يعرض 1 - 10 نتائج من 622 نتيجة بحث عن '"Bouhouche A"', وقت الاستعلام: 2.14s تنقيح النتائج
  1. 1
    مؤتمر
    Low Frequency Noise Study of X-ray Irradiated Si/SiGe:C BiCMOS Technology Bipolar Transistors

    المؤلفون: Belie, A. Adebabay, El Beyrouthy, J., Pascal, F., Boch, J., Maraine, T., Hoffmann, A., Bouhouche, M., Sagnes, B., Haendler, S., Chevalier, P., Gloria, D.

    المصدر: 2023 International Conference on Noise and Fluctuations (ICNF) Noise and Fluctuations (ICNF), 2023 International Conference on. :1-4 Oct, 2023

    Relation: 2023 International Conference on Noise and Fluctuations (ICNF)

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  2. 2
    دورية أكاديمية
    Association of Renin–Angiotensin Pathway Gene Polymorphisms with COVID-19 Susceptibility and Severity in Moroccans: A Case–Control Study

    المؤلفون: El Yousfi, Fatima-Zahra, El Hilali, SamiaAff2, Aff3, Belayachi, JihaneAff2, Aff4, Ennibi, Khalid, Razine, RachidAff2, Aff3, Abouqal, RedouaneAff2, Aff3, Bouhouche, AhmedAff1, Aff6, IDs10528024108136_cor7

    المصدر: Biochemical Genetics. :1-19

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  3. 3
    دورية أكاديمية
    Sustainable Corrosion Inhibition: Maceration of Green Tea Waste for Improved Performance—An Electrochemical and Theoretical Exploration

    المؤلفون: Bouhouche, Ichraq, Bouiti, Khalid, Chraka, Anas, El Hamil, Abdelilah, Labjar, NajouaAff1, IDs4073502400847z_cor5, Damour, HoudaAff3, Aff4, Dahrouch, Abdelouahed, Nasrellah, Hamid, Benmessaoud, Mohammed, El Hajjaji, Souad

    المصدر: Journal of Bio- and Tribo-Corrosion. 10(3)

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  4. 4
    دورية أكاديمية
    Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection

    المؤلفون: Yousfi, Fatima Zahra El, Haroun, Abbas ErmiloAff2, Aff3, Nebhani, Chaimae, Belayachi, JihaneAff2, Aff4, Askander, Omar, Fahime, Elmostafa El, Fares, Hakima, Ennibi, Khalid, Abouqal, RedouaneAff2, Aff3, Razine, RachidAff2, Aff3, Bouhouche, AhmedAff1, Aff9, IDs0070502406038y_cor11

    المصدر: Archives of Virology: Official Journal of the Virology Division of the International Union of Microbiological Societies. 169(5)

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  5. 5
    دورية أكاديمية
    Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients

    المؤلفون: Smaili, Imane, Tibar, Houyam, Rahmani, MouniaAff1, Aff3, Machkour, Najlaa, Razine, Rachid, Darai, Hajar Naciri, Bouslam, Naima, Benomar, AliAff1, Aff2, Regragui, WafaAff1, Aff2, Bouhouche, AhmedAff1, Aff2, IDs12031023021289_cor10

    المصدر: Journal of Molecular Neuroscience. 73(6):391-402

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  6. 6
    كتاب إلكتروني
    A New Collective Simulated Annealing with Adapted Objective Function for Web Service Selection

    المؤلفون: Bouhouche, AbdelouahidAff14, Benmohammed, MohamedAff15

    المساهمون: Kacprzyk, Janusz, Series EditorAff1, Gomide, Fernando, Advisory EditorAff2, Kaynak, Okyay, Advisory EditorAff3, Liu, Derong, Advisory EditorAff4, Pedrycz, Witold, Advisory EditorAff5, Polycarpou, Marios M., Advisory EditorAff6, Rudas, Imre J., Advisory EditorAff7, Wang, Jun, Advisory EditorAff8, Laouar, Mohamed Ridda, editorAff9, Balas, Valentina Emilia, editorAff10, Lejdel, Brahim, editorAff11, Eom, Sean, editorAff12, Boudia, Mohamed Amine, editorAff13

    المصدر: 12th International Conference on Information Systems and Advanced Technologies “ICISAT 2022” : Intelligent Information, Data Science and Decision Support System. 624:8-17

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  7. 7
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  8. 8
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

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  9. 9
    دورية أكاديمية
    An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3

    المؤلفون: Bouhouche Ahmed, Benomar Ali, Errguig Leila, Lachhab Lamiae, Bouslam Naima, Aasfara Jehanne, Sefiani Sanaa, Chabraoui Layachi, El Fahime Elmostafa, El Quessar Abdeljalil, Jiddane Mohamed, Yahyaoui Mohamed

    المصدر: BMC Medical Genetics, Vol 13, Iss 1, p 18 (2012)

    مصطلحات موضوعية: Internal medicine, RC31-1245, Genetics, QH426-470

    وصف الملف: electronic resource

    Relation: http://www.biomedcentral.com/1471-2350/13/18; https://doaj.org/toc/1471-2350

    URL الوصول: https://doaj.org/article/2e7a896a67fe4b86bd07ff2c4c4f5bab

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  10. 10
    دورية أكاديمية
    Homozygous mutation in the ADH6 gene, involved in alcohol metabolism, associated with a multisystem disorder, analogous to the fetal alcohol syndrome

    المؤلفون: Ahmed Bouhouche, Omar Askander, Hicham Charoute, Mouna Sabib, Abdeljalil El Quessar, Amine El Hassani, Naima Erreimi

    المصدر: Journal of Clinical and Translational Endocrinology Case Reports, Vol 28, Iss , Pp 100144- (2023)

    مصطلحات موضوعية: Whole exome sequencing, Novel mutation, ADH6, Alcohol metabolism, Genetic disorder, Diseases of the endocrine glands. Clinical endocrinology, RC648-665

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S2214624523000060; https://doaj.org/toc/2214-6245

    URL الوصول: https://doaj.org/article/128eb9956a514944882c508dfe0c2a06

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