Works by Amri, Yessine

Results: 17

Artificial intelligence in vestibular disorder diagnosis.

Published in:

Bulletin of Electrical Engineering & Informatics, 2025, v. 14, n. 3, p. 1901, doi. 10.11591/eei.v14i3.7160

By:

Slama, Amine Ben;
Sahli, Hanene;
Amri, Yessine;
Labidi, Salam

Publication type:

Article

BTS-ADCNN: brain tumor segmentation based on rapid anisotropic diffusion function combined with convolutional neural network using MR images.

Published in:

Journal of Supercomputing, 2024, v. 80, n. 9, p. 13272, doi. 10.1007/s11227-024-05985-2

By:

Mbarki, Zouhair;
Ben Slama, Amine;
Amri, Yessine;
Trabelsi, Hedi;
Seddik, Hassene

Publication type:

Article

Epidemiological and molecular study of hemoglobinopathies in Mauritanian patients.

Published in:

Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2048

By:

Mahmoud, Taher;
Sahli, Chaima;
Hadj Fredj, Sondess;
Amri, Yessine;
Othmani, Rim;
Mohamed, Ghaber S.;
Zein, Ekhtelbenina;
Messaoud, Taieb

Publication type:

Article

Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia.

Published in:

BMC Genomics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s12864-024-11060-0

By:

Chkioua, Latifa;
Amri, Yessine;
Sahli, Chayma;
Nasri, Tawfik;
Miladi, Mohamed Omar;
Massoud, Taieb;
Laradi, Sandrine;
Ghorbel, Mohamed;
Ben Abdennebi, Hassen

Publication type:

Article

Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations.

Published in:

Molecular Biology Reports, 2021, v. 48, n. 8, p. 5923, doi. 10.1007/s11033-021-06592-7

By:

Kasmi, Chaima;
Amri, Yessine;
Hadj-Fredj, Sondess;
Oueslati, Sabrine;
Dabboussi, Malek;
Mahjoub, Rahma;
Hammami, Sana;
Aljane, Imen;
Mami, Faika Ben;
Jamoussi, Henda;
Messaoud, Taieb;
Bibi, Amina

Publication type:

Article

Inherited bisalbuminemia with growth hormone deficiency.

Published in:

2019

By:

Dabboubi, Rym;
Amri, Yessine;
Sahli, Chaima;
Fredj, Sondess Hadj;
Essaddam, Leila;
Zoghlami, Ala;
Ben Becher, Saida;
Messaoud, Taieb

Publication type:

Case Study

Comprehensive analysis of a novel LYST mutation in a Tunisian patient with Chediak-Higashi syndrome.

Published in:

BMC Medical Genomics, 2025, v. 18, n. 1, p. 1, doi. 10.1186/s12920-025-02145-0

By:

Amri, Yessine;
Chouchene, Saoussen;
Foddha, Hajer;
Abderahmene, Amani;
Kooli, Ikbel;
Toumi, Adnen;
Hadj Khalifa, Kawthar;
Mezrigui, Rihem;
Messaoud, Taieb;
Hassine, Mohsen;
Dabboubi, Rym

Publication type:

Article

Contribution of HLA class I (A, B, C) and HLA class II (DRB1, DQA1, DQB1) alleles and haplotypes in exploring ethnic origin of central Tunisians.

Published in:

BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01821-x

By:

Ben Bnina, Amène;
Yessine, Amri;
El Bahri, Yasmine;
Chouchene, Saoussen;
Ben Lazrek, Nada;
Mimouna, Mariem;
Mlika, Zeineb;
Messoudi, Aziza;
Zellama, Dorsaf;
Sahtout, Wissal;
Bouatay, Amina

Publication type:

Article

Congenital analbuminemia associated with compound heterozygous novel nucleotide variations in a young adult with coronary thrombosis.

Published in:

Annales de Biologie Clinique, 2023, v. 81, n. 2, p. 204, doi. 10.1684/abc.2023.1806

By:

Amri, Yessine;
Aboulkacem, Sana;
Dabboubi, Rym;
Ayoub, Manel;
Lamine, Oussema;
Othmani, Mariem;
Aouni, Zied;
Messaoud, Taieb;
Mazigh, Chakib

Publication type:

Article

Glucose-6-phosphate dehydrogenase deficiency in Tunisian jaundiced neonates.

Published in:

Annales de Biologie Clinique, 2020, v. 78, n. 4, p. 411, doi. 10.1684/abc.2020.1558

By:

Dabboubi, Rym;
Amri, Yessine;
Hamdi, Soumaya;
Jouini, Hamida;
Sahli, Chaima;
Fredj, Sondess Hadj;
Salem, Kamel Ben;
ElhoudaToumi, Nour;
Messaoud, Taieb

Publication type:

Article

Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6‐10_16delTTTG deletion.

Published in:

Haemophilia, 2020, v. 26, n. 4, p. e194, doi. 10.1111/hae.13974

By:

Amri, Yessine;
Dabboubi, Rym;
Mghaieth, Fathia;
Zili, Mohamed;
Messaoud, Taieb;
Casini, Alessandro;
De Moerloose, Philippe;
Toumi, Nour El Houda

Publication type:

Article

Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b.

Published in:

Diabetology & Metabolic Syndrome, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13098-023-01065-2

By:

Chkioua, Latifa;
Amri, Yessine;
Sahli, Chayma;
Rhouma, Ferdawes Ben;
Chehida, Amel Ben;
Tebib, Neji;
Messaoud, Taieb;
Abdennebi, Hassen Ben;
Laradi, Sandrine

Publication type:

Article

Molecular characterization of CTNS mutations in Tunisian patients with ocular cystinosis.

Published in:

Diagnostic Pathology, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13000-022-01221-8

By:

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

Publication type:

Article

Catalyzing precision: unraveling the diagnostic conundrum of tunisian familial hypophosphatasia case through integrative clinical and molecular approaches.

Published in:

Molecular Genetics & Genomics, 2024, v. 299, n. 1, p. 1, doi. 10.1007/s00438-024-02157-y

By:

Amri, Yessine;
Dabboubi, Rym;
Khemiri, Monia;
Jebabli, Elham;
Hadj Fredj, Sondess;
Ahmed, Sarra Ben;
Jouini, Yosr;
Ouali, Faida;
Messaoud, Taieb

Publication type:

Article

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

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3

By:

Chkioua, Latifa;
Amri, Yessine;
Chaima, Sahli;
Fenni, Ferdawes;
Boudabous, Hela;
Ben Turkia, Hadhami;
Messaoud, Taieb;
Tebib, Neji;
Laradi, Sandrine

Publication type:

Article

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

Published in:

2021

By:

Chkioua, Latifa;
Amri, Yessine;
Chaima, Sahli;
Fenni, Ferdawes;
Boudabous, Hela;
Ben Turkia, Hadhami;
Messaoud, Taieb;
Tebib, Neji;
Laradi, Sandrine

Publication type:

Correction Notice

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

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01061-3

By:

Chkioua, Latifa;
Amri, Yessine;
Saheli, Chayma;
Fenni, Ferdawes;
Boudabous, Hela;
Ben Turkia, Hadhami;
Messaoud, Taieb;
Tebib, Neji;
Laradi, Sandrine

Publication type:

Article