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PUBMED FOR HANDHELDS

Journal Abstract Search


279 related items for PubMed ID: 31990487

  • 1. Systemic hypertension followed by insidious stroke in a 12-year-old boy with childhood neurofibromatosis type 1 presenting with renal and cerebral artery vasculopathy.
    Lee ML, Chang TM, Yang RC, Yang AD, Chen M.
    Turk J Pediatr; 2019; 61(4):629-634. PubMed ID: 31990487
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  • 4. Revascularization in a 17-Year-Old Girl with Neurofibromatosis and Severe Hypertension Caused by Renal Artery Stenosis.
    Beladan CC, Geavlete OD, Botezatu S, Postu M, Popescu BA, Ginghina C, Coman IM.
    Tex Heart Inst J; 2017 Feb; 44(1):50-54. PubMed ID: 28265213
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  • 5. De Novo Renal Artery Stenosis Developed in Initially Normal Renal Arteries during the Long-Term Follow-Up of Patients with Moyamoya Disease.
    Hara S, Shimizu K, Nariai T, Kishino M, Kudo T, Umemoto T, Inaji M, Maehara T.
    J Stroke Cerebrovasc Dis; 2020 Aug; 29(8):104786. PubMed ID: 32229075
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  • 6. Moyamoya syndrome associated with neurofibromatosis Type 1: perioperative and long-term outcome after surgical revascularization.
    Koss M, Scott RM, Irons MB, Smith ER, Ullrich NJ.
    J Neurosurg Pediatr; 2013 Apr; 11(4):417-25. PubMed ID: 23373626
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  • 7. Moyamoya syndrome and neurofibromatosis type 1.
    Vargiami E, Sapountzi E, Samakovitis D, Batzios S, Kyriazi M, Anastasiou A, Zafeiriou DI.
    Ital J Pediatr; 2014 Jun 21; 40():59. PubMed ID: 24952383
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  • 8. Endovascular Management of Neurofibromatosis Type I-Associated Vasculopathy: A Case Series and Brief Review of the Literature.
    Raborn J, McCafferty BJ, Gunn AJ, Moawad S, Mahmoud K, Aal AKA, Saddekni S.
    Vasc Endovascular Surg; 2020 Feb 21; 54(2):182-190. PubMed ID: 31672102
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  • 10. Moyamoya disease presenting with tubular dysfunction in a child: pitfalls in diagnosing an atypical hyponatremic-hypertensive syndrome.
    Conte ML, La Scola C, Mencarelli F, Filippini B, Fabbri E, Ragnoni V, Ravaioli E, Pasini A, Vergine G.
    BMC Pediatr; 2023 May 08; 23(1):227. PubMed ID: 37150827
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  • 11. How commonly do children with complex cerebral arteriopathy have renovascular disease?
    Willsher A, Roebuck DJ, Ng J, Ganesan V.
    Dev Med Child Neurol; 2013 Apr 08; 55(4):335-40. PubMed ID: 23253043
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  • 12. [High blood pressure due to aortic coarctation and renal artery stenosis in a teenager with type 1 neurofibromatosis].
    Pardo R, Somalo L, Málaga S, Santos F.
    Nefrologia; 2008 Apr 08; 28(2):216-7. PubMed ID: 18454714
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  • 13. Renal artery stenosis due to neurofibromatosis type 1: case report and literature review.
    Duan L, Feng K, Tong A, Liang Z.
    Eur J Med Res; 2014 Mar 28; 19(1):17. PubMed ID: 24678641
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  • 14. Renovascular hypertension in moyamoya syndrome. Therapeutic response to percutaneous transluminal angioplasty.
    Halley SE, White WB, Ramsby GR, Voytovich AE.
    Am J Hypertens; 1988 Oct 28; 1(4 Pt 1):348-52. PubMed ID: 2975177
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  • 15. [Moyamoya disease associated with stenosis of extracranial arteries: a case report and review of the literature].
    Kaczorowska M, Jóźwiak S, Litwin M, Kmieć T, Kuczyński D, Jurkiewicz E, Kościerza I.
    Neurol Neurochir Pol; 2005 Oct 28; 39(3):242-6. PubMed ID: 15981166
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  • 16. Neurofibromatosis, stroke and basilar impression. Case report.
    Piovesan EJ, Scola RH, Werneck LC, Zétola VH, Nóvak EM, Iwamoto FM, Piovesan LM.
    Arq Neuropsiquiatr; 1999 Jun 28; 57(2B):484-8. PubMed ID: 10450358
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  • 18. Ask-Upmark kidney in a girl with neurofibromatosis type 1.
    Dote Y, Kibe T, Murakami T, Awazu M.
    CEN Case Rep; 2020 Aug 28; 9(3):285-288. PubMed ID: 32277359
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  • 19. Temporal profile of de novo development of moyamoya vasculopathy in an adult: case report.
    Shimoda Y, Fujimura M, Inoue T, Shimizu H, Tominaga T.
    Neurol Med Chir (Tokyo); 2012 Aug 28; 52(5):339-42. PubMed ID: 22688072
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  • 20. Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
    Santoro C, Di Rocco F, Kossorotoff M, Zerah M, Boddaert N, Calmon R, Vidaud D, Cirillo M, Cinalli G, Mirone G, Giugliano T, Piluso G, D'Amico A, Capra V, Pavanello M, Cama A, Nobili B, Lyonnet S, Perrotta S.
    Am J Med Genet A; 2017 Jun 28; 173(6):1521-1530. PubMed ID: 28422438
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