Zobrazeno 1 - 10
of 25
pro vyhledávání: '"ouns naija"'
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
Akademický článek
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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
Patients with systemic lupus erythematous (SLE) are at higher risk of malignant lymphomas, particularly non-Hodgkin lymphoma. Primary central nervous system lymphoma (PCNSL) is a rare form of extranodal non-Hodgkin lymphoma. In adults, about twenty c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55798ce74ddda0b4aa5e3958d4b4de9e
https://doi.org/10.22541/au.164792968.89601655/v1
https://doi.org/10.22541/au.164792968.89601655/v1
Autor:
Manel, Jellouli, Asma, Ben Mansour, Kamel, Abidi, Meriem, Ferjani, Ouns, Naija, Yousra, Hammi, Chokri, Zarrouk, Tahar, Gargah
Publikováno v:
La Tunisie medicale. 94(6)
Background - Vesicoureteral reflux (VUR) is a common pediatric urologic disorder. After the first urinary tract infection (UTI), imaging studies are recommended, starting with a renal ultrasound (US) and voiding cystourethrography (VCUG). We propose
Autor:
Manel, Jellouli, Meriem, Brika, Kamel, Abidi, Meriem, Ferjani, Ouns, Naija, Yousra, Hammi, Tahar, Gargah
Publikováno v:
La Tunisie medicale. 94(7)
Background - Most patients with idiopathic nephrotic syndrome are steroid-responsive, about 50% relapse and often become steroid-dependent and exposed to long-term steroid complications. The aim of this study was to determine predictive risk factors
Autor:
Manel, Jellouli, Meriem, Ferjani, Amal, Oueslati, Kamel, Abidi, Ouns, Naija, Yousra, Hammi, Taieb, Ben Abdallah, Tahar, Gargah
Publikováno v:
La Tunisie medicale. 94(5)
Introduction Peritoneal dialysis (PD) is still the most common modality used in treatment for children with End Stage Renal Disease (ESRD). The objective of this study was to identify the epidemiological, clinical, and microbiological factors affecti
Autor:
Manel, Jellouli, Kamel, Abidi, Mouna, Askri, Meriem, Ferjani, Ouns, Naija, Yousra, Hammi, Rym, Goucha, Tahar, Gargah
Publikováno v:
La Tunisie medicale. 94(5)
Background Focal segmental glomerulosclerosis (FSGS) represents 20% of nephrotic syndrome in children. The clinical course and prognosis is heterogeneous in children. The aim of this study was to analyze treatment and outcome of children with FSGS. M
Autor:
Manel, Jellouli, Wiem, Karoui, Kamel, Abidi, Yousra, Hammi, Ouns, Naija, Chokri, Zarrouk, Jaouida, Abdelmoula, Tahar, Gargah
Publikováno v:
La Tunisie medicale. 94(4)
Background Nephrocalcinosis is rare in children. Its etiologies are multiple. The aim of this study was to analyze the etiology of nephrocalcinosis in Tunisian children. Methods This retrospective study was conducted in the department of pediatrics i