Search Results - "Nouf, Alballa"

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.

“…BACKGROUND: The introduction of biological treatments has revolutionized the management of moderate-to-severe psoriasis. Multiple clinical trials have…”
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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

“…Background/Aim: Instrument-based image-enhanced endoscopy (IEE) is of benefit in detecting and characterizing lesions during colonoscopy. We aimed to study the…”
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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

“…Narcolepsy type 1 (NT1) is thought to have a chronic persistent course. This study aimed to assess the natural course of cataplexy in patients with NT1 at 2,…”
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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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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.

“…Almeneessier AS, Alballa NS, Alsalman BH, Aleissi S, OlaishAH, BaHammam AS. Nat Sci Sleep. 2019;11:231- 239. The authors have advised affiliation 1 on page 231…”
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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

“…Abstract LEOPARD syndrome (LS) is a rare autosomal dominant disorder that is characterized by multiple lentigines and various congenital anomalies. The…”
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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

“…Adalimumab is a human monoclonal antibody which targets tumor necrosis factor (TNF)-alpha. It is produced by recombinant DNA technology, using a mammalian cell…”
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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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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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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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