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Hela Boudabous

Observed names: Boudabous, Hela, H Boudabous, H. Boudabous, Héla Boudabous, hela Boudabous
Observed institutions: Tunis University, Institut Salah-Azaïz, Hôpital La Rabta, Hôpital Charles-Nicolle, Faculté de médecine de Tunis, Tunis El Manar University
ORCID: 0000-0002-4368-927X
Observed ORCID: 0000-0002-4368-927X
OpenAlex ID: A5055463793
Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
2017 · Rim Ben Abdelaziz, Habiba Hafsi, et al. · BMC Pediatrics · 118
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Large-scale screening of lipase acid deficiency in at risk population
2021 · Abdellah Tebani, Bénédicte Sudrié-Arnaud, et al. · Clinica Chimica Acta · 17
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A Novel Mutation c.153 C>A in a Tunisian Girl With Wolman Disease and Unusual Presentation: Hemophagocytic Lymphohistiocytosis
2018 · Faten Tinsa, Manel Ben Romdhane, et al. · Journal of Pediatric Hematology/Oncology · 17
Fucosidosis in Tunisian patients: mutational analysis and homology-based modeling of FUCA1 enzyme
2021 · Latifa Chkioua, Yessine Amri, et al. · BMC Medical Genomics · 12
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The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients
2020 · L Chkioua, O Grissa, et al. · BMC Medical Genetics · 12
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Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients
2018 · Sana Ben Messaoud, Rim Ben Abdelaziz, et al. · Neuropediatrics · 11
A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients
2018 · Amel Ben Chehida, Sana Ben Messaoud, et al. · Journal of Pediatric Endocrinology and Metabolism · 11
Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
2018 · Rim Ben Abdelaziz, Habiba Hafsi, et al. · BMC Pediatrics · 7
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High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness
2018 · Amel Ben Chehida, Sana Ben Messaoud, et al. · Journal of Tropical Pediatrics · 7
Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa
2024 · Latifa Chkioua, Houda El Fissi, et al. · BMC Genomics · 6
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Novel RAB3GAP1 Mutation in the First Tunisian Family With Warburg Micro Syndrome
2022 · Nesrine Kerkeni, Maher Kharrat, et al. · Journal of Clinical Neurology · 6
Self-Reported Anxiety, Depression and Coping in Parents of Children with Phenylketonuria
2019 · Rim Ben Abdelaziz, Amel Ben Chehida, et al. · Journal of Developmental and Physical Disabilities · 6
Novel splice site IDUA gene mutation in Tunisian pedigrees with hurler syndrome
2018 · Latifa Chkioua, Hela Boudabous, et al. · Diagnostic Pathology · 6
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Transcript Long‐Read Sequencing Unveils the Molecular Complexity of a Novel ROGDI Splicing Variant in a Tunisian Family With Kohlschütter‐Tönz Syndrome
2025 · Miriam Essid, Sana Karoui, et al. · Clinical Genetics · 3
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Homozygous pArg610del Mutation Unusually Associated With Severe Delay of Growth in 2 Acid Sphingomyelinase Deficiency–affected Sibs
2019 · Manel Naifar, Faten Kallel, et al. · Journal of Pediatric Hematology/Oncology · 3
Role play for genetic counseling learning: Value and students perceptions.
2019 · Rim Ben Abdelaziz, Hela Boudabous, et al. · PubMed · 3
Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis
2022 · Latifa Chkioua, Yessine Amri, et al. · Diagnostic Pathology · 2
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Factors predictive of prognosis of infantile spasms. A retrospective study in a low-income country
2018 · R. Ben Abdelaziz, A. Ben Chehida, et al. · Archives de Pédiatrie · 2
Patient-management Problem (PMP) for paediatrics learning: Value and students perceptions.
2018 · Rim Ben Abdelaziz, Hela Hajji, et al. · PubMed · 2
Genetic variations in the IDUA gene in Tunisian MPS I families: Identification of a novel microdeletion disrupting substrate binding and structural insights
2025 · Mariem Rebai, Yessine Amri, et al. · Molecular Genetics and Metabolism Reports · 1
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À propos de six cas de paragangliome cervical
2010 · C. Nasr, L. Kochbati, et al. · Cancer/Radiothérapie · 1
Dual Urea Cycle Dysfunction Caused by Coexisting Argininosuccinic Aciduria and Citrin Deficiency: Clinical, Biochemical, and Molecular Insights From an Exceptional Case
2026 · Mouna Zribi, Mariem Bhouri, et al. · JIMD Reports
Case Report: Primary bile acid synthesis defect: first cases series from Tunisia
2026 · Mouna Zribi, Safa Khatrouch, et al. · Frontiers in Pediatrics
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Mucopolysaccharidosis type II in tunisian families: IDS gene variations disrupting substrate binding and a novel deep intronic deletion reducing IDS expression
2026 · Roua Ltaifa, Chayma Jellali, et al. · Molecular Biology Reports
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Integrated exome and mitochondrial genome sequencing reveals the genetic landscape of primary mitochondrial diseases: findings from a large Tunisian cohort
2026 · Ismail Gouiza, Aymane Bouzidi, et al. · Mitochondrion
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Works count: 45
Citation count: 253
H-index: 7
I10-index: 7
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