Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Tahar, Gargah"'
Autor:
Maryem Ferjani, Mounira El Euch, Mariem Boumediene, Mariem Jrad, Fethi Ben Hamida, Sami Turki, Tahar Gargah
Publikováno v:
Journal of Medical Case Reports, Vol 17, Iss 1, Pp 1-4 (2023)
Abstract Background Takayasu arteritis is a rare and chronic granulomatous vasculitis that affects the large vessels. Takayasu arteritis targets the aorta and its branches and is still of unknown etiology. It often affects female patients under 50 ye
Externí odkaz:
https://doaj.org/article/a61fd3dc79634860840dbd844107a8d5
Publikováno v:
Urology Case Reports, Vol 49, Iss , Pp 102429- (2023)
Neuroblastoma is the most common extracranial solid tumor in children, often manifests in the retroperitoneal region. We present a case of a 3-year-old boy with no previous medical history, presented for abdominal distension. Physical examination rev
Externí odkaz:
https://doaj.org/article/62b5667ca54943bb9d0a2bf0003595b1
Autor:
Abir Boussetta, Dalia Louati, Manel Jellouli, Hanen Gaied, Sameh Mabrouk, Bayen Maalej, Karim Zouaghi, Rym Goucha, Tahar Gargah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 33, Iss 3, Pp 440-448 (2022)
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disorder of unknown etiology. Lupus nephritis (LN) is one of the most severe clinical manifestations observed in patients with SLE; it is more frequent and more severe in children than in
Externí odkaz:
https://doaj.org/article/4c433c06bae6402bb58442581a8ee629
Autor:
Maryem Ferjani, Mounira El Euch, Yousra Hammi, Taha Sayari, Ouns Naija, Fethi Ben Hamida, Sami Turki, Tahar Gargah
Publikováno v:
Clinical Case Reports, Vol 10, Iss 2, Pp n/a-n/a (2022)
Abstract Acute pancreatitis may be the first manifestation in systemic lupus erythematosus or occur during evolution. It is a rare complication, which is often associated with other visceral manifestations. Outcome is usually favorable but can be ser
Externí odkaz:
https://doaj.org/article/54cd23633d414ad997dab0a348b2ed3d
Autor:
Meryam Ferjani, Malek Ben Slimane, Taha Sayari, Yosra Hammi, Noureddine Litaiem, Ouns Naija, Faten Zeglaoui, Tahar Gargah
Publikováno v:
Clinical Case Reports, Vol 9, Iss 7, Pp n/a-n/a (2021)
Abstract Cutaneous manifestations of childhood COVID‐19 differ from those of adults. Maculopapular rash is not specific and could be mistaken with other viral exanthema. A nasopharyngeal swab is strongly recommended to confirm the possible COVID‐
Externí odkaz:
https://doaj.org/article/ababa11f2c1b4b96a838e1eb6b1ff773
Publikováno v:
Egyptian Pediatric Association Gazette; 4/25/2024, Vol. 72 Issue 1, p1-7, 7p
Publikováno v:
Néphrologie & Thérapeutique. 18:541-548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e203b536971f78f4f56f54043fad86fe
https://doi.org/10.1016/j.nephro.2022.03.006
https://doi.org/10.1016/j.nephro.2022.03.006
Autor:
Manel Jellouli, Meriem Ferjani, Kamel Abidi, Chokri Zarrouk, Jaouida Abdelmoula, Tahar Gargah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 28, Iss 5, Pp 1180-1183 (2017)
Cystinosis is an autosomal recessive, lysosomal storage disease characterised by the accumulation of the amino acid cystine in different organs and tissues. It is a multisystemic disease that can present with renal and extra-renal manifestations. In
Externí odkaz:
https://doaj.org/article/11ece3ae0b49469d80d023f3aa48ca26
Autor:
Manel Jellouli, Mariem Ferjani, Kamel Abidi, Chokri Zarrouk, Ouns Naija, J Abdelmoula, Tahar Gargah
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 27, Iss 3, Pp 526-532 (2016)
The infantile form of primary hyperoxaluria type-1 (PH-1) is characterized by a rapid progression to the end-stage renal disease (ESRD) due to both increased oxalate load and reduced glomerular filtration rate. In the literature, data on this form ar
Externí odkaz:
https://doaj.org/article/09a54e2c65f24e1cb5527d0c95dff7fc
Publikováno v:
Journal of Nephrology. 35:1731-1735
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cd3475afc42a32ea31bb25d13f8c001
https://doi.org/10.1007/s40620-021-01190-z
https://doi.org/10.1007/s40620-021-01190-z