يعرض 1 - 11 نتائج من 11 نتيجة بحث عن '"Almatrafi, Ahmed"', وقت الاستعلام: 0.38s تنقيح النتائج
  1. 1
    Academic Journal
    Precautions Compliance Among Respiratory Therapist, Radiology, Laboratory, Pharmacist And Nursing Teams, During COVID-19 Pandemic

    المؤلفون: Kumil Habib Mohammed Al Jumaia , Samar Jaber Almatrafi , Ahmed Ali Wadani , Amal Hussain Hamed Alalasi , Shurooq Najeeb Aladwani , Faisal Ahmed Almami , Maha Hussein Shararah , Helal Abdulmatlub Alhajuj, Maha Abdulrahman Alofi , Abdul Karim Abdullah Alhazmi , Emad Abdulkhaliq Huwaykim , Ahmed Khalaf Bahdal Al-Shammari, Fahd Bostan Alrweli , Muhammad Khamis Fahad Alwasmi , Hassan Ali Salman Al Gazwi , Ali Abdullah Alghafli , Hussain Salman Alhassan

    المصدر: Journal of Positive Psychology and Wellbeing; Vol. 6 No. 3 (2022): Journal of Positive Psychology and Wellbeing; 734-738 ; 2587-0130

    وصف الملف: application/pdf

    Relation: https://journalppw.com/index.php/jppw/article/view/18383/11514; https://journalppw.com/index.php/jppw/article/view/18383

    الاتاحة: https://journalppw.com/index.php/jppw/article/view/18383

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  2. 2
    Dissertation/ Thesis
    Identification and functional characterisation of potential novel cancer-testis genes in human cancer cells

    المؤلفون: Almatrafi, Ahmed Mubrik

    مصطلحات موضوعية: 570

    الاتاحة: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665628

    View record in Networked Digital Library of Theses & Dissertations

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  3. 3
    Academic Journal
    Exome Sequencing to Identify Novel Variants Associated with Secondary Amenorrhea and Premature Ovarian Insufficiency (POI) in Saudi Women.

    المؤلفون: Almatrafi, Ahmed M., Hibshi, Ali M., Basit, Sulman

    المصدر: Biomedicines; Apr2024, Vol. 12 Issue 4, p785, 11p

    مصطلحات موضوعية: PREMATURE ovarian failure, SAUDI Arabians, AMENORRHEA, GONADAL diseases, FEMALE infertility, GENETIC disorders

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  4. 4
    Academic Journal
    Investigating the pathogenic SNPs in BLM helicase and their biological consequences by computational approach

    المؤلفون: Alzahrani, Faisal A., Ahmed, Firoz, Sharma, Monika, Rehan, Mohd, Mahfuz, Maryam, Baeshen, Mohammed N., Hawsawi, Yousef, Almatrafi, Ahmed, Alsagaby, Suliman Abdallah, Kamal, Mohammad Azhar, Warsi, Mohiuddin Khan, Choudhry, Hani, Jamal, Mohammad Sarwar

    المصدر: Scientific Reports ; volume 10, issue 1 ; ISSN 2045-2322

    الاتاحة: http://dx.doi.org/10.1038/s41598-020-69033-8
    https://www.nature.com/articles/s41598-020-69033-8.pdf
    https://www.nature.com/articles/s41598-020-69033-8

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  5. 5
    Academic Journal
    KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption

    المؤلفون: Assiry, Ali A., Albalawi, Alia M., Zafar, Muhammad S., Khan, Siraj D., Ullah, Anhar, Almatrafi, Ahmed, Ramzan, Khushnooda, Basit, Sulman

    المصدر: Scientific Reports ; volume 9, issue 1 ; ISSN 2045-2322

    الاتاحة: http://dx.doi.org/10.1038/s41598-019-52935-7
    https://www.nature.com/articles/s41598-019-52935-7.pdf
    https://www.nature.com/articles/s41598-019-52935-7

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  6. 6
    Academic Journal
    Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency.

    المؤلفون: Almatrafi, Ahmed M., Hibshi, Ali M., Basit, Sulman

    المصدر: Medicina (1010660X); Mar2023, Vol. 59 Issue 3, p474, 10p

    مصطلحات موضوعية: HORMONE deficiencies, PITUITARY hormones, STEPFAMILIES, PITUITARY dwarfism, PITUITARY gland, SHORT stature

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  7. 7
    Academic Journal
    Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family

    المؤلفون: Hashmi, Jamil A., Fadhli, Fatima, Almatrafi, Ahmed, Afzal, Sibtain, Ramzan, Khushnooda, Thiele, Holger, Nuernberg, Peter, Basit, Sulman

    مصطلحات موضوعية: ddc:no

    Relation: Hashmi, Jamil A., Fadhli, Fatima, Almatrafi, Ahmed, Afzal, Sibtain, Ramzan, Khushnooda, Thiele, Holger orcid:0000-0002-0169-998X , Nuernberg, Peter and Basit, Sulman orcid:0000-0003-4294-6825 (2020). Homozygosity mapping and whole exome sequencing provide exact diagnosis of Cohen syndrome in a Saudi family. Brain Dev., 42 (8). S. 587 - 594. AMSTERDAM: ELSEVIER. ISSN 1872-7131

    الاتاحة: https://kups.ub.uni-koeln.de/32222/

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  8. 8
    Academic Journal
    Clinical and Molecular Genetic Characterization of Waardenburg Syndrome.

    المؤلفون: Almatrafi, Ahmed M.1 a.m.almatrafi@gmail.com

    المصدر: Egyptian Academic Journal of Biological Sciences, C Physiology & Molecular Biology. Jan2022, Vol. 14 Issue 1, p277-292. 16p.

    مصطلحات موضوعية: *HEARING disorders, *GENETIC disorders, *IRIS (Eye), *SYNDROMES, *SOX transcription factors, *FAMILIAL spastic paraplegia, *HUMAN skin color


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  9. 9
    Academic Journal
    Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa

    المؤلفون: Hashmi, Jamil Amjad, Albarry, Maan Abdullah, Almatrafi, Ahmed M., Albalawi, Alia M., Mahmood, Amer, Basit, Sulman

    المصدر: Congenital Anomalies ; volume 58, issue 1, page 10-15 ; ISSN 0914-3505 1741-4520

    الاتاحة: http://dx.doi.org/10.1111/cga.12225
    https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fcga.12225
    https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12225

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  10. 10
    Academic Journal
    Whole exome sequencing identified a novel single base pair insertion mutation in the EYS gene in a six generation family with retinitis pigmentosa.

    المؤلفون: Hashmi, Jamil Amjad, Albarry, Maan Abdullah, Almatrafi, Ahmed M., Albalawi, Alia M., Mahmood, Amer, Basit, Sulman

    المصدر: Congenital Anomalies; Jan2018, Vol. 58 Issue 1, p10-15, 6p


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  11. 11
    Dissertation/ Thesis
    Identification and functional characterisation of potential novel cancer-testis genes in human cancer cells

    المؤلفون: Almatrafi, Ahmed

    المصدر: synchronisedUnifiedStudentThesis

    Relation: https://research.bangor.ac.uk/portal/en/theses/identification-and-functional-characterisation-of-potential-novel-cancertestis-genes-in-human-cancer-cells(a368f7ee-0b71-47d3-979c-4233f0d256c8).html

    الاتاحة: https://research.bangor.ac.uk/portal/en/theses/identification-and-functional-characterisation-of-potential-novel-cancertestis-genes-in-human-cancer-cells(a368f7ee-0b71-47d3-979c-4233f0d256c8).html

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