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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 30690789)

  • 1. Delayed diagnosis of hereditary angioedema with C1-inhibitor deficiency in iranian children and adolescents.
    Ayazi M; Fazlollahi MR; Mohammadzadeh I; Fayezi A; Nabavi M; Mahdaviani SA; Movahedi M; Heidarzadeh M; Saghafi S; Shokouhi Shoormasti R; Mohammadian S; Farkas H; Pourpak Z
    Pediatr Allergy Immunol; 2019 May; 30(3):395-398. PubMed ID: 30690789
    [No Abstract]   [Full Text] [Related]  

  • 2. Delayed diagnosis of hereditary angioedema.
    Maskatia ZK; Orson FM
    Am J Med Sci; 2010 Jul; 340(1):82-3. PubMed ID: 20531165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 3(2):200-5. PubMed ID: 25609336
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Baseline level of functional C1-inhibitor correlates with disease severity scores in hereditary angioedema.
    Kelemen Z; Moldovan D; Mihály E; Visy B; Széplaki G; Csuka D; Füst G; Farkas H; Varga L
    Clin Immunol; 2010 Mar; 134(3):354-8. PubMed ID: 19945350
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recurrent attacks of hereditary angioedema: a case of delayed diagnosis.
    Jacobs J
    Allergy Asthma Proc; 2011; 32 Suppl 1():23-26. PubMed ID: 22195758
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pediatric angioedema: Essential features and preliminary results from the Hereditary Angioedema Global Registry in Italy.
    Cancian M; Perego F; Senter R; Arcoleo F; De Pasquale T; Zoli A; Cicardi M; Zanichelli A
    Pediatr Allergy Immunol; 2020 Feb; 31 Suppl 24():22-24. PubMed ID: 32017221
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary angioedema in children and adolescents.
    Mansour E; Veronez CL; Craig T; Grumach AS
    Allergol Immunopathol (Madr); 2022; 50(S Pt 1):1-6. PubMed ID: 35726485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Type I and Type II Hereditary Angioedema: Clinical and Laboratory Findings in Iranian Patients.
    Kargarsharif F; Mehranmehr N; Zahedi Fard S; Fazlollahi MR; Ayazi M; Mohammadzadeh I; Nabavi M; Bemanian MH; Fayezi A; Movahedi M; Heidarzadeh M; Kalantari N; Arefimehr S; Saghafi S; Pourpak Z
    Arch Iran Med; 2015 Jul; 18(7):425-9. PubMed ID: 26161706
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Acute Genital Swelling Heralding C1 Esterase Inhibitor Deficiency in a Child.
    Murad A; Leahy TR; Lenane P
    Pediatr Dermatol; 2017 Sep; 34(5):e277-e278. PubMed ID: 28730616
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Delayed diagnosis of hereditary angioedema: Thirty-nine years of inadequate treatment.
    Martinez-Saguer I; Escuriola Ettingshausen C
    Ann Allergy Asthma Immunol; 2016 Nov; 117(5):554-556. PubMed ID: 27593101
    [No Abstract]   [Full Text] [Related]  

  • 11. 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; 185(3):332-7. PubMed ID: 27271546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study.
    Steiner UC; Weber-Chrysochoou C; Helbling A; Scherer K; Grendelmeier PS; Wuillemin WA
    Orphanet J Rare Dis; 2016 Apr; 11():43. PubMed ID: 27101900
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary angioedema with normal C1 inhibitor.
    Bork K
    Immunol Allergy Clin North Am; 2013 Nov; 33(4):457-70. PubMed ID: 24176211
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hereditary angioedema biological diagnosis].
    Ponard D
    Presse Med; 2015 Jan; 44(1):57-64. PubMed ID: 25511654
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Pediatric Hereditary Angioedema: Onset, Diagnostic Delay, and Disease Severity.
    Christiansen SC; Davis DK; Castaldo AJ; Zuraw BL
    Clin Pediatr (Phila); 2016 Sep; 55(10):935-42. PubMed ID: 26581355
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary angioedema in Austria: prevalence and regional peculiarities.
    Schöffl C; Wiednig M; Koch L; Blagojevic D; Duschet P; Hawranek T; Kinaciyan T; Öllinger A; Aberer W
    J Dtsch Dermatol Ges; 2019 Apr; 17(4):416-423. PubMed ID: 30883006
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Report on the First Survey of Iranian Patients with Hereditary Angioedema.
    Shahinpour S; Tavakol M; Abolhassani H; Mohammadinejad P; Movahedi M; Arshi S; Aghamohammadi A
    Iran J Immunol; 2015 Sep; 12(3):209-18. PubMed ID: 26412639
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary angioedema: Repeated attacks in a 10-year-old boy.
    Otani T; Hoshika S; Horiuchi T; Hashimura C; Sugihara S
    Pediatr Int; 2019 Jan; 61(1):101-103. PubMed ID: 30734432
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.