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Comparative Study of High-Resolution Multifrequency Ultrasound of the Plantar Skin in Patients with Various Types of Hereditary Palmoplantar Keratoderma.
Published in:
Dermatology (10188665), 2013, v. 226, n. 4, p. 365, doi. 10.1159/000351321
By:
- Goldberg, I.;
- Sprecher, E.;
- Schwartz, M.E.;
- Gaitini, D.
Publication type:
Article
Best treatment practices for pachyonychia congenita.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2014, v. 28, n. 3, p. 279, doi. 10.1111/jdv.12098
By:
- Goldberg, I.;
- Fruchter, D.;
- Meilick, A.;
- Schwartz, M.E.;
- Sprecher, E.
Publication type:
Article
Transmission of factor VII deficiency through liver transplantation.
Published in:
Transplant International, 1999, v. 12, n. 4, p. 278, doi. 10.1111/j.1432-2277.1999.tb01214.x
By:
- Guy, S.R.;
- Magliocca, J. F.;
- Fruchtman, S.;
- McDonough, P.;
- Emre, S.;
- Kim-Schluger, L.;
- Sheiner, P. A.;
- Fishbein, T. M.;
- Schwartz, M. E.;
- Miller, C. M.;
- Schwartz, M.E.;
- Miller, CM.
Publication type:
Article
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children.
Published in:
British Journal of Dermatology, 2020, v. 182, n. 3, p. 708, doi. 10.1111/bjd.18742
By:
- Goldberg, I.;
- Mashiah, J.;
- Kutz, A.;
- Derowe, A.;
- Warshauer, E.;
- Schwartz, M.E.;
- Smith, F.;
- Sprecher, E.;
- Hansen, C.D.
Publication type:
Article
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening.
Published in:
British Journal of Dermatology, 2017, v. 176, n. 5, p. 1345, doi. 10.1111/bjd.14973
By:
- LovgrEN, M. ‐ L.;
- McAleer, M.A.;
- Irvine, A.D.;
- Wilson, N.J.;
- Tavadia, S.;
- Schwartz, M.E.;
- Cole, C.;
- Sandilands, A.;
- Smith, F.J.D.;
- Zamiri, M.
Publication type:
Article
Mutations in GJB6 causing phenotype resembling pachyonychia congenita.
Published in:
British Journal of Dermatology, 2015, v. 172, n. 5, p. 1447, doi. 10.1111/bjd.13520
By:
- Hale, G.I.;
- Wilson, N.J.;
- Smith, F.J.D.;
- Wylie, G.;
- Schwartz, M.E.;
- Zamiri, M.
Publication type:
Article
Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting.
Published in:
British Journal of Dermatology, 2014, v. 171, n. 5, p. 974, doi. 10.1111/bjd.13341
By:
- O'Toole, E.A.;
- Kaspar, R.L.;
- Sprecher, E.;
- Schwartz, M.E.;
- Rittié, L.
Publication type:
Article
The molecular genetic analysis of the expanding pachyonychia congenita case collection.
Published in:
British Journal of Dermatology, 2014, v. 171, n. 2, p. 343, doi. 10.1111/bjd.12958
By:
- Wilson, N.J.;
- O'Toole, E.A.;
- Milstone, L.M.;
- Hansen, C.D.;
- Shepherd, A.A.;
- Al‐Asadi, E.;
- Schwartz, M.E.;
- McLean, W.H.I.;
- Sprecher, E.;
- Smith, F.J.D.
Publication type:
Article
Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma.
Published in:
British Journal of Dermatology, 2013, v. 169, n. 6, p. 1357, doi. 10.1111/bjd.12574
By:
- Higgins, E.;
- Capra, M.;
- Schwartz, M.E.;
- Smith, F.J.D.;
- McLean, W.H.I.;
- Irvine, A.D.
Publication type:
Article
Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16.
Published in:
British Journal of Dermatology, 2012, v. 166, n. 4, p. 875, doi. 10.1111/j.1365-2133.2011.10745.x
By:
- Spaunhurst, K.M.;
- Hogendorf, A.M.;
- Smith, F.J.D.;
- Lingala, B.;
- Schwartz, M.E.;
- Cywinska-Bernas, A.;
- Zeman, K.J.;
- Tang, J.Y.
Publication type:
Article

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