Search Results - Al-Allaf, Faisal Ahmad

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  1. 1
    Combined therapy with oncolytic adenoviruses encoding TRAIL and IL-12 genes markedly suppressed human hepatocellular carcinoma both in vitro and in an orthotopic transplanted mouse model

    Combined therapy with oncolytic adenoviruses encoding TRAIL and IL-12 genes markedly suppressed human hepatocellular carcinoma both in vitro and in an orthotopic transplanted mouse... by El-Shemi, Adel Galal, Ashshi, Ahmad Mohammed, Na, Youjin, Li, Yan, Basalamah, Mohammed, Al-Allaf, Faisal Ahmad, Oh, Eonju, Jung, Bo-Kyeong, Yun, Chae-Ok

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  2. 2
    Erratum to: Combined therapy with oncolytic adenoviruses encoding TRAIL and IL-12 genes markedly suppressed human hepatocellular carcinoma both in vitro and in an orthotopic transplanted mouse model

    Erratum to: Combined therapy with oncolytic adenoviruses encoding TRAIL and IL-12 genes markedly suppressed human hepatocellular carcinoma both in vitro and in an orthotopic transp... by El-Shemi, Adel Galal, Ashshi, Ahmad Mohammed, Na, Youjin, Li, Yan, Basalamah, Mohammed, Al-Allaf, Faisal Ahmad, Oh, Eonju, Jung, Bo-Kyeong, Yun, Chae-Ok

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  3. 3
    Familial Hypercholesterolemia in the Arabian Gulf Region: Clinical results of the Gulf FH Registry

    Familial Hypercholesterolemia in the Arabian Gulf Region: Clinical results of the Gulf FH Registry by Alhabib, Khalid F, Al-Rasadi, Khalid, Almigbal, Turky H, Batais, Mohammed A, Al-Zakwani, Ibrahim, Al-Allaf, Faisal A, Al-Waili, Khalid, Zadjali, Fahad, Alghamdi, Mohammad, Alnouri, Fahad, Awan, Zuhier, Kinsara, Abdulhalim J, AlQudaimi, Ahmed, Almahmeed, Wael, Sabbour, Hani, Traina, Mahmoud, Atallah, Bassam, Al-Jarallah, Mohammed, AlSarraf, Ahmad, AlSayed, Nasreen, Amin, Haitham, Altaradi, Hani

    Published in PloS one
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  4. 4
    Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs33)) causing familial hypercholesterolemia in Saudi Arab homozygous children

    Identification of a recurrent frameshift mutation at the LDLR exon 14 (c.2027delG, p.(G676Afs33)) causing familial hypercholesterolemia in Saudi Arab homozygous children by Al-Allaf, Faisal A., Alashwal, Abdullah, Abduljaleel, Zainularifeen, Taher, Mohiuddin M., Siddiqui, Shahid S., Bouazzaoui, Abdellatif, Abalkhail, Hala, Aun, Rakan, Al-Allaf, Ahmad F., AbuMansour, Iman, Azhar, Zohor, Ba-Hammam, Faisal A., Khan, Wajahatullah, Athar, Mohammad

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  5. 5
    Neuromyelitis Optica Spectrum Disorder and Autoimmune Rheumatological Diseases: A Report of Two Cases and Literature Review

    Neuromyelitis Optica Spectrum Disorder and Autoimmune Rheumatological Diseases: A Report of Two Cases and Literature Review by Faisal, Mohannad, Matarneh, Ahmad, Alshahwani, Israa, Al-Allaf, Omar, Al-Allaf, Abdul-wahab

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  6. 6
    4. Identification of a novel nonsense variant C.1332DUP, P. (D445) in the LDLR gene that causes familial hypercholesterolemia

    4. Identification of a novel nonsense variant C.1332DUP, P. (D445) in the LDLR gene that causes familial hypercholesterolemia by Al-Allaf, Faisal, Athar, Mohammad, Abduljaleel, Zainularifeen, Bouazzaoui, Abdellatif, Mohiuddin, Taher, Own, Rakan, Al-Allaf, Ahmad, Abumansour, Iman, Azhar, Zohor, Ba-Hammam, Faisal, Abalkhail, Halah, Alashwal, Abdullah

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  7. 7
    Identification of a novel nonsense variant c.1332dup, p.(D445) in the LDLR gene that causes familial hypercholesterolemia

    Identification of a novel nonsense variant c.1332dup, p.(D445) in the LDLR gene that causes familial hypercholesterolemia by Al-Allaf, Faisal A, Athar, Mohammad, Abduljaleel, Zainularifeen, Bouazzaoui, Abdellatif, Taher, Mohiuddin M, Own, Rakan, Al-Allaf, Ahmad F, AbuMansour, Iman, Azhar, Zohor, Ba-hammam, Faisal A, Abalkhail, Hala, Alashwal, Abdullah

    Published in Human genome variation
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  8. 8
    1. Founder mutation identified in the LDLR gene causing familial hypercholesterolemia associated with increased risk of coronary heart disease

    1. Founder mutation identified in the LDLR gene causing familial hypercholesterolemia associated with increased risk of coronary heart disease by Al-Allaf, Faisal, Athar, Mohammad, Alashwal, Abdullah, Abduljaleel, Zainularifeen, Mohiuddin, Taher, Bouazzaoui, Abdellatif, Abalkhail, Halah, Own, Rakan, Al-Allaf, Ahmad, Abumansour, Iman, Azhar, Zohor, Alnouri, Fahad, Toonsi, Mawaddah

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  9. 9
    Neuromyelitis Optica Spectrum Disorder and Autoimmune Rheumatological Diseases: A Report of Two Cases and Literature Review

    Neuromyelitis Optica Spectrum Disorder and Autoimmune Rheumatological Diseases: A Report of Two Cases and Literature Review by Faisal, Mohannad, Matarneh, Ahmad, Alshahwani, Israa, Al-Allaf, Omar, Al-Allaf, Abdul-Wahab

    Published in Cureus
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