Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Pawinee, Rerknimitr"'
Autor:
Pawinee Rerknimitr
Publikováno v:
Annals, Academy of Medicine, Singapore, Vol 53, Iss 11, Pp 641-643 (2024)
Atopic dermatitis (AD) is a chronic, relapsing inflammatory skin condition characterised by dysregulated type 2 immune responses, skin barrier dysfunction and intense pruritus (itching). The disease burden of AD is substantial, affecting at least 171
Externí odkaz:
https://doaj.org/article/0e4ad21b52df47f38f26992728ec0693
Autor:
Gaidganok Sornsamdang, Patompong Satapornpong, Pimonpan Jinda, Thawinee Jantararoungtong, Napatrupron Koomdee, Therdpong Tempark, Jettanong Klaewsongkram, Ticha Rerkpattanapipat, Pawinee Rerknimitr, Papapit Tuchinda, Leena Chularojanamontri, Napatra Tovanabutra, Kumutnart Chanprapaph, Wareeporn Disphanurat, Panlop Chakkavittumrong, Chutika Srisuttiyakorn, Yuttana Srinoulprasert, Shobana John, Mohitosh Biswas, Chonlaphat Sukasem
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Allopurinol has been causing substantial morbidity and mortality particularly in Asian population by producing cutaneous adverse drug reactions (cADRs). Nonetheless, there are no data describing whether other genetics are a valid
Externí odkaz:
https://doaj.org/article/29c4a501e9b74a8faf9ce920ccb509c1
Publikováno v:
JAAD Case Reports, Vol 48, Iss , Pp 128-130 (2024)
Externí odkaz:
https://doaj.org/article/061e8ac8d1ef41efa0eb38045e5ab4b4
Autor:
Donlaporn Chuenwipasakul, Chanudda Washrawirul, Rawiphan Panpruk, Jade Wititsuwannakul, Kridipop Charoenchaipiyakul, Supranee Buranapraditkun, Vilavun Puangsricharern, Jettanong Klaewsongkram, Pawinee Rerknimitr
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe dermatological emergencies. The role of cytokines and chemokines in the pathogenesis, progression of the disease, and histopathologic features is not fully eluc
Externí odkaz:
https://doaj.org/article/6c5bb21fb0694e878130f6bb47a514ac
Autor:
Patapong Towiwat, Suppachai Lawanaskol, Wichittra Tassaneeyakul, Chonlaphat Sukasem, Niwat Saksit, Nontaya Nakkam, Duangkamon Poolpun, Ticha Rerkpattanapipat, Jettanong Klaewsongkram, Pawinee Rerknimitr, Worawit Louthrenoo
Publikováno v:
Journal of Clinical Rheumatology and Immunology, Vol 24, Iss supp01, Pp 151-152 (2024)
Background The side effect of allopurinol was severe allopurinol hypersensitivity (SAH). There are two major causes including genetic risk factor, HLA-B*58:01 and non-genetic risk factors including female, old age, renal impairment, inadequate starti
Externí odkaz:
https://doaj.org/article/dfbeffa3510546848dae1414dc4322f0
Autor:
Rawiphan Panpruk, Vilavun Puangsricharern, Jettanong Klaewsongkram, Pawinee Rerknimitr, Thanachaporn Kittipibul, Yuda Chongpison, Supranee Buranapraditkun
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe cutaneous adverse drug reactions with high mortality rates. Its sequelae, such as blindness, persist even after recovery. Patients with SJS/TEN should be accurate
Externí odkaz:
https://doaj.org/article/c56202b9ffee40f18ef1364492fba47e
Publikováno v:
JAAD Case Reports, Vol 18, Iss , Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/79f08a551ebe4ab9afd5e64027d21dfd
Autor:
Therdpong Tempark, Shobana John, Pawinee Rerknimitr, Patompong Satapornpong, Chonlaphat Sukasem
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
SCARs are rare and life-threatening hypersensitivity reactions. In general, the increased duration of hospital stays and the associated cost burden are common issues, and in the worst-case scenario, they can result in mortality. SCARs are delayed T c
Externí odkaz:
https://doaj.org/article/fdb8c01806a1478c9aadde281a15ff29
Autor:
Chankiat Songsantiphap, Jirat Suwanwatana, Chupong Ittiwut, Pravit Asawanonda, Pawinee Rerknimitr, Vorasuk Shotelersuk
Publikováno v:
Case Reports in Dermatology, Vol 12, Iss 3, Pp 241-248 (2020)
Nagashima-type palmoplantar keratosis (NPPK) is a diffuse, non-syndromic (isolated), autosomal recessive palmoplantar keratoderma (PPK) with transgredients. It is characterized by non-progressive mild to moderate transgredient PPK. The mutation in SE
Externí odkaz:
https://doaj.org/article/e3db016bd72241b38e3a26e6fefcc631
Autor:
Pattamon Lertpichitkul, MD, Jade Wititsuwannakul, MD, Pravit Asawanonda, MD, DSc, Pawinee Rerknimitr, MD, MSc
Publikováno v:
JAAD Case Reports, Vol 6, Iss 2, Pp 86-88 (2020)
Externí odkaz:
https://doaj.org/article/c2fd7071a08b4b9da2ff311cb6c5240c