Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nucha Niumpradit"'
Autor:
Kuanjira Wongkietkachorn, Julphat Intarasupht, Chutika Srisuttiyakorn, Kobkul Aunhachoke, Artit Nakakes, Nucha Niumpradit
Publikováno v:
Case Reports in Dermatology, Vol 5, Iss 1, Pp 11-14 (2013)
Linear atrophoderma of Moulin (LAM) is a rare dermatosis in childhood and early adolescence. The exact etiology of LAM is still obscure. Several treatment modalities were reported but none was consistently successful. We report a case of LAM in which
Externí odkaz:
https://doaj.org/article/92d0a8ba3ec3416eab5aad0cfd8e9df4
Autor:
Sawanya Buranaphalin, Artit Nakakes, Nucha Niumpradit, Chotinand Piriyanand, Kittisak Payapvipapong
Publikováno v:
Journal of Cosmetic Dermatology. 14:83-90
Summary Intralesional injection with corticosteroid remains the mainstay of therapy for hypertrophic scars and keloids, however some lesions are unresponsive or may result in skin atrophy. Intralesional bleomycin injection is an alternative therapy t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bce50992317f7ddffb13c35be2cd5e6
https://doi.org/10.1111/jocd.12132
https://doi.org/10.1111/jocd.12132
Autor:
Kobkul Aunhachoke, Julphat Intarasupht, Kuanjira Wongkietkachorn, Chutika Srisuttiyakorn, Artit Nakakes, Nucha Niumpradit
Publikováno v:
Case Reports in Dermatology
Case Reports in Dermatology, Vol 5, Iss 1, Pp 11-14 (2013)
Case Reports in Dermatology, Vol 5, Iss 1, Pp 11-14 (2013)
Linear atrophoderma of Moulin (LAM) is a rare dermatosis in childhood and early adolescence. The exact etiology of LAM is still obscure. Several treatment modalities were reported but none was consistently successful. We report a case of LAM in which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7b2806c56d7b93e4fa5d642f667b15d
http://europepmc.org/articles/PMC3573794
http://europepmc.org/articles/PMC3573794
A rare case of acquired partial lipodystrophy (Barraquer-Simons syndrome) with localized scleroderma
Publikováno v:
International Journal of Dermatology. 53:82-84
IntroductionLipodystrophy is a group of adipose tissue disorders classi-fied into genetic/acquired or generalized/partial lack ofadipose tissue (lipoatrophy). Acquired partial lipodystro-phy (APL) or Barraquer–Simons syndrome presents withlate ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b9bd1b0ce9ca0d463eebf96a217f0e0
https://doi.org/10.1111/j.1365-4632.2011.05435.x
https://doi.org/10.1111/j.1365-4632.2011.05435.x
A rare case of acquired partial lipodystrophy (Barraquer-Simons syndrome) with localized scleroderma
Publikováno v:
International journal of dermatology. 53(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c3cc8ea21ba8ab76e07d70252302ae2
https://pubmed.ncbi.nlm.nih.gov/23675994
https://pubmed.ncbi.nlm.nih.gov/23675994
Autor:
Rajyani, Kanechorn Na Ayuthaya, Nonthaya, Patthamapasphong, Thanyachai, Sura, Nucha, Niumpradit, Objoon, Trachoo
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 91
Ehlers-Danlos syndrome has many subtypes. The vascular type (type IV) is characterized by thin, translucent skin, easy bruising, characteristic facial appearance, and arterial, intestinal, and/or uterine fragility.To encourage a better understanding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::998f063bde392f8d3a509c061fb8c511
https://pubmed.ncbi.nlm.nih.gov/18672610
https://pubmed.ncbi.nlm.nih.gov/18672610
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 88
Rat-bite fever is an uncommon disease known for its endemicity to occur worldwide. Although most patients tend to develop mild symptoms with improvement from conventional antibiotics, it can progress with severe complications with a mortality rate as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbfa712261cb124987e0361ba1d84b52
https://pubmed.ncbi.nlm.nih.gov/16858964
https://pubmed.ncbi.nlm.nih.gov/16858964