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H Traupe

Showing results (131-140 of 166) with videos related to

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Acta Neurologica Scandinavica|November 18, 2000
CD45RA+ ICAM-3+ lymphocytes in cerebrospinal fluid and blood as markers of disease activity in patients with multiple sclerosisJ Kraus, P Oschmann, B Engelhardt, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Human Genetics|March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphismH Traupe, U Vetter, R Happle, et al.
The British Journal of Dermatology|April 3, 2016
Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in IL36RN in German patientsS Löhr, S Uebe, F Behrens, et al.
The British Journal of Dermatology|September 18, 2008
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubulesG Grimberg, I Hausser, F B Müller, et al.
Nature Genetics|August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of SiemensJ A Rothnagel, H Traupe, S Wojcik, et al.
American Journal of Medical Genetics|August 26, 1998
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: clinical and neuropathological observations in a 33-year-old manK Keyvani, W Paulus, H Traupe, et al.
The Journal of Investigative Dermatology|April 14, 1999
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium testN Jacob, F Rüschendorf, M Schmitt-Egenolf, et al.
The Journal of Investigative Dermatology|March 1, 1997
A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythrodermaG Y Joh, H Traupe, D Metze, et al.
The British Journal of Dermatology|August 23, 2003
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasisP Hensen, K Asadullah, C Windemuth, et al.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Acta Neurologica Scandinavica|November 18, 2000
CD45RA+ ICAM-3+ lymphocytes in cerebrospinal fluid and blood as markers of disease activity in patients with multiple sclerosisJ Kraus, P Oschmann, B Engelhardt, et al.
Human Genetics|August 1, 1992
Exclusion mapping of the X-linked dominant chondrodysplasia punctata/ichthyosis/cataract/short stature (Happle) syndrome: possible involvement of an unstable pre-mutationH Traupe, D Müller, D Atherton, et al.
Human Genetics|March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphismH Traupe, U Vetter, R Happle, et al.
The British Journal of Dermatology|April 3, 2016
Association analysis of psoriasis vulgaris and psoriatic arthritis with loss-of-function mutations in IL36RN in German patientsS Löhr, S Uebe, F Behrens, et al.
The British Journal of Dermatology|September 18, 2008
Novel and recurrent mutations in the 1B domain of keratin 1 in palmoplantar keratoderma with tonotubulesG Grimberg, I Hausser, F B Müller, et al.
Nature Genetics|August 1, 1994
Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of SiemensJ A Rothnagel, H Traupe, S Wojcik, et al.
American Journal of Medical Genetics|August 26, 1998
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: clinical and neuropathological observations in a 33-year-old manK Keyvani, W Paulus, H Traupe, et al.
The Journal of Investigative Dermatology|April 14, 1999
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium testN Jacob, F Rüschendorf, M Schmitt-Egenolf, et al.
The Journal of Investigative Dermatology|March 1, 1997
A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythrodermaG Y Joh, H Traupe, D Metze, et al.
The British Journal of Dermatology|August 23, 2003
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasisP Hensen, K Asadullah, C Windemuth, et al.
Pageof 17