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G Pohla

Showing results (11-20 of 29) with videos related to

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Journal of Cutaneous Pathology|September 26, 2003
Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderC M Lanschuetzer, W H Muss, M Emberger, 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.
The American Journal of Gastroenterology|April 9, 2009
Transient autoimmune hepatitis induced by a thymomaE Aigner, C P Strassburg, M Strasser, 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.
Human Genetics|August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, KoebnerC 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 KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
The British Journal of Dermatology|December 3, 1999
Ocular involvement in IgA-epidermolysis bullosa acquisitaJ W Bauer, H Schaeppi, D Metze, et al.
Wiener Klinische Wochenschrift|January 1, 1992
[Quality control in the allergy laboratory--4 years "Allergy Ring Trial" in Austria]W Aberer, H Ebner, F Horak, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Journal of Cutaneous Pathology|September 26, 2003
Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorderC M Lanschuetzer, W H Muss, M Emberger, 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.
The American Journal of Gastroenterology|April 9, 2009
Transient autoimmune hepatitis induced by a thymomaE Aigner, C P Strassburg, M Strasser, 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.
Human Genetics|August 11, 2004
Gene symbol: KRT14. Disease: epidermolysis bullosa simplex, KoebnerC 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 KöbnerC M Lanschuetzer, A Klausegger, G Pohla-Gubo, et al.
The British Journal of Dermatology|December 3, 1999
Ocular involvement in IgA-epidermolysis bullosa acquisitaJ W Bauer, H Schaeppi, D Metze, et al.
Wiener Klinische Wochenschrift|January 1, 1992
[Quality control in the allergy laboratory--4 years "Allergy Ring Trial" in Austria]W Aberer, H Ebner, F Horak, et al.
Pageof 3