Search Results - Maâlej, Bayen

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  1. 1
    Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneys

    Custom Next‐Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the t... by Said, Mariem Ben, Ayed, Ikhlas Ben, Elloumi, Ines, Hasnaoui, Mehdi, Souissi, Amal, Idriss, Nabil, Aloulou, Hajer, Chabchoub, Imen, Maâlej, Bayen, Driss, Dorra, Masmoudi, Saber

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  2. 2
    Rituximab in The Management of Pediatric Steroid-Resistant Nephrotic Syndrome: A Systematic Review

    Rituximab in The Management of Pediatric Steroid-Resistant Nephrotic Syndrome: A Systematic Review by Jellouli, Manel, Charfi, Rim, Maalej, Bayen, Mahfoud, Abdelmajid, Trabelsi, Sameh, Gargah, Tahar

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  3. 3
    P660 Abscess of the kidney, a diagnosis not always evident

    P660 Abscess of the kidney, a diagnosis not always evident by Safi, Faiza, Gargouri, Lamia, Hsairi, Manel, Regaieg, Chiraz, Maalej, Bayen, Mahfoudh, Abdelmajid

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  4. 4
    Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients

    Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients by Ammar, Sawssan, Kanoun, Houda, Kammoun, Khawla, Domingo-Gallego, Andrea, Ruiz, Patricia, Lorente-Grandoso, Laura, Pybus, Marc, Maalej, Bayen, Boudawara, Tahya, Kamoun, Hassen, Ben Hmida, Mohamed, Ars, Elisabet, Jarraya, Faiçal

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  5. 5
    Lupus Nephritis in Tunisian Children: Predictive Factors of Poor Outcomes

    Lupus Nephritis in Tunisian Children: Predictive Factors of Poor Outcomes by Boussetta, Abir, Louati, Dalia, Jellouli, Manel, Gaied, Hanen, Mabrouk, Sameh, Maalej, Bayen, Zouaghi, Karim, Goucha, Rym, Gargah, Tahar

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  6. 6
    Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations

    Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations by Kanoun, Houda, Jarraya, Faiçal, Maalej, Bayen, Lahiani, Amina, Mahfoudh, Hichem, Makni, Fatma, Hachicha, Jamil, Fakhfakh, Faiza

    Published in BMC nephrology
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  7. 7
    An unusual case of pediatric acute nicotine poisoning due to a dermal exposure

    An unusual case of pediatric acute nicotine poisoning due to a dermal exposure by Manel Weli, Mouna Jerbi, Olfa Chakroun-Walha, Bayen Maalej, Lamia Gargouri, Noureddine Rekik, Abdelmajid Mahfoudh

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  8. 8
    Genetic insights into fetal kidney development: Variants in HNF1A and PKHD1 genes

    Genetic insights into fetal kidney development: Variants in HNF1A and PKHD1 genes by Abdelwahed, Mayssa, Benoit, Valerie, Maalej, Bayen, Hilbert, Pascale, Calemard, Laurence Michel, Kamoun, Hassen, Ammar-Keskes, Leila, Belguith, Neila

    Published in Gene
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  9. 9
    Complications mécaniques de la dialyse péritonéale chez l’enfant tunisien

    Complications mécaniques de la dialyse péritonéale chez l’enfant tunisien by Jellouli, Manel, Abdellatif, Abir, Bousetta, Abir, Hlel, Youssef, Daib, Aida, Kaabar, Nejib, Kerkeni, Yousra, Houas, Yasmine, Jouini, Riadh, Jlidi, Said, Gargah, Tahar, Maalej, Bayen, Sahli, Sondes

    Published in Tunisie Medicale
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