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K Bork

Showing results (151-160 of 159) with videos related to

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The British Journal of Dermatology|December 10, 2020
A germline mutation in the platelet-derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosisA Onoufriadis, B Boulouadnine, G Dachy, et al.
Allergy|August 10, 2016
International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiencyH Farkas, I Martinez-Saguer, K Bork, et al.
Allergy|June 1, 2011
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian familyM F Ferraro, A S Moreno, E C Castelli, et al.
Allergy|July 17, 2018
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedemaA E Germenis, G Loules, M Zamanakou, et al.
Allergy|March 29, 2014
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working GroupM Cicardi, W Aberer, A Banerji, et al.
Allergy|January 11, 2018
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and updateM Maurer, M Magerl, I Ansotegui, et al.
Arerugi = [Allergy]|March 17, 2023
M Maurer, M Magerl, I Ansotegui, et al.
Arerugi = [Allergy]|September 20, 2023
M Maurer, M Magerl, S Betschel, et al.
Arerugi = [Allergy]|May 24, 2023
M Maurer, M Magerl, S Betschel, et al.
Pageof 16

Showing results (151-160 of 159) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 159 results.
The British Journal of Dermatology|December 10, 2020
A germline mutation in the platelet-derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosisA Onoufriadis, B Boulouadnine, G Dachy, et al.
Allergy|August 10, 2016
International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiencyH Farkas, I Martinez-Saguer, K Bork, et al.
Allergy|June 1, 2011
A single nucleotide deletion at the C1 inhibitor gene as the cause of hereditary angioedema: insights from a Brazilian familyM F Ferraro, A S Moreno, E C Castelli, et al.
Allergy|July 17, 2018
On the pathogenicity of the plasminogen K330E mutation for hereditary angioedemaA E Germenis, G Loules, M Zamanakou, et al.
Allergy|March 29, 2014
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working GroupM Cicardi, W Aberer, A Banerji, et al.
Allergy|January 11, 2018
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2017 revision and updateM Maurer, M Magerl, I Ansotegui, et al.
Arerugi = [Allergy]|March 17, 2023
M Maurer, M Magerl, I Ansotegui, et al.
Arerugi = [Allergy]|September 20, 2023
M Maurer, M Magerl, S Betschel, et al.
Arerugi = [Allergy]|May 24, 2023
M Maurer, M Magerl, S Betschel, et al.
Pageof 16