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K

Konrad Bork

johannes gutenberg university

63H指数
354论文数
1.8W被引数
收录论文 110
发表时间
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Algorithms in Allergy: Hereditary Angioedema
errAllergy
IF12
err2026-02-02
err0
errOAAI
errKonrad Bork; Markus Magerl; Emel Aygören-Pürsün; Henriette Farkas
err分享
err收藏
Treatment of Hereditary Angioedema With Plasma-Derived C1 Inhibitor: A Review
errCLINICAL AND TRANSLATIONAL ALLERGY
IF4
err2025-12-17
err0
errOAAI
errMartinez-Saguer, Inmaculada; Pragst, Ingo; Worrall, Beverley; Bork, Konrad
err分享
err收藏
Insights from the first 820 patients from the Brazilian Multicenter Registry of Hereditary Angioedema: the key role of genetic testing and targeted therapies.来自巴西遗传性血管性水肿多中心登记研究前820例患者的见解：基因检测和靶向治疗的关键作用。
errThe Journal of Allergy and Clinical Immunology: In Practice
IF0
err2025-09-03
err0
errOAAI
errMariana P.L. Ferriani; José Eduardo S Lemos; L.Karla Arruda; Fernanda L. Nunes; Marina M. Dias; Maitê L. Kolarik; Persio Roxo-Junior; Maria Fernanda Ferraro; Maria Eduarda T Zanetti; Faradiba S. Serpa FS; Herberto J. Chong Neto; Fernanda G. Minafra; Solange O.R. Valle; Régis A. Campos; Jane da Silva; Eli Mansour; Rozana F. Gonçalves; Eliana C. Toledo; Fernanda C. Marcelino; Iramirton F. Moreira; Adriana Azoubel-Antunes; Janaira F.S. Ferreira; Gabriela A.C. Dias; Marcelo V. Aun; Ana Paula; Maria Luiza O Alonso; Vanessa A. Batigalia; Clarissa Ltsv Tavares; Albertina V. Capelo; Therezinha R. Moyses; Nelson A. Rosário Filho; Lucca NP Jannuzzi; Nyla TML Fragnan; Joanemile P. de Figueiredo; Joice T. da Fonseca; Ana Julia R Teixeira; Nayara MF Nasser; Natasha R. Ferraroni; Leonardo O. Mendonça; Márcia T. Iwashita; Alex I.F. Prado; Melissa T. Tumelero; Julianne A. Machado; Tsukiyo O. Kamoi; Luciana M. Ferrel; Adriana MSC Barbosa; Caroline GFB de Moraes; Tatielly Kruk; Mariana R. Figueiredo; Maria Stela Y Moraes; Adriana S. Moreno; Luana SM Maia; Fabiola Traina; Patricia C. Ruy PC; João B. Pesquero; Konrad Bork; Sven Cichon; Davi C. Aragon; Pedro Giavina-Bianchi; Anete S. Grumach AS
err分享
err收藏
Garadacimab in hereditary angioedema due to normal C1INH with F12/PLG mutationsGaradacimab 在C1INH正常的F12/PLG突变型遗传性血管性水肿中的应用
errJournal of Allergy and Clinical Immunology
IF11.2
err2025-08-26
err0
PREAI
errDanny M. Cohn; Avner Reshef; Petra Staubach; William R. Lumry; Henrike Feuersenger; Iris Jacobs; Ingo Pragst; Bruce Zuraw; Konrad Bork
err分享
err收藏
Hypertension risk in patients having hereditary angioedema with plasminogen gene mutation K330E遗传性血管性水肿伴plasminogen基因K330E突变患者的 hypertension 风险
errThe Journal of Allergy and Clinical Immunology: In Practice
IF0
err2025-05-15
err0
PREAI
errKonrad Bork; Karin Wulff; Peter Meinke; Thomas Machnig; Jochen Hardt
err分享
err收藏
Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N-acylethanolamines in patients with hereditary angioedema due to FXII mutation
errALLERGY
IF12
err2024-06-27
err0
PREAI
errFerrara, Anne Lise; Palestra, Francesco; Piscitelli, Fabiana; Petraroli, Angelica; Suffritti, Chiara; Firinu, Davide; Lopez-Lera, Alberto; Caballero, Teresa; Bork, Konrad; Spadaro, Giuseppe; Marone, Gianni; Di Marzo, Vincenzo; Bova, Maria; Loffredo, Stefania
err分享
err收藏
Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 Inhibitor具有正常C1抑制剂的孤立性血管性水肿患者中与遗传性血管性水肿相关的基因突变
errJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
IF6.6
err2023-08-01
err8
PREAI
errBork, Konrad; Wulff, Karin; Witzke, Gunther; Staubach, Petra; Hardt, Jochen; Meinke, Peter
err分享
err收藏
Angioedema With Normal Complement Studies: What Do We Know?
errJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
IF6.6
err2023-08-01
err1
PREAI
errKatelaris, Constance H.; Grumach, Anete S.; Bork, Konrad
err分享
err收藏
Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin
errFRONTIERS IN PHYSIOLOGY
IF3.4
err2023-01-05
err12
errOAAI
errHintze, Stefan; Moehl, Britta S.; Beyerl, Jessica; Wulff, Karin; Wieser, Andreas; Bork, Konrad; Meinke, Peter
err分享
err收藏
Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development遗传性血管性水肿的遗传模式表明早期胚胎发育过程中的突变依赖性选择性作用
errJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
IF6.6
err2022-04-01
err4
PREAI
errBork, Konrad; Wulff, Karin; Witzke, Guenther; Hardt, Jochen; Meinke, Peter
err分享
err收藏
The international WAO/EAACI guideline for the management of hereditary angioedema - The 2021 revision and update
errWORLD ALLERGY ORGANIZATION JOURNAL
IF4.3
err2022-03-01
err53
errOAAI
errMaurer, Marcus; Magerl, Markus; Betschel, Stephen; Aberer, Werner; Ansotegui, Ignacio J.; Aygoeren-Puersuen, Emel; Banerji, Aleena; Bara, Noemi-Anna; Boccon-Gibod, Isabelle; Bork, Konrad; Bouillet, Laurence; Boysenl, Henrik Balle; Brodszki, Nicholas; Busse, Paula J.; Bygum, Anette; Caballero, Teresa; Cancian, Mauro; Castaldol, Anthony J.; Cohn, Danny M.; Csuka, Dorottya; Farkas, Henriette; Gompels, Mark; Gower, Richard; Grumach, Anete S.; Guidos-Fogelbach, Guillermo; Hide, Michihiro; Kang, Hye-Ryun; Kaplan, Allen P.; Katelaris, Constance H.; Kiani-Alikhan, Sorena; Lei, Wei-Te; Lockey, Richard F.; Longhurst, Hilary; Lumry, William; MacGinnitie, Andrew; Malbran, Alejandro; Martinez Saguer, Inmaculada; Matta Campos, Juan Jose; Nast, Alexander; Dinh Nguyen; Nieto-Martinez, Sandra A.; Pawankar, Ruby; Peter, Jonathan; Porebski, Grzegorz; Prior, Nieves; Reshef, Avner; Riedl, Marc; Ritchie, Bruce; Sheikh, Farrukh Rafique; Smith, William B.; Spaeth, Peter J.; Stobiecki, Marcin; Toubi, Elias; Varga, Lilian Agnes; Weller, Karsten; Zanichelli, Andrea; Zhi, Yuxiang; Zuraw, Bruce; Craig, Timothy
err分享
err收藏
The international WAO/EAACI guideline for the management of hereditary angioedema-The 2021 revision and update
errALLERGY
IF12
err2022-02-03
err224
errOAAI
errMaurer, Marcus; Magerl, Markus; Betschel, Stephen; Aberer, Werner; Ansotegui, Ignacio J.; Aygoeren-Puersuen, Emel; Banerji, Aleena; Bara, Noemi-Anna; Boccon-Gibod, Isabelle; Bork, Konrad; Bouillet, Laurence; Boysen, Henrik Balle; Brodszki, Nicholas; Busse, Paula J.; Bygum, Anette; Caballero, Teresa; Cancian, Mauro; Castaldo, Anthony; Cohn, Danny M.; Csuka, Dorrottya; Farkas, Henriette; Gompels, Mark; Gower, Richard; Grumach, Anete S.; Guidos-Fogelbach, Guillermo; Hide, Michihiro; Kang, Hye-Ryun; Kaplan, Allen Phillip; Katelaris, Constance; Kiani-Alikhan, Sorena; Lei, Wei-Te; Lockey, Richard; Longhurst, Hilary; Lumry, William R.; MacGinnitie, Andrew; Malbran, Alejandro; Saguer, Inmaculada Martinez; Matta, Juan Jose; Nast, Alexander; Nguyen, Dinh; Nieto-Martinez, Sandra A.; Pawankar, Ruby; Peter, Jonathan; Porebski, Grzegorz; Prior, Nieves; Reshef, Avner; Riedl, Marc; Ritchie, Bruce; Sheikh, Farrukh Rafique; Smith, William R.; Spaeth, Peter J.; Stobiecki, Marcin; Toubi, Elias; Varga, Lilian Agnes; Weller, Karsten; Zanichelli, Andrea; Zhi, Yuxiang; Zuraw, Bruce; Craig, Timothy
err分享
err收藏
Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation
errJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
IF11.2
err2021-10-01
err62
PREAI
errBork, Konrad; Wulff, Karin; Moehl, Britta S.; Steinmueller-Magin, Lars; Witzke, Gunther; Hardt, Jochen; Meinke, Peter
err分享
err收藏
Analysis of cold activation of the contact system in hereditary angioedema with normal C1 inhibitor
errMOLECULAR IMMUNOLOGY
IF3
err2021-08-01
err6
PREAI
errLarrauri, Blas; Hester, C. Garren; Jiang, Haixiang; Miletic, Vojislav D.; Malbran, Alejandro; Bork, Konrad; Kaplan, Allen; Frank, Michael
err分享
err收藏
Uncommon Signs Associated With Hereditary Angioedema With Normal C1 Inhibitor
errJOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY
IF4.8
err2021-06-23
err3
errOAAI
errTaya, J.; Veronez, C. L.; Pesquero, J. B.; Bork, K.; Grumach, A. S.
err分享
err收藏
The Expanding Spectrum of Mutations in Hereditary Angioedema遗传性血管性水肿中突变谱的扩展
errJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE
IF6.6
err2021-06-01
err43
PREAI
errVeronez, Camila Lopes; Csuka, Dorottya; Sheikh, Farrukh R.; Zuraw, Bruce L.; Farkas, Henriette; Bork, Konrad
err分享
err收藏
A germline mutation in the platelet-derived growth factor receptor beta gene may be implicated in hereditary progressive mucinous histiocytosis
errBRITISH JOURNAL OF DERMATOLOGY
IF9.6
err2021-02-05
err6
PREAI
errOnoufriadis, A.; Boulouadnine, B.; Dachy, G.; Higashino, T.; Huang, H. Y.; Hsu, C. K.; Simpson, M. A.; Bork, K.; Demoulin, J. B.; McGrath, J. A.
err分享
err收藏
Current and Prospective Targets of Pharmacologic Treatment of Hereditary Angioedema Types 1 and 2
errCLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY
IF11.3
err2021-01-09
err30
errOAAI
errFijen, Laure M.; Bork, Konrad; Cohn, Danny M.
err分享
err收藏
Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2020-10-15
err67
errOAAI
errBork, Konrad; Machnig, Thomas; Wulff, Karin; Witzke, Guenther; Prusty, Subhransu; Hardt, Jochen
err分享
err收藏
Measurement of Bradykinin Formation and Degradation in Blood Plasma: Relevance for Acquired Angioedema Associated With Angiotensin Converting Enzyme Inhibition and for Hereditary Angioedema Due to Factor XII or Plasminogen Gene Variants
errFRONTIERS IN MEDICINE
IF3
err2020-07-17
err17
errOAAI
errMarceau, Francois; Rivard, Georges E.; Gauthier, Julie M.; Binkley, Karen E.; Bonnefoy, Arnaud; Boccon-Gibod, Isabelle; Bouillet, Laurence; Picard, Matthieu; Levesque, Ghislain; Elfassy, Hannah Laure; Bachelard, Helene; Hebert, Jacques; Bork, Konrad
err分享
err收藏

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