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A Bygum

Showing results (31-40 of 46) with videos related to

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Allergy|September 5, 2014
A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymesK Joseph, S Bains, B G Tholanikunnel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 10, 2021
Variability of disease activity in patients with hereditary angioedema type 1/2: longitudinal data from the Icatibant Outcome SurveyM Maurer, T Caballero, W Aberer, et al.
Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.
Clinical and Experimental Immunology|March 16, 2011
Novel assays to assess the functional capacity of the classical, the alternative and the lectin pathways of the complement systemY Palarasah, C Nielsen, U Sprogøe, et al.
Bone|March 11, 2020
Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variantsM Frost, E T Rahbek, C Ejersted, et al.
The British Journal of Dermatology|August 18, 2009
A randomized controlled trial of R-salbutamol for topical treatment of discoid lupus erythematosusG B E Jemec, S Ullman, M Goodfield, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
American Journal of Human Genetics|May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3R C Betz, Y A Lee, A Bygum, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2022
Proposal for a 6-step approach for differential diagnosis of neonatal erythrodermaE Cuperus, A Bygum, L Boeckmann, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Allergy|September 5, 2014
A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymesK Joseph, S Bains, B G Tholanikunnel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 10, 2021
Variability of disease activity in patients with hereditary angioedema type 1/2: longitudinal data from the Icatibant Outcome SurveyM Maurer, T Caballero, W Aberer, et al.
Journal of Human Genetics|September 2, 2006
A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype associationM Melin, J Klar, T Jr Gedde-Dahl, et al.
Clinical and Experimental Immunology|March 16, 2011
Novel assays to assess the functional capacity of the classical, the alternative and the lectin pathways of the complement systemY Palarasah, C Nielsen, U Sprogøe, et al.
Bone|March 11, 2020
Modeling-based bone formation transforms trabeculae to cortical bone in the sclerotic areas in Buschke-Ollendorff syndrome. A case study of two females with LEMD3 variantsM Frost, E T Rahbek, C Ejersted, et al.
The British Journal of Dermatology|August 18, 2009
A randomized controlled trial of R-salbutamol for topical treatment of discoid lupus erythematosusG B E Jemec, S Ullman, M Goodfield, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Molecular Syndromology|October 30, 2013
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedemaA Mendola, M J Schlögel, A Ghalamkarpour, et al.
American Journal of Human Genetics|May 4, 2000
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3R C Betz, Y A Lee, A Bygum, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2022
Proposal for a 6-step approach for differential diagnosis of neonatal erythrodermaE Cuperus, A Bygum, L Boeckmann, et al.
Pageof 5