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H Hintner

Showing results (71-80 of 121) with videos related to

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Der Urologe. Ausg. A|November 1, 1989
[Benign prostatic hyperplasia: a stromal disease]G Bartsch, A Brüngger, U Schweikert, et al.
The Journal of Clinical Investigation|May 20, 1999
Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutationT N Darling, C Yee, J W Bauer, et al.
The Journal of Investigative Dermatology|February 1, 1987
Phagocytosis of keratin filament aggregates following opsonization with IgG-anti-keratin filament autoantibodiesH Hintner, N Romani, U Stanzl, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|October 27, 2009
[Orogenital and conjunctival involvement in hereditary and autoimmune blistering diseases]M Laimer, C M Lanschützer, M Emberger, et al.
Human Pathology|June 1, 1992
Life history of cutaneous vascular lesions in Sneddon's syndromeB Zelger, N Sepp, K W Schmid, et al.
Archives of Dermatological Research|April 27, 2011
Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's diseaseA Klausegger, E Nischler, R N Wagner, et al.
The British Journal of Dermatology|May 22, 2001
Human papillomavirus infection in Netherton's syndromeF Weber, P G Fuchs, H J Pfister, et al.
Clinical Nephrology|March 1, 1993
Hereditary complete deficiency of the fourth component of complement: effects on the kidneyK Lhotta, W Thoenes, J Glatzl, et al.
The Journal of Investigative Dermatology|February 1, 1981
Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseasesH Hintner, G Stingl, G Schuler, et al.
The Journal of Investigative Dermatology|July 1, 1988
Amyloid P component binds to keratin bodies in human skin and to isolated keratin filament aggregates in vitroH Hintner, J Booker, J Ashworth, et al.
Pageof 13

Showing results (71-80 of 121) with videos related to

Sort By:
Pageof 13
Der Urologe. Ausg. A|November 1, 1989
[Benign prostatic hyperplasia: a stromal disease]G Bartsch, A Brüngger, U Schweikert, et al.
The Journal of Clinical Investigation|May 20, 1999
Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutationT N Darling, C Yee, J W Bauer, et al.
The Journal of Investigative Dermatology|February 1, 1987
Phagocytosis of keratin filament aggregates following opsonization with IgG-anti-keratin filament autoantibodiesH Hintner, N Romani, U Stanzl, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|October 27, 2009
[Orogenital and conjunctival involvement in hereditary and autoimmune blistering diseases]M Laimer, C M Lanschützer, M Emberger, et al.
Human Pathology|June 1, 1992
Life history of cutaneous vascular lesions in Sneddon's syndromeB Zelger, N Sepp, K W Schmid, et al.
Archives of Dermatological Research|April 27, 2011
Seven novel mutations in the ATP2A2 gene of Austrian patients with Darier's diseaseA Klausegger, E Nischler, R N Wagner, et al.
The British Journal of Dermatology|May 22, 2001
Human papillomavirus infection in Netherton's syndromeF Weber, P G Fuchs, H J Pfister, et al.
Clinical Nephrology|March 1, 1993
Hereditary complete deficiency of the fourth component of complement: effects on the kidneyK Lhotta, W Thoenes, J Glatzl, et al.
The Journal of Investigative Dermatology|February 1, 1981
Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseasesH Hintner, G Stingl, G Schuler, et al.
The Journal of Investigative Dermatology|July 1, 1988
Amyloid P component binds to keratin bodies in human skin and to isolated keratin filament aggregates in vitroH Hintner, J Booker, J Ashworth, et al.
Pageof 13