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The Journal of Investigative Dermatology
|
March 7, 2001
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
A Klausegger, L Pulkkinen, G Pohla-Gubo, et al.
Microbiology (Reading, England)
|
September 7, 2010
Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target
M Haim, A Trost, C J Maier, et al.
The British Journal of Dermatology
|
June 29, 2007
Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab
E Sadler, B Schafleitner, C Lanschuetzer, 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 Köbner
C M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Journal of Telemedicine and Telecare
|
March 10, 2004
Telepathology using immunofluorescence/immunoperoxidase microscopy
C 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 bullosa
J 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 diseases
G Dallinger, M Puttaraju, L G Mitchell, et al.
Human Genetics
|
August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, Koebner
C M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 121) with videos related to
Sort By:
Page
of 13
The Journal of Investigative Dermatology
|
March 7, 2001
Is screening of the candidate gene necessary in unrelated partners of members of families with Herlitz junctional epidermolysis bullosa?
A Klausegger, L Pulkkinen, G Pohla-Gubo, et al.
Microbiology (Reading, England)
|
September 7, 2010
Cytokeratin 8 interacts with clumping factor B: a new possible virulence factor target
M Haim, A Trost, C J Maier, et al.
The British Journal of Dermatology
|
June 29, 2007
Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab
E Sadler, B Schafleitner, C Lanschuetzer, 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 Köbner
C M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Journal of Telemedicine and Telecare
|
March 10, 2004
Telepathology using immunofluorescence/immunoperoxidase microscopy
C 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 bullosa
J 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 diseases
G Dallinger, M Puttaraju, L G Mitchell, et al.
Human Genetics
|
August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, Koebner
C M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
Page
of 13