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M F Jonkman

Showing results (111-120 of 151) with videos related to

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The British Journal of Dermatology|June 21, 2007
Acquired palmoplantar keratoderma and immunobullous disease associated with antibodies to desmocollin 3M 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 formK 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 plectinJ 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 collagenA M G Pasmooij, G van der Steege, H H Pas, et al.
The British Journal of Dermatology|June 26, 2013
Laboratory diagnosis of paraneoplastic pemphigusA 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 mutationD 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 230M 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 mappingM 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 2S P Covello, F J Smith, J H Sillevis Smitt, et al.
Pageof 16

Showing results (111-120 of 151) with videos related to

Sort By:
Pageof 16
The British Journal of Dermatology|June 21, 2007
Acquired palmoplantar keratoderma and immunobullous disease associated with antibodies to desmocollin 3M 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 formK 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 plectinJ 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 collagenA M G Pasmooij, G van der Steege, H H Pas, et al.
The British Journal of Dermatology|June 26, 2013
Laboratory diagnosis of paraneoplastic pemphigusA 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 mutationD 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 230M 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 mappingM 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 2S P Covello, F J Smith, J H Sillevis Smitt, et al.
Pageof 16