Ljerka Lapic-Karadza
Sibenik, Croatia
Last Updated: 09/26/2026
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Found 9 publications
Validation and Cross-Cultural Adaptation of Croatian Self-Evaluation of Communication Experiences after Laryngectomy Questionnaire.
Journal: Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP)
Published: July 26, 2022
HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA - FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES.
Journal: Acta clinica Croatica
Published: August 01, 2019
Recombinant human C1 esterase inhibitor as short-term prophylaxis in patients with hereditary angioedema.
Journal: The journal of allergy and clinical immunology. In practice
Published: April 25, 2019
The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE.
Journal: Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology
Published: March 11, 2019
Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
Journal: Annals of medicine
Published: March 08, 2018
The Incidence and Frequency of Various Causes of Angioedema in Emergency Medicine.
Journal: Acta medica academica
Published: December 29, 2017
Hereditary angioedema - rare disease, complex problems.
Journal: Lijecnicki vjesnik
Published: November 01, 2016
Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1.
Journal: Annals of medicine
Published: May 18, 2016
Guidelines for the diagnosis and treatment of hereditary angioedema
Journal: Lijecnicki vjesnik
Published: August 27, 2014
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Last Updated: 09/26/2026