Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Hela, Fourati"'
Autor:
Raghda Bouazra, Afef Feki, Imen Sellami, Chema Zribi, Zouhour Gassara, Samar Ben Djemaa, Mariam Ezzeddine, Mohamed Hédi Kallel, Hela Fourati, Sofien Baklouti
Publikováno v:
SAGE Open Medical Case Reports, Vol 12 (2024)
Osteomyelitis of the pubic symphysis is a rare infectious disease commonly caused by the opportunistic bacteria Staphylococcus aureus and Pseudomonas aeruginosa . The clinical context includes fever, and pubic, or abdominal pain, thus should prompt a
Externí odkaz:
https://doaj.org/article/bba89a3a2d0141d8a5475e356def4ac1
Autor:
Afef Feki, Cyrine Abid, Samar Ben Djemaa, Zouhour Gassara, Ezzeddine Mariam, Mohamed Hedi Kallel, Akrout Rim, Hela Fourati, Sofien Baklouti
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key Clinical Message Hydatidosis is a parasitic infection caused by the larval form of “Echinococcus granulosis.” Bone localization is rare even in endemic areas. We report an unusual case of an extensive hydatidosis of the right sacrum and femur
Externí odkaz:
https://doaj.org/article/e01d83d805d5470a9aac50e1e883d81f
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:
Afef Feki, Imen Sellami, Zouhour Gassara, Samar Ben Djemaa, Mariam Ezzeddine, Mohamed Hedi Kallel, Hela Fourati, Rim Akrout, Sofien Baklouti
Publikováno v:
Clinical Case Reports, Vol 10, Iss 8, Pp n/a-n/a (2022)
Abstract Cord compression and ischemic non‐compressive myelopathy are a complication of spinal Paget's disease (SPD). SPD usually touches a single spine level. We report an unusual case with bilevel spinal cord compression and dysfunction which was
Externí odkaz:
https://doaj.org/article/65cc65ea55144ff18d83bfcea0fb34ec
Autor:
Imen Maaloul, Marwa Moussaoui, Ameni Salah, Wiem Feki, Hela Fourati, Nadia Charfi, Zeineb Mnif
Publikováno v:
Case Reports in Radiology, Vol 2021 (2021)
Introduction. Meningeal melanocytoma (MM) is a very rare neuroectodermal neoplasm arising from the leptomeninges. Primary suprasellar melanocytomas are exceedingly rare, with only a handful of cases reported. The systemic spread of a nontransformed m
Externí odkaz:
https://doaj.org/article/29fac0d6032a4663b33bcdd1b5ae6722
Autor:
Karim Masmoudi, Emna Elleuch, Rim Akrout, Afef Feki, Mariam Ezzeddine, Hela Fourati, Dorra Lahiani, Mounir Ben Jemaâ, Sofiène Baklouti
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-5 (2018)
Abstract Background Septic arthritis is an infectious disease that commonly affects weight-bearing or proximal joints such as the knee and the hip. The sternoclavicular joint is an unusual site of this entity. It usually occurs in patients with diabe
Externí odkaz:
https://doaj.org/article/6e855e8ae8fc4eb9bc5d2bef5f482680
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 37, Iss 1, Pp 87.e1-87.e5 (2018)
Coronary subclavian steal syndrome is an uncommon cause of ischemia recurrence after coronary artery bypass grafting. Endovascular treatment of subclavian artery stenosis or occlusion is increasingly common and appears to offer a safe and effective a
Externí odkaz:
https://doaj.org/article/ad74b3e636c54e5eba92cb9f6dd7af1c
Publikováno v:
Case Reports in Radiology
Case Reports in Radiology, Vol 2021 (2021)
Case Reports in Radiology, Vol 2021 (2021)
Introduction. Meningeal melanocytoma (MM) is a very rare neuroectodermal neoplasm arising from the leptomeninges. Primary suprasellar melanocytomas are exceedingly rare, with only a handful of cases reported. The systemic spread of a nontransformed m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9597b61931a24b24952b07f4e69c0c
https://doi.org/10.1155/2021/7306432
https://doi.org/10.1155/2021/7306432
Autor:
Mouna Feki Mnif, Mahdi Kamoun, Fatma Mnif, Nadia Charfi, Nozha Kallel, Nabila Rekik, Basma Ben Naceur, Hela Fourati, Emna Daoud, Zainab Mnif, Mohamed Habib Sfar, Samia Younes-Mhenni, Mohamed Tahar Sfar, Mongia Hachicha, Mohamed Abid
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 17, Iss 1, Pp 121-127 (2013)
Background: Congenital adrenal hyperplasia (CAH) is an inherited recessive disorder of adrenal steroidogenesis. The enzymes most commonly affected are 21-hydroxylase. Past reports suggested brain magnetic resonance imaging (MRI) abnormalities in CAH
Externí odkaz:
https://doaj.org/article/3fa499640002449e8efeaed951b32800
Autor:
Hanen Loukil, Mouna Snoussi, Hela Fourati, Faten Frikha, Raida Ben Salah, Moez Jallouli, Sameh Marzouk, Zeineb Mnif, Zouhir Bahloul
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 326 (2016)
Patiente âgée de 48 ans était hospitalisée pour une cholestase asymptomatique hépatique. Elle rapportait une histoire personnelle et familiale d'récidivante. Le bilan biologique révélait une anémie ferriprive et une cholestase modérée. Les
Externí odkaz:
https://doaj.org/article/9a6d4e62d7394473bfc9e28137167b0f