Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Hamza Dallali"'
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hajer Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, CRYSTEL Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/d1f20ca9f1e041b5805610de30e16616
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Background:Chronic pain is a major socioeconomic burden in the Mediterranean region. However, we noticed an under-representation of these populations in the pharmacogenetics of pain management studies. In this context, we aimed 1) to decipher the pha
Externí odkaz:
https://doaj.org/article/49783d55ee74468d8f67ee730c36aeed
Autor:
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Maroua Boujemaa, Hamza Dallali, Marwa Sayeb, Saida Lahbib, Hager Jaouadi, Hela Boudabbous, Lotfi Zekri, Mariem Chargui, Olfa Messaoud, Meriem Elyounsi, Ichraf Kraoua, Anissa Zaouak, Ilhem Turki, Mourad Mokni, Sophie Boucher, Christine Petit, Fabrice Giraudet, Chiraz Mbarek, Ghazi Besbes, Soumeyya Halayem, Rim Zainine, Hamida Turki, Amel Tounsi, Crystel Bonnet, Ridha Mrad, Sonia Abdelhak, Mediha Trabelsi, Cherine Charfeddine
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Hearing impairment (HI) is a prevalent neurosensory condition globally, impacting 5% of the population, with over 50% of congenital cases attributed to genetic etiologies. In Tunisia, HI underdiagnosis prevails, primarily due to limited access to com
Externí odkaz:
https://doaj.org/article/d53f3da42b5b4e8f9503ec02796dd375
Autor:
Ismail Gouiza, Meriem Hechmi, Abir Zioudi, Hamza Dallali, Nadia Kheriji, Majida Charif, Morgane Le Mao, Said Galai, Lilia Kraoua, Ilhem Ben Youssef-Turki, Ichraf Kraoua, Guy Lenaers, Rym Kefi
Publikováno v:
Frontiers in Genetics, Vol 14 (2024)
Introduction: Inherited mitochondrial diseases are the most common group of metabolic disorders caused by a defect in oxidative phosphorylation. They are characterized by a wide clinical and genetic spectrum and can manifest at any age. In this study
Externí odkaz:
https://doaj.org/article/d0d0662ffbeb44a0b3f31c44fdd41dc5
Autor:
Hamza Dallali, Wided Boukhalfa, Nadia Kheriji, Meriem Fassatoui, Haifa Jmel, Meriem Hechmi, Ismail Gouiza, Mariem Gharbi, Wafa Kammoun, Mehdi Mrad, Marouen Taoueb, Asma Krir, Hajer Trabelsi, Afef Bahlous, Henda Jamoussi, Olfa Messaoud, Abdelmajid Abid, Rym Kefi
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionType 2 diabetes (T2D) is a multifactorial disease involving genetic and environmental components. Several genome-wide association studies (GWAS) have been conducted to decipher potential genetic aberrations promoting the onset of this met
Externí odkaz:
https://doaj.org/article/ec2f2977e6d94ae5b458346728bffc4e
Autor:
Nadia Kheriji, Hamza Dallali, Ismail Gouiza, Meriem Hechmi, Faten Mahjoub, Mehdi Mrad, Asma Krir, Manel Soltani, Hajer Trabelsi, Walid Hamdi, Afef Bahlous, Melika Ben Ahmed, Henda Jamoussi, Rym Kefi
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Monogenic diabetes (MD) accounts for 3%–6% of all cases of diabetes. This prevalence is underestimated due to its overlapping clinical features with type 1 and type 2 diabetes. Hence, genetic testing is the most appropriate tool for o
Externí odkaz:
https://doaj.org/article/85bbbf73920242eda3ed84cba86223cf
Autor:
Wided Boukhalfa, Haifa Jmel, Nadia Kheriji, Ismail Gouiza, Hamza Dallali, Mariem Hechmi, Rym Kefi
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
IntroductionAlzheimer’s disease (AD) and Type 2 diabetes (T2D) are both age-associated diseases. Identification of shared genes could help develop early diagnosis and preventive strategies. Although genetic background plays a crucial role in these
Externí odkaz:
https://doaj.org/article/5f80903f20c0495fbab32361a26d42d6
Autor:
Hamza Dallali, Meriem Hechmi, Imane Morjane, Sahar Elouej, Haifa Jmel, Yosra Ben Halima, Abdelmajid Abid, Afef Bahlous, Abdelhamid Barakat, Henda Jamoussi, Sonia Abdelhak, Rym Kefi
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-11 (2022)
Abstract Background Variants in the Hepatocyte Nuclear Factor 1 Alpha gene (HNF1A) are associated with lipoproteins levels and type 2 diabetes. In this study, we aimed to assess the association of HNF1A gene and haplotypes with the metabolic syndrome
Externí odkaz:
https://doaj.org/article/83976765788742f1a3bf0aa0de69fd51
Autor:
Lilia Romdhane, Nessrine Mezzi, Hamza Dallali, Olfa Messaoud, Jingxuan Shan, Khalid A. Fakhro, Rym Kefi, Lotfi Chouchane, Sonia Abdelhak
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-18 (2021)
Abstract Copy number variation (CNV) is considered as the most frequent type of structural variation in the human genome. Some CNVs can act on human phenotype diversity, encompassing rare Mendelian diseases and genomic disorders. The North African po
Externí odkaz:
https://doaj.org/article/399d7564503448b8a9d14b264646b319
Autor:
Hamza Dallali, Nadia Kheriji, Wafa Kammoun, Mehdi Mrad, Manel Soltani, Hajer Trabelsi, Walid Hamdi, Afef Bahlous, Melika Ben Ahmed, Faten Mahjoub, Henda Jamoussi, Sonia Abdelhak, Rym Kefi
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Juvenile-onset diabetes may occur in the context of a rare syndromic presentation, suggesting a monogenic etiology rather than a common multifactorial diabetes. In the present study, we report the case of a young diabetic Tunisian patient presenting
Externí odkaz:
https://doaj.org/article/ad233d3064ed4150bbaef109375d9e5a