Zobrazeno 1 - 10
of 139
pro vyhledávání: '"Abdelhamid Barakat"'
Autor:
Yosr Hamdi, Maroua Boujemaa, Jihenne Ben Aissa-Haj, Fouzia Radouani, Meriem Khyatti, Najah Mighri, Mariem Hannachi, Kais Ghedira, Oussema Souiai, Chaima Hkimi, Mohamed Selim Kammoun, Nesrine Mejri, Hanen Bouaziz, Mohamed Amine Beloufa, Hicham Charoute, Abdelhamid Barakat, Imène Najjar, Hiroaki Taniguchi, Natalia Pietrosemoli, Koussay Dellagi, Sonia Abdelhak, Mohamed Samir Boubaker, Claudia Chica, Etienne Rouleau, Abdellatif benider, Adil El-hamouchi, AIT YOUNES Sonia, Alia Ben Kahla, AMIMER Abdelmalik, AMIR Zine, charif, Amira Jaballah, Amira Louiza, Amina GIHBID, BACHIR Achouak, BELABDI Djihad, BELHADEF Said, BELNOUI Rafika, Belarbi Ayed, Benchakroune Nadia, Benchakroun Nadia, BENINAL Meriem, BENKALI Radja, BENSIHAMDI Asma, BENYOUCEF Hichem, BENDIMRED Thouraya, Bensouf Nadir, BENNOUI Rafika, Berrazegua Yosra, Biskri Latefa, BOUAOUNI Saida, BOUANIKA Meriem, Bouamra Abderezzak, Bouaziz Hanen, Boudinar Fatma Zohra, Bouhara Sabrina, Boussouf Nadir, Boutayeb Saber, BOUNEDJAR Adda, Chabati Omar, Charfeddine Cherine, Chilla Dalia, Chiraz Mehemmai, Cyrine Bouabid, Dahnane Souad, DIAB Soraya, Dib Hocine Adlane, Dorra Wider, DERRAR Fawzi, ELKEBOUB Amina, EL ATTAR Hicham, EL FAHIME Elmostafa, ELHADEF Djazia, Emna Fehri, Farid Hakkou, Farida Hadjam, Fanny Mamboisse, GAIS Widad, GHARNAOUT Merzak, Guessoum Amir Nidhal, HADJAM Farida, HADJ SAHRAOUI, Haifa Rachdi, Hamza Yaiche, HANNACHI Leila, Hassan Mahfouf, Hend Bouguerra, Hicham El Attar, Hichem Ben Hassine, Houda Filali, Houda Harmak, Houda Kanaane, Ichrak Benamri, Imane El Alami, KASSA Reda, Karima Bendahhou, Khaoula Errafii, Khalid El Bairi, Khaali Wafaa, KARKOURI Mehdi, Kabbage Maria, Kammoun Wafa, Kanaane Houda, Kassa Reda, LAOUAR Narimane, Latefa Biskri, Louiza Amira, Louise Marie, Charion Chevalier, MALOUM Nabila, Marc Monot, Mariem Saadi, Mario Campone, Mehdi Mrad, MEHDI KARKOURI, MELIZI Mohamed, Meriem Saadi, Meriem CHAHER, Monia Ardhaoui, Mourad TALEB, Nadia Ben Jmiaa, Nadia Benchakroun, Najet Hadhri, Nawel SALHI, Nezha Taoufiq, Nouha Jandoubi, OUAHIOUNE Wahiba, OULDSLIMANE Salima, Rafika BELNOUI, Rahman Amira Louiza, Rym Benkhalifa, Saber Boutaib, Saber Boutayeb, Samia Menif, Salima OULDSLIMANE, Samuel Valcke, SLIMANI Assia, Sonia Ben Nasr, Sonia Maatoug, Sonia Ait Younes, Souad BENCHEHIDA, Souad BEKOUACI, Souha Sahraoui, Tali Maamar Hassiba, Talha Soraya, TALEB Mourad, TERKMANI Fella, TALHA Soraya, TOUISI Wassila, Wafa Kammoun, Wahiba OUAHIOUNE, Yosra Berrazegua, ZEMMOUR Amel, ZEROUAL Sarah, Zine Charif AMIR, Zineb Zouafi
Publikováno v:
Translational Oncology, Vol 44, Iss , Pp 101940- (2024)
Precision Medicine is being increasingly used in the developed world to improve health care. While several Precision Medicine (PM) initiatives have been launched worldwide, their implementations have proven to be more challenging particularly in low-
Externí odkaz:
https://doaj.org/article/a76edd34ed914c7887c2118049e17ad9
Autor:
Aymane Bouzidi, Hicham Charoute, Majida Charif, Ghita Amalou, Mostafa Kandil, Abdelhamid Barakat, Guy Lenaers
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-21 (2022)
Abstract Background Inherited retinal dystrophies (IRD) and optic neuropathies (ION) are the two major causes world-wide of early visual impairment, frequently leading to legal blindness. These two groups of pathologies are highly heterogeneous and r
Externí odkaz:
https://doaj.org/article/db52d4935dcd4f328ef4486bf0a50f6e
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:
Imane Morjane, Hicham Charoute, Sanaa Ouatou, Lamiae Elkhattabi, Houda Benrahma, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Cardiology Research and Practice, Vol 2020 (2020)
Purpose. Coronary artery diseases (CAD) are clinical cardiovascular events associated with dyslipidemia in common. The interaction between environmental and genetic factors can be responsible for CAD. The present paper aimed to examine the associatio
Externí odkaz:
https://doaj.org/article/4ae80b7ce2d74100ad093ab5b8f8a891
Autor:
Zineb Kindil, Mohamed Amine Senhaji, Amina Bakhchane, Hicham Charoute, Soumia Chihab, Sellama Nadifi, Abdelhamid Barakat
Publikováno v:
BMC Research Notes, Vol 10, Iss 1, Pp 1-6 (2017)
Abstract Objective Xeroderma pigmentosum (XP) is a genetically and clinically heterogeneous disease, associated with an inherited defect in one of eight different genes (XPA to XPG and XPV). In addition to the early onset of the skin manifestations,
Externí odkaz:
https://doaj.org/article/0add5980e7164b9a8a081a7cfa58c7cb
Autor:
Soukaina Essadssi, Al Mehdi Krami, Lamiae Elkhattabi, Zouhair Elkarhat, Ghita Amalou, Houria Abdelghaffar, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Immunology Research, Vol 2019 (2019)
Severe combined immunodeficiency (SCID) is the most severe form of primary immunodeficiency (PID), characterized by fatal opportunistic infections. The ADA gene encodes adenosine deaminase, an enzyme that catalyzes the irreversible deamination of ade
Externí odkaz:
https://doaj.org/article/e85042a2409444ac95a68039de425c73
Autor:
Lamiae Elkhattabi, Imane Morjane, Hicham Charoute, Soumaya Amghar, Hind Bouafi, Zouhair Elkarhat, Rachid Saile, Hassan Rouba, Abdelhamid Barakat
Publikováno v:
Journal of Diabetes Research, Vol 2019 (2019)
Resistin (RETN) is a gene coding for proinflammatory adipokine called resistin secreted by macrophages in humans. Single nucleotide polymorphisms (SNPs) in RETN are linked to obesity and insulin resistance in various populations. Using dbSNP, 78 nons
Externí odkaz:
https://doaj.org/article/41e98608f08d48dd86d2f849c1857432
Autor:
Sara Haydar, Florin Grigorescu, Mădălina Vintilă, Yannick Cogne, Corinne Lautier, Yildiz Tutuncu, Jean Frederic Brun, Jean Marie Robine, Michel Pugeat, Christophe Normand, Patrick Poucheret, Monica Livia Gheorghiu, Carmen Georgescu, Corin Badiu, Nicoleta Băculescu, Eric Renard, Dorina Ylli, Stephanie Badiou, Thibault Sutra, Jean Paul Cristol, Jacques Mercier, Ramon Gomis, Josep Maria Macias, Serghey Litvinov, Elza Khusnutdinova, Catalina Poiana, Renato Pasquali, Davide Lauro, Giorgio Sesti, Sabrina Prudente, Vincenzo Trischitta, Agathocles Tsatsoulis, Sonia Abdelhak, Abdelhamid Barakat, Akila Zenati, Agron Ylli, Ilhan Satman, Timo Kanninen, Yves Rinato, Sasa Missoni
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0214122 (2019)
Branched chain amino acids (BCAA) are essential elements of the human diet, which display increased plasma levels in obesity and regained particular interest as potential biomarkers for development of diabetes. To define determinants of insulin resis
Externí odkaz:
https://doaj.org/article/8c27de3eae724884a16e3faed7dfd99e
Publikováno v:
Case Reports in Medicine, Vol 2018 (2018)
Gullo’s syndrome is a singular physiological phenomenon defined by an abnormal increase in serum pancreatic enzyme levels that may occur in healthy subjects in the absence of pancreatic disorders. During routine health examination in a 54-year-old
Externí odkaz:
https://doaj.org/article/aa78139d5d5244039cbd3ca879bba223
Autor:
Amina Bakhchane, Majida Charif, Amale Bousfiha, Redouane Boulouiz, Halima Nahili, Hassan Rouba, Hicham Charoute, Guy Lenaers, Abdelhamid Barakat
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176516 (2017)
The MYO7A gene encodes a protein belonging to the unconventional myosin super family. Mutations within MYO7A can lead to either non syndromic hearing loss or to the Usher syndrome type 1B (USH1B). Here, we report the results of genetic analyses perfo
Externí odkaz:
https://doaj.org/article/82f455cff15345659651dafe589d5c76