Quality of life and clinical characteristics of self‐improving congenital ichthyosis within the disease spectrum of autosomal‐recessive congenital ichthyosis
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.
Published in Journal of the European Academy of Dermatology and Venereology (01.04.2022)
Published in Journal of the European Academy of Dermatology and Venereology (01.04.2022)
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The importance of genetic susceptibility in Dupuytren's disease
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.
Published in Clinical genetics (01.05.2015)
Published in Clinical genetics (01.05.2015)
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Journal Article
Towards characterization of palmoplantar keratoderma caused by gain‐of‐function mutation in loricrin: analysis of a family and review of the literature
Gedicke, M.M., Traupe, H., Fischer, B., Tinschert, S., Hennies, H.C.
Published in British journal of dermatology (1951) (01.01.2006)
Published in British journal of dermatology (1951) (01.01.2006)
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Neurotological and Neuroanatomical Changes in the Connexin-26-Related HID/KID Syndrome
Todt, I., Hennies, H.C., Küster, W., Smolle, J., Rademacher, G., Mutze, S., Basta, D., Eisenschenk, A., Ernst, A.
Published in Audiology & neurotology (01.01.2006)
Published in Audiology & neurotology (01.01.2006)
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CEDNIK syndrome results from loss-of-function mutations in SNAP29
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.
Published in British journal of dermatology (1951) (01.03.2011)
Published in British journal of dermatology (1951) (01.03.2011)
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Journal Article
Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations
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.
Published in British journal of dermatology (1951) (01.04.2017)
Published in British journal of dermatology (1951) (01.04.2017)
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Journal Article
Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss‐of‐function mutation in CSTA
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.
Published in British journal of dermatology (1951) (01.06.2015)
Published in British journal of dermatology (1951) (01.06.2015)
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Journal Article
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene: Correspondence
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.
Published in British journal of dermatology (1951) (01.06.2013)
Published in British journal of dermatology (1951) (01.06.2013)
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Journal Article
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene
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.
Published in British journal of dermatology (1951) (01.06.2013)
Published in British journal of dermatology (1951) (01.06.2013)
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Journal Article
CEDNIK syndrome results from loss-of-function mutations in SNAP29: CEDNIK syndrome
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.
Published in British journal of dermatology (1951) (01.02.2011)
Published in British journal of dermatology (1951) (01.02.2011)
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Journal Article
Towards characterization of palmoplantar keratoderma caused by gain-of-function mutation in loricrin: analysis of a family and review of the literature: Palmoplantar keratoderma with mutation in loricrin
Gedicke, M.M., Traupe, H., Fischer, B., Tinschert, S., Hennies, H.C.
Published in British journal of dermatology (1951) (01.01.2006)
Published in British journal of dermatology (1951) (01.01.2006)
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Journal Article
HID and KID syndromes are associated with the same connexin 26 mutation
Van Geel, M., Van Steensel, M.A.M., Küster, W., Hennies, H.C., Happle, R., Steijlen, P.M., König‡, A.
Published in British journal of dermatology (1951) (01.06.2002)
Published in British journal of dermatology (1951) (01.06.2002)
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Journal Article
Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTA
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.
Published in British Journal of Dermatology (01.06.2015)
Published in British Journal of Dermatology (01.06.2015)
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