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Wajdi Safi

Observed names: Safi Wajdi, W. Safi, wajdi Safi
ORCID: 0009-0002-6533-2308
Observed ORCID: 0009-0002-6533-2308
OpenAlex ID: A5031438381
Ovarian Steroid Cell Tumor (Not Otherwise Specified): A Case Report of Ovarian Hyperandrogenism
2020 · Hadjkacem Faten, Ghorbel Dorra, et al. · Case Reports in Oncological Medicine · 17
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The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes
2020 · Mouna Tabebi, Wajdi Safi, et al. · Molecular Genetics & Genomic Medicine · 8
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Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation
2021 · Mariam Moalla, Wajdi Safi, et al. · Frontiers in Endocrinology · 7
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Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency
2022 · Mariam Moalla, Mouna Mnif-Feki, et al. · Journal of Clinical Medicine · 3
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Potential role of liver enzyme levels as predictive markers of glucose metabolism disorders in a Tunisian population
2018 · Houda Bouhajja, Rania Abdelhedi, et al. · Canadian Journal of Physiology and Pharmacology · 3
Molecular mechanisms underlying the defects of two novel mutations in the HSD17B3 gene found in the Tunisian population
2022 · Bochra Ben Rhouma, Manuel Kley, et al. · The Journal of Steroid Biochemistry and Molecular Biology · 2
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigations
2022 · Marwa Ammar, Wajdi Safi, et al. · International Journal of Developmental Neuroscience · 2
Occurrence of Hypopituitarism in Tunisian Turner Syndrome patients: familial versus sporadic cases
2021 · M. Mnif-Feki, W. Safi, et al. · Gynecological Endocrinology · 2
Screening of MKRN3, DLK1, KISS1, KISS1R, and PROKR2 genes sequences in related girls with central precocious puberty for a personalized management
2025 · Ayah Alhusseni, Mariam Moalla, et al. · Endocrine and Metabolic Science · 1
Genetic investigation of thyroid dyshormonogenesis in a Tunisian consanguineous family
2021 · Wajdi Safi, Kacem Faten Hadj, et al. · Endocrine Abstracts · 1
Simulation Based Learning in internal medicine students.
2021 · Melek Kechida, Syrine Daadaa, et al. · PubMed Central · 1
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Screening of MKRN3, DLK1, KISS1, KISS1R, and PROKR2 genes sequences in related girls with precocious puberty for a personalized management
2024 · A. Alhusseni, M. Moalla, et al. · Annales d Endocrinologie
Hypogonadotropic hypogonadism, phenotype genotype correlation
2024 · Hana Charfi, Hamdi Frikha, et al. · Endocrine Abstracts
Congenital hypopituitarism in familial Turner syndrome cases caused by a highly prevalent PROP1 gene mutation in Tunisia
2024 · Hassen Hadj Kacem, Mariam Moalla, et al. · Endocrine and Metabolic Science
Prevalence and associated factors related to combined hypopituitarism in patients with congenital Growth Hormone deficiency
2023 · Kacem Akid Faten Haj, Wafa Belabed, et al. · Endocrine Abstracts
Morphological pituitary abnormalities in patients with congenital Growth Hormone deficiency
2023 · Faten Haj Kacem Akid, Abdel Mouhaymen Missaoui, et al. · Endocrine Abstracts
Growth hormone deficiency in pseudohypoparathyroidism type 1a: a case report
2023 · Kacem Akid Faten Haj, Wafa Belabed, et al. · Endocrine Abstracts
Predictive clinical factors of stature gain in congenital growth hormone deficiency treated patients
2023 · Kacem Akid Faten Haj, Wafa Belabed, et al. · Endocrine Abstracts
Molecular Mechanisms Underlying the Defects of Two Novel Mutations in the Hsd17b3 Gene Found in the Tunisian Population
2022 · Bochra Ben Rhouma, Manuel Kley, et al. · SSRN Electronic Journal
Les atteintes thyroïdiennes des polyendocrinopathies auto-immunes
2021 · D. Bensalah, A. Salah, et al. · Annales d Endocrinologie
Besoins en éducation thérapeutique du patient selon le type du diabète
2021 · M. Elleuch, H. Frikha, et al. · Annales d Endocrinologie
Oral and dental manifestation of Allgrove syndrome: A case report
2021 · Ben Salah Dhoha, Hana Charfi, et al. · Endocrine Abstracts
Syndromic mitochondrial diabetes: About three Tunisian families
2021 · Wajdi Safi, Mouna Tabbebi, et al. · Endocrine Abstracts
Phenotypic expression of a defects in androgen synthesis of action
2021 · Wajdi Safi, Rhouma Bochra Ben, et al. · Endocrine Abstracts
Social phobia and predictive factors in obese adults
2021 · Salah Dhouha Ben, Ameni Salah, et al. · Endocrine Abstracts
Works count: 64
Citation count: 47
H-index: 3
I10-index: 1
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