Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Manel Jellouli"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 5, Pp n/a-n/a (2023)
Key Clinical Message Genetic counseling and genetic screening for hyperoxaluria should be recommended for children with urinary lithiasis for early management to avoid progression to oxalosis especially if there is a family history of lithiasis. Prim
Externí odkaz:
https://doaj.org/article/f58a51b0f87f4c97b5242cfe5165590d
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
Publikováno v:
Clinical Case Reports, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Spontaneous hemothorax occurs in the absence of trauma or iatrogenic causes. Etiologies of spontaneous hemothorax in children include connective tissue disease, neoplasia and coagulopathy, which is associated with thromboembolic events. We p
Externí odkaz:
https://doaj.org/article/fe62259b767b416e827f04edf8a20404
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
Autor:
Manel Jellouli, Tahar Gargah
Publikováno v:
The Pan African Medical Journal, Vol 23, Iss 155 (2016)
La calcinose tumorale est une affection bénigne rare, qui se caractérise par le dépôt de matériel calcique dans les tissus mous extra-articulaires prenant une forme tumorale. Elle peut être primitive ou secondaire à une insuffisance rénale ch
Externí odkaz:
https://doaj.org/article/aa5ac4c4daa74596a2d48df5ce98ef75
Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 348 (2015)
La cystinose est une maladie rare qui résulte d'un défaut d'expression de la cystinosine transporteur de la cystine du lysosome. La forme infantile est la plus fréquente et la plus sévère. Elle conduit en dehors du traitement à l'insuffisance r
Externí odkaz:
https://doaj.org/article/b02b6506431647eb879b5e747fe13820
Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 302 (2015)
Recipients of solid organ transplantation are, because of immunosuppressive therapy, at high risk to develop opportunistic infections including tuberculosis (TB). The incidence, clinical manifestations, and optimal diagnostic tests of this disease in
Externí odkaz:
https://doaj.org/article/05b4fc4a11f944319a36282334692b95
Autor:
Manel Jellouli, Tahar Gargah
Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 287 (2015)
Le syndrome d'encéphalopathie postérieure réversible (SEPR) est une entité rare, d'étiopathogénie inconnue; le diagnostic est radio-clinique qui associe des signes neurologiques avec des anomalies radiologiques cérébrales bilatérales classiq
Externí odkaz:
https://doaj.org/article/284686c65008448d956cc16e3c0db3e0
Publikováno v:
The Pan African Medical Journal, Vol 22, Iss 276 (2015)
Williams-Beuren syndrome is a rare neurodevelopmental disorder, characterized by congenital heart defects, abnormal facial features, mental retardation with specific cognitive and behavioral profile, growth hormone deficiency, renal and skeletal anom
Externí odkaz:
https://doaj.org/article/3a22270357bb48a9bd6510116fef1d00