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Journal Abstract Search

109 related items for PubMed ID: 16369843

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  • 5. 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; 41(11):981-988. PubMed ID: 30209282
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  • 6. Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly.
    Naraghi R, Schuster H, Toka HR, Bähring S, Toka O, Oztekin O, Bilginturan N, Knoblauch H, Wienker TF, Busjahn A, Haller H, Fahlbusch R, Luft FC.
    Stroke; 1997 Sep; 28(9):1749-54. PubMed ID: 9303020
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  • 7. PDE3A variant associated with hypertension and brachydactyly syndrome in a patient with ischemic stroke caused by spontaneous intracranial artery dissection: A review of the clinical and molecular genetic features.
    Lee CG, Kang K, Yoon RG, Seo JY, Park JM.
    Eur J Med Genet; 2020 Apr; 63(4):103781. PubMed ID: 31589936
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  • 8. 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; 26(3):295-298. PubMed ID: 38319596
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  • 9. A PDE3A mutation in familial hypertension and brachydactyly syndrome.
    Boda H, Uchida H, Takaiso N, Ouchi Y, Fujita N, Kuno A, Hata T, Nagatani A, Funamoto Y, Miyata M, Yoshikawa T, Kurahashi H, Inagaki H.
    J Hum Genet; 2016 Aug; 61(8):701-3. PubMed ID: 27053290
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  • 10. Familial syndrome of progressive arterial occlusive disease consistent with fibromuscular dysplasia, hypertension, congenital cardiac defects, bone fragility, brachysyndactyly, and learning disabilities.
    Grange DK, Balfour IC, Chen SC, Wood EG.
    Am J Med Genet; 1998 Feb 17; 75(5):469-80. PubMed ID: 9489789
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  • 11. [Surgery of abdominal aorta with horseshoe kidney].
    Lotina SL, Davidović LB, Kostić DM, Velimirović DV, Petrović PLj, Perisić-Savić MV, KovacevićN S.
    Srp Arh Celok Lek; 1997 Feb 17; 125(1-2):36-44. PubMed ID: 17974353
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  • 12. Childhood hypertension in autosomal-dominant hypertension with brachydactyly.
    Toka O, Maass PG, Aydin A, Toka H, Hübner N, Rüschendorf F, Gong M, Luft FC, Bähring S.
    Hypertension; 2010 Nov 17; 56(5):988-94. PubMed ID: 20837885
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  • 13. Disproportionate short stature, type E brachydactyly and exostoses of tibiae in a patient with an XYY karyotype. A 'new' syndrome?
    Ikegawa S, Nagano A, Kurokawa T.
    Clin Dysmorphol; 1992 Oct 17; 1(4):217-9. PubMed ID: 1342873
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  • 14. 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
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  • 15. 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
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  • 16. Ulnar/fibular ray defect and brachydactyly in a family: a possible new autosomal dominant syndrome.
    Morava E, Czakó M, Kárteszi J, Cser B, Weissbecker K, Méhes K.
    Clin Dysmorphol; 2003 Jul 05; 12(3):161-5. PubMed ID: 14564152
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  • 17. A distinctive autosomal recessive syndrome of severe disproportionate short stature with short long bones, brachydactyly, and hypotrichosis in two consanguineous Arab families.
    Shalev SA, Spiegel R, Borochowitz ZU.
    Eur J Med Genet; 2012 Apr 05; 55(4):256-64. PubMed ID: 22440536
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  • 18. [A congenital vascular anomaly--arteriovenous shunt to the right kidney with an aneurysm of the inferior right branch of the renal artery as a cause of asymptomatic hematuria and vasorenal hypertension].
    Dimitrakova D, Velkova K, Simeonov S.
    Vutr Boles; 1990 Apr 05; 29(4):101-3. PubMed ID: 2281652
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  • 19. 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
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  • 20. Natural history and life-threatening complications in Myhre syndrome and review of the literature.
    Garavelli L, Maini I, Baccilieri F, Ivanovski I, Pollazzon M, Rosato S, Iughetti L, Unger S, Superti-Furga A, Tartaglia M.
    Eur J Pediatr; 2016 Oct 28; 175(10):1307-15. PubMed ID: 27562837
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