Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Z Fitouri"'
Autor:
R Guedri, C Dghaies, H Hrizi, H Fraj, M Rebhi, L Essaddam, M Dahmouni, A Abdelaali, Z Fitouri, S Ben Becher
Publikováno v:
Rheumatology. 61
Background Methotrexate (MTX) is the anti-rheumatic drug of choice in juvenile idiopathic arthritis (JIA). Its adverse effects such as intolerance occur frequently, potentially hindering its efficacy Objective To describe the frequency of MTX intoler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c58b7a75bc08a54d8520fb1bd5879ee
https://doi.org/10.1093/rheumatology/keac496.028
https://doi.org/10.1093/rheumatology/keac496.028
Autor:
C Dghaies, H Hrizi, R Guedri, M Rebhi, H Fraj, L Essaddam, M Dahmouni, A Abdelaali, Z Fitouri, S Ben Becher
Publikováno v:
Rheumatology. 61
Background Oligoarticular juvenile idiopathic arthritis (JIA) is a rare inflammatory disease that occur in children under the age of 16. JIA associated uveitis is the most frequent extra-articular manifestation. The uveitis can be sight-threatening a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8adc89bf5bc9ceaa564a3d32a58283f
https://doi.org/10.1093/rheumatology/keac496.029
https://doi.org/10.1093/rheumatology/keac496.029
Autor:
C Dghaies, R Guedri, M Rebhi, H Hrizi, L Essaddam, M Dahmouni, A Abdelaali, Z Fitouri, S Ben Becher
Publikováno v:
Rheumatology. 61
Background Juvenile idiopathic arthritis (JIA) is an acquired autoinflammatory disease characterised by arthritis of unknown origin with onset before age of 16 years. JIA comprises a group of heterogeneous diseases further divided into various catego
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99b059e462795e9fb5de150e94459e53
https://doi.org/10.1093/rheumatology/keac496.027
https://doi.org/10.1093/rheumatology/keac496.027
Publikováno v:
Rheumatology. 60
Background Multisystem inflammatory syndrome in children (MIS-C) is a severe immune-mediated syndrome that occurs after COVID-19 infection. It mainly affects children and presents several clinical aspects. The cutaneous and mucous signs are very much
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ac7fc462796a78e9627004ab5bcaec0
https://doi.org/10.1093/rheumatology/keab722.071
https://doi.org/10.1093/rheumatology/keab722.071
Akademický článek
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Autor:
Emna Cherifi, L. Essaddam, Wafa Kallali, R. Guedri, Z. Fitouri, Saayda Ben Becher, Nadia Mattoussi
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 2, Pp 74-77 (2020)
International Journal of Pediatrics and Adolescent Medicine, Vol 7, Iss 2, Pp 74-77 (2020)
Background Short stature is a common reason for referral to pediatric endocrinology clinics. It may be a manifestation of a pathological condition requiring early treatment. The aim of this study was to describe the characteristics and etiologies of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9045a4792af8c1d174abe71b333be4a5
https://pubmed.ncbi.nlm.nih.gov/32642540
https://pubmed.ncbi.nlm.nih.gov/32642540
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Revue Française d'Allergologie. 54:30-33
Resume L’anaphylaxie alimentaire induite par l’exercice est une forme rare mais deroutante de l’allergie alimentaire. Nous rapportons deux observations d’anaphylaxie alimentaire induite par l’exercice a la farine de ble chez un garcon de 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18130049f206d8638cb9fd33cf839f0d
https://doi.org/10.1016/j.reval.2013.08.001
https://doi.org/10.1016/j.reval.2013.08.001
Autor:
Kais Douzi, M. Jaouani, Miniar Kalai, Maria Leticia Ribeiro, SK Macedo, I. Boudriga, Imen Darragi, R. van Wijk, Alexandra Silva, Z. Fitouri, Salem Abbes, Leila Chaouch, Licínio Manco, Dorra Chaouachi
Publikováno v:
International Journal of Laboratory Hematology
International Journal of Laboratory Hematology, Wiley, 2017, 39 (2), pp.223-231. ⟨10.1111/ijlh.12610⟩
International Journal of Laboratory Hematology, Wiley, 2017, 39 (2), pp.223-231. ⟨10.1111/ijlh.12610⟩
International audience; INTRODUCTION:Pyruvate kinase (PK) deficiency is one of the most common hereditary nonspherocytic hemolytic anemias worldwide with clinical manifestations ranging from mild to severe hemolysis. However, investigation of this en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e02887226fae2daa68cd62d4261cb1b
https://pubmed.ncbi.nlm.nih.gov/28133914
https://pubmed.ncbi.nlm.nih.gov/28133914
Publikováno v:
Annales d'Endocrinologie. 69:231-239
Resume Le diabete insipide central est rare chez l’enfant. Il se manifeste par un syndrome polyuropolydipsique secondaire a un deficit en ADH dont le diagnostic etiologique pose des problemes variables d’un enfant a un autre. Le but de cette etud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d82f0a51db2d7ffad0c5ada8e16bc3fe
https://doi.org/10.1016/j.ando.2007.11.003
https://doi.org/10.1016/j.ando.2007.11.003