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

273 related items for PubMed ID: 17505266

  • 1. Association of hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome) and malignant melanoma in two patients.
    Kluger N, Riviére S, Coupier I, Bessis D, Guillot B.
    Melanoma Res; 2007 Jun; 17(3):201-3. PubMed ID: 17505266
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary hemorrhagic telangiectasia. Report of a pediatric case].
    Maaloul I, Aloulou H, Fourati H, Sfaihi L, Chabchoub I, Kamoun T, Mnif Z, Hachicha M.
    Arch Pediatr; 2014 Jul; 21(7):768-71. PubMed ID: 24935454
    [Abstract] [Full Text] [Related]

  • 3. Rendu-Osler-Weber disease: update of medical and dental considerations.
    te Veldhuis EC, te Veldhuis AH, van Dijk FS, Kwee ML, van Hagen JM, Baart JA, van der Waal I.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2008 Feb; 105(2):e38-41. PubMed ID: 18230376
    [Abstract] [Full Text] [Related]

  • 4. [Hereditary hemorrhagic telangiectasia].
    Pérez del Molino A, Zarrabeitia R, Fernández A.
    Med Clin (Barc); 2005 Apr 23; 124(15):583-7. PubMed ID: 15860174
    [Abstract] [Full Text] [Related]

  • 5. [Rendu-Osler-Weber syndrome: an rare cause of hypoxemia in children].
    Balza OR, García-Guereta L, Vidal MD, Marín MJ, Pajares MP.
    An Pediatr (Barc); 2010 Nov 23; 73(5):272-6. PubMed ID: 20813596
    [Abstract] [Full Text] [Related]

  • 6. Hereditary HaemorrhagicTelangiectasia--A Rare Cause of Severe Anaemia.
    Deshpande P, Bhat S, Karmarkar A.
    J Assoc Physicians India; 2014 Dec 23; 62(12):48-51. PubMed ID: 26259423
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Mutation analysis in hereditary haemorrhagic telangiectasia in Germany reveals 11 novel ENG and 12 novel ACVRL1/ALK1 mutations.
    Wehner LE, Folz BJ, Argyriou L, Twelkemeyer S, Teske U, Geisthoff UW, Werner JA, Engel W, Nayernia K.
    Clin Genet; 2006 Mar 23; 69(3):239-45. PubMed ID: 16542389
    [Abstract] [Full Text] [Related]

  • 10. [Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): clinical manifestations and multidisciplinary management].
    Frigerio C, Aebischer N, Baud D, Bonafe L, Fellmanne F, Ikonomidis C, Mazzolai L, Michel P, Nichita C, Qanadli SD, Lazor R.
    Rev Med Suisse; 2016 May 04; 12(517):896-901. PubMed ID: 27323484
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis.
    McDonald J, Bayrak-Toydemir P, Pyeritz RE.
    Genet Med; 2011 Jul 04; 13(7):607-16. PubMed ID: 21546842
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Pulmonary hypertension and hepatic encephalopathy: lethal complications of Rendu-Osler-Weber disease.
    Ford TJ, Fong MW, Cheah BC, Alexopolous C.
    J R Coll Physicians Edinb; 2014 Jul 04; 44(2):126-9. PubMed ID: 24999773
    [Abstract] [Full Text] [Related]

  • 19. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype.
    Bossler AD, Richards J, George C, Godmilow L, Ganguly A.
    Hum Mutat; 2006 Jul 04; 27(7):667-75. PubMed ID: 16752392
    [Abstract] [Full Text] [Related]

  • 20. Hepatic manifestation is associated with ALK1 in hereditary hemorrhagic telangiectasia: identification of five novel ALK1 and one novel ENG mutations.
    Kuehl HK, Caselitz M, Hasenkamp S, Wagner S, El-Harith el-HA, Manns MP, Stuhrmann M.
    Hum Mutat; 2005 Mar 04; 25(3):320. PubMed ID: 15712270
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.