BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 29058329)

  • 1. Presymptomatic genetic diagnosis of two siblings with hereditary angioedema, presenting with unusual normal levels of serum C4.
    Kasami S; Sowa-Osako J; Fukai K; Tokimasa S; Kaga SI; Saito R; Tanaka A; Hide M; Tsuruta D
    J Dermatol; 2018 Feb; 45(2):e31-32. PubMed ID: 29058329
    [No Abstract]   [Full Text] [Related]  

  • 2. A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis.
    Yokoyama K; Horiuchi T; Hashimura C; Yoshida A
    Allergol Int; 2020 Jan; 69(1):148-149. PubMed ID: 31409531
    [No Abstract]   [Full Text] [Related]  

  • 3. 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; 37(3):154-161. PubMed ID: 30118244
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recurrent Acute Abdomen as the Main Manifestation of Hereditary Angioedema.
    Iwanami K; Okano T; Ohara O; Morio T
    Intern Med; 2019 Jan; 58(2):213-216. PubMed ID: 30146609
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 38(3):294-299. PubMed ID: 29623547
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pearls and pitfalls in the diagnosis of hereditary angioedema.
    Li HH
    Allergy Asthma Proc; 2019 Jul; 40(4):282-284. PubMed ID: 31262383
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary angioedema in a family presenting as transient periarthritis.
    Adhikesavan LG; Olenginski TP
    J Clin Rheumatol; 2008 Oct; 14(5):289-91. PubMed ID: 18824924
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary angioedema].
    Kreuz W
    Kinderkrankenschwester; 2009 Dec; 28(12):520-1. PubMed ID: 20063658
    [No Abstract]   [Full Text] [Related]  

  • 9. 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; 178(1):50-59. PubMed ID: 30278448
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deficiency of plasminogen activator inhibitor 2 in plasma of patients with hereditary angioedema with normal C1 inhibitor levels.
    Joseph K; Tholanikunnel BG; Wolf B; Bork K; Kaplan AP
    J Allergy Clin Immunol; 2016 Jun; 137(6):1822-1829.e1. PubMed ID: 26395818
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hereditary angioedema causing colocolic intussusception].
    Sanchez A; Ecochard A; Maestracci M; Rodiere M
    Arch Pediatr; 2008 Mar; 15(3):271-4. PubMed ID: 18329867
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The relationship between complement levels and disease activity in Japanese family cases of hereditary angioedema with C1-INH deficiency.
    Fukunaga A; Tsuchiyama S; Lee K; Washio K; Hashimura C; Horiuchi T; Nishigori C
    Allergol Int; 2018 Oct; 67(4):518-520. PubMed ID: 29661499
    [No Abstract]   [Full Text] [Related]  

  • 13. Hereditary angioedema in childhood: a challenging diagnosis you cannot afford to miss.
    Kjaer L; Bygum A
    Pediatr Dermatol; 2013; 30(1):94-6. PubMed ID: 22276768
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic features of hereditary angioedema with and without C1-inhibitor (C1-INH) deficiency in Japan.
    Hashimura C; Kiyohara C; Fukushi JI; Hirose T; Ohsawa I; Tahira T; Horiuchi T
    Allergy; 2021 Nov; 76(11):3529-3534. PubMed ID: 34343365
    [No Abstract]   [Full Text] [Related]  

  • 15. 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; 50(3):269-276. PubMed ID: 29513108
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hereditary angioedema: Differential diagnosis, diagnostic tests, and family screening.
    Manning ME
    Allergy Asthma Proc; 2020 Nov; 41(Suppl 1):S22-S25. PubMed ID: 33109321
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Analysis of genetic impact on smell impairment in patients with hereditary angioedema type 1 and 2.
    Förster-Ruhrmann U; Pierchalla G; Stieber C; Heilmann-Heimbach S; Cichon S; Nöthen MM; Ellrich A; Olze H; Maurer M; Magerl M
    J Dtsch Dermatol Ges; 2021 Jul; 19(7):1060-1062. PubMed ID: 34015192
    [No Abstract]   [Full Text] [Related]  

  • 18. Newly found C1 inhibitor gene mutation in hereditary angioedema patients.
    Tang R; Zhang HY
    Chin Med Sci J; 2009 Dec; 24(4):252. PubMed ID: 20120775
    [No Abstract]   [Full Text] [Related]  

  • 19. Hereditary C1 inhibitor deficiency is associated with high spontaneous amidase activity.
    Charignon D; Ghannam A; Ponard D; Drouet C
    Mol Immunol; 2017 May; 85():120-122. PubMed ID: 28222330
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema.
    Aabom A; Andersen KE; Fagerberg C; Fisker N; Jakobsen MA; Bygum A
    Orphanet J Rare Dis; 2017 Mar; 12(1):55. PubMed ID: 28302171
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.