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Journal Abstract Search

169 related items for PubMed ID: 31549136

  • 1. 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]

  • 2. 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 22; 41(11):981-988. PubMed ID: 30209282
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  • 3. 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 22; 61(8):701-3. PubMed ID: 27053290
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  • 4. Whole-exome sequencing identifies a de novo PDE3A variant causing autosomal dominant hypertension with brachydactyly type E syndrome: a case report.
    Li X, Li Z, Chen P, Wang Y, Wang DW, Wang DW.
    BMC Med Genet; 2020 Jul 06; 21(1):144. PubMed ID: 32631253
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  • 6. 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 06; 63(4):103781. PubMed ID: 31589936
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  • 8. The Case| A handful of hypertension.
    van den Born BJ, Oskam LC, Zidane M, Schächterle C, Klussmann E, Bähring S, Luft FC.
    Kidney Int; 2016 Oct 06; 90(4):911-3. PubMed ID: 27633875
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  • 10. Phosphodiesterase 3A and Arterial Hypertension.
    Ercu M, Markó L, Schächterle C, Tsvetkov D, Cui Y, Maghsodi S, Bartolomaeus TUP, Maass PG, Zühlke K, Gregersen N, Hübner N, Hodge R, Mühl A, Pohl B, Illas RM, Geelhaar A, Walter S, Napieczynska H, Schelenz S, Taube M, Heuser A, Anistan YM, Qadri F, Todiras M, Plehm R, Popova E, Langanki R, Eichhorst J, Lehmann M, Wiesner B, Russwurm M, Forslund SK, Kamer I, Müller DN, Gollasch M, Aydin A, Bähring S, Bader M, Luft FC, Klussmann E.
    Circulation; 2020 Jul 14; 142(2):133-149. PubMed ID: 32524868
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  • 12. 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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  • 13. A novel variant of IHH in a Chinese family with brachydactyly type 1.
    Yang Q, Wang J, Tian X, Shen F, Lan J, Zhang Q, Fan X, Yi S, Li M, Shen Y.
    BMC Med Genet; 2020 Mar 24; 21(1):60. PubMed ID: 32209048
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  • 14. 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 24; 21(3):390-3. PubMed ID: 16369843
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  • 17. Clinical and Molecular Perspectives of Monogenic Hypertension.
    Levanovich PE, Diaczok A, Rossi NF.
    Curr Hypertens Rev; 2020 Mar 24; 16(2):91-107. PubMed ID: 30963979
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  • 19. Variable expressivity of the phenotype in two families with brachydactyly type E, craniofacial dysmorphism, short stature and delayed bone age caused by novel heterozygous mutations in the PTHLH gene.
    Jamsheer A, Sowińska-Seidler A, Olech EM, Socha M, Kozłowski K, Pyrkosz A, Trzeciak T, Materna-Kiryluk A, Latos-Bieleńska A.
    J Hum Genet; 2016 May 24; 61(5):457-61. PubMed ID: 26763883
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