These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

334 related items for PubMed ID: 29753808

  • 21. Genetics of Hereditary Angioedema Revisited.
    Germenis AE, Speletas M.
    Clin Rev Allergy Immunol; 2016 Oct; 51(2):170-82. PubMed ID: 27116602
    [Abstract] [Full Text] [Related]

  • 22. Genetic variants of SERPING1 gene in Polish patients with hereditary angioedema due to C1 inhibitor deficiency.
    Obtulowicz K, KsiĄŻek T, Bogdali A, Dyga W, Czarnobilska E, Juchacz A.
    Cent Eur J Immunol; 2020 Oct; 45(3):301-309. PubMed ID: 33437182
    [Abstract] [Full Text] [Related]

  • 23. Deletions in SERPING1 Lead to Lower C1 Inhibitor Function: Lower C1 Inhibitor Function Can Predict Disease Severity.
    Mete Gökmen N, Gülbahar O, Onay H, Peker Koc Z, Özgül S, Köse T, Gelincik A, Büyüköztürk S, Sin AZ.
    Int Arch Allergy Immunol; 2019 Oct; 178(1):50-59. PubMed ID: 30278448
    [Abstract] [Full Text] [Related]

  • 24. Psychology and hereditary angioedema: A systematic review.
    Savarese L, Mormile I, Bova M, Petraroli A, Maiello A, Spadaro G, Freda MF.
    Allergy Asthma Proc; 2021 Jan 01; 42(1):e1-e7. PubMed ID: 33404395
    [Abstract] [Full Text] [Related]

  • 25. In Search of an Association Between Genotype and Phenotype in Hereditary Angioedema due to C1-INH Deficiency.
    Loli-Ausejo D, López-Lera A, Drouet C, Lluncor M, Phillips-Anglés E, Pedrosa M, Cabañas R, Caballero T.
    Clin Rev Allergy Immunol; 2021 Aug 01; 61(1):1-14. PubMed ID: 33469833
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. The Expanding Spectrum of Mutations in Hereditary Angioedema.
    Veronez CL, Csuka D, Sheikh FR, Zuraw BL, Farkas H, Bork K.
    J Allergy Clin Immunol Pract; 2021 Jun 01; 9(6):2229-2234. PubMed ID: 33746090
    [Abstract] [Full Text] [Related]

  • 28. Hereditary angioedema in a single family with specific mutations in both plasminogen and SERPING1 genes.
    Bork K, Zibat A, Ferrari DM, Wollnik B, Schön MP, Wulff K, Lippert U.
    J Dtsch Dermatol Ges; 2020 Mar 01; 18(3):215-223. PubMed ID: 32065705
    [Abstract] [Full Text] [Related]

  • 29. New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema.
    Cagini N, Veronez CL, Constantino-Silva RN, Buzolin M, Martin RP, Grumach AS, Velloso LA, Mansour E, Pesquero JB.
    Biol Chem; 2016 Apr 01; 397(4):337-44. PubMed ID: 26812872
    [Abstract] [Full Text] [Related]

  • 30. First Analysis of SERPING1 Gene in Patients with Hereditary Angioedema in Colombia Reveals Two Genotypic Variants in a Highly Symptomatic Individual.
    Rodríguez JA, Narváez CF.
    J Clin Immunol; 2018 Apr 01; 38(3):294-299. PubMed ID: 29623547
    [Abstract] [Full Text] [Related]

  • 31. The Panorama of Primary Angioedema in the Brazilian Population.
    Veronez CL, Mendes AR, Leite CS, Gomes CP, Grumach AS, Pesquero JB, Hereditary Angioedema Brazilian Study Group (GEBRAEH).
    J Allergy Clin Immunol Pract; 2021 Jun 01; 9(6):2293-2304.e5. PubMed ID: 33276216
    [Abstract] [Full Text] [Related]

  • 32. Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing.
    Veronez CL, da Silva ED, Lima Teixeira PV, Cagini N, Constantino-Silva RN, Grumach AS, Mansour E, Velloso LA, Pesquero JB.
    Biol Chem; 2016 Apr 01; 397(4):315-22. PubMed ID: 26751894
    [Abstract] [Full Text] [Related]

  • 33. A hereditary angioedema screening on an index case: Turkey.
    Ozkars MY, Keskin O, Bayram N, Keskin M, Bayram H, Sahin Y, Kucukosmanoglu E, Attila N, Kirik SK.
    Asian Pac J Allergy Immunol; 2019 Sep 01; 37(3):154-161. PubMed ID: 30118244
    [Abstract] [Full Text] [Related]

  • 34. Novel SERPING1 gene mutations and clinical experience of type 1 hereditary angioedema from North India.
    Jindal AK, Rawat A, Kaur A, Sharma D, Suri D, Gupta A, Garg R, Dogra S, Saikia B, Minz RW, Singh S.
    Pediatr Allergy Immunol; 2021 Apr 01; 32(3):599-611. PubMed ID: 33220126
    [Abstract] [Full Text] [Related]

  • 35. Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1.
    Kajdácsi E, Jani PK, Csuka D, Varga L, Prohászka Z, Farkas H, Cervenak L.
    J Clin Immunol; 2016 Feb 01; 36(2):160-70. PubMed ID: 26873707
    [Abstract] [Full Text] [Related]

  • 36. Parallel comparison of three methodologies for measuring functional C1-inhibitor in Hereditary angioedema patients.
    Kapoor A, Garg BK, Zhou Z, Lu P, Chockalingam PS.
    Int Immunopharmacol; 2020 Apr 01; 81():106348. PubMed ID: 32143147
    [Abstract] [Full Text] [Related]

  • 37. The Genetics of Hereditary Angioedema: A Review.
    Santacroce R, D'Andrea G, Maffione AB, Margaglione M, d'Apolito M.
    J Clin Med; 2021 May 09; 10(9):. PubMed ID: 34065094
    [Abstract] [Full Text] [Related]

  • 38. Hereditary angioedema: Historical aspects, classification, pathophysiology, clinical presentation, and laboratory diagnosis.
    Khan DA.
    Allergy Asthma Proc; 2011 May 09; 32(1):1-10. PubMed ID: 21262092
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency.
    López-Lera A, Pernia O, López-Trascasa M, Ibanez de Caceres I.
    Orphanet J Rare Dis; 2014 Jul 22; 9():103. PubMed ID: 25053016
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 17.