Search Results - Alballa, Nouf S.

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  1. 1
    Monitoring the effect of TNF-alpha inhibitors on laboratory parameters and adverse effects in different diseases: a retrospective, single-center study

    Monitoring the effect of TNF-alpha inhibitors on laboratory parameters and adverse effects in different diseases: a retrospective, single-center study by Madani, Abdulaziz N., Al-Saif, Fahad M., Alzamil, Lama R., Almazroua, Aljohara M., Alfurayh, Nuha A., Aldokhayel, Sara D., Almuhaideb, Qais A., Alballa, Nouf S., Daham, Nujud A., Alkharashi, Abdulrahman A.

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  2. 2
    Use of image-enhanced endoscopy in the characterization of colorectal polyps: Still some ways to go

    Use of image-enhanced endoscopy in the characterization of colorectal polyps: Still some ways to go by Alharbi, Othman, Alballa, Nouf, AlRajeh, Areej, Alturki, Lulwah, Alfuraih, Ibrahim, Jamalaldeen, Mouhab, Almadi, Majid

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  3. 3
    A 10-Year Longitudinal Observational Study Of Cataplexy In A Cohort Of Narcolepsy Type 1 Patients

    A 10-Year Longitudinal Observational Study Of Cataplexy In A Cohort Of Narcolepsy Type 1 Patients by Almeneessier, Aljohara S, Alballa, Nouf S, Alsalman, Budoor H, Aleissi, Salih, Olaish, Awad H, BaHammam, Ahmed S

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  4. 4
    A 10-Year Longitudinal Observational Study of Cataplexy in a Cohort of Narcolepsy Type 1 Patients [Corrigendum]

    A 10-Year Longitudinal Observational Study of Cataplexy in a Cohort of Narcolepsy Type 1 Patients [Corrigendum] by Almeneessier, Aljohara S., Alballa, Nouf S., Alsalman, Budoor, Alessie, Salih, Olaish, Awad H., BaHammam, Ahmed S.

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  5. 5
    A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

    A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family by Aldokhayel, Sara, Nouf, Alballa, Khalid, Aleedan, Faisal, Alsaif, Maram, Alotaibi, Ahmed, Alhumidi, Fahad, Alsaif

    Published in JAAD Case Reports
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  6. 6
    LEOPARD Syndrome with PTPN11 Gene Mutation in Three Family Members Presenting with Different Phenotypes

    LEOPARD Syndrome with PTPN11 Gene Mutation in Three Family Members Presenting with Different Phenotypes by Alfurayh, Nuha, Alsaif, Fahad, Alballa, Nouf, Zeitouni, Leena, Ramzan, Khushnooda, Imtiaz, Faiqa, Alakeel, Abdullah

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  7. 7
    Hodgkin's lymphoma in a patient on adalimumab treatment for psoriasis

    Hodgkin's lymphoma in a patient on adalimumab treatment for psoriasis by Alballa, Nouf, Alyousef, Alanoud, Alamari, Albatool, Alhumidi, Ahmed Abdullah, Zayed, Mohammed Ayesh, Zeitouni, Leena, Alsaif, Fahad Mohammed

    Published in AME case reports
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  8. 8
    A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family

    A novel mutation in ABCB6 associated with dyschromatosis universalis hereditaria in a Saudi family by Aldokhayel, Sara, Nouf, Alballa, Khalid, Aleedan, Faisal, Alsaif, Maram, Alotaibi, Ahmed, Alhumidi, Fahad, Alsaif

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  9. 9
    LEOPARD Syndrome with PTPN11 Gene Mutation in Three Family Members Presenting with Different Phenotypes

    LEOPARD Syndrome with PTPN11 Gene Mutation in Three Family Members Presenting with Different Phenotypes by Alfurayh, Nuha, Alsaif, Fahad, Alballa, Nouf, Zeitouni, Leena, Ramzan, Khushnooda, Imtiaz, Faiqa, Alakeel, Abdullah

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  10. 10
    Hodgkin's lymphoma in a patient on adalimumab treatment for psoriasis

    Hodgkin's lymphoma in a patient on adalimumab treatment for psoriasis by Alballa, Nouf, Alyousef, Alanoud, Alamari, Albatool, Alhumidi, Ahmed Abdullah, Zayed, Mohammed Ayesh, Zeitouni, Leena, Alsaif, Fahad Mohammed

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