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Kamel Abidi

Showing results (11-20 of 20) with videos related to

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Nephrologie & Therapeutique|July 25, 2015
[Outcome of rapidly progressive glomerulonephritis post-streptococcal disease in children]Manel Jellouli, Sondos Maghraoui, Kamel Abidi, et al.
La Tunisie Medicale|October 6, 2016
Nephrocalcinosis in Tunisian childrenManel Jellouli, Wiem Karoui, Kamel Abidi, et al.
La Tunisie Medicale|November 2, 2016
Focal segmental glomerulosclerosis in childrenManel Jellouli, Kamel Abidi, Mouna Askri, et al.
La Tunisie Medicale|November 2, 2016
Peritoneal dialysis: Experience of the department of pediatrics of the hospital Charles Nicolle of TunisManel Jellouli, Meriem Ferjani, Amal Oueslati, et al.
La Tunisie Medicale|January 5, 2017
Contribution of ultrasound scans in the first episode of urinary tract infection in childrenManel Jellouli, Asma Ben Mansour, Kamel Abidi, et al.
Nephrologie & Therapeutique|February 25, 2016
[Etiologies of end-stage renal disease of children in Tunisia]Manel Jellouli, Abir Boussetta, Kamel Abidi, et al.
Nephrologie & Therapeutique|November 2, 2015
[Peritonitis in pediatric patients receiving peritoneal dialysis]Manel Jellouli, Meriem Ferjani, Kamel Abidi, et al.
Journal of Clinical Laboratory Analysis|August 27, 2016
HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian PatientsSaoussen M'dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
Journal of Genetics|September 24, 2016
A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlationSaoussen M'Dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
Clinical Biochemistry|May 23, 2012
Detection of a novel splicing mutation causing analbuminemia in a Libyan familyAmina Bibi, Latifa Jouini, Chaima Abdelhafidh Sahli, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Nephrologie & Therapeutique|July 25, 2015
[Outcome of rapidly progressive glomerulonephritis post-streptococcal disease in children]Manel Jellouli, Sondos Maghraoui, Kamel Abidi, et al.
La Tunisie Medicale|October 6, 2016
Nephrocalcinosis in Tunisian childrenManel Jellouli, Wiem Karoui, Kamel Abidi, et al.
La Tunisie Medicale|November 2, 2016
Focal segmental glomerulosclerosis in childrenManel Jellouli, Kamel Abidi, Mouna Askri, et al.
La Tunisie Medicale|November 2, 2016
Peritoneal dialysis: Experience of the department of pediatrics of the hospital Charles Nicolle of TunisManel Jellouli, Meriem Ferjani, Amal Oueslati, et al.
La Tunisie Medicale|January 5, 2017
Contribution of ultrasound scans in the first episode of urinary tract infection in childrenManel Jellouli, Asma Ben Mansour, Kamel Abidi, et al.
Nephrologie & Therapeutique|February 25, 2016
[Etiologies of end-stage renal disease of children in Tunisia]Manel Jellouli, Abir Boussetta, Kamel Abidi, et al.
Nephrologie & Therapeutique|November 2, 2015
[Peritonitis in pediatric patients receiving peritoneal dialysis]Manel Jellouli, Meriem Ferjani, Kamel Abidi, et al.
Journal of Clinical Laboratory Analysis|August 27, 2016
HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian PatientsSaoussen M'dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
Journal of Genetics|September 24, 2016
A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlationSaoussen M'Dimegh, Cécile Aquaviva-Bourdain, Asma Omezzine, et al.
Clinical Biochemistry|May 23, 2012
Detection of a novel splicing mutation causing analbuminemia in a Libyan familyAmina Bibi, Latifa Jouini, Chaima Abdelhafidh Sahli, et al.
Pageof 2