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M Schmuth

Showing results (31-40 of 45) with videos related to

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Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1996
[Rare variants of cutaneous T-cell lymphomas]S Goerdt, C Trautmann, B Kütting, et al.
The Journal of Investigative Dermatology|August 22, 2000
Permeability barrier disorder in Niemann-Pick disease: sphingomyelin-ceramide processing required for normal barrier homeostasisM Schmuth, M Q Man, F Weber, et al.
The British Journal of Dermatology|June 20, 2002
Topical corticosteroid therapy for acute radiation dermatitis: a prospective, randomized, double-blind studyM Schmuth, M A Wimmer, S Hofer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 21, 2000
Production of IL-12 by human monocyte-derived dendritic cells is optimal when the stimulus is given at the onset of maturation, and is further enhanced by IL-4S Ebner, G Ratzinger, B Krösbacher, et al.
The British Journal of Dermatology|December 11, 2008
Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysisK A Giehl, M A Rogers, M Radivojkov, et al.
The Journal of Investigative Dermatology|October 26, 2001
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosisM Schmuth, G Yosipovitch, M L Williams, et al.
The British Journal of Dermatology|November 18, 2014
Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTAV Moosbrugger-Martinz, A Jalili, A S Schossig, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2016
Systematic review of surgical treatment of pyoderma gangrenosum with negative pressure wound therapy or skin graftingM Pichler, T Thuile, B Gatscher, et al.
The British Journal of Dermatology|July 25, 2016
Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutationsR Gruber, G Rainer, A Weiss, et al.
The Journal of Investigative Dermatology|December 14, 1999
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichiaR Kruse, S Cichon, M Anker, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|February 1, 1996
[Rare variants of cutaneous T-cell lymphomas]S Goerdt, C Trautmann, B Kütting, et al.
The Journal of Investigative Dermatology|August 22, 2000
Permeability barrier disorder in Niemann-Pick disease: sphingomyelin-ceramide processing required for normal barrier homeostasisM Schmuth, M Q Man, F Weber, et al.
The British Journal of Dermatology|June 20, 2002
Topical corticosteroid therapy for acute radiation dermatitis: a prospective, randomized, double-blind studyM Schmuth, M A Wimmer, S Hofer, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 21, 2000
Production of IL-12 by human monocyte-derived dendritic cells is optimal when the stimulus is given at the onset of maturation, and is further enhanced by IL-4S Ebner, G Ratzinger, B Krösbacher, et al.
The British Journal of Dermatology|December 11, 2008
Pili annulati: refinement of the locus on chromosome 12q24.33 to a 2.9-Mb interval and candidate gene analysisK A Giehl, M A Rogers, M Radivojkov, et al.
The Journal of Investigative Dermatology|October 26, 2001
Pathogenesis of the permeability barrier abnormality in epidermolytic hyperkeratosisM Schmuth, G Yosipovitch, M L Williams, et al.
The British Journal of Dermatology|November 18, 2014
Epidermal barrier abnormalities in exfoliative ichthyosis with a novel homozygous loss-of-function mutation in CSTAV Moosbrugger-Martinz, A Jalili, A S Schossig, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 27, 2016
Systematic review of surgical treatment of pyoderma gangrenosum with negative pressure wound therapy or skin graftingM Pichler, T Thuile, B Gatscher, et al.
The British Journal of Dermatology|July 25, 2016
Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutationsR Gruber, G Rainer, A Weiss, et al.
The Journal of Investigative Dermatology|December 14, 1999
Novel Hairless mutations in two kindreds with autosomal recessive papular atrichiaR Kruse, S Cichon, M Anker, et al.
Pageof 5