Pavel Kuklı́nek

Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation

Pavla Hujová, Přemysl Souček, Lucie Grodecká et al. · Journal of Clinical Immunology · 2020 · 33 citations

Life Sciences, Genetics, Molecular Genetics +4

Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy

Roman Hakl, Pavel Kuklı́nek, Irena Krčmová et al. · Journal of Clinical Immunology · 2018 · 27 citations

Medicine, Pharmacology, Pharmacotherapy +8

Acquired Angioedema with C1 Inhibitor Deficiency: Occurrence, Clinical Features, and Management: A Nationwide Retrospective Study in the Czech Republic Patients

Marta Sobotková, Radana Zachová, Roman Hakl et al. · International Archives of Allergy and Immunology · 2021 · 26 citations · Full text

Medicine, Internal Medicine, Clinical Pharmacology +10

Five novel mutations in the C1 inhibitor gene (C1NH) leading to a premature stop codon in patients with type I hereditary angioedema

Tomáš Freiberger, Lenka Kolářová, Pavel Mejstřík et al. · Human Mutation · 2002 · 25 citations

Life Sciences, Genetics, Molecular Genetics +12

Exon 1 polymorphism of the B2BKR gene does not influence the clinical status of patients with hereditary angioedema

Tomáš Freiberger, Martina Vyskočilová, Lenka Kolářová et al. · Human Immunology · 2002 · 20 citations

Life Sciences, Genetics, Molecular Genetics +4