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Journal Abstract Search

94 related items for PubMed ID: 20837885

  • 1. 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; 56(5):988-94. PubMed ID: 20837885
    [Abstract] [Full Text] [Related]

  • 2. Clinical and Molecular Description of 16 Families With Heterozygous IHH Variants.
    Sentchordi-Montané L, Benito-Sanz S, Aza-Carmona M, Pereda A, Parrón-Pajares M, de la Torre C, Vasques GA, Funari MFA, Travessa AM, Dias P, Suarez-Ortega L, González-Buitrago J, Portillo-Najera NE, Llano-Rivas I, Martín-Frías M, Ramírez-Fernández J, Sánchez Del Pozo J, Garzón-Lorenzo L, Martos-Moreno GA, Alfaro-Iznaola C, Mulero-Collantes I, Ruiz-Ocaña P, Casano-Sancho P, Portela A, Ruiz-Pérez L, Del Pozo A, Vallespín E, Solís M, Lerario AM, González-Casado I, Ros-Pérez P, Pérez de Nanclares G, Jorge AAL, Heath KE.
    J Clin Endocrinol Metab; 2020 Aug 01; 105(8):. PubMed ID: 32311039
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  • 3. 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
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  • 4. The growth hormone receptor exon 3-deleted/full-length polymorphism and response to growth hormone therapy in prepubertal idiopathic short children.
    Hellgren G, Glad CA, Jonsson B, Johannsson G, Albertsson-Wikland K.
    Growth Horm IGF Res; 2015 Jun 19; 25(3):127-35. PubMed ID: 25742716
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  • 5. Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension.
    Toka HR, Bähring S, Chitayat D, Melby JC, Whitehead R, Jeschke E, Wienker TF, Toka O, Schuster H, Luft FC.
    Ann Intern Med; 1998 Aug 01; 129(3):204-8. PubMed ID: 9696728
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  • 6. A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly.
    Schuster H, Toka O, Toka HR, Busjahn A, Oztekin O, Wienker TF, Bilginturan N, Bähring S, Skrabal F, Haller H, Luft FC.
    Kidney Int; 1998 Jan 01; 53(1):167-72. PubMed ID: 9453014
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  • 7. Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA.
    Bähring S, Kann M, Neuenfeld Y, Gong M, Chitayat D, Toka HR, Toka O, Plessis G, Maass P, Rauch A, Aydin A, Luft FC.
    Hypertension; 2008 Feb 01; 51(2):426-31. PubMed ID: 18086950
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  • 8. 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 01; 41(11):981-988. PubMed ID: 30209282
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  • 11. 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 01; 61(8):701-3. PubMed ID: 27053290
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  • 12. [Clinical investigation of a family with brachydactyly type A1 and the identification of the disease gene].
    Ke X, Dong AL, Liu QJ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun 01; 26(3):267-71. PubMed ID: 19504437
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  • 13. 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 01; 55(4):256-64. PubMed ID: 22440536
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  • 14. PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
    Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S.
    Nat Genet; 2015 Jun 01; 47(6):647-53. PubMed ID: 25961942
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  • 15. 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 01; 21(3):390-3. PubMed ID: 16369843
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  • 16. New Developments in the Genetics of Hypertension: What Should Clinicians Know?
    Geller DS.
    Curr Cardiol Rep; 2015 Dec 01; 17(12):122. PubMed ID: 26521239
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  • 20. Effect of age and affection status on blood pressure, serum potassium and stature in familial hyperkalaemia and hypertension.
    Farfel A, Mayan H, Melnikov S, Holtzman EJ, Pinhas-Hamiel O, Farfel Z.
    Nephrol Dial Transplant; 2011 May 01; 26(5):1547-53. PubMed ID: 20956807
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