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H Traupe

Showing results (111-120 of 166) with videos related to

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Cerebrovascular Diseases (Basel, Switzerland)|May 27, 2003
Contrast media effect on cerebral blood flow regulation after performance of cerebral or coronary angiographyB Rosengarten, M K Steen-Müller, A Müller, et al.
Human Genetics|April 17, 1998
Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosisH C Hennies, M Raghunath, V Wiebe, et al.
The British Journal of Dermatology|October 10, 2013
Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trialA Vahlquist, S Blockhuys, P Steijlen, et al.
American Journal of Medical Genetics|March 1, 1992
Psoriasis vulgaris, fetal growth, and genomic imprintingH Traupe, P J van Gurp, R Happle, et al.
The British Journal of Dermatology|January 29, 2011
Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosisM J Arin, V Oji, S Emmert, et al.
The British Journal of Dermatology|April 26, 2006
Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1V Oji, M E Oji, N Adamini, et al.
Human Molecular Genetics|August 15, 2000
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicismC Has, L Bruckner-Tuderman, D Müller, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 1, 1993
[Incontinentia pigmenti in a male infant]K H Vehring, G Kurlemann, H Traupe, et al.
The British Journal of Dermatology|June 9, 2009
Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutationJ Mazereeuw-Hautier, K Aufenvenne, C Deraison, et al.
Archives of Dermatological Research|December 22, 1998
A novel in situ method for the detection of deficient transglutaminase activity in the skinM Raghunath, H C Hennies, F Velten, et al.
Pageof 17

Showing results (111-120 of 166) with videos related to

Sort By:
Pageof 17
Cerebrovascular Diseases (Basel, Switzerland)|May 27, 2003
Contrast media effect on cerebral blood flow regulation after performance of cerebral or coronary angiographyB Rosengarten, M K Steen-Müller, A Müller, et al.
Human Genetics|April 17, 1998
Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosisH C Hennies, M Raghunath, V Wiebe, et al.
The British Journal of Dermatology|October 10, 2013
Oral liarozole in the treatment of patients with moderate/severe lamellar ichthyosis: results of a randomized, double-blind, multinational, placebo-controlled phase II/III trialA Vahlquist, S Blockhuys, P Steijlen, et al.
American Journal of Medical Genetics|March 1, 1992
Psoriasis vulgaris, fetal growth, and genomic imprintingH Traupe, P J van Gurp, R Happle, et al.
The British Journal of Dermatology|January 29, 2011
Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosisM J Arin, V Oji, S Emmert, et al.
The British Journal of Dermatology|April 26, 2006
Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1V Oji, M E Oji, N Adamini, et al.
Human Molecular Genetics|August 15, 2000
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicismC Has, L Bruckner-Tuderman, D Müller, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 1, 1993
[Incontinentia pigmenti in a male infant]K H Vehring, G Kurlemann, H Traupe, et al.
The British Journal of Dermatology|June 9, 2009
Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutationJ Mazereeuw-Hautier, K Aufenvenne, C Deraison, et al.
Archives of Dermatological Research|December 22, 1998
A novel in situ method for the detection of deficient transglutaminase activity in the skinM Raghunath, H C Hennies, F Velten, et al.
Pageof 17