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Archives of Dermatological Research|May 16, 2012
A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformitiesKatalin Farkas, Nikoletta Nagy, Agnes Kinyó, et al.Orvosi Hetilap|April 5, 2012
[Allopurinol-induced hypersensitivity syndrome]Agnes Kinyó, Anna Lakatos, Anita Varga, et al.Acta Dermato-Venereologica|May 9, 2012
Successful treatment of multiple basaliomas with bleomycin-based electrochemotherapy: a case series of three patients with Gorlin-Goltz syndromeErika Kis, Eszter Baltás, Agnes Kinyó, et al.The Journal of Investigative Dermatology|September 11, 2009
COP1 contributes to UVB-induced signaling in human keratinocytesAgnes Kinyó, Zsuzsanna Kiss-László, Szabolcs Hambalkó, et al.Archives of Dermatological Research|August 31, 2013
A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ-Siemens-Touraine syndromeAgnes Kinyó, Péter Vályi, Katalin Farkas, et al.Pageof 1