Browsing by UP Author "Jacyk, Witold Kamil"

Browsing by UP Author "Jacyk, Witold Kamil"

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  • Chronic ulcerative stomatitis and lichen planus : just a coincidence or a direct link between the two diseases? 
    Jacyk, Witold Kamil; Fourie, Jeanine; Van Heerden, Willem Francois Petrus (Cornetis Publishing House, 2012)
    Chronic ulcerative dermatitis (CUS) is characterized by painful exacerbating and remitting oral erosions and ulcerations. A very characteristic direct immunofluorescence (DIF) pattern differentiates CUS from other ...
  • A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex Iidicates the Importance of the amino acid located at the boundary site between the H1 and coil 1A domains 
    Shinkuma, Satoru; Nishie, Wataru; Jacyk, Witold Kamil; Natsuga, Ken; Ujiie, Hideyuki; Nakamura, Hideki; Akiyama, Masashi; Shimizu, Hiroshi (Medical Journals, 2013-09)
    No abstract
  • Pagetoid reticulosis with CD30 positivity and cytotoxic/suppressor cells 
    Jacyk, Witold Kamil; Grayson, Wayne; Dinkel, Jurgen Erich; Requena, Luis (Blackwell, 2007-08)
    Pagetoid reticulosis (PR), also named Woringer-Kolopp disease, is a low-grade primary cutaneous T-cell lymphoma that usually presents as a solitary, slowly enlarging erythematous or hyperkeratotic plaque on the distal areas ...
  • Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and Barber-Say syndromes 
    Jacyk, Witold Kamil; Marchegiani, Shannon; Davis, Taylor; Tessadori, Federico; Van Haaften, Gijs; Brancati, Francesco; Hoischen, Alexander; Huang, Haigen; Valkanas, Elise; Pusey, Barbara; Schanze, Denny; Zerfas, Patricia M.; Zambruno, Giovanna; Kariminejad, Ariana; Sabbagh-Kermani, Farahnaz; Lee, Janice; Tsokos, Maria G.; Lee, Chyi-Chia R.; Ferraz, Victor; Da Silva, Eduarda Morgana; Stevens, Cathy A.; Roche, Nathalie; Bartsch, Oliver; Farndon, Peter; Bermejo-Sanchez, Eva; Brooks, Brian P.; Maduro, Valerie; Dallapiccola, Bruno; Ramos, Feliciano J.; Chung, Hon-Yin Brian; Le Caignec, Cedric; Martins, Fabiana; Mazzanti, Laura; Brunner, Han G.; Bakkers, Jeroen; Lin, Shuo; Malicdan, May Christine V.; Boerkoel, Cornelius F.; Gahl, William A.; De Vries, Bert B.A.; Van Haelst, Mieke M.; Zenker, Martin; Markello, Thomas C.; Venselaar, Hanka (Cell Press, 2015-07)
    Ablepharon macrostomia syndrome (AMS) and Barber-Say syndrome (BSS) are rare congenital ectodermal dysplasias characterized by similar clinical features. To establish the genetic basis of AMS and BSS, we performed extensive ...
  • Revised nomenclature and classification of inherited ichthyoses : results of the first ichthyosis consensus conference in Sorèze 2009 
    Oji, Vinzenz; Tadini, Gianluca; Akiyama, Masashi; Bardon, Claudine Blanchet; Bodemer, Christine; Bourrat, Emmanuelle; Coudiere, Philippe; DiGiovanna, John J.; Elias, Peter; Fischer, Judith; Fleckman, Philip; Gina, Michal; Harper, John; Hashimoto, Takashi; Hausser, Ingrid; Hennies, Hans Christian; Hohl, Daniel; Hovnanian, Alain; Ishida-Yamamoto, Akemi; Jacyk, Witold Kamil; Leachman, Sancy; Leigh, Irene; Mazereeuw-Hautier, Juliette; Milstone, Leonard; Morice-Picard, Fanny; Paller, Amy S.; Richard, Gabriele; Schmuth, Matthias; Shimizu, Hiroshi; Sprecher, Eli; Van Steensel, Maurice; Taieb, Alain; Toro, Jorge R.; Vabres, Pierre; Vahlquist, Anders; Williams, Mary; Traupe, Heiko (American Academy of Dermatology, 2010-10)
    BACKGROUND: Inherited ichthyoses belong to a large, clinically and etiologically heterogeneous group of mendelian disorders of cornification, typically involving the entire integument. Over the recent years, much progress ...