Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Faten Frikha"'
Autor:
Donia Chebbi, Raida Ben Salah, Faten Frikha, Hela Fourati, Mariem Ghribi, Zeineb Mnif, Zouhir Bahloul
Publikováno v:
Acta Medica Iranica, Vol 61, Iss 3 (2023)
Sarcoidosis is a systemic disease histologically characterized by the presence of non-caseating granulomas. Granulomas can affect all structures of the body, giving heterogeneous manifestations and making the diagnosis of this disease a real challeng
Externí odkaz:
https://doaj.org/article/194fae6666344826a329a1a7f54cbcba
Autor:
Patrice Cacoub, Arsène Mekinian, David Saadoun, Pavel I Novikov, Savino Sciascia, Corrado Campochiaro, Olivier Fain, Ilya Smitienko, Nicolas Schleinitz, Patrick Jégo, Francesco Muratore, Carlo Salvarani, Elena Galli, Sabine Berthier, Marc Lambert, François Maurier, Isabelle Kone-Paut, Sergey Moiseev, Masataka Kuwana, Alexandre Belot, Martin Michaud, Francis Gaches, Achille Aouba, Xavier Puechal, Karim Sacre, Tiphaine Goulenok, Alessandro Tomelleri, Thomas Sené, Elena Marina Baldissera, Luigi Boiardi, Abid Awisat, Ygal Benhamou, Vahan Mukuchyan, Mathieu Vautier, Azeddine Dellal, Lucie Biard, Julie Seguier, José Hernández-Rodríguez, Olivier Espitia, Sebastien Humbert, Guillaume Denis, Nolan Hassold, Dagna Lorenzo, Helene Munoz Pons, Jean Baptiste Gaultier, Le Mouel Edwige, Antoinette Perlat, Bertrand Lioger, Jonathan Broner, Virginie Dufrost, Faten Frikha, Alexandra Audemard-Verger, Pascal Woaye-Hune, Pierre Zeminsky, Moya Alvarado, Matheus Vieira, Alberto Lo Gullo
Publikováno v:
RMD Open, Vol 9, Iss 2 (2023)
Objectives In this large multicentre study, we compared the effectiveness and safety of tocilizumab intravenous versus subcutaneous (SC) in 109 Takayasu arteritis (TAK) patients.Methods We conducted a retrospective multicentre study in referral centr
Externí odkaz:
https://doaj.org/article/516d057fd503452483e4b0dac563dcdb
Autor:
Donia Chebbi, Sameh Marzouk, Imen Krichen, Ikram El Ahmer, Mouna Snoussi, Chifa Dammak, Faten Frikha, Raida Ben Salah, Choumous Kallel, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 11, Iss 3, Pp n/a-n/a (2023)
Abstract Acquired hemophilia A (AHA) is a potentially life‐threatening hemorrhagic disorder with many etiologies. We report the first case in the literature describing the association of AHA with adult‐onset Still's disease (AOSD).
Externí odkaz:
https://doaj.org/article/daa42fd1724343808b78e7030a7b8129
Autor:
Imen Chabchoub, Mouna Snoussi, Rania Ammar, Raida Ben Salah, Chifa Dammak, Faten Frikha, Mounir Bouaziz, Tahia Boudawara, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Guillain–Barré syndrome (GBS) and polymyositis (PM) are two rare autoimmune diseases, one of which affects the peripheral nervous system and other the muscle. We report the case of a young woman with no previous medical history who was ho
Externí odkaz:
https://doaj.org/article/651a94b8972941d48a776b0653229cdf
Autor:
Olfa Frikha, Raida Ben Salah, Ansar Mefteh, Faten Frikha, Mouna Snoussi, Sameh Marzouk, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Agranulocytosis is a rare acute condition characterized by severe a
Externí odkaz:
https://doaj.org/article/bdb3a4dda1584b9a97d3518a228ecbb3
Autor:
Donia Chebbi, Chifa Damak, Faten Frikha, Walid Abid, Mohamed Rebai, Mouna Snoussi, Raida Ben Salah, Sameh Marzouk, Abdessalem Hentati, Zouhir Bahloul
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Pulmonary artery aneurysm must be evoked in front of any hemoptysis in a patient with Behçet disease as it requires urgent immunosuppressive therapy and often surgery.
Externí odkaz:
https://doaj.org/article/a907ce10286a4388b4e0db47b67694db
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract The association of Thrombotic thrombocytopenic purpura (TTP) and adult‐onset Still's disease (AOSD) is very uncommon. Hereby, we present a case of TTP occurring in patient with a known AOSD and the successful outcome after plasma exchanges
Externí odkaz:
https://doaj.org/article/c5be4a97fe4544cc9ca2613a59e57ea6
Autor:
Mariem Ghribi, Faten Frikha, Abir Derbel, Sameh Marzouk, Raida Ben Salah, Mouna Snoussi, Zouhir Bahloul
Publikováno v:
PAMJ Clinical Medicine, Vol 3, Iss 191 (2020)
L´atteinte neurologique pseudotumorale au cours de la maladie de Behçet est rare. Quelques cas ont été rapportés dans la littérature. L´imagerie par résonance magnétique, montre un aspect pseudotumoral de localisation capsulothalamique. Le t
Externí odkaz:
https://doaj.org/article/1fa1dc683c7644ca805429ce456668b2
Publikováno v:
PAMJ Clinical Medicine, Vol 2, Iss 114 (2020)
Le lupus érythémateux chronique est une dermatose auto-immune touchant habituellement le visage et le cuir chevelu. La localisation palpébrale sous la forme d´une blépharite chronique est rare. Nous rapportons un cas de blépharite lupique au co
Externí odkaz:
https://doaj.org/article/c8a6ea04bd26413fa10c009ab3545967
Pyélonéphrite emphysémateuse associée à une fibrose rétropéritonéale et un pseudo-anévrysme aortique
Publikováno v:
PAMJ Clinical Medicine, Vol 1, Iss 44 (2019)
La pyélonéphrite emphysémateuse est une forme rare de suppuration rénale définie par la présence de pus et de gaz au sein du parenchyme rénal. C’est une affection grave survenant préférentiellement chez le diabétique et qui peut engager l
Externí odkaz:
https://doaj.org/article/dcbb245954a94fc88a2ed14ac0a3999b