Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Hammadi Ayadi"'
Autor:
Mohamed Abid, Romain Legrand, Hammadi Ayadi, Houda Bouhajja, Srini V. Kaveri, Nicolas Lucas, Sergueï O. Fetissov, Rim Marrakchi, Noura Bougacha-Elleuch, Mouna Mnif-Feki, Kamel Jamoussi
Publikováno v:
Nutrition & Diabetes
Nutrition & Diabetes, Springer Nature, 2018, 8 (1), ⟨10.1038/s41387-018-0044-y⟩
Nutrition & Diabetes, 2018, 8 (1), ⟨10.1038/s41387-018-0044-y⟩
Nutrition & Diabetes, Vol 8, Iss 1, Pp 1-5 (2018)
Nutrition & Diabetes, Springer Nature, 2018, 8 (1), ⟨10.1038/s41387-018-0044-y⟩
Nutrition & Diabetes, 2018, 8 (1), ⟨10.1038/s41387-018-0044-y⟩
Nutrition & Diabetes, Vol 8, Iss 1, Pp 1-5 (2018)
Obese subjects display elevated plasma levels of leptin reflecting the phenomenon of leptin resistance. Here, we aimed to determine whether leptin-reactive immunoglobulins (Ig) are present in obese and type 2 diabetes (T2D) patients and whether their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edb08d31fbdba3246b731f9495de7603
https://hal-normandie-univ.archives-ouvertes.fr/hal-02315360/file/s41387-018-0044-y.pdf
https://hal-normandie-univ.archives-ouvertes.fr/hal-02315360/file/s41387-018-0044-y.pdf
Autor:
Houda Bouhajja, Faten Hadj Kacem, Mohamed Abid, Nadia Charfi, Salwa Bensassi, Mouna Mnif-Feki, Kamel Jamoussi, Houcem Mrabet, M. Fourati, Wajdi Safi, Noura Bougacha-Elleuch, Rania Abdelhedi, Hammadi Ayadi, Ali Amouri, Rim Marrakchi, Lassaad Chtourou
Publikováno v:
Canadian journal of physiology and pharmacology. 96(11)
The relationship between liver enzymes and T2D risk is inconclusive. We aimed to evaluate the association between liver markers and risk of carbohydrate metabolism disorders, as well as their discriminatory power, for T2D prediction. This cross-secti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f79697f3c1834df52cffc82f5ab12f
https://pubmed.ncbi.nlm.nih.gov/29527933
https://pubmed.ncbi.nlm.nih.gov/29527933
Autor:
Ilhem Charfeddine, Joël Lachuer, Magali Roche, Christine Petit, Hammadi Ayadi, Abdullah A.Y. Gibriel, I. Achour, Ibtihel Smeti, Abdelmonem Ghorbel, Aida Khalfallah, Leila Dhouib, Saber Masmoudi, Amal Bouzid
Publikováno v:
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals. 23(4)
Presbycusis, an age-related hearing impairment (ARHI), represents the most common sensory disability in adults. Today, the molecular mechanisms underlying presbycusis remain unclear. This is in particular due to the fact that ARHI is a multifactorial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78ac6f88c55e79d56b461bcdc161a8dd
https://pubmed.ncbi.nlm.nih.gov/29325454
https://pubmed.ncbi.nlm.nih.gov/29325454
Autor:
Nadia Charfi, Nabil Miled, Houda Bouhajja, Paula Jaurge, Noura Bougacha-Elleuch, Mongia Hachicha, Mouna Mnif, Mohamed Abid, Nessrine Chikhrouhou, Hammadi Ayadi, Neila Belguith
Publikováno v:
European Journal of Pediatrics. 174:1491-1501
We aimed to identify causal mutation(s) in 13 patients with thyroid dyshormonogenesis (TD) from three consanguineous Tunisian families. A 12-year clinical follow-up showed phenotypic variability ranging from the presence to the absence of goiter, sen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07aa6abf8f0c5bad7ac99caa3eb71aae
https://doi.org/10.1007/s00431-015-2550-4
https://doi.org/10.1007/s00431-015-2550-4
Autor:
Noura Bougacha-Elleuch, Nadia Charfi, Mohamed Abid, Maha Kammoun-Krichen, Ghazi Chabchoub, Salima Belguith-Maalej, Fatma Ayadi, Najla Kharrat, Hammadi Ayadi, Abdellatif Maalej, Mouna Mnif, Ahmed Rebai
Publikováno v:
Meta Gene
Autoimmune thyroid diseases (AITD), which include Hashimoto thyroiditis (HT), Graves' disease (GD) and primary idiopathic myxoedema (PIM), are recognized by their clinical and genetic heterogeneity. In this study, we have carried on a global approach
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1c2ab7338d2ab701d75343c0720346
Autor:
Hammadi Ayadi, Kamel Jamoussi, Faten Hadj Kacem, Mohamed Abid, Rim Marrakchi, Ahmed Rebai, Marwa Ncir, Jordan D. Dimitrov, Mouna Mnif-Feki, Noura Bougacha-Elleuch, Rania Abdelhedi, Abdelfattah El Feki, Houda Bouhajja, Srini V. Kaveri
Publikováno v:
Canadian journal of diabetes. 42(3)
We evaluated the potential clinical relevance of malondialdehyde (MDA) and autoantibodies to copper oxidized low-density lipoprotein (CuOx-LDL) in type 2 diabetes occurrence.This cross-sectional study enrolled 69 normoglycemic subjects, 18 prediabeti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2c48afd78d7ee460d128ce898f6487e
https://pubmed.ncbi.nlm.nih.gov/28734952
https://pubmed.ncbi.nlm.nih.gov/28734952
Autor:
Peter Söderkvist, Salma Ben Salem, Ebtissem Chouchène, Hammadi Ayadi, Walid Bouassida, Zeineb Benzina, Mariem Ben Said, Kods Daoud, Leila El Matri, Mounira Hmani-Aifa, L. Largueche
Publikováno v:
Gene. 528:288-294
Congenital microphthalmia (CMIC) is a common developmental ocular disorder characterized by a small, and sometimes malformed, eye. Posterior microphthalmia (PM) and nanophthalmia are two rare subtypes of isolated CMIC characterized by extreme hyperop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a07b3a07ccd12c20564f827285e45a3
https://doi.org/10.1016/j.gene.2013.06.045
https://doi.org/10.1016/j.gene.2013.06.045
Autor:
Fakhri Kallabi, Hammadi Ayadi, Ghada Ben Salah, Nourhene Fendri-Kriaa, Emna Mkaouar-Rebai, Hassen Kamoun, Amine Fourati, Faiza Fakhfakh
Publikováno v:
Molecular Biology Reports. 39:9639-9647
Genetic polymorphisms in DNA repair genes might influence the repair activities of the enzymes predisposing individuals to cancer risk. Owing to the presence of these genetic variants, interethnic differences in DNA repair capacity have been observed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fab3d9980ba5a9e652ef65c8ce70415e
https://doi.org/10.1007/s11033-012-1829-z
https://doi.org/10.1007/s11033-012-1829-z
Autor:
Saber Masmoudi, Mounira Hmani-Aifa, Mariem Ben Said, Houria Dhouib, Hammadi Ayadi, Felipe Moreno, Abdelmoneem Ghorbel, Zeineb Benzina
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 76:832-836
Objective Recessive mutations of the SLC26A4 (PDS) gene on chromosome 7q31 can cause sensorineural hearing loss with goiter (Pendred syndrome) or non-syndromic autosomal recessive hearing loss (DFNB4). Furthermore, mutations in the GJB2 gene results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a10bb575472c5a9dfcaa37ec10e5e67d
https://doi.org/10.1016/j.ijporl.2012.02.053
https://doi.org/10.1016/j.ijporl.2012.02.053
Autor:
Melek Mnejja, Mariem Ben Said, Ayda Khalfallah, Zeineb Benzina, Ignacio del Castillo, Khalil Turki, Leila Ayedi, Bochra Hakim, Mounira Hmani Aifa, Abdelmonem Ghorbel, Hammadi Ayadi, Ilhem Charfeddine, Saber Masmoudi, Chamseddine Khifagi
Publikováno v:
European Journal of Medical Genetics. 54:e535-e541
Autosomal recessive non-syndromic hearing loss (ARNSHL) is a genetically heterogenous disorder with 41 genes so far identified. Among these genes, ESRRB whose mutations are responsible for DFNB35 hearing loss in Pakistani and Turkish families. This g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::455349c487509409a3eb3780be26f8f8
https://doi.org/10.1016/j.ejmg.2011.06.008
https://doi.org/10.1016/j.ejmg.2011.06.008