Search Results - Jihene, Chelly

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  1. 1
    Case Report: Cerebral venous thrombosis revealing celiac disease [version 2; peer review: 2 approved]

    Case Report: Cerebral venous thrombosis revealing celiac disease [version 2; peer review: 2 approved] by Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Olfa, Jomaa, Sonia, Hammami, Karima, Hmida, Fatma, El Arbi, Olfa, Berriche

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  2. 2
    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? (a case report)

    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? (a case report) by Olfa, Berriche, Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Fatma, El Arbi, Wafa, Alaya

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  3. 3
    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? A case report

    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? A case report by Olfa, Berriche, Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Fatma, El Arbi, Wafa, Alaya

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  4. 4
    Case Report: Cerebral venous thrombosis revealing celiac disease [version 1; peer review: 2 approved with reservations]

    Case Report: Cerebral venous thrombosis revealing celiac disease [version 1; peer review: 2 approved with reservations] by Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Olfa, Jomaa, Sonia, Hammami, Karima, Hmida, Fatma, El Arbi, Olfa, Berriche

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  5. 5
    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? (a case report)

    Granulomatosis with polyangiitis and neurofibromatosis type 1: a fortuitous association? (a case report) by Olfa, Berriche, Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Fatma, El Arbi, Wafa, Alaya

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  6. 6
    Case Report: Cerebral venous thrombosis revealing celiac disease

    Case Report: Cerebral venous thrombosis revealing celiac disease by Wiem, Romdhane, Sondess, Arfa, Jihene, Chelly, Olfa, Jomaa, Sonia, Hammami, Karima, Hmida, Fatma, El Arbi, Olfa, Berriche

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  7. 7
    Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment

    Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment by Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Turki Ben Youssef, Ilhem, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha

    Published in PloS one
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