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Journal Abstract Search

179 related items for PubMed ID: 33419752

  • 21. Osler-Rendu-Weber syndrome: congenital arteriovenous intrapulmonary fistula treated using a percutaneous Amplatzer plug.
    Conti V, Fiorucci F, Serpilli M, Patrizi A, Paone G, Neri P, Giannunzio G, Pirozzo MG, Fiorucci C, Lucantoni G.
    Eur Rev Med Pharmacol Sci; 2008; 12(3):213-6. PubMed ID: 18700694
    [Abstract] [Full Text] [Related]

  • 22. Embolotherapy for pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).
    Andersen PE, Kjeldsen AD, Oxhøj H, Vase P, White RI.
    Acta Radiol; 1998 Nov; 39(6):723-6. PubMed ID: 9817050
    [Abstract] [Full Text] [Related]

  • 23. [Hereditary haemorrhagic telangiectasia diagnosed in connection with a traffic accident].
    Sivapalan P, Demény AK, Almind M, Kjeldsen AD.
    Ugeskr Laeger; 2014 Feb 17; 176(8A):V10130614. PubMed ID: 25350308
    [Abstract] [Full Text] [Related]

  • 24. An update on the ophthalmic features in hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).
    Abdolrahimzadeh S, Formisano M, Marani C, Rahimi S.
    Int Ophthalmol; 2022 Jun 17; 42(6):1987-1995. PubMed ID: 35034241
    [Abstract] [Full Text] [Related]

  • 25. 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 17; 69(3):239-45. PubMed ID: 16542389
    [Abstract] [Full Text] [Related]

  • 26. [Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu syndrome) Part I. Pathophysiology, clinical symptoms and recommend screening for vascular malformations].
    Adam Z, Brančiková D, Romanová G, Pour L, Krejčí M, König J, Nebeský T, Adamová Z, Štork M, Krejčí M, Ševčíková S, Eid M, Král Z.
    Vnitr Lek; 2021 Mar 17; 67(6):339-344. PubMed ID: 35459376
    [Abstract] [Full Text] [Related]

  • 27. Estimates of maternal risks of pregnancy for women with hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): suggested approach for obstetric services.
    Shovlin CL, Sodhi V, McCarthy A, Lasjaunias P, Jackson JE, Sheppard MN.
    BJOG; 2008 Aug 17; 115(9):1108-15. PubMed ID: 18518871
    [Abstract] [Full Text] [Related]

  • 28. [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 17; 21(7):768-71. PubMed ID: 24935454
    [Abstract] [Full Text] [Related]

  • 29. Definite hereditary hemorrhagic telangiectasia in a 60-year-old black Kenyan woman: a case report.
    Kiyeng JC, Siika A, Koech C, Bloomfield GS.
    J Med Case Rep; 2016 May 25; 10(1):126. PubMed ID: 27225226
    [Abstract] [Full Text] [Related]

  • 30. Characterization of pulmonary arteriovenous malformations in ACVRL1 versus ENG mutation carriers in hereditary hemorrhagic telangiectasia.
    Mu W, Cordner ZA, Yuqi Wang K, Reed K, Robinson G, Mitchell S, Lin D.
    Genet Med; 2018 Jun 25; 20(6):639-644. PubMed ID: 29048420
    [Abstract] [Full Text] [Related]

  • 31. Pulmonary Arteriovenous Malformations Are Associated with Silent Brain Infarcts in Hereditary Hemorrhagic Telangiectasia Patients.
    Brinjikji W, Nasr DM, Wood CP, Iyer VN.
    Cerebrovasc Dis; 2017 Jun 25; 44(3-4):179-185. PubMed ID: 28746925
    [Abstract] [Full Text] [Related]

  • 32. Clinical and molecular characterization of patients with hereditary hemorrhagic telangiectasia: Experience from an HHT Center of Excellence.
    Latif MA, Sobreira NLD, Guthrie KS, Motaghi M, Robinson GM, Shafaat O, Gong AJ, Weiss CR.
    Am J Med Genet A; 2021 Jul 25; 185(7):1981-1990. PubMed ID: 33768677
    [Abstract] [Full Text] [Related]

  • 33. Subcutaneous temporal abscess as a clinical manifestation of pulmonary arteriovenous malformations in a patient with hereditary haemorrhagic telangiectasia (Rendu-Osler-Weber disease).
    Haarmann S, Budihardja AS, Hölzle F, Wolff KD.
    Int J Oral Maxillofac Surg; 2007 Dec 25; 36(12):1211-4. PubMed ID: 17681734
    [Abstract] [Full Text] [Related]

  • 34. 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 25; 118(3-4):72-80. PubMed ID: 16703249
    [Abstract] [Full Text] [Related]

  • 35. Follow-up interval for small untreated pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia.
    Ryan DJ, O'Connor TM, Murphy MM, Brady AP.
    Clin Radiol; 2017 Mar 25; 72(3):236-241. PubMed ID: 28040200
    [Abstract] [Full Text] [Related]

  • 36. Pulmonary arteriovenous malformations: a clinical review.
    Iqbal M, Rossoff LJ, Steinberg HN, Marzouk KA, Siegel DN.
    Postgrad Med J; 2000 Jul 25; 76(897):390-4. PubMed ID: 10878194
    [Abstract] [Full Text] [Related]

  • 37. Rendu-Osler-Weber syndrome.
    Benítez-Rivero S, Camacho Romero J, Eiroa D.
    Med Clin (Barc); 2019 Jun 07; 152(11):e65. PubMed ID: 30392695
    [No Abstract] [Full Text] [Related]

  • 38. Pulmonary arteriovenous malformation in Osler-Weber-Rendu syndrome.
    Chen QK, Jiang GN, Chen C, Chen XF.
    Asian Cardiovasc Thorac Ann; 2011 Oct 07; 19(5):370. PubMed ID: 22100937
    [No Abstract] [Full Text] [Related]

  • 39. Hereditary haemorrhagic telangiectasia with pulmonary arteriovenous malformations: a treatable cause of thromboembolic cerebral events.
    Yoong JK, Htoo MM, Jeyaseelan V, Ng DC.
    Singapore Med J; 2004 Jul 07; 45(7):334-6. PubMed ID: 15221050
    [Abstract] [Full Text] [Related]

  • 40. Pulmonary gas exchange in hereditary hemorrhagic telangiectasia patients with liver arteriovenous malformations.
    de Picciotto C, El Hajjam M, Karam C, Chinet T, Bonay M.
    Respir Res; 2019 Jul 04; 20(1):137. PubMed ID: 31272464
    [Abstract] [Full Text] [Related]

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