Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Fahad M Alsaif"'
Publikováno v:
Indian Journal of Dermatology, Vol 67, Iss 1, Pp 1-4 (2022)
Background: The use of tumor necrosis factor-α inhibitors (TNFi) has been associated with an increased risk latent tuberculosis (TB) reactivation. The role of TB screening assays in monitoring patients during TNFi therapy remains uncertain. Spontane
Externí odkaz:
https://doaj.org/article/a9b47eeca10841d9a120634459d7c37b
Autor:
Norah A. AlSubait, MD, Hessah F. BinJadeed, MD, Muneera R. AlSaleh, MD, Fawziyah S. AlFaifi, MD, Fahad M. AlSaif, PhD, Mariah A. Arafah, MD
Publikováno v:
JAAD Case Reports, Vol 14, Iss , Pp 116-119 (2021)
Externí odkaz:
https://doaj.org/article/8f4a1fab91f64385826919774a5daccd
Autor:
Monira Abdullah Alnasser, Nour Marwan AlKhawajah, Nada Ghazi AlQadri, Asem Mustafa Shadid, Fahad M. Alsaif
Publikováno v:
Case Reports in Oncology, Vol 14, Iss 1, Pp 256-261 (2021)
Cutaneous T-cell lymphoma (CTCL) describes a group of lymphoproliferative disorders characterized by localization of neoplastic T lymphocytes to the skin. Mycosis fungoides (MF) represents the most common type of CTCL and accounts for ∼60% of all p
Externí odkaz:
https://doaj.org/article/c73ade423f0e487a80a300015ced44c7
Autor:
Hanan H. Alsalman, MD, Rama A. Alhallaf, MD, Abdulrahman Alhuzaimi, MD, Ahmed A. Alhumidi, MD, Abdullah Alakeel, MD, Fahad M. Alsaif, MD
Publikováno v:
JAAD Case Reports, Vol 6, Iss 10, Pp 1116-1118 (2020)
Externí odkaz:
https://doaj.org/article/4e3162f074fb4c02a60f8e9776dfeed1
Publikováno v:
Case Reports in Oncology, Vol 12, Iss 2, Pp 411-417 (2019)
Papillon–Lefèvre syndrome (PLS) is a rare autosomal recessive disorder characterized by palmoplantar keratoderma and early-onset periodontitis. It was first described by Papillon and Lefèvre in 1924. PLS is caused by mutations in the cathepsin-C
Externí odkaz:
https://doaj.org/article/48657250b7b444d19049e2a1634998e9
Autor:
Monira Abdullah Alnasser, Nour Marwan AlKhawajah, Nada Al-Qadri, Asem Mustafa Shadid, Fahad M. Alsaif
Publikováno v:
Kompass Dermatologie. 10:45-47
Unter dem Begriff der kutanen T-Zell-Lymphome (CTCL) wird eine Gruppe lymphoproliferativer Erkrankungen zusammengefasst, die durch Lokalisation neoplastischer T-Lymphozyten in der Haut gekennzeichnet sind. Die Mycosis fungoides (MF) ist die häufigst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42dc37c1c6529fdebf0109fac407fe5
https://doi.org/10.1159/000521432
https://doi.org/10.1159/000521432
Autor:
Ghadah F. Alotaibi, Hanan H. Alsalman, Rama A. Alhallaf, Rayan A. Ahmad, Hashem A. Alshareef, Jumanah Meshari Muammar, Fahad M. Alsaif, Felwah F. Alotaibi, Mohamed F. Balaha, Nehad J. Ahmed, El-Sayed Khafagy, Hadil F. Alotaibi, Rahaf Alshammari, Sarah Fatani
Publikováno v:
Healthcare
Volume 11
Issue 3
Pages: 427
Volume 11
Issue 3
Pages: 427
Contact dermatitis is a chronic inflammatory skin disorder with a highly variable prevalence worldwide. Smoking plays a crucial role in mediating inflammatory skin conditions such as contact dermatitis. The present study aimed to investigate the asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c97bd561c270da44798ddf6fa97e2782
https://doi.org/10.3390/healthcare11030427
https://doi.org/10.3390/healthcare11030427
Autor:
A Mesut Erzurumluoglu, Muslim M Alsaadi, Santiago Rodriguez, Tahani S Alotaibi, Philip A I Guthrie, Sian Lewis, Aasiya Ginwalla, Tom R Gaunt, Khalid K Alharbi, Fahad M Alsaif, Basma M Alsaadi, Ian N M Day
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0121351 (2015)
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early onset periodontitis and palmoplantar hyperkeratosis. A previously reported missense mutation in the CTSC gene (NM_001814.4:c.899G>A:p.(G300D)) was identi
Externí odkaz:
https://doaj.org/article/4e81a7a0ca9541c1a339d1172f47cfc5
Publikováno v:
Biologics : Targets & Therapy
Atopic dermatitis (eczema) is a common chronic disease that is described as severe itching associated with recurrent eczematous lesions. In 2017 the US Food and Drug Administration approved dupilumab for treatment of adults with moderate to severe at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ff7b1543b348f88265d5dc2b6d82111
https://pubmed.ncbi.nlm.nih.gov/31190731
https://pubmed.ncbi.nlm.nih.gov/31190731
Autor:
A Mesut, Erzurumluoglu, Muslim M, Alsaadi, Santiago, Rodriguez, Tahani S, Alotaibi, Philip A I, Guthrie, Sian, Lewis, Aasiya, Ginwalla, Tom R, Gaunt, Khalid K, Alharbi, Fahad M, Alsaif, Basma M, Alsaadi, Ian N M, Day
Publikováno v:
PLoS ONE
Papillon-Lefevre syndrome (PLS) is an autosomal recessive disorder characterised by severe early onset periodontitis and palmoplantar hyperkeratosis. A previously reported missense mutation in the CTSC gene (NM_001814.4:c.899G>A:p.(G300D)) was identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4b5fe40647a1fd45d88980720c102c8e
https://pubmed.ncbi.nlm.nih.gov/25799584
https://pubmed.ncbi.nlm.nih.gov/25799584