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The importance of genetic susceptibility in Dupuytren's disease.
Published in:
Clinical Genetics, 2015, v. 87, n. 5, p. 483, doi. 10.1111/cge.12410
By:
- Becker, K.;
- Tinschert, S.;
- Lienert, A.;
- Bleuler, P.E.;
- Staub, F.;
- Meinel, A.;
- Rößler, J.;
- Wach, W.;
- Hoffmann, R.;
- Kühnel, F.;
- Damert, H.‐G.;
- Nick, H.‐E.;
- Spicher, R.;
- Lenze, W.;
- Langer, M.;
- Nürnberg, P.;
- Hennies, H.C.
Publication type:
Article
Kartierung und molekulare Analyse erblicher Hautkrankheiten Stand der Forschung.
Published in:
Der Hautarzt, 2000, v. 51, n. 12, p. 906, doi. 10.1007/s001050051238
By:
- Küster, W.;
- Hennies, H.C.;
- Happle, R.
Publication type:
Article
Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 4, p. 582, doi. 10.1111/jdv.17873
By:
- Hake, L.;
- Süßmuth, K.;
- Komlosi, K.;
- Kopp, J.;
- Drerup, C.;
- Metze, D.;
- Traupe, H.;
- Hausser, I.;
- Eckl, K.M.;
- Hennies, H.C.;
- Fischer, J.;
- Oji, V.
Publication type:
Article
Correspondence.
Published in:
1999
By:
- Stevens, H.P.;
- Choon, S.E.;
- Hennies, H.C.;
- Kelsell, D.P.;
- Schmidt, E.;
- Herzele, K.;
- Schumann, H.;
- Wesselmann, U.;
- Chimanovitch, I.;
- Bruckner-Tuderman, L.;
- Brocker, E.-B.;
- Guidice, G.J.;
- Zillikens, S.;
- Von Kobyletzki, G.;
- Pieck, C.;
- Hoxtermann, S.;
- Freitag, M.;
- Altmeyer, P.;
- Lee, N.H.
Publication type:
Letter
Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations.
Published in:
British Journal of Dermatology, 2017, v. 176, n. 4, p. 1068, doi. 10.1111/bjd.14860
By:
- Gruber, R.;
- Rainer, G.;
- Weiss, A.;
- Udvardi, A.;
- Thiele, H.;
- Eckl, K.M.;
- Schupart, R.;
- Nürnberg, P.;
- Zschocke, J.;
- Schmuth, M.;
- Volc ‐ Platzer, B.;
- Hennies, H.C.
Publication type:
Article
Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTA.
Published in:
British Journal of Dermatology, 2015, v. 172, n. 6, p. 1628, doi. 10.1111/bjd.13545
By:
- Moosbrugger‐Martinz, V.;
- Jalili, A.;
- Schossig, A.S.;
- Jahn‐Bassler, K.;
- Zschocke, J.;
- Schmuth, M.;
- Stingl, G.;
- Eckl, K.M.;
- Hennies, H.C.;
- Gruber, R.
Publication type:
Article
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene.
Published in:
British Journal of Dermatology, 2013, v. 168, n. 6, p. 1372, doi. 10.1111/bjd.12203
By:
- Nellen, R.G.L.;
- Steijlen, P.M.;
- Hennies, H.C.;
- Fischer, J.;
- Munro, C.S.;
- Jonkman, M.F.;
- van Steensel, M.A.M.;
- van Geel, M.
Publication type:
Article
CEDNIK syndrome results from loss-of-function mutations in SNAP29.
Published in:
British Journal of Dermatology, 2011, v. 164, n. 3, p. 610, doi. 10.1111/j.1365-2133.2010.10133.x
By:
- Fuchs-Telem, D.;
- Stewart, H.;
- Rapaport, D.;
- Nousbeck, J.;
- Gat, A.;
- Gini, M.;
- Lugassy, Y.;
- Emmert, S.;
- Eckl, K.;
- Hennies, H.C.;
- Sarig, O.;
- Goldsher, D.;
- Meilik, B.;
- Ishida-Yamamoto, A.;
- Horowitz, M.;
- Sprecher, E.
Publication type:
Article
HID and KID syndromes are associated with the same connexin 26 mutation.
Published in:
British Journal of Dermatology, 2002, v. 146, n. 6, p. 938, doi. 10.1046/j.1365-2133.2002.04893.x
By:
- Van Geel, M.;
- Van Steensel, M.A.M.;
- Küster, W.;
- Hennies, H.C.;
- Happle, R.;
- Steijlen, P.M.;
- König‡, A.
Publication type:
Article
Krankheitsspezifische Hautmodelle.
Published in:
Medizinische Genetik, 2009, v. 21, n. 4, p. 487, doi. 10.1007/s11825-009-0195-2
By:
- Eckl, K.-M.;
- Hennies, H.C.
Publication type:
Article
Molekulare Charakterisierung der Ichthyosen.
Published in:
Medizinische Genetik, 2009, v. 21, n. 4, p. 479, doi. 10.1007/s11825-009-0194-3
By:
- Oji, V.;
- Traupe, H.;
- Hennies, H.C.
Publication type:
Article

Found: 11