P. Kuklínek

发表

Serotonin transporter gene (SLC6A4) variability in patients with recurrent aphthous stomatitis.

J. Bartova, A. Fassmann, P. Bořilová Linhartová, 2019, Archives of oral biology.

Association of the angiotensin I converting enzyme (ACE) gene polymorphisms with recurrent aphthous stomatitis in the Czech population: case–control study

L. Dušek, J. Bartova, A. Fassmann, 2022, BMC oral health.

Association study of interleukin‐1 family, interleukin‐6, and its receptor gene polymorphisms in patients with recurrent aphthous stomatitis

J. Bartova, A. Fassmann, P. Bořilová Linhartová, 2017, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

Recurrent aphthous stomatitis and gene variability in selected interleukins: a case–control study

L. Dušek, J. Bartova, A. Fassmann, 2018, European journal of oral sciences.

Change in Referral Diagnoses and Diagnostic Delay in Hypogammaglobulinaemic Patients during 28 Years in a Single Referral Centre

J. Litzman, T. Pavlík, V. Thon, 2010, International Archives of Allergy and Immunology.

Sequence variants of the TNFRSF13B gene in Czech CVID and IgAD patients in the context of other populations.

J. Litzman, B. Ravčuková, Jirí Jarkovský, 2012, Human immunology.

Paracentesis vs. intraperitoneal reinfusion of concentrated ascites — effect on opsonic activity of ascites

I. Novotný, J. Lata, J. Prášek, 1999 .

Lack of dehydroepiandrosterone in type I and II hereditary angioedema and role of danazol in steroid hormone conversion

J. Schölmerich, R. Straub, V. Thon, 2007, Allergy.

Gene variability in matrix metalloproteinases in patients with recurrent aphthous stomatitis.

L. Dušek, J. Bartova, A. Fassmann, 2020, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

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

M. Vlková, P. Kralickova, J. Litzman, 2018, Journal of Clinical Immunology.

Association of the NOD‐like receptor 3 (NLRP3) gene variability with recurrent aphthous stomatitis in the Czech population

L. Dušek, J. Bartova, A. Fassmann, 2018, Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology.

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

M. Vlková, P. Kralickova, J. Litzman, 2018, Journal of Clinical Immunology.

Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre.

J. Litzman, P. Kadlecová, P. Kuklínek, 2016, Allergologia et immunopathologia.

No Evidence for Linkage between the Hereditary Angiooedema Clinical Phenotype and the BDKR1, BDKR2, ACE or MBL2 gene

J. Litzman, B. Ravčuková, Jirí Jarkovský, 2011, Scandinavian journal of immunology.

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

J. Litzman, L. Kolářová, T. Freiberger, 2002, Human immunology.

Registry‐based analysis of Icatibant and C1‐inhibitor use in treatment of laryngeal attacks of hereditary angioedema

P. Kralickova, J. Litzman, M. Svoboda, 2022, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

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

J. Litzman, P. Mejstrik, L. Kolářová, 2002, Human mutation.

Abstracts from the 10th C1-inhibitor deficiency workshop

William H. Yang, A. Szilágyi, M. Margaglione, 2017, Allergy, Asthma & Clinical Immunology.

Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation

J. Litzman, B. Ravčuková, P. Souček, 2020, Journal of Clinical Immunology.

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

P. Kralickova, I. Krčmová, J. Bartunkova, 2021, International Archives of Allergy and Immunology.

Hereditary angioedema in Czechoslovakia. Clinical, immunological, genetic and therapeutic studies of 16 families.

J. Čáp, J. Štefanovič, J. Lokaj, 1988, Allergie und Immunologie.

Incidence of primary immunodeficiencies in a population of south Moravia, Czechoslovakia.

J. Litzman, J. Lokaj, P. Kuklínek, 1995, Advances in Experimental Medicine and Biology.

Systematic Approach Revealed SERPING1 Splicing-Affecting Variants to be Highly Represented in the Czech National HAE Cohort

P. Kralickova, J. Litzman, B. Ravčuková, 2023, Journal of Clinical Immunology.