Ezzeddine Abderrahim
Overview
Explore the profile of Ezzeddine Abderrahim including associated specialties, affiliations and a list of published articles.
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Articles
49
Citations
58
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Recent Articles
1.
Younsi M, Achour A, Kraoua L, Nesrine M, Sayari T, Abderrahim E, et al.
Pediatr Nephrol
. 2024 Aug;
40(1):103-116.
PMID: 39138691
Background: Alport syndrome is a genetic disorder affecting the kidneys, ears, and eyes, causing chronic kidney disease, sensorineural hearing loss, and ocular abnormalities. It results from pathogenic variants in the...
2.
Boussetta A, Jellouli M, Gargah T, Hajji M, Hedri H, Abderrahim E
Tunis Med
. 2024 Mar;
102(1):38-43.
PMID: 38545728
Introduction: Pediatric end-stage renal disease is a rare but severe condition that causes numerous complications and impairs the quality of life of children. Kidney transplantation is the therapy of choice...
3.
Hajji M, Saied S, Mami I, Khadhar Y, Ben Ayed T, Gorsane I, et al.
Case Rep Nephrol
. 2024 Mar;
2024:5219914.
PMID: 38525052
Introduction: Longer survival in dialysis led to a higher incidence of vascular access complications and failure. With the limited access to kidney transplantation programs and peritoneal dialysis, exhaustion of vascular...
4.
Kefi A, Helali W, Ben Abdelghani K, Euch M, Sassi C, Turki S, et al.
Tunis Med
. 2024 Mar;
101(10):765-769.
PMID: 38465758
Introduction: Sarcoidosis is a systemic granulomatosis that can be associated with large-scale physical and mental disability, affecting the health related quality-of-life (HRQoL) of patients. Aim: To evaluate the HRQoL of...
5.
Charfi R, Bacha M, Ben Fadhal M, Ferchichi K, El Jebari H, Gaies E, et al.
Tunis Med
. 2024 Mar;
101(10):738-744.
PMID: 38465753
Introduction: Tacrolimus, exhibits interindividual pharmacokinetic variability and a narrow therapeutic index. The influence of the CYP3A5 6986A>G single nucleotide polymorphism (SNP) on this variability remains a topic of debate. Aim:...
6.
Meriam H, Kaaroud H, Karray R, Ben Hamida F, Bouzid K, Abderrahim E
Case Rep Nephrol
. 2024 Feb;
2024:1265364.
PMID: 38419822
Background: Urinary lithiasis constitutes a recurrent pathology affecting a relatively young population. The risk of progression to chronic renal failure and the cost of treatment are the most important issues....
7.
Boussetta A, Jellouli M, Hajji M, Rekaya S, Ouederni M, Abderrahim E, et al.
J Nephrol
. 2023 Dec;
37(3):821-825.
PMID: 38055151
No abstract available.
8.
Hajji M, Barbouch S, Kaaroud H, Ben Abdelghani K, Ben Hamida F, Harzallah A, et al.
Clin Med Insights Case Rep
. 2023 Nov;
16:11795476231210137.
PMID: 37920369
Introduction: Hemophagocytic lymphohistiocytosis (HLH) is a disease of multi-organ dysfunction due to excessive immune activation causing widespread inflammation and tissue destruction. It is a severe condition associated with high morbidity...
9.
Boussetta A, Jellouli M, Hajji M, Abderrahim E, Gargah T
Pediatr Nephrol
. 2023 Sep;
39(2):451-453.
PMID: 37737906
Polyuria-polydipsia syndrome is a frequent symptom in pediatrics, primarily attributed to diabetes mellitus. In the context of diabetes insipidus, this syndrome can stem from central or nephrogenic factors. Sjögren's syndrome,...
10.
Meriam H, Bettaieb A, Kaaroud H, Ben Hamida F, Gargeh T, Mrad R, et al.
Int J Nephrol
. 2023 Jul;
2023:2874414.
PMID: 37521011
Introduction: Primary hyperoxaluria type 1 (PH1) is a rare and inherited condition of urolithiasis. The aim of our study was to analyze clinical, paraclinical, and evolutionary aspects of PH1 in...