Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Houssam Boulenouar"'
Autor:
Houssam Boulenouar, Fatima-Zohra Moghtit, Amine Mellouk, Khaldia Belhadj-djellou, Hadjira Ouhaibi Djelloul, Mohamed Benmansour, Sarah Lardjam Hetrai, Faouzia Zemani Fodil, Nadhira Saidi Mehtar, Sounnia Mediene Benchekor
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 1 (2024)
Résumé La Dystrophie Musculaire de Duchenne (DMD) est la plus sévère et la plus fréquente des dystrophies musculaires, atteignant une naissance mâle sur 5000 dans la population mondiale. Elle se caractérise par une dégénérescence musculai
Externí odkaz:
https://doaj.org/article/6ded61d88476488aa36b2867249840ac
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-12 (2022)
Abstract Background Schizophrenia is a psychotic disorder that impacts around 0.5% to 1.2% of the world's population. It has been well established that heredity plays an essential role in the causation of schizophrenia, with genetic heritability of u
Externí odkaz:
https://doaj.org/article/62d952c74ceb4e7393545ed34114c503
Autor:
Houssam BOULENOUAR, Fatima-Zohra MOGHTIT, Amine MELLOUK, Khaldia BENLHADJ-DJELLOUL, Hadjira OUHAIBI DJELLOULI, Mohamed BENMANSOUR, Sarah LARJAM HETRAF, Faouzia ZEMANI FODIL, Nadhira SAIDI MEHTAR, Sounnia MEDIENE BENCHEKOR
Publikováno v:
Journal de la Faculté de Médecine d'Oran, Vol 1, Iss 1 (2022)
Duchenne Muscular Dystrophy (DMD) is the most common and severe form of muscular dystrophy, reaching one out of every 5000 male births in the world population. It is characterized by progressive muscular degeneration from a young age and leads to ser
Externí odkaz:
https://doaj.org/article/6a96e06cad3a48e88d5f857e2594e8aa
Autor:
Houssam Boulenouar, Sounnia Mediene Benchekor, Hadjira Ouhaibi Djellouli, Sarah Aicha Larjam Hetraf, Leila Houti, Imane Hammani-Medjaoui
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
Abstract Background Metabolic syndrome (MetS) represents a combination of at least three primary metabolic abnormalities among which obesity, hyperglycemia, dyslipidemia, and high blood pressure (HBP); once combined, they increase the cardiovascular
Externí odkaz:
https://doaj.org/article/d9a9acf703f04c3e96f1337ec7b73275
Autor:
Mohammed Nassim Boukli, Yassamina Tabet Zatla, Meriem Saker, Zoubeyr Abbou, Amina Youcef, Houssam Boulenouar, Hakima Fekir, Khawla Khaldi, Nawel Brikci-Nigassa, Ali Lounici, Kaouel Meguenni
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Introduction:adherence to drugs is critical for achieving the best clinical results in the treatment of chronic diseases. Adherence to chronic drugs might be influenced by beliefs about medications and other variables. The goal of this study was to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0527719ac52aafc0ee4d25409ce4f292
https://pubmed.ncbi.nlm.nih.gov/35573427
https://pubmed.ncbi.nlm.nih.gov/35573427
Autor:
Youssouf Kachekouche, Majda Dali-Sahi, Hamza N.M. Boudia, Nouria Dennouni-Medjati, Houssam Boulenouar
Publikováno v:
The Open Hypertension Journal. 11:6-10
Background: The existing literature reports results on the association of lipid parameters with the level of insulin secretion and the risk of arterial hypertension. Objective: This study evaluated the role of the insulin dosage and lipid fractions i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::167eb372b0a1c9b407c60f88340fb3bf
https://doi.org/10.2174/1876526201911010006
https://doi.org/10.2174/1876526201911010006
Autor:
Magellan Guewo-Fokeng, Arnaud D. Kaze, Houssam Boulenouar, Ambroise Wonkam, Jean Jacques Noubiap, Edith Pascale Mofo Mato
Publikováno v:
OMICS: A Journal of Integrative Biology. 22:749-758
Identification of genetic/genomic factors contributing to dyslipidemia is of great interest to prevention and reduction of the onset and burden of cardiovascular diseases in Africa. This systematic review summarizes available data on genetic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf2ab4904858acbadff22e855953d341
https://doi.org/10.1089/omi.2018.0158
https://doi.org/10.1089/omi.2018.0158
Autor:
Majda Dali-Sahi, Nouria Dennouni-Medjati, Yasmine Benslama, Houssam Boulenouar, Yahia Harek, Fatima Zohra Meziane, Youssouf Kachekouche
Publikováno v:
Diabetesmetabolic syndrome. 14(6)
Background and aims Type 1 diabetes (T1D) is a multifactorial autoimmune disease that combines genetics and environmental factors. The aim of this study is to determine the environmental risk factors and to investigate how virals infections are risks
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::713ff6ad4bc1501f5baa2d910985db41
https://pubmed.ncbi.nlm.nih.gov/32947109
https://pubmed.ncbi.nlm.nih.gov/32947109
Autor:
Sounnia Mediene Benchekor, Hadjira Ouhaibi Djellouli, Imane Hammani-Medjaoui, Leila Houti, Sarah Aicha Larjam Hetraf, Houssam Boulenouar
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-8 (2019)
Background Metabolic syndrome (MetS) represents a combination of at least three primary metabolic abnormalities among which obesity, hyperglycemia, dyslipidemia, and high blood pressure (HBP); once combined, they increase the cardiovascular risk sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9fc477a16cf45c951adc4b1c5f75bd2
https://doi.org/10.1186/s43042-019-0013-6
https://doi.org/10.1186/s43042-019-0013-6
Autor:
Sounnia Mediene-Benchekor, Aline Meirhaeghe, I. Hamani-Medjaoui, Hadjira Ouhaibi-Djellouli, Philippe Amouyel, Houssam Boulenouar, Djabaria Naïma Meroufel, Leila Houti, Sarah Aïcha Lardjam-Hetraf, Xavier Hermant, Benjamin Grenier-Boley, Louisa Goumidi, Nadhira Saidi-Mehtar
Publikováno v:
Gene. 567:159-163
article i nfo Background: In European populations, the NPPB rs198389 single nucleotide polymorphism (SNP) is associated with a reduced risk of type 2 diabetes mellitus (T2DM). We investigated the putative associations between NPPB rs198389, the T2DM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b8759b04dfc31eb1a644d7ecb89ee67
https://doi.org/10.1016/j.gene.2015.04.073
https://doi.org/10.1016/j.gene.2015.04.073