Zobrazeno 1 - 10
of 15
pro vyhledávání: '"S Ladj"'
Autor:
Raed Alzyoud, Nermeen El-Kholy, Yousra Arab, Nadine Choueiter, Ashraf S. Harahsheh, Adnan Salem Aselan, Alyaa Kotby, Asma Bouaziz, Aso F. Salih, Awatif Abushhaiwia, Fahad Alahmadi, Hala M. Agha, Hala M. Elmarsafawy, Hanifa Alrabte, Hesham Al-Saloos, Houda Boudiaf, Issa Hijazi, Kenza Bouayed, Khalfan Salim Al Senaidi, Lamia Boughammoura, Maryam Jalal, Mohamed S. Ladj, Mohammed E. Abu-Shukair, Mona M. ElGanzoury, Nacera Hammadouche, Nora Elsamman, Pierre Mouawad, Rachida Boukari, Nassiba Benalikhoudja, Salima Jdour, Sima Y. Abu Al-Saoud, Soued Nabila Touri, Thouraya Kammoun, Zohra Fitouri, Nagib Dahdah
Kawasaki Disease (KD) is still the most common acquired heart disease in children below the age of five years; it has been well described in the developed world; however, data from the Arab world are limited to case reports or single-center case seri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe84407cd023c5838fd93c370f67a0d9
https://doi.org/10.21203/rs.3.rs-2628492/v1
https://doi.org/10.21203/rs.3.rs-2628492/v1
Autor:
N Ayad, M Gherbi, O Gacem, H Falek, L Labboun, L Amirat, M Chouli, K Abba, H Benmakhlouf, M Achir, M. S Ladj
Publikováno v:
Rheumatology. 61
Background Juvenile dermatomyositis (JDM) is a very rare inflammatory myopathy with an approximate incidence of 2–4 per million. The discovery of specific circulating autoantibodies present in about 60% of cases has allowed them to be classified ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05379f4fe533afa50de3f3b5d7e6ab12
https://doi.org/10.1093/rheumatology/keac496.078
https://doi.org/10.1093/rheumatology/keac496.078
Autor:
Yousra Arab, Nadine Choueiter, Nagib Dahdah, Nermeen El-Kholy, Sima Y. Abu Al-Saoud, Mohammed E. Abu-Shukair, Hala M. Agha, Hesham Al-Saloos, Khalfan Salim Al Senaidi, Raed Alzyoud, Asma Bouaziz, Rachida Boukari, Mona M. El Ganzoury, Hala M. Elmarsafawy, Najat ELrugige, Zohra Fitouri, Mohamed S. Ladj, Pierre Mouawad, Aso F. Salih, Rocio G. Rojas, Ashraf S. Harahsheh
Publikováno v:
Pediatric cardiology. 43(6)
Studies on Kawasaki disease (KD) in Arab countries are scarce, often providing incomplete data. This along with the benefits of multicenter research collaboratives led to the creation of the KD Arab Initiative [Kawarabi] consortium. An anonymous surv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9514098eb7987b58bcf1369487109627
https://pubmed.ncbi.nlm.nih.gov/35624313
https://pubmed.ncbi.nlm.nih.gov/35624313
Autor:
O Gacem, N Hamadouche, N Mansouri, N Mehaba, K Abba, H Chouiki, M S Ladj, N Hadjyoucef, F Boukandoura, K Ouahbi, H Benmekhmouf, Moussa Achir
Publikováno v:
Rheumatology. 60
Background Mevalonate kinase deficiency (MKD) is a rare autosomal recessive auto inflammatory disease. The clinical spectrum of this disease is a continuum ranging from the moderate form of Hyper-IgD syndrome (HIDS) to lethal forms of mevalonic acidu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccc49c8d72551c901c2a5a47f61de0d2
https://doi.org/10.1093/rheumatology/keab722.076
https://doi.org/10.1093/rheumatology/keab722.076
Publikováno v:
Rheumatology. 60
Background Pediatric Systemic Lupus Erythematosus (pSLE) is a chronic mutisystemic autoimmune disease with complex clinical manifestations whose diagnosis is not always easy and the course is generally severe and the treatment is not very well codifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd76fab582af1ba6d25cc98c5b3eecd2
https://doi.org/10.1093/rheumatology/keab722.033
https://doi.org/10.1093/rheumatology/keab722.033
Publikováno v:
Rheumatology. 60
Background Pediatric Systemic Lupus Erythematosus (pSLE) is a severe autoimmune disease due to its serious multi-visceral disorders, its morbidity causing deleterious and sometimes permanent effects. The objective is to determine the prognostic predi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::334e58b718f83f7abab4668221d29433
https://doi.org/10.1093/rheumatology/keab722.035
https://doi.org/10.1093/rheumatology/keab722.035
Publikováno v:
Rheumatology. 60
Background Systemic lupus erythematosus (SLE) is an autoimmune disorder affecting multiple organ systems. Kidney involvement is one of the most frequent and severe manifestations of pediatric systemic lupus erythematosus (pSLE), seriously affecting t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38acff9d590624fa085b0e261191cd0d
https://doi.org/10.1093/rheumatology/keab723.003
https://doi.org/10.1093/rheumatology/keab723.003
Autor:
Nabila Attal, Y. Ferhani, N. Abdellaoui, L. Kedji, K. Saidani, S. Sedfi, Nadia Kechout, A. Dehimi, S. Ladj, R. Boukari, N. Benmesbah, H. Hadji, K. Okka, N. Touri
Publikováno v:
Meta Gene. 25:100746
Leukocyte adhesion deficiency type I (LAD-I) is an autosomal recessive disease characterized by impaired leukocyte diapedesis to sites of infection. The disorder is caused by mutations in the ITGB2 (integrin beta-2) gene. Herein, we report the first
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::097cd80880d124d90b6d43414802e164
https://doi.org/10.1016/j.mgene.2020.100746
https://doi.org/10.1016/j.mgene.2020.100746
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc4b1fd92ef3c7b845df81353d161be0
https://doi.org/10.1182/blood-2018-99-114094
https://doi.org/10.1182/blood-2018-99-114094
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