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M F Jonkman

Showing results (131-140 of 151) with videos related to

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European Journal of Dermatology : EJD|July 3, 1998
The use of skin substrates deficient in basement membrane molecules for the diagnosis of subepidermal autoimmune bullous diseaseR M Vodegel, M Kiss, M Cjm De Jong, et al.
Archives of Dermatology|February 1, 1996
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiencyM F Jonkman, M C de Jong, K Heeres, et al.
The British Journal of Dermatology|January 8, 2013
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 geneR G L Nellen, P M Steijlen, H C Hennies, et al.
Journal of Dermatological Science|November 1, 2011
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndromeJ J A J van der Velden, M F Jonkman, W H I McLean, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 15, 2020
IgE autoantibodies in serum and skin of non-bullous and bullous pemphigoid patientsA Lamberts, N Kotnik, G F H Diercks, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2015
Surgery under general anaesthesia in severe hidradenitis suppurativa: a study of 363 primary operations in 113 patientsJ L Blok, M Boersma, J B Terra, et al.
Allergy|October 21, 2009
Filaggrin mutations in the onset of eczema, sensitization, asthma, hay fever and the interaction with cat exposureM L A Schuttelaar, M Kerkhof, M F Jonkman, et al.
Oral Oncology|July 19, 2000
Paraneoplastic pemphigus caused by an epithelioid leiomyosarcoma and associated with fatal respiratory failureR I van der Waal, H H Pas, H C Nousari, et al.
The Journal of Investigative Dermatology|September 1, 1997
LAD-1 is absent in a subset of junctional epidermolysis bullosa patientsM P Marinkovich, H H Tran, S K Rao, et al.
Human Genetics|August 1, 1997
Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosaH Scheffer, R P Stulp, E Verlind, et al.
Pageof 16

Showing results (131-140 of 151) with videos related to

Sort By:
Pageof 16
European Journal of Dermatology : EJD|July 3, 1998
The use of skin substrates deficient in basement membrane molecules for the diagnosis of subepidermal autoimmune bullous diseaseR M Vodegel, M Kiss, M Cjm De Jong, et al.
Archives of Dermatology|February 1, 1996
Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiencyM F Jonkman, M C de Jong, K Heeres, et al.
The British Journal of Dermatology|January 8, 2013
Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 geneR G L Nellen, P M Steijlen, H C Hennies, et al.
Journal of Dermatological Science|November 1, 2011
A recurrent mutation in the TGM5 gene in European patients with acral peeling skin syndromeJ J A J van der Velden, M F Jonkman, W H I McLean, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 15, 2020
IgE autoantibodies in serum and skin of non-bullous and bullous pemphigoid patientsA Lamberts, N Kotnik, G F H Diercks, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 16, 2015
Surgery under general anaesthesia in severe hidradenitis suppurativa: a study of 363 primary operations in 113 patientsJ L Blok, M Boersma, J B Terra, et al.
Allergy|October 21, 2009
Filaggrin mutations in the onset of eczema, sensitization, asthma, hay fever and the interaction with cat exposureM L A Schuttelaar, M Kerkhof, M F Jonkman, et al.
Oral Oncology|July 19, 2000
Paraneoplastic pemphigus caused by an epithelioid leiomyosarcoma and associated with fatal respiratory failureR I van der Waal, H H Pas, H C Nousari, et al.
The Journal of Investigative Dermatology|September 1, 1997
LAD-1 is absent in a subset of junctional epidermolysis bullosa patientsM P Marinkovich, H H Tran, S K Rao, et al.
Human Genetics|August 1, 1997
Implications of intragenic marker homozygosity and haplotype sharing in a rare autosomal recessive disorder: the example of the collagen type XVII (COL17A1) locus in generalised atrophic benign epidermolysis bullosaH Scheffer, R P Stulp, E Verlind, et al.
Pageof 16