. Hemostasis studies show low fibrinogen level, elevated D-dimers, d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1881edca07b7dfdc77c1592f8ee04747
https://doi.org/10.1016/s0369-8114(01)00134-1
https://doi.org/10.1016/s0369-8114(01)00134-1
Autor:
S, Hadiji Mseddi, L, Kammoun, H, Bellaaj, Y, Ben Youssef, L, Aissaoui, L, Torjemane, F, Telmoudi, A, Amouri, H, Elghezal, M, Ouederni, Y, Ben Abdennebi, S, Hammemi, T, Ben Othmen, H, Ben Abid, M, Bejaoui, S, Abdelhak, M, Hachicha, K, Dellagi, M, Frikha, H, Slama
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 19(5)
Fanconi anemia (FA) is a genetically and phenotypically heterogeneous inherited disease. Many groups have established FA registries. In Tunisia, in collaboration with the Tunisian Fanconi Anemia Study Group (TFASG), we set up the Tunisian Fanconi Ane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1cbc68aa6305e7ad021eeab67c5589b9
https://pubmed.ncbi.nlm.nih.gov/22480464
https://pubmed.ncbi.nlm.nih.gov/22480464
Autor:
W. Bouteraa, Lamia Aissaoui, Amel Turki, Karima Kacem, R. Ben Lakhal, Balkis Meddeb, R. Ben Amor, Y. Ben Abdennebi, Zaher Belhadjali, Ramzi Jeddi, H. Ben Abid, Hela Ghedira
Publikováno v:
International Journal of Infectious Diseases. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea3aee19ed10c12b087242c044bcd547
Autor:
Lamia Aissaoui, Karima Kacem, W. Bouteraa, Balkis Meddeb, R. Ben Amor, Ramzi Jeddi, R. Ben Lakhal, Amel Turki, H. Ben Abid, Z. Bel Hadjali, Hela Ghedira, Y. Ben Abdennebi
Publikováno v:
International Journal of Infectious Diseases. 14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94cd4a9a6b8930e33144fee39053c337
Autor:
Emna Gouider, Samia Mnif, H. Ben Abid, Zaher Belhadjali, Balkis Meddeb, H. Benneji, Ramzi Jeddi
Publikováno v:
Pathologie-biologie. 56(3)
Current APL chemotherapy protocols usually include high-dose anthracyclines, mitoxantrone, and epipodophillotoxins, which are topoisomerase II inhibitors of high leukemogenic potential. In the last years, several case reports of myelodysplastic syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c33bc7555beddda0f8eb57030e73b3
https://pubmed.ncbi.nlm.nih.gov/18178033
https://pubmed.ncbi.nlm.nih.gov/18178033
Autor:
Balkis Meddeb, Ramzi Jeddi, S. Hdeiji, Moez Elloumi, N. Ben Alaya, A. Khlif, S. Zarrouki, Samia Menif, K. Dellagi, Z. Belhadj Ali, H. Ben Abid
Publikováno v:
Pathologie-biologie. 57(5)
The optimal management of malignant haematological disorders depend on the degree of tumor load reduction after therapy. Chronic myeloid leukemia constitutes a clinical model for molecular detection and therapy surveillance of malignant disease since
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1601022d32da4279bc1af28c763dfc
https://pubmed.ncbi.nlm.nih.gov/18387753
https://pubmed.ncbi.nlm.nih.gov/18387753
Publikováno v:
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. 13(6)
Background Some patients with autoimmune hemolytic anemia (AIHA) have in their sera autohemolysins able to hemolyze RBCs in vitro by activation of complement. We describe three autohemolysins in patients with AIHA and we study clinical correlations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99ba0f212c723f4825fe002c90ca874e
https://pubmed.ncbi.nlm.nih.gov/17306584
https://pubmed.ncbi.nlm.nih.gov/17306584