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 *

321 related articles for article (PubMed ID: 12843319)

  • 1. Visceral manifestations in hereditary haemorrhagic telangiectasia type 2.
    Abdalla SA; Geisthoff UW; Bonneau D; Plauchu H; McDonald J; Kennedy S; Faughnan ME; Letarte M
    J Med Genet; 2003 Jul; 40(7):494-502. PubMed ID: 12843319
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia.
    Kjeldsen AD; Møller TR; Brusgaard K; Vase P; Andersen PE
    J Intern Med; 2005 Oct; 258(4):349-55. PubMed ID: 16164574
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers.
    Sabbà C; Pasculli G; Lenato GM; Suppressa P; Lastella P; Memeo M; Dicuonzo F; Guant G
    J Thromb Haemost; 2007 Jun; 5(6):1149-57. PubMed ID: 17388964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-phenotype correlations in hereditary hemorrhagic telangiectasia: data from the French-Italian HHT network.
    Lesca G; Olivieri C; Burnichon N; Pagella F; Carette MF; Gilbert-Dussardier B; Goizet C; Roume J; Rabilloud M; Saurin JC; Cottin V; Honnorat J; Coulet F; Giraud S; Calender A; Danesino C; Buscarini E; Plauchu H;
    Genet Med; 2007 Jan; 9(1):14-22. PubMed ID: 17224686
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University Hospital.
    Karlsson T; Cherif H
    Ups J Med Sci; 2018 Sep; 123(3):153-157. PubMed ID: 30251589
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations.
    Berg J; Porteous M; Reinhardt D; Gallione C; Holloway S; Umasunthar T; Lux A; McKinnon W; Marchuk D; Guttmacher A
    J Med Genet; 2003 Aug; 40(8):585-90. PubMed ID: 12920067
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Non-invasive CT screening for pulmonary arteriovenous malformations in children with confirmed hereditary hemorrhagic telangiectasia: Results from two pediatric centers.
    Soysal N; Eyries M; Verlhac S; Escabasse V; Remus N; Tamalet A; Rioux JY; Franchi-Abella S; Vasile M; Robert S; Delestrain C; Hau I; Ducou-Le Pointe H; Soubrier F; Carette MF; Epaud R
    Pediatr Pulmonol; 2017 May; 52(5):642-649. PubMed ID: 28165669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genotype-phenotype correlation in hereditary hemorrhagic telangiectasia: mutations and manifestations.
    Bayrak-Toydemir P; McDonald J; Markewitz B; Lewin S; Miller F; Chou LS; Gedge F; Tang W; Coon H; Mao R
    Am J Med Genet A; 2006 Mar; 140(5):463-70. PubMed ID: 16470787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype relationship in hereditary haemorrhagic telangiectasia.
    Letteboer TG; Mager JJ; Snijder RJ; Koeleman BP; Lindhout D; Ploos van Amstel JK; Westermann CJ
    J Med Genet; 2006 Apr; 43(4):371-7. PubMed ID: 16155196
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary hemorrhagic telangiectasia in Japanese patients.
    Komiyama M; Ishiguro T; Yamada O; Morisaki H; Morisaki T
    J Hum Genet; 2014 Jan; 59(1):37-41. PubMed ID: 24196379
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia.
    van Tuyl SA; Letteboer TG; Rogge-Wolf C; Kuipers EJ; Snijder RJ; Westermann CJ; Stolk MF
    Eur J Gastroenterol Hepatol; 2007 Feb; 19(2):153-8. PubMed ID: 17273001
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Heart failure and pulmonary arteriovenous malformations in a patient with hereditary hemorrhagic telangiectasia type 2.
    Du J; Zhu Y; Zhang YL; Li S; Huang J; Luo XH; Liu L
    J Thromb Thrombolysis; 2015 Nov; 40(4):515-9. PubMed ID: 26245826
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary hemorrhagic telangiectasia: an update on clinical manifestations and diagnostic measures.
    Sadick H; Sadick M; Götte K; Naim R; Riedel F; Bran G; Hörmann K
    Wien Klin Wochenschr; 2006 Mar; 118(3-4):72-80. PubMed ID: 16703249
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Symptomatic children with hereditary hemorrhagic telangiectasia: a pediatric center experience.
    Mei-Zahav M; Letarte M; Faughnan ME; Abdalla SA; Cymerman U; MacLusky IB
    Arch Pediatr Adolesc Med; 2006 Jun; 160(6):596-601. PubMed ID: 16754821
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening for children from families with Rendu-Osler-Weber disease: from geneticist to clinician.
    Giordano P; Nigro A; Lenato GM; Guanti G; Suppressa P; Lastella P; DE Mattia D; Sabbà C
    J Thromb Haemost; 2006 Jun; 4(6):1237-45. PubMed ID: 16706966
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-phenotype relationship for localization and age distribution of telangiectases in hereditary hemorrhagic telangiectasia.
    Letteboer TG; Mager HJ; Snijder RJ; Lindhout D; Ploos van Amstel HK; Zanen P; Westermann KJ
    Am J Med Genet A; 2008 Nov; 146A(21):2733-9. PubMed ID: 18831062
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients.
    Letteboer TG; Zewald RA; Kamping EJ; de Haas G; Mager JJ; Snijder RJ; Lindhout D; Hennekam FA; Westermann CJ; Ploos van Amstel JK
    Hum Genet; 2005 Jan; 116(1-2):8-16. PubMed ID: 15517393
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Neuroradiological Manifestations of Hereditary Hemorrhagic Telangiectasia in 139 Japanese Patients.
    Komiyama M; Terada A; Ishiguro T; Watanabe Y; Nakajima H; Yamada O; Morisaki H
    Neurol Med Chir (Tokyo); 2015; 55(6):479-86. PubMed ID: 26041630
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ALK-1 mutations in liver transplanted patients with hereditary hemorrhagic telangiectasia.
    Argyriou L; Pfitzmann R; Wehner LE; Twelkemeyer S; Neuhaus P; Nayernia K; Engel W
    Liver Transpl; 2005 Sep; 11(9):1132-5. PubMed ID: 16123970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hepatic angiodynamic profile in paediatric patients with hereditary haemorrhagic telangiectasia type 1 and type 2.
    Giordano P; Francavilla M; Buonamico P; Suppressa P; Lastella P; Sangerardi M; Miniello VL; Scardapane A; Lenato GM; Sabbà C
    Vasa; 2017 May; 46(3):195-202. PubMed ID: 28248153
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.