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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
|
December 18, 1998
Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling
F Rouan, L Pulkkinen, M F Jonkman, 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.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 26, 2018
Increased tumour cell PD-L1 expression, macrophage and dendritic cell infiltration characterise the tumour microenvironment of ulcerated primary melanomas
P Koelblinger, M Emberger, M Drach, 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.
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.
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 bullosa
T 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 allele
T N Darling, B B Koh, S J Bale, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 64) with videos related to
Sort By:
Page
of 7
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
|
December 18, 1998
Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling
F Rouan, L Pulkkinen, M F Jonkman, 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.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 26, 2018
Increased tumour cell PD-L1 expression, macrophage and dendritic cell infiltration characterise the tumour microenvironment of ulcerated primary melanomas
P Koelblinger, M Emberger, M Drach, 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.
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.
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 bullosa
T 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 allele
T N Darling, B B Koh, S J Bale, et al.
Page
of 7