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Investigation of the functional variant c.-169T > C of the Fc receptor-like 3 ( FCRL3) gene in alopecia areata.
Published in:
International Journal of Immunogenetics, 2006, v. 33, n. 6, p. 393, doi. 10.1111/j.1744-313X.2006.00633.x
By:
- Schäfer, N.;
- Blaumeiser, B.;
- Becker, T.;
- Freudenberg-Hua, Y.;
- Hanneken, S.;
- Eigelshoven, S.;
- Schmael, C.;
- Lambert, J.;
- De Weert, J.;
- Kruse, R.;
- Nöthen, M. M.;
- Betz, R. C.
Publication type:
Article
Haaranomalien bei syndromalen Erkrankungen.
Published in:
Der Hautarzt, 2019, v. 70, n. 7, p. 514, doi. 10.1007/s00105-019-4440-6
By:
- Frank, J.;
- Betz, R. C.
Publication type:
Article
Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2023, v. 37, n. 8, p. 1547, doi. 10.1111/jdv.18921
By:
- Foo, J. C.;
- Redler, S.;
- Forstner, A. J.;
- Basmanav, F. B.;
- Pethukova, L.;
- Guo, J.;
- Streit, F.;
- Witt, S. H.;
- Sirignano, L.;
- Zillich, L.;
- Awasthi, S.;
- Ripke, S.;
- Christiano, A. M.;
- Tesch, F.;
- Schmitt, J.;
- Nöthen, M. M.;
- Betz, R. C.;
- Rietschel, M.;
- Frank, J.
Publication type:
Article
Cole disease due to a novel pathogenic variant in the ENPP1 gene.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 7, p. e559, doi. 10.1111/jdv.18028
By:
- Nanda, A.;
- Xiong, X.;
- AlLafi, A.;
- Cesarato, N.;
- Betz, R. C.
Publication type:
Article
An insertion mutation in <italic>HOXC13</italic> underlies pure hair and nail ectodermal dysplasia with lacrimal duct obstruction.
Published in:
2018
By:
- Humbatova, A.;
- Maroofian, R.;
- Romano, M.‐T.;
- Tafazzoli, A.;
- Behnam, M.;
- Dilaver, N.;
- Nouri, N.;
- Salehi, M.;
- Wolf, S.;
- Frank, J.;
- Kokordelis, P.;
- Betz, R. C.
Publication type:
Letter to the Editor
Functional implications of novel <italic>ADAM10</italic> mutations in reticulate acropigmentation of Kitamura.
Published in:
2017
By:
- Ralser, D. J.;
- Lestringant, G. G.;
- Du‐Thanh, A.;
- Kokordelis, P.;
- Fischer, J.;
- Basmanav, F.B.Ünalan;
- Wolf, S.;
- Thiele, H.;
- Altmüller, J.;
- Nürnberg, P.;
- Oji, V.;
- Fritz, G.;
- Frank, J.;
- Betz, R. C.
Publication type:
Letter to the Editor
Investigation of variants of the aromatase gene ( CYP19A1) in female pattern hair loss.
Published in:
British Journal of Dermatology, 2011, v. 165, n. 3, p. 703, doi. 10.1111/j.1365-2133.2011.10456.x
By:
- Redler, S.;
- Birch, M. P.;
- Drichel, D.;
- Dobson, K.;
- Brockschmidt, F.F.;
- Tazi-Ahnini, R.;
- Giehl, K.A.;
- Kluck, N.;
- Kruse, R.;
- Lutz, G.;
- Wolff, H.;
- Becker, T.;
- Nöthen, M. M.;
- Messenger, A. G.;
- Betz, R. C.
Publication type:
Article
Systematic mutation screening of KRT5 supports the hypothesis that Galli–Galli disease is a variant of Dowling–Degos disease.
Published in:
British Journal of Dermatology, 2010, v. 163, n. 1, p. 197, doi. 10.1111/j.1365-2133.2010.09741.x
By:
- Hanneken, S.;
- Rütten, A.;
- Pasternack, S. M.;
- Eigelshoven, S.;
- El Shabrawi-Caelen, L.;
- Wenzel, J.;
- Braun-Falco, M.;
- Ruzicka, T.;
- Nöthen, M. M.;
- Kruse, R.;
- Betz, R. C.
Publication type:
Article
A non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalp.
Published in:
British Journal of Dermatology, 2005, v. 153, n. 6, p. 1216, doi. 10.1111/j.1365-2133.2005.06958.x
By:
- Dávalos, N. O.;
- García-Vargas, A.;
- Pforr, J.;
- Dávalos, I. P.;
- Picos-Cárdenas, V. J.;
- García-Cruz, D.;
- Kruse, R.;
- Figuera, L. E.;
- Nöthen, M. M.;
- Betz, R. C.
Publication type:
Article
Isolated recessive nail dysplasia caused by FZD6 mutations: report of three families and review of the literature.
Published in:
Clinical & Experimental Dermatology, 2016, v. 41, n. 8, p. 884, doi. 10.1111/ced.12934
By:
- Kasparis, C.;
- Reid, D.;
- Wilson, N. J.;
- Okur, V.;
- Cole, C.;
- Hansen, C. D.;
- Bosse, K.;
- Betz, R. C.;
- Khan, M.;
- Smith, F. J. D.
Publication type:
Article
A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.
Published in:
Clinical & Experimental Dermatology, 2015, v. 40, n. 7, p. 781, doi. 10.1111/ced.12631
By:
- Redler, S.;
- Pasternack, S. M.;
- Wolf, S.;
- Stienen, D.;
- Wenzel, J.;
- Nöthen, M. M.;
- Betz, R. C.
Publication type:
Article
Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
Published in:
Clinical & Experimental Dermatology, 2009, v. 34, n. 8, p. e953, doi. 10.1111/j.1365-2230.2009.03644.x
By:
- Düzenli, S.;
- Redler, S.;
- Müller, M.;
- Polat, M.;
- Dogruer, D.;
- Pasternack, S. M.;
- Betz, R. C.
Publication type:
Article

Found: 12