MUDr. Roman Hakl, Ph.D.
Assistant professor, Department of Clinical Immunology and Allergology
Total number of publications: 30
2018
-
A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema
Year: 2018, type:
-
Hereditární angioedém laryngealní ataky: data z Národního registru primárních imunodeficiencí
Year: 2018, type: Conference abstract
-
Perioperative management of Hereditary Angioedema
Year: 2018, type:
-
Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy
Journal of Clinical Immunology, year: 2018, volume: 38, edition: 7, DOI
2017
-
Clinical and molecular characterisation of czech hereditary angioedema patients.
Year: 2017, type: Appeared in Conference without Proceedings
-
New deep intronic mutation c.1029+384 A>G in SERPING1 gene creates de novo donor splice site and causes aberrant splicing
Year: 2017, type: Conference abstract
2016
-
Hereditary angio-oedema with C1 inhibitor deficiency: Characteristics and diagnostic delay of Czech patients from one centre
Allergologia et immunopathologia, year: 2016, volume: 44, edition: 3, DOI
-
Současné možnosti léčby hereditárního angioedému
Vnitřní lékařství, year: 2016, volume: 62, edition: 9
2015
-
A novel STAT3 gene mutation revealed in a patient with hyper IgE syndrome and severe eczema
Year: 2015, type: Conference abstract
-
Activation of granulocytes in common variable immunodeficiency and hereditary angioedema
Year: 2015, type: Conference abstract