Search research articles
Contact Us
Filters
Showing results (31-40 of 45) with videos related to
Page
of 5
Sort By:
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 homeostasis
M 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 study
M 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-4
S 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 analysis
K 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 hyperkeratosis
M 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 CSTA
V 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 grafting
M 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 mutations
R 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 atrichia
R Kruse, S Cichon, M Anker, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 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 homeostasis
M 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 study
M 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-4
S 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 analysis
K 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 hyperkeratosis
M 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 CSTA
V 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 grafting
M 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 mutations
R 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 atrichia
R Kruse, S Cichon, M Anker, et al.
Page
of 5