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Journal Abstract Search

110 related items for PubMed ID: 32617206

  • 1. Hypertension With Brachydactyly Syndrome: A Case Report.
    Asim R, Reddy A, Grigorieva Olson O, Ronen JA, Prasad V.
    Cureus; 2020 May 28; 12(5):e8329. PubMed ID: 32617206
    [Abstract] [Full Text] [Related]

  • 2. Reversal of cardiac and renal damage in a teenager with hypertension: A case report.
    Du H, Gao S, Dong W, Huang Q, Qu H, Zhang C, Guo L, Liu Z, Liu M.
    J Clin Hypertens (Greenwich); 2024 Mar 28; 26(3):295-298. PubMed ID: 38319596
    [Abstract] [Full Text] [Related]

  • 3. PDE3A gene screening improves diagnostics for patients with Bilginturan syndrome (hypertension and brachydactyly syndrome).
    Renkema KY, Westermann JM, Nievelstein RAJ, Lo-A-Njoe SM, van der Zwaag B, Manshande ME, van Haelst MM.
    Hypertens Res; 2018 Nov 28; 41(11):981-988. PubMed ID: 30209282
    [Abstract] [Full Text] [Related]

  • 4. Hypertension and Brachydactyly Syndrome Associated With Vertebral Artery Malformation Caused by a PDE3A Missense Mutation.
    Fan P, Zhang D, Yang KQ, Zhang QY, Luo F, Lou Y, Liu YX, Zhang HM, Song L, Cai J, Wu HY, Zhou XL.
    Am J Hypertens; 2020 Feb 22; 33(2):190-197. PubMed ID: 31549136
    [Abstract] [Full Text] [Related]

  • 5. Brachydactyly short-stature hypertension syndrome: a case with associated vascular malformations.
    Derbent M, Baskin E, Ağildere M, Agras PI, Saatçi U.
    Pediatr Nephrol; 2006 Mar 22; 21(3):390-3. PubMed ID: 16369843
    [Abstract] [Full Text] [Related]

  • 6. Hypertension and Brachydactyly Syndrome: Genetic Insights and a Novel Presentation.
    Shahid A, Shetty NS, Patel N, McClinchey T, Arora G, Arora P.
    JACC Case Rep; 2024 Jun 05; 29(11):102343. PubMed ID: 38689596
    [Abstract] [Full Text] [Related]

  • 7. Arterial hypertension with brachydactyly in a 15-year-old boy.
    Litwin M, Jurkiewicz E, Nowak K, Kościesza A, Grenda R, Malczyk K, Kościesza I.
    Pediatr Nephrol; 2003 Aug 05; 18(8):814-9. PubMed ID: 12811651
    [Abstract] [Full Text] [Related]

  • 8. Brachydactyly E: isolated or as a feature of a syndrome.
    Pereda A, Garin I, Garcia-Barcina M, Gener B, Beristain E, Ibañez AM, Perez de Nanclares G.
    Orphanet J Rare Dis; 2013 Sep 12; 8():141. PubMed ID: 24028571
    [Abstract] [Full Text] [Related]

  • 9. Hyperphalangism accompanied by brachydactyly of the feet: a case report.
    Suresh SS, Abraham R.
    Acta Orthop Traumatol Turc; 2010 Sep 12; 44(1):79-81. PubMed ID: 20513996
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  • 11. Brachydactyly-short stature-hypertension (Bilginturan) syndrome: report on two families.
    Chitayat D, Grix A, Balfe JW, Abramowicz JS, Garza J, Fong CT, Silver MM, Saller DN, Bresnick GH, Giedion A, Lachman RS, Rimoin DL.
    Am J Med Genet; 1997 Dec 19; 73(3):279-85. PubMed ID: 9415685
    [Abstract] [Full Text] [Related]

  • 12. Congenital anonychia and brachydactyly of the left foot - Cooks syndrome variant: Case report and review of literature.
    Chatterjee D.
    Indian J Hum Genet; 2014 Apr 19; 20(2):206-8. PubMed ID: 25400355
    [Abstract] [Full Text] [Related]

  • 13. [Psychiatric manifestations of lupus erythematosus systemic and Sjogren's syndrome].
    Ampélas JF, Wattiaux MJ, Van Amerongen AP.
    Encephale; 2001 Apr 19; 27(6):588-99. PubMed ID: 11865567
    [Abstract] [Full Text] [Related]

  • 14. A case of symbrachydactyly with oligodactyly.
    Seven M, Yuksel A, Ozkilic A.
    Genet Couns; 2001 Apr 19; 12(1):77-83. PubMed ID: 11332981
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  • 18. Brachydactyly type B: case report and further evidence for clinical heterogeneity.
    Slavotinek A, Clayton-Smith J.
    Clin Dysmorphol; 1999 Jul 19; 8(3):165-71. PubMed ID: 10457848
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  • 19. Two novel disease-causing variants in BMPR1B are associated with brachydactyly type A1.
    Racacho L, Byrnes AM, MacDonald H, Dranse HJ, Nikkel SM, Allanson J, Rosser E, Underhill TM, Bulman DE.
    Eur J Hum Genet; 2015 Dec 19; 23(12):1640-5. PubMed ID: 25758993
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