MUDr. Roman Hakl, Ph.D.
Assistant professor, Department of Clinical Immunology and Allergology
Total number of publications: 33
2020
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The splicing pattern of PLAUR gene changes during monocyte differentiation in patients with hereditary angioedema.
Year: 2020, type: Conference abstract
2019
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Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period
Mediators of Inflammation, year: 2019, volume: 2019, edition: 9515628, DOI
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Safety of recombinant human C1 esterase inhibitor for hereditary angioedema attacks during pregnancy
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, year: 2019, volume: 7, edition: 8, DOI
2018
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A new deep intronic mutation caused aberrant splicing in a family diagnosed with hereditary angioedema
Year: 2018, type:
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Hereditární angioedém laryngealní ataky: data z Národního registru primárních imunodeficiencí
Year: 2018, type: Conference abstract
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Perioperative management of Hereditary Angioedema
Year: 2018, type:
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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
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Clinical and molecular characterisation of czech hereditary angioedema patients.
Year: 2017, type: Appeared in Conference without Proceedings
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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
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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