Zobrazeno 1 - 10
of 34
pro vyhledávání: '"R Guedri"'
Autor:
J.B. Monfort, S. Deshayes, P. Dusser, R. Bourguiba, L. Savey, C. Vinit, I. Koné-Paut, G. Amaryan, K. Theodoropoulou, R. Guedri, J. Pachlopnik, A. Belot, I. Melki, N. Perveen Maldar, V. Hentgen, S. Georgin-Lavialle, C. Wouters, A. Woerner, D. Kaiser, G. Berthet, E. Merlin, P. Pillet, O. Richer, C. Barbier, C. Ballot, I. Bolt, H. Wittkowski, K. Rotornaz, A.L. Jurquet, S. Poignant, U. Meinzer, F. Vanoni, D. Dan, J.C. Lega, J. Brunner, A. Aouba, F. Uettwiller, G. Kaplanski, S. Ardois, N. Schleinitz, J. Dehoorne
Publikováno v:
Journal of the American Academy of Dermatology. 87:1391-1394
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
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
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
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
Autor:
J.B. Monfort, S. Deshayes, P. Dusser, R. Bourguiba, L. Savey, C. Vinit, I. Kone-Paut, G. Amaryan, K. Theodoropoulou, R. Guedri, J. Pachlopnik, A. Belot, I. Melki, N. Perveen-Maldar, V. Hentgen, S. Georgin-Lavialle
Publikováno v:
Annales de Dermatologie et de Vénéréologie - FMC. 2:A73
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Clinical Case Reports
Clinical Case Reports
Congenital Methemoglobinemia is a rare condition that may mimic congenital heart diseases. There are two types of congenital Methemoglobinemia. The type I is usually benign. The enzyme deficiency is limited to red blood cells. Clinically, the patient
Akademický článek
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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