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536 related items for PubMed ID: 31363336
1. HEREDITARY ANGIOEDEMA DUE TO C1-INHIBITOR DEFICIENCY IN PEDIATRIC PATIENTS IN CROATIA - FIRST NATIONAL STUDY, DIAGNOSTIC AND PROPHYLACTIC CHALLENGES. Karadža-Lapić L, Barešić M, Vrsalović R, Ivković-Jureković I, Sršen S, Prkačin I, Rijavec M, Cikojević D. Acta Clin Croat; 2019 Mar; 58(1):139-146. PubMed ID: 31363336 [Abstract] [Full Text] [Related]
2. [Guidelines for the diagnosis and treatment of hereditary angioedema]. Marković AS, Rozmanić V, Anić B, Aberle N, Racić G, Novak S, Sunara D, Grdinić B, Karadza-Lapić L, Radas MR, Karanović B, Kvenić B. Lijec Vjesn; 2014 Mar; 136(5-6):117-29. PubMed ID: 25154179 [Abstract] [Full Text] [Related]
3. Diagnosis and treatment of hereditary angioedema. Canonica GW, Rossi O. Panminerva Med; 2012 Sep; 54(3):241-53. PubMed ID: 22801442 [Abstract] [Full Text] [Related]
7. Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype. Grivčeva-Panovska V, Košnik M, Korošec P, Andrejević S, Karadža-Lapić L, Rijavec M. Ann Med; 2018 May 01; 50(3):269-276. PubMed ID: 29513108 [Abstract] [Full Text] [Related]
8. Hereditary angioedema with normal C1 inhibitor and factor XII mutation: a series of 57 patients from the French National Center of Reference for Angioedema. Deroux A, Boccon-Gibod I, Fain O, Pralong P, Ollivier Y, Pagnier A, Djenouhat K, Du-Thanh A, Gompel A, Faisant C, Launay D, Bouillet L. Clin Exp Immunol; 2016 Sep 01; 185(3):332-7. PubMed ID: 27271546 [Abstract] [Full Text] [Related]
9. Bradykinin mediated gastrointestinal edema as a cause of abdominal attacks in patients with hereditary angioedema due to C1-inhibitor deficiency. Obtulowicz P, Piotrowicz-Wojcik K, Dyga W, Stobiecki M, Popiela T, Obtulowicz K. J Physiol Pharmacol; 2022 Apr 01; 73(2):. PubMed ID: 36193964 [Abstract] [Full Text] [Related]
10. Comparison of chromogenic and ELISA functional C1 inhibitor tests in diagnosing hereditary angioedema. Li HH, Busse P, Lumry WR, Frazer-Abel A, Levy H, Steele T, Dayno J, Riedl M. J Allergy Clin Immunol Pract; 2015 Apr 01; 3(2):200-5. PubMed ID: 25609336 [Abstract] [Full Text] [Related]
11. Pasteurized and nanofiltered, plasma-derived C1 esterase inhibitor concentrate for the treatment of hereditary angioedema. Bork K. Immunotherapy; 2014 Apr 01; 6(5):533-51. PubMed ID: 24635050 [Abstract] [Full Text] [Related]
12. The safety of treatments for angioedema with hereditary C1 inhibitor deficiency. Zanichelli A, Wu MA, Andreoli A, Mansi M, Cicardi M. Expert Opin Drug Saf; 2015 Apr 01; 14(11):1725-36. PubMed ID: 26429506 [Abstract] [Full Text] [Related]
13. Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy. Hakl R, Kuklínek P, Krčmová I, Králíčková P, Freiberger T, Janků P, Vlková M, Litzman J. J Clin Immunol; 2018 Oct 01; 38(7):810-815. PubMed ID: 30280305 [Abstract] [Full Text] [Related]
14. Hereditary and acquired C1-inhibitor-dependent angioedema: from pathophysiology to treatment. Zeerleder S, Levi M. Ann Med; 2016 Oct 01; 48(4):256-67. PubMed ID: 27018196 [Abstract] [Full Text] [Related]
15. Frequent life-threatening laryngeal attacks in two Croatian families with hereditary angioedema due to C1 inhibitor deficiency harbouring a novel frameshift mutation in SERPING1. Karadža-Lapić L, Korošec P, Šilar M, Košnik M, Cikojević D, Lozić B, Rijavec M. Ann Med; 2016 Nov 01; 48(7):485-491. PubMed ID: 27187751 [Abstract] [Full Text] [Related]
16. Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families. Veronez CL, Moreno AS, Constantino-Silva RN, Maia LSM, Ferriani MPL, Castro FFM, Valle SR, Nakamura VK, Cagini N, Gonçalves RF, Mansour E, Serpa FS, Coelho Dias GA, Piccirillo MA, Toledo E, de Souza Bernardes M, Cichon S, Stieber C, Arruda LK, Pesquero JB, Grumach AS. J Allergy Clin Immunol Pract; 2018 Nov 01; 6(4):1209-1216.e8. PubMed ID: 29128335 [Abstract] [Full Text] [Related]
17. Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema. Andrási N, Veszeli N, Kőhalmi KV, Csuka D, Temesszentandrási G, Varga L, Farkas H. J Allergy Clin Immunol Pract; 2018 Nov 01; 6(4):1205-1208. PubMed ID: 29715562 [Abstract] [Full Text] [Related]
18. Hereditary angioedema in children and adolescents - A consensus update on therapeutic strategies for German-speaking countries. Wahn V, Aberer W, Aygören-Pürsün E, Bork K, Eberl W, Faßhauer M, Krüger R, Magerl M, Martinez-Saguer I, Späth P, Staubach-Renz P, Weber-Chrysochoou C. Pediatr Allergy Immunol; 2020 Nov 01; 31(8):974-989. PubMed ID: 32524650 [Abstract] [Full Text] [Related]
19. Health-related quality of life among children with hereditary angioedema. Engel-Yeger B, Farkas H, Kivity S, Veszeli N, Kőhalmi KV, Kessel A. Pediatr Allergy Immunol; 2017 Jun 01; 28(4):370-376. PubMed ID: 28258590 [Abstract] [Full Text] [Related]
20. Recombinant human C1 esterase inhibitor in the management of hereditary angioedema. Riedl M. Clin Drug Investig; 2015 Jul 01; 35(7):407-17. PubMed ID: 26091744 [Abstract] [Full Text] [Related] Page: [Next] [New Search]