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Wiener Medizinische Wochenschrift (1946)|November 17, 1998
[Computer-assisted diagnosis in mammography: the R2 ImageChecker System in detection of spiculated lesions]M Funovics, S Schamp, B Lackner, et al.
Clinical and Experimental Dermatology|February 1, 2003
A novel homozygous nonsense deletion/insertion mutation in the keratin 14 gene (Y248X; 744delC/insAG) causes recessive epidermolysis bullosa simplex type KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Journal of Telemedicine and Telecare|March 10, 2004
Telepathology using immunofluorescence/immunoperoxidase microscopyC M Lanschuetzer, G Pohla-Gubo, B Schafleitner, et al.
The Journal of Investigative Dermatology|April 1, 1996
A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosaJ A McGrath, T Darling, B Gatalica, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|September 11, 2002
[Unilateral blepharochalasis with IgA-deposits]H Schaeppi, M Emberger, U Wieland, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|May 12, 2009
[Hereditary blistering diseases. Symptoms, diagnosis and treatment of epidermolysis bullosa]M Laimer, C M Lanschützer, E Nischler, et al.
Experimental Dermatology|March 13, 2003
Development of spliceosome-mediated RNA trans-splicing (SMaRT) for the correction of inherited skin diseasesG Dallinger, M Puttaraju, L G Mitchell, et al.
Allergy|October 18, 2008
Array-based profiling of ragweed and mugwort pollen allergensG Gadermaier, N Wopfner, M Wallner, et al.
The Journal of Investigative Dermatology|February 11, 1998
Cycloheximide facilitates the identification of aberrant transcripts resulting from a novel splice-site mutation in COL17A1 in a patient with generalized atrophic benign epidermolysis bullosaT N Darling, C Yee, B Koh, et al.
The Journal of Investigative Dermatology|February 11, 1998
A deletion mutation in COL17A1 in five Austrian families with generalized atrophic benign epidermolysis bullosa represents propagation of an ancestral alleleT N Darling, B B Koh, S J Bale, et al.
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