Zobrazeno 1 - 10
of 103
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
Publikováno v:
Clinical Case Reports. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94a81e1eb6e2c237ea988b02cb0bdd89
https://doi.org/10.1002/ccr3.6613
https://doi.org/10.1002/ccr3.6613
Autor:
Manel Jellouli, Abir Boussetta, Meriem Hajji, Yosra Falfoul, Linda Hadj Kacem, Ezzeddine Abderrahim, Tahar Gargah
Publikováno v:
Pediatric Nephrology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8074cfdc0e015462054f461738065d0
https://doi.org/10.1007/s00467-022-05767-z
https://doi.org/10.1007/s00467-022-05767-z
Autor:
Manel Jellouli, Abir Boussetta, Meriem Hajji, Yosra Falfoul, Linda Hadj Kacem, Ezzeddine Abderrahim, Tahar Gargah
Publikováno v:
Pediatric Nephrology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ad7add3b18016d36c20814b19c72754
https://doi.org/10.1007/s00467-022-05766-0
https://doi.org/10.1007/s00467-022-05766-0
Publikováno v:
La Tunisie medicale. 100(5)
To describe the clinical, biochemical and evolutive profile of monogenic urinary lithiasis in Tunisian children followed up in a reference service, during a 25 years period.This was a single-center retrospective observational study of children with u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a194e50c4e5ebb343b9e3564dcc006b0
https://pubmed.ncbi.nlm.nih.gov/36206091
https://pubmed.ncbi.nlm.nih.gov/36206091
Publikováno v:
La Tunisie medicale. 100(1)
Nephrotic syndrome is a common pathology in children. Despite its good prognosis, it can become complicated and threaten the patient's vital and functional prognosis. Thromboembolic complications are rare but serious.To study the main thromboembolic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4cc44ce1420ea4edabbd4a5408fab5c
https://pubmed.ncbi.nlm.nih.gov/35822329
https://pubmed.ncbi.nlm.nih.gov/35822329