Infantile Parotid Hemangioma With Diagnostic Dilemma: A Case Report von Abidi, Kamel T, Kamal, Naglaa M, Althobaiti, Khaled A, Althobaiti, Sami D, Halabi, Yasser A, Alalyani, Saad A

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Sjogren–Larsson Syndrome: A case series of five members from an extended family with a novel mutation von Abidi, Kamel T., Kamal, Naglaa M., Bakkar A., Ayman A., Alotaibi, Maram, Asseri, Haifa, Bokari, Kawthar A.

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Diffuse Mesangial Sclerosis in a Child With Dyskeratosis Congenita Leading to End-stage Renal Disease von Abidi, Kamel, Sayari, Taha, Jallouli, Manel, Hammi, Yousra, Louzir, Rim Goucha, Gargah, Tahar

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Primary hyperoxaluria in infants von Jellouli, Manel, Firjani, Maryam, Abidi, Kamil, Zarruq, Shukri, Naija, Ouns, Abd al-Mawla, J., Gargah, Tahar

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Infantile cystinosis : from dialysis to renal transplantation von Abd al-Mawla, Juwaydah, Zarruq, Shukri, Abidi, Kamil, Jellouli, Manel, Gargah, Tahar, Farjani, Maryam

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Tuberculosis following kidney transplantation: report of paediatric case von Abidi, Kamel, Jellouli, Manel, Hammi, Yousra, Gargah, Tahar

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Williams-Beuren syndrome associated with single kidney and nephrocalcinosis: a case report von Abidi, Kamel, Jellouli, Manel, Ben Rabeh, Rania, Hammi, Yousra, Gargah, Tahar

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Persistent Hypertransaminasemia Uncovered Occult Limb-Girdle-Muscle Dystrophy-Type-2C in a Saudi Child von Kamal, Naglaa M, Alghamdi, Hamed A, Halabi, Abdulrahman, Alharbi, Abdullah O, Rafque, Muhammad, Abidi, Kamel, El-Shabrawi, Mortada H.H, Eskander, Ayman E, Mansour, Hala, Sherief, Laila M

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Syndrome de Protée: à propos d'une observation pédiatrique von Kamel Abidi, Manel Jellouli, Abir Boussetta, Yousra Hammi, Tahar Gargah

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Particularité de la cystinose infantile chez l'enfant tunisien von Jellouli, Manel, Turkia, Hadhami Ben, Abidi, Kamel, Hammi, Yosra, Gargah, Tahar

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Caractéristiques bactériologiques des infections de liquide de dialyse péritonéale von Jellouli, Manel, Ferjani, Meriem, Abidi, Kamel, Hammi, Yosra, Abdallah, Taieb Ben, Gargah, Tahar

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HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients von M'dimegh, Saoussen, Aquaviva‐bourdain, Cécile, Omezzine, Asma, Souche, Geneviéve, M'barek, Ibtihel, Abidi, Kamel, Gargah, Tahar, Abroug, Saoussen, Bouslama, Ali

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Persistance de la veine cave supérieure gauche: à propos d’un cas von Abidi, Kamel, Jellouli, Manel, Hammi, Yousra, Gargah, Tahar

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Focal segmental glomerulosclerosis in children von Jellouli, Manel, Abidi, Kamel, Askri, Mouna, Ferjani, Meriem, Naija, Ouns, Hammi, Yousra, Goucha, Rym, Gargah, Tahar

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Nephrotic syndrome in children: risk factors for steroid dependence von Jellouli, Manel, Brika, Meriem, Abidi, Kamel, Ferjani, Meriem, Naija, Ouns, Hammi, Yousra, Gargah, Tahar

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A novel mutation in the AGXT gene causing primary hyperoxaluria type I: genotype–phenotype correlation von M’DIMEGH, SAOUSSEN, AQUAVIVA-BOURDAIN, CÉCILE, OMEZZINE, ASMA, M’BAREK, IBTIHEL, SOUCHE, GENEVIÉVE, ZELLAMA, DORSAF, ABIDI, KAMEL, ACHOUR, ABDELATTIF, GARGAH, TAHAR, ABROUG, SAOUSSEN, BOUSLAMA, ALI

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Nephrocalcinosis in Tunisian children von Jellouli, Manel, Karoui, Wiem, Abidi, Kamel, Hammi, Yousra, Naija, Ouns, Zarrouk, Chokri, Abdelmoula, Jaouida, Gargah, Tahar

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Mycophenolate mofetil in treatment of childhood steroid-dependent nephrotic syndrome von Jellouli, Manel, Fitouhi, Sonia, Abidi, Kamel, Hammi, Yousra, Naija, Ouns, Zarrouk, Chokri, Gargah, Tahar

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Sclerosing Encapsulating Peritonitis due to Peritoneal Dialysis Successfully Treated with Tamoxifen von Abidi, Kamel, Ferjani, Merieme, Jallouli, Manel, Gargah, Tahar

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Peritoneal dialysis: Experience of the department of pediatrics of the hospital Charles Nicolle of Tunis von Jellouli, Manel, Ferjani, Meriem, Oueslati, Amal, Abidi, Kamel, Naija, Ouns, Hammi, Yousra, Ben Abdallah, Taieb, Gargah, Tahar

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