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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.
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|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.
Tissue Antigens|September 15, 2001
Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German familiesM Schmitt-Egenolf, C Windemuth, H C Hennies, et al.
Acta Neurologica Scandinavica|April 10, 2002
Serum cytokine levels do not correlate with disease activity and severity assessed by brain MRI in multiple sclerosisJ Kraus, B S Kuehne, J Tofighi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 10, 2013
Complete filaggrin deficiency in ichthyosis vulgaris is associated with only moderate changes in epidermal permeability barrier function profileA M Perusquía-Ortiz, V Oji, M C Sauerland, et al.
American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.
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