Search research articles
Contact Us
Filters
Showing results (61-70 of 74) with videos related to
Page
of 8
Sort By:
Journal of Leukocyte Biology
|
July 20, 2018
The role of IL-23/IL-17 axis in human kidney allograft rejection
Youssra Haouami, Tarak Dhaouadi, Imen Sfar, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 19, 2026
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalence
Ridha M'rad, Mahdi Kammoun, Ahlem Achour, et al.
The Pan African Medical Journal
|
June 22, 2026
Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department
Asma Bettaieb, Meriam Hajji, Hayet Kaaroud, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 21, 2022
Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis
Mariem El Younsi, Médiha Trabelsi, Sandra Ben Youssef, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation
|
March 7, 2017
Thirty Years of Experience at the First Tunisian Kidney Transplant Center
Ezzedine Abderrahim, Asma Zammouri, Mohamed Mongi Bacha, et al.
Journal of Genetics
|
September 24, 2016
A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation
Saoussen M'Dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
La Tunisie Medicale
|
March 11, 2024
Manel Jellouli, Abir Abdellatif, Abir Bousetta, et al.
La Tunisie Medicale
|
October 23, 2024
Changes in echocardiographic parameters after hemodialysis session in a North African pediatric population with end-stage renal disease and without known heart disease
Faten El Ayech Boudiche, Malek Elarbi, Selim Boudiche, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 14, 2024
Genetic study of Alport syndrome in Tunisia
Mariem El Younsi, Ahlem Achour, Lilia Kraoua, et al.
La Tunisie Medicale
|
March 15, 2026
Epileptic child in remission: Ceiling effect of valproic acid
Mariem Kammoun, Rim Charfi, Abir Boussetta, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 74) with videos related to
Sort By:
Page
of 8
Journal of Leukocyte Biology
|
July 20, 2018
The role of IL-23/IL-17 axis in human kidney allograft rejection
Youssra Haouami, Tarak Dhaouadi, Imen Sfar, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 19, 2026
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalence
Ridha M'rad, Mahdi Kammoun, Ahlem Achour, et al.
The Pan African Medical Journal
|
June 22, 2026
Renal survival in hereditary urolithiasis: a monocentric cohort study from a Tunisian nephrology department
Asma Bettaieb, Meriam Hajji, Hayet Kaaroud, et al.
Pediatric Nephrology (Berlin, Germany)
|
April 21, 2022
Clinical and genetic characteristics of Tunisian children with infantile nephropathic cystinosis
Mariem El Younsi, Médiha Trabelsi, Sandra Ben Youssef, et al.
Experimental and Clinical Transplantation : Official Journal of the Middle East Society for Organ Transplantation
|
March 7, 2017
Thirty Years of Experience at the First Tunisian Kidney Transplant Center
Ezzedine Abderrahim, Asma Zammouri, Mohamed Mongi Bacha, et al.
Journal of Genetics
|
September 24, 2016
A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation
Saoussen M'Dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
La Tunisie Medicale
|
March 11, 2024
Manel Jellouli, Abir Abdellatif, Abir Bousetta, et al.
La Tunisie Medicale
|
October 23, 2024
Changes in echocardiographic parameters after hemodialysis session in a North African pediatric population with end-stage renal disease and without known heart disease
Faten El Ayech Boudiche, Malek Elarbi, Selim Boudiche, et al.
Pediatric Nephrology (Berlin, Germany)
|
August 14, 2024
Genetic study of Alport syndrome in Tunisia
Mariem El Younsi, Ahlem Achour, Lilia Kraoua, et al.
La Tunisie Medicale
|
March 15, 2026
Epileptic child in remission: Ceiling effect of valproic acid
Mariem Kammoun, Rim Charfi, Abir Boussetta, et al.
Page
of 8