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9 results for Boudabous,+Hela

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ArticlesPeer ReviewedFull Text
Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa
Author / Creator:Chkioua, Latifa ; El Fissi, Houda ; Amri, Yessine ; Sahli, Chayma ; Bouzid, Fadoua ; Boudabous, Hela ; Tbib, Neji ; Ferchichi, Salima ; Massoud, Taieb ; Alif, Najat ; Laradi, Sandrine ; Ben Abdennebi, Hassen
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2024-10, Vol.25 (1), p.948-9, Article 948
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Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
Author / Creator:Ben Abdelaziz, Rim ; Hafsi, Habiba ; Hajji, Hela ; Boudabous, Hela ; Ben Chehida, Amel ; Mrabet, Ali ; Boussetta, Khadija ; Barsaoui, Sihem ; Sammoud, Azza ; Hamzaoui, Mourad ; Azzouz, Hatem ; Tebib, Néji
Publisher:London: BioMed Central Ltd
Journal title:BMC pediatrics, 2017-12, Vol.17 (1), p.1-11, Article 208
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Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
Author / Creator:Chkioua, Latifa ; Amri, Yessine ; Chaima, Sahli ; Fenni, Ferdawes ; Boudabous, Hela ; Ben Turkia, Hadhami ; Messaoud, Taieb ; Tebib, Neji ; Laradi, Sandrine
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2021-08, Vol.14 (1), p.208-11, Article 208
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Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
Author / Creator:Chkioua, Latifa ; Amri, Yessine ; Chaima, Sahli ; Fenni, Ferdawes ; Boudabous, Hela ; Ben Turkia, Hadhami ; Messaoud, Taieb ; Tebib, Neji ; Laradi, Sandrine
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2021-12, Vol.14 (1), p.293-1, Article 293
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Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis
Author / Creator:Chkioua, Latifa ; Amri, Yessine ; Saheli, Chaima ; Mili, Wassila ; Mabrouk, Sameh ; Chabchoub, Imen ; Boudabous, Hela ; Azzouz, Wissem Ben ; Turkia, Hadhami Ben ; Ferchichi, Salima ; Tebib, Neji ; Massoud, Taieb ; Ghorbel, Mohamed ; Laradi, Sandrine
Publisher:England: BioMed Central Ltd
Journal title:Diagnostic pathology, 2022-05, Vol.17 (1), p.44-44, Article 44
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Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome
Author / Creator:Chkioua, Latifa ; Boudabous, Hela ; Jaballi, Ibtissem ; Grissa, Oussama ; Turkia, Hadhami Ben ; Tebib, Neji ; Laradi, Sandrine
Publisher:England: BioMed Central Ltd
Journal title:Diagnostic pathology, 2018-05, Vol.13 (1), p.35-35, Article 35
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Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
Author / Creator:Ben Abdelaziz, Rim ; Hafsi, Habiba ; Hajji, Hela ; Boudabous, Hela ; Ben Chehida, Amel ; Mrabet, Ali ; Boussetta, Khadija ; Barsaoui, Sihem ; Sammoud, Azza ; Hamzaoui, Mourad ; Azzouz, Hatem ; Tebib, Néji
Publisher:England: BioMed Central Ltd
Journal title:BMC pediatrics, 2018-09, Vol.18 (1), p.307-307, Article 307
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Self-Reported Anxiety, Depression and Coping in Parents of Children with Phenylketonuria
Author / Creator:Abdelaziz, Rim Ben ; Chehida, Amel Ben ; Chakchouk, Henda Kachouri ; Messaoud, Sana Ben ; Hajji, Hela ; Boudabous, Hela ; Ferchichi, Maherzia ; Azzouz, Hatem ; Tebib, Néji
Publisher:New York: Springer US
Journal title:Journal of developmental and physical disabilities, 2019-12, Vol.31 (6), p.753-776
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ArticlesPeer ReviewedFull Text
Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
Author / Creator:Ben Abdelaziz, Rim ; Hafsi, Habiba ; Hajji, Hela ; Boudabous, Hela ; Ben Chehida, Amel ; Mrabet, Ali ; Boussetta, Khadija ; Barsaoui, Sihem ; Sammoud, Azza ; Hamzaoui, Mourad ; Azzouz, Hatem ; Tebib, Néji
Publisher:England
Journal title:BMC pediatrics, 2017-12, Vol.17 (1), p.208-208
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Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa

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Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study

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Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme

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Correction to: Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme

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Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis

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Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome

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Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study

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Self-Reported Anxiety, Depression and Coping in Parents of Children with Phenylketonuria

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Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study

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