Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Chavalit Supsrisunjai"'
Publikováno v:
Journal of Health Science and Medical Research (JHSMR), Vol 41, Iss 3, Pp e2022914-e2022914 (2023)
Epidermolytic ichthyosis (EI) is a rare genodermatosis disorder. We report a 39-year-old woman with EI, who presented with generalized erythroderma since birth, followed by generalized hyperkeratosis later in life. The physical examination revealed g
Externí odkaz:
https://doaj.org/article/8a005b5b72ea4895b1fe6baa6b0f8a32
Validity and Reliability of the Topical Corticosteroid Phobia (TOPICOP©) Questionnaire: Thai Version
Publikováno v:
Siriraj Medical Journal, Vol 75, Iss 2 (2023)
Objective: To determine the validity and reliability of the Thai version of the Topical Corticosteroid Phobia (TOPICOP©) questionnaire, which is used to evaluate topical corticosteroid (TCS) phobia in atopic dermatitis (AD). Materials & Methods: T
Externí odkaz:
https://doaj.org/article/c1bd0719c91c4764a0b8ab13c0e4807c
Autor:
Purich Kosidcanasap, Monton Tanabodee, Thareena Bunnag, Prapaipit Chaowalit, Pailin Puangpet, Chavalit Supsrisunjai
Publikováno v:
Australasian Journal of Dermatology. 63:258-261
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d13cf0e244667e3c4bb9d955338ff899
https://doi.org/10.1111/ajd.13837
https://doi.org/10.1111/ajd.13837
Publikováno v:
Siriraj Medical Journal, Vol 68, Iss 3, Pp 155-159 (2016)
Background: The most common cause of hair loss seen in women is female pattern hair loss (FPHL), also known as female androgenetic alopecia. It affects the central part of the scalp, but spares the frontal hairline. Frontal accentuation was also de
Externí odkaz:
https://doaj.org/article/9356b94a9be44405a6e0ca34c38306aa
Publikováno v:
Journal of Health Science and Medical Research.
Epidermolytic ichthyosis (EI) is a rare genodermatosis disorder. We report a 39-year-old woman with EI, who presented with generalized erythroderma since birth, followed by generalized hyperkeratosis later in life. The physical examination revealed g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac1a298331f284f2efd5793c9469d95e
https://doi.org/10.31584/jhsmr.2022914
https://doi.org/10.31584/jhsmr.2022914
Autor:
Jongjin Suwanthaweemeesuk, Chatip Phunmanee, Sasathorn Singthong, Oraya Kwangsukstid, Chavalit Supsrisunjai
Publikováno v:
International Journal of Dermatology and Venereology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a46806257813e67c9c0df85426d44f59
https://doi.org/10.1097/jd9.0000000000000235
https://doi.org/10.1097/jd9.0000000000000235
Autor:
Eduardo Calonje, Hsin Yu Huang, Chavalit Supsrisunjai, Roberto A. Steiner, Magdalene Michael, Hsing San Yang, John A. McGrath, Chao Kai Hsu, Ofer Sarig, Robert A. S. Ariëns, Eli Sprecher, Michael A. Simpson, Maddy Parsons, Thitiwat Chaikul, Cédric Duval, Curt P. Samlaska, John Y.W. Lee, M. Eskin-Schwartz, Alexandros Onoufriadis
Publikováno v:
King's College London
Dermatofibromas are common benign skin lesions, the etiology of which is poorly understood. We identified two unrelated pedigrees in which there was autosomal dominant transmission of multiple dermatofibromas. Whole exome sequencing revealed a rare s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338864fa06a2e1634164abafe05dd524
Publikováno v:
Medical Science and Discovery. 8:289-290
Basal cell nevus syndrome is a rare inherited autosomal dominant syndrome characterized by developmental defects and tumor predisposition. There are more than 400 reported PTCH1 mutations, including frameshift, nonsense, missense, deletions, duplicat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::028e9a3866499ee1fcf2216d571635ed
https://doi.org/10.36472/msd.v8i4.519
https://doi.org/10.36472/msd.v8i4.519
Autor:
Vesarat Wessagowit, Prapaipit Chaowalit, Tanawatt Kootiratrakarn, Pailin Puangpet, Chavalit Supsrisunjai, Thareena Bunnag
Publikováno v:
The American Journal of Tropical Medicine and Hygiene. :16-0472
Several case reports of autochthonous leishmaniasis in Thailand have been published since 1996. Most of the previous cases presented with visceral leishmaniasis (VL) and were mostly reported in southern part of Thailand. Recently, it has been evident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81cc77939362c80cdb1aa701aaa958cf
https://doi.org/10.4269/ajtmh.16-0472
https://doi.org/10.4269/ajtmh.16-0472
Autor:
Chao Kai Hsu, Jean-Philippe Lacour, Pascal Del Giudice, John A. McGrath, Chavalit Supsrisunjai, Azzam Alkhalifah, Lu Liu, Christine Chiaverini, Alexandra Charlesworth
Publikováno v:
Alkhalifah, A, Chiaverini, C, Del Giudice, P, Supsrisunjai, C, Hsu, C-K, Liu, L, Charlesworth, A, McGrath, J A & Lacour, J-P 2017, ' PLACK syndrome resulting from a new homozygous insertion mutation in CAST ', Journal of Dermatological Science . https://doi.org/10.1016/j.jdermsci.2017.06.004
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::613480659b9162a965325a58327b3b7b
https://doi.org/10.1016/j.jdermsci.2017.06.004
https://doi.org/10.1016/j.jdermsci.2017.06.004