Related content

A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)

By Kato A.   Fukai K.   Oiso N.   Hosomi N.   Saitoh S.   Wada T.   Shimizu H.   Ishii M.  

Journal of Dermatological Science, Vol. 31, Iss. 3, 2003-05 ,pp. : 189-192

Elsevier

Access to resources Recommend Favorite

LPS induces melanogenesis through p38 MAPK activation in human melanocytes

By Ahn Joo  

Archives of Dermatological Research, Vol. 300, Iss. 6, 2008-07 ,pp. : 325-329

Springer Publishing Company

Access to resources Recommend Favorite

Hereditary Gelsolin Amyloidosis: A New Japanese Case with Cutis Laxa as a Diagnostic Clue

By Asahina Akihiko   Yokoyama Teruo   Ueda Mitsuharu   Ando Yukio   Ohshima Noboru   Saito Ikuo   Tadokoro Etsuko   Hasegawa Kazuko  

Acta Dermato-Venereologica, Vol. 91, Iss. 2, 2011-03 ,pp. : 201-203

Medical Journals Limited

Access to resources Recommend Favorite

Characterization of Two Cases of Bullous Pemphigoid Reactive Only with BP230 on Japanese Enzyme-linked Immunosorbent Assays

By  

Acta Dermato-Venereologica, Vol. 94, Iss. 6, 2014-11 ,pp. : 734-736

Medical Journals Limited

Access to resources Recommend Favorite

Extensive Human Papillomavirus Type 7-Associated Orofacial Warts in an Immunocompetent Patient

By Ritzkowsky Andreas   Weissenborn Sönke   Krieg Thomas   Pfister Herbert   Wieland Ulrike  

Acta Dermato-Venereologica, Vol. 81, Iss. 2, 2001-03 ,pp. : 130-133

Medical Journals Limited

Access to resources Recommend Favorite