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The British Journal of Dermatology
|
June 21, 2007
Acquired palmoplantar keratoderma and immunobullous disease associated with antibodies to desmocollin 3
M C Bolling, J R Mekkes, W F M Goldschmidt, et al.
Clinical and Experimental Dermatology
|
February 15, 2000
Two type XVII collagen (BP180) mRNA transcripts in human keratinocytes: a long and a short form
K Molnar, G van der Steege, M F Jonkman, et al.
Clinical and Experimental Dermatology
|
July 28, 2005
Inflammatory epidermolysis bullosa acquisita with coexistent IgA antibodies to plectin
J J A Buijsrogge, M C J M de Jong, H J Meijer, et al.
The British Journal of Dermatology
|
September 21, 2004
Features of epidermolysis bullosa simplex due to mutations in the ectodomain of type XVII collagen
A M G Pasmooij, G van der Steege, H H Pas, et al.
The British Journal of Dermatology
|
June 26, 2013
Laboratory diagnosis of paraneoplastic pemphigus
A M Poot, G F H Diercks, D Kramer, et al.
Acta Dermato-Venereologica
|
June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation
D Koss-Harnes, B Høyheim, M F Jonkman, et al.
The British Journal of Dermatology
|
March 20, 2002
Cicatricial pemphigoid with circulating autoantibodies to beta4 integrin, bullous pemphigoid 180 and bullous pemphigoid 230
M Leverkus, K Bhol, Y Hirako, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 23, 2020
Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?
R Baardman, V K Yenamandra, J C Duipmans, et al.
Archives of Dermatology
|
February 1, 1996
Bullous pemphigoid and epidermolysis bullosa acquisita. Differentiation by fluorescence overlay antigen mapping
M C De Jong, S Bruins, K Heeres, et al.
The British Journal of Dermatology
|
October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
S P Covello, F J Smith, J H Sillevis Smitt, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 151) with videos related to
Sort By:
Page
of 16
The British Journal of Dermatology
|
June 21, 2007
Acquired palmoplantar keratoderma and immunobullous disease associated with antibodies to desmocollin 3
M C Bolling, J R Mekkes, W F M Goldschmidt, et al.
Clinical and Experimental Dermatology
|
February 15, 2000
Two type XVII collagen (BP180) mRNA transcripts in human keratinocytes: a long and a short form
K Molnar, G van der Steege, M F Jonkman, et al.
Clinical and Experimental Dermatology
|
July 28, 2005
Inflammatory epidermolysis bullosa acquisita with coexistent IgA antibodies to plectin
J J A Buijsrogge, M C J M de Jong, H J Meijer, et al.
The British Journal of Dermatology
|
September 21, 2004
Features of epidermolysis bullosa simplex due to mutations in the ectodomain of type XVII collagen
A M G Pasmooij, G van der Steege, H H Pas, et al.
The British Journal of Dermatology
|
June 26, 2013
Laboratory diagnosis of paraneoplastic pemphigus
A M Poot, G F H Diercks, D Kramer, et al.
Acta Dermato-Venereologica
|
June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutation
D Koss-Harnes, B Høyheim, M F Jonkman, et al.
The British Journal of Dermatology
|
March 20, 2002
Cicatricial pemphigoid with circulating autoantibodies to beta4 integrin, bullous pemphigoid 180 and bullous pemphigoid 230
M Leverkus, K Bhol, Y Hirako, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
October 23, 2020
Novel insights into the epidemiology of epidermolysis bullosa (EB) from the Dutch EB Registry: EB more common than previously assumed?
R Baardman, V K Yenamandra, J C Duipmans, et al.
Archives of Dermatology
|
February 1, 1996
Bullous pemphigoid and epidermolysis bullosa acquisita. Differentiation by fluorescence overlay antigen mapping
M C De Jong, S Bruins, K Heeres, et al.
The British Journal of Dermatology
|
October 10, 1998
Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
S P Covello, F J Smith, J H Sillevis Smitt, et al.
Page
of 16