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Items: 1 to 20 of 57


Evaluation of a CIAP session for students in Medicine, Pediatrics module.

Jellouli M, Ben Hamida E, Hammi Y, Ferjani M, Gargah T.

Tunis Med. 2018 Mar;96(3):161-164.


WDR73-related galloway mowat syndrome with collapsing glomerulopathy.

El Younsi M, Kraoua L, Meddeb R, Ferjani M, Trabelsi M, Ouertani I, Maazoul F, Abid N, Gargah T, M'rad R.

Eur J Med Genet. 2018 Oct 10. pii: S1769-7212(18)30141-1. doi: 10.1016/j.ejmg.2018.10.002. [Epub ahead of print]


The role of IL-23/IL-17 axis in human kidney allograft rejection.

Haouami Y, Dhaouadi T, Sfar I, Bacha M, Gargah T, Bardi R, Abderrahim E, Goucha R, Ben Abdallah T, Gorgi Y.

J Leukoc Biol. 2018 Dec;104(6):1229-1239. doi: 10.1002/JLB.5AB0318-148R. Epub 2018 Jul 19.


Rituximab in The Management of Pediatric Steroid-Resistant Nephrotic Syndrome: A Systematic Review.

Jellouli M, Charfi R, Maalej B, Mahfoud A, Trabelsi S, Gargah T.

J Pediatr. 2018 Jun;197:191-197.e1. doi: 10.1016/j.jpeds.2018.01.008. Epub 2018 Apr 18.


Infantile cystinosis: From dialysis to renal transplantation.

Jellouli M, Ferjani M, Abidi K, Zarrouk C, Abdelmoula J, Gargah T.

Saudi J Kidney Dis Transpl. 2017 Sep-Oct;28(5):1180-1183. doi: 10.4103/1319-2442.215119.


Efficacy and Safety of Rituximab in the Management of Pediatric Systemic Lupus Erythematosus: A Systematic Review.

Mahmoud I, Jellouli M, Boukhris I, Charfi R, Ben Tekaya A, Saidane O, Ferjani M, Hammi Y, Trabelsi S, Khalfallah N, Tekaya R, Gargah T, Abdelmoula L.

J Pediatr. 2017 Aug;187:213-219.e2. doi: 10.1016/j.jpeds.2017.05.002. Review.


Thirty Years of Experience at the First Tunisian Kidney Transplant Center.

Abderrahim E, Zammouri A, Bacha MM, Ounissi M, Gargah T, Hedri H, Ben Slama R, Bardi R, Chebil M, Ben Abdallah T.

Exp Clin Transplant. 2017 Feb;15(Suppl 1):84-89.


Nephrotic syndrome in children: risk factors for steroid dependence.

Jellouli M, Brika M, Abidi K, Ferjani M, Naija O, Hammi Y, Gargah T.

Tunis Med. 2016 Jul;94(7):401-405.


Contribution of ultrasound scans in the first episode of urinary tract infection in children.

Jellouli M, Ben Mansour A, Abidi K, Ferjani M, Naija O, Hammi Y, Zarrouk C, Gargah T.

Tunis Med. 2016 Jun;94(6):167-170.


Diffuse Mesangial Sclerosis in a Child With Dyskeratosis Congenita Leading to End-stage Renal Disease.

Kamel A, Sayari T, Jellouli M, Hammi Y, Louzir RG, Gargah T.

Iran J Kidney Dis. 2016 Nov;10(6):416-418.


Peritoneal dialysis: Experience of the department of pediatrics of the hospital Charles Nicolle of Tunis.

Jellouli M, Ferjani M, Oueslati A, Abidi K, Naija O, Hammi Y, Ben Abdallah T, Gargah T.

Tunis Med. 2016 May;94(5):368-374.


Focal segmental glomerulosclerosis in children.

Jellouli M, Abidi K, Askri M, Ferjani M, Naija O, Hammi Y, Goucha R, Gargah T.

Tunis Med. 2016 May;94(5):356-359.


Nephrocalcinosis in Tunisian children.

Jellouli M, Karoui W, Abidi K, Hammi Y, Naija O, Zarrouk C, Abdelmoula J, Gargah T.

Tunis Med. 2016 Apr;94(4):167-170.


A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype-phenotype correlation.

M'Dimegh S, Aquaviva-Bourdain C, Omezzine A, M'Barek I, Souche G, Zellama D, Abidi K, Achour A, Gargah T, Abroug S, Bouslama A.

J Genet. 2016 Sep;95(3):659-66.


Mycophenolate mofetil in treatment of childhood steroid-dependent nephrotic syndrome.

Jellouli M, Fitouhi S, Abidi K, Hammi Y, Naija O, Zarrouk C, Gargah T.

Tunis Med. 2016 Mar;94(3):221-5.


HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.

M'dimegh S, Aquaviva-Bourdain C, Omezzine A, Souche G, M'barek I, Abidi K, Gargah T, Abroug S, Bouslama A.

J Clin Lab Anal. 2017 May;31(3). doi: 10.1002/jcla.22053. Epub 2016 Aug 26.


[Tumoral calcinosis in a patient on hemodialysis].

Jellouli M, Gargah T.

Pan Afr Med J. 2016 Mar 31;23:155. doi: 10.11604/pamj.2016.23.155.8335. eCollection 2016. French. No abstract available.


Primary hyperoxaluria in infants.

Jellouli M, Ferjani M, Abidi K, Zarrouk C, Naija O, Abdelmoula J, Gargah T.

Saudi J Kidney Dis Transpl. 2016 May;27(3):526-32. doi: 10.4103/1319-2442.182389.


X-Linked Agammagobulinemia in a Large Series of North African Patients: Frequency, Clinical Features and Novel BTK Mutations.

Aadam Z, Kechout N, Barakat A, Chan KW, Ben-Ali M, Ben-Mustapha I, Zidi F, Ailal F, Attal N, Doudou F, Abbadi MC, Kaddache C, Smati L, Touri N, Chemli J, Gargah T, Brini I, Bakhchane A, Charoute H, Jeddane L, El Atiqi S, El Hafidi N, Hida M, Saile R, Alj HS, Boukari R, Bejaoui M, Najib J, Barbouche MR, Lau YL, Mellouli F, Bousfiha AA.

J Clin Immunol. 2016 Apr;36(3):187-94. doi: 10.1007/s10875-016-0251-z. Epub 2016 Mar 1.


[Etiologies of end-stage renal disease of children in Tunisia].

Jellouli M, Boussetta A, Abidi K, Maalej B, Naija O, Hammi Y, Zarrouk C, Mahfoudh A, Gargah T.

Nephrol Ther. 2016 Jun;12(3):166-70. doi: 10.1016/j.nephro.2015.09.001. Epub 2016 Feb 20. French.


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