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Diagnosing Pediatric Patients With Hereditary C1-Inhibitor Deficiency-Experience From the Hungarian Angioedema Center of Reference and Excellence.
Andrási, Noémi; Balla, Zsuzsanna; Visy, Beáta; Szilágyi, Ágnes; Csuka, Dorottya; Varga, Lilian; Farkas, Henriette.
Affiliation
  • Andrási N; Department of Internal Medicine and Haematology, Hungarian Angioedema Center of Reference and Excellence, Semmelweis University, Budapest, Hungary.
  • Balla Z; School of Ph.D. Studies, Semmelweis University, Budapest, Hungary.
  • Visy B; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Szilágyi Á; Department of Internal Medicine and Haematology, Hungarian Angioedema Center of Reference and Excellence, Semmelweis University, Budapest, Hungary.
  • Csuka D; School of Ph.D. Studies, Semmelweis University, Budapest, Hungary.
  • Varga L; Department of Internal Medicine and Haematology, Hungarian Angioedema Center of Reference and Excellence, Semmelweis University, Budapest, Hungary.
  • Farkas H; Department of Infectious Diseases, Heim Pál Children's Hospital, Budapest, Hungary.
Front Allergy ; 3: 860355, 2022.
Article in En | MEDLINE | ID: mdl-35769571
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Language: En Journal: Front Allergy Year: 2022 Document type: Article Affiliation country: Hungary Country of publication: Switzerland
Fulltext
Add to My VHL
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XML
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Language: En Journal: Front Allergy Year: 2022 Document type: Article Affiliation country: Hungary Country of publication: Switzerland