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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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.
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Published in Journal of the European Academy of Dermatology and Venereology (01.04.2022)
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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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Pharmacokinetics of temocapril and temocaprilat after 14 once daily oral doses of temocapril in hypertensive patients with varying degrees of renal impairment
Püchler, K., Eckl, K. M., Fritsche, L., Renneisen, K., Neumayer, H.‐H., Sierakowski, B., Lavrijssen, A. T. J., Thomsen, T., Roots, I.
Published in British journal of clinical pharmacology (01.12.1997)
Published in British journal of clinical pharmacology (01.12.1997)
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Voglibose has no effect on the pharmacokinetics of hydrochlorothiazide
KLEIST, P, SUZUKI, Y, THOMSEN, T, MÖLLER, M, RÖMER, A, HUCKE, H. P, KUROWSKI, M, ECKL, K. M
Published in European journal of clinical pharmacology (01.05.1998)
Published in European journal of clinical pharmacology (01.05.1998)
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The pharmacokinetics of paroxetine in patients with liver cirrhosis
Krastev, Z, Terziivanov, D, Vlahov, V, Maleev, A, Greb, W H, Eckl, K M, Dierdorf, H D, Wolf, D
Published in Acta psychiatrica Scandinavica. Supplementum (01.01.1989)
Published in Acta psychiatrica Scandinavica. Supplementum (01.01.1989)
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Safety and immunogenicity of IMVAMUNE, a promising candidate as a third generation smallpox vaccine
Vollmar, Jens, Arndtz, Nathaly, Eckl, Karl M., Thomsen, Torben, Petzold, Barbara, Mateo, Luis, Schlereth, Bernd, Handley, Amanda, King, Lynette, Hülsemann, Vanessa, Tzatzaris, Maria, Merkl, Karin, Wulff, Niels, Chaplin, Paul
Published in Vaccine (15.03.2006)
Published in Vaccine (15.03.2006)
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Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis
Eckl, Katja-Martina, Krieg, Peter, Küster, Wolfgang, Traupe, Heiko, André, Françoise, Wittstruck, Nadine, Fürstenberger, Gerhard, Hennies, Hans Christian
Published in Human mutation (01.10.2005)
Published in Human mutation (01.10.2005)
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Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome
HENNIES, Hans Christian, RAUCH, Anita, GIUGLIANI, Roberto, NEUMANN, Thomas E, ECKL, Katja M, KARBASIYAN, Mohsen, REIS, André, HORN, Denise, SEIFERT, Wenke, SCHUMI, Christian, MOSER, Elisabeth, AL-TAJI, Eva, TARIVERDIAN, Gholamali, CHRZANOWSKA, Krystyna H, KRAJEWSKA-WALASEK, Malgorzata, RAJAB, Anna
Published in American journal of human genetics (01.07.2004)
Published in American journal of human genetics (01.07.2004)
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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates
ECKL, Katja Martina, STEVENS, Howard P, REIS, André, HENNIES, Hans Christian, LESTRINGANT, Gilles G, WESTENBERGER-TREUMANN, Margaretha, TRAUPE, Heiko, HINZ, Britta, FROSSARD, Philippe M, STADLER, Rudolf, LEIGH, Irene M, NÜRNBERG, Peter
Published in Human genetics (2003)
Published in Human genetics (2003)
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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 The British journal of dermatology (01.04.2017)
Published in The British journal of dermatology (01.04.2017)
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Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies
Pichler, Robert, Stelzer, Christoph, Berg, Jörg, Holzinger, Carl, Eckl, Katja Martina, Hennies, Hans Christian, Auböck, Josef
Published in Archives of Dermatological Research (01.06.2005)
Published in Archives of Dermatological Research (01.06.2005)
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