Publications by authors named "Karin Wulff"

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Hypertension risk in patients having hereditary angioedema with plasminogen gene mutation K330E.
Konrad Bork, Karin Wulff, Peter Meinke, Thomas Machnig, Jochen Hardt

J Allergy Clin Immunol Pract· August 2025

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Gene Mutations Linked to Hereditary Angioedema in Solitary Angioedema Patients With Normal C1 Inhibitor.
Konrad Bork, Karin Wulff, Günther Witzke, Petra Staubach, Jochen Hardt

J Allergy Clin Immunol Pract· August 2023

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Mutant plasminogen in hereditary angioedema is bypassing FXII/kallikrein to generate bradykinin.
Stefan Hintze, Britta S Möhl, Jessica Beyerl, Karin Wulff, Andreas Wieser

Front Physiol· January 2023

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Inheritance Pattern of Hereditary Angioedema Indicates Mutation-Dependent Selective Effects During Early Embryonic Development.
Konrad Bork, Karin Wulff, Günther Witzke, Jochen Hardt, Peter Meinke

J Allergy Clin Immunol Pract· April 2022

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Novel hereditary angioedema linked with a heparan sulfate 3-O-sulfotransferase 6 gene mutation.
Konrad Bork, Karin Wulff, Britta S Möhl, Lars Steinmüller-Magin, Günther Witzke

J Allergy Clin Immunol· October 2021

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Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence.
Konrad Bork, Thomas Machnig, Karin Wulff, Guenther Witzke, Subhransu Prusty

Orphanet J Rare Dis· October 2020

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Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
Konrad Bork, Arne Zibat, David M Ferrari, Bernd Wollnik, Michael P Schön, Karin Wulff

J Dtsch Dermatol Ges· March 2020

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[Not Available].
Konrad Bork, Arne Zibat, David M Ferrari, Bernd Wollnik, Michael P Schön, Karin Wulff

J Dtsch Dermatol Ges· March 2020

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Treatment of patients with hereditary angioedema with the c.988A>G (p.Lys330Glu) variant in the plasminogen gene.
Konrad Bork, Karin Wulff, Guenther Witzke, Thomas Machnig, Jochen Hardt

Orphanet J Rare Dis· February 2020

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Hereditary angioedema cosegregating with a novel kininogen 1 gene mutation changing the N-terminal cleavage site of bradykinin.
Konrad Bork, Karin Wulff, Heidi Rossmann, Lars Steinmüller-Magin, Ingrid Braenne

Allergy· December 2019

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Antihistamine-resistant angioedema in women with negative family history: estrogens and F12 gene mutations.
Konrad Bork, Karin Wulff, Günther Witzke, Christian Stanger, Peter Lohse

Am J Med· December 2013

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A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.
Konrad Bork, Karin Wulff, Peter Meinke, Nicola Wagner, Jochen Hardt

Clin Immunol· October 2011

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Hereditary angioedema caused by missense mutations in the factor XII gene: clinical features, trigger factors, and therapy.
Konrad Bork, Karin Wulff, Jochen Hardt, Günther Witzke, Petra Staubach

J Allergy Clin Immunol· July 2009

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Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V.
Falko H Herrmann, Karin Wulff, Rüdiger Strey, Annelie Siegemund, Jan Astermark

Haematologica· August 2008

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The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients.
Lizbeth Salazar-Sánchez, Maria Paz Leon, Mayra Cartin, Gudrun Schuster, Karin Wulff

Cell Biochem Funct· January 2008

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Analysis of the novel factor X gene mutation Glu51Lys in two families with factor X-Riyadh anomaly.
Akram Al-Hilali, Karin Wulff, Hikmat Abdel-Razeq, Khalida Abu Saud, Fateh Al-Gaili

Thromb Haemost· April 2007

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Influence of factor V HR2 on thrombin generation and clinical manifestation in rare bleeding disorders.
Rüdiger F Strey, Annelie Siegemund, Thomas Siegemund, Christine Schubert, Gudrun Schuster, Karin Wulff

Pathophysiol Haemost Thromb· July 2006

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Common polymorphisms and cardiovascular factors in patients with myocardial infarction of Costa Rica.
Lizbeth Salazar-Sánchez, Lilliana Chaves, Mayra Cartin, Gudrun Schuster, Karin Wulff

Rev Biol Trop· March 2006

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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency.
Guglielmo Mariani, Falko H Herrmann, Alberto Dolce, Angelika Batorova, Daniela Etro, Karin Wulff

Thromb Haemost· March 2005

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Homozygous Factor X gene mutations Gly380Arg and Tyr163delAT are associated with perinatal intracranial hemorrhage.
Falko H Herrmann, Marta Navarette, Lizbeth Salazar-Sanchez, Juan M Carillo, Guenter Auerswald, Karin Wulff

J Pediatr· January 2005

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Molecular diagnosis of hemophilia A and B. Report of five families from Costa Rica.
Lizbeth Salazar-Sánchez, Guillermo Jiménez-Cruz, Pilar Chaverri, Winnie Schröder, Karin Wulff

Rev Biol Trop· September 2004

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Prevalence of eight molecular markers associated with thrombotic diseases in six Amerindian tribes and two African groups of Costa Rica.
Falko H Herrmann, Lizbeth Salazar-Sánchez, Gudrun Schuster, Gerardo Jiménez-Arce, Rita Grimm, Karin Wulff

Am J Hum Biol· April 2004

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The Gly331Ser mutation in factor VII in Europe and the Middle East.
Daniela Etro, Mirko Pinotti, Karin Wulff, Giovanna Marchetti, Angiola Rocino

Haematologica· December 2003

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Early onset of cardiomyopathy in two brothers with X-linked Emery-Dreifuss muscular dystrophy.
Ulvi Astra Talkop, Inga Talvik, Margit Sõnajalg, Hiljar Sibul, Anneli Kolk, Karin Wulff

Neuromuscul Disord· November 2002

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