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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

360 related items for PubMed ID: 22447508

  • 21. Possible Holt-Oram Syndrome: Missed Prenatal Diagnosis and Sub-Optimal Management in a Poor-Resourced Hospital.
    Osonuga A, Arhin JK, Okoye GC, Da’Costa A.
    Balkan Med J; 2019 May 10; 36(3):192-193. PubMed ID: 30873826
    [No Abstract] [Full Text] [Related]

  • 22. Novel TBX5 duplication in a Japanese family with Holt-Oram syndrome.
    Kimura M, Kikuchi A, Ichinoi N, Kure S.
    Pediatr Cardiol; 2015 Jan 10; 36(1):244-7. PubMed ID: 25274398
    [Abstract] [Full Text] [Related]

  • 23. A novel missense mutation in the TBX5 gene in a Saudi infant with Holt-Oram syndrome.
    Al-Qattan MM, Abou Al-Shaar H.
    Saudi Med J; 2015 Aug 10; 36(8):980-2. PubMed ID: 26219450
    [Abstract] [Full Text] [Related]

  • 24. KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5.
    Darwich R, Li W, Yamak A, Komati H, Andelfinger G, Sun K, Nemer M.
    Hum Mol Genet; 2017 Mar 01; 26(5):942-954. PubMed ID: 28164238
    [Abstract] [Full Text] [Related]

  • 25. Holt-Oram syndrome: contribution of prenatal 3-dimensional sonography in an index case.
    Sepulveda W, Enriquez G, Martinez JL, Mejia R.
    J Ultrasound Med; 2004 Jul 01; 23(7):983-7. PubMed ID: 15292570
    [No Abstract] [Full Text] [Related]

  • 26. Defining Features of the Upper Extremity in Holt-Oram Syndrome.
    Wall LB, Piper SL, Habenicht R, Oishi SN, Ezaki M, Goldfarb CA.
    J Hand Surg Am; 2015 Sep 01; 40(9):1764-8. PubMed ID: 26243320
    [Abstract] [Full Text] [Related]

  • 27. Holt Oram syndrome: a case report and review of the literature.
    Virdis G, Dessole M, Dessole S, Ambrosini G, Cosmi E, Cherchil PL, Capobianco G.
    Clin Exp Obstet Gynecol; 2016 Sep 01; 43(1):137-9. PubMed ID: 27048037
    [Abstract] [Full Text] [Related]

  • 28. Holt-Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: functional characterization of a de novo TBX5 mutation.
    Baban A, Pitto L, Pulignani S, Cresci M, Mariani L, Gambacciani C, Digilio MC, Pongiglione G, Albanese S.
    Am J Med Genet A; 2014 Jun 01; 164A(6):1419-24. PubMed ID: 24664498
    [Abstract] [Full Text] [Related]

  • 29. Malignant hyperthermia-like manifestations in a two-month-old child with Holt-Oram syndrome undergoing cardiac surgery.
    Franklin AD, Lorinc AN, Donahue BS.
    J Cardiothorac Vasc Anesth; 2014 Oct 01; 28(5):1326-7. PubMed ID: 24011877
    [No Abstract] [Full Text] [Related]

  • 30. Functional analysis of two novel TBX5 variants present in individuals with Holt-Oram syndrome with different clinical manifestations.
    Varela D, Varela T, Conceição N, Ferreira Â, Marques N, Silva AP, Azevedo P, Pereira S, Camacho A, de Jesus I, Cancela ML.
    Mol Genet Genomics; 2021 Jul 01; 296(4):809-821. PubMed ID: 33866394
    [Abstract] [Full Text] [Related]

  • 31. An Unusual Finding of a Double Orifice Mitral Valve in a Patient With Holt-Oram Syndrome.
    Verma KP, Healy S, Teng J, Nerlekar N.
    Heart Lung Circ; 2019 Apr 01; 28(4):e99-e100. PubMed ID: 30555010
    [No Abstract] [Full Text] [Related]

  • 32. [Holt-Oram syndrome: study of 7 cases].
    Martínez-García M, Lorda-Sanchez I, García-Hoyos M, Ramos C, Ayuso C, Trujillo-Tiebas MJ.
    Med Clin (Barc); 2010 Nov 13; 135(14):653-7. PubMed ID: 21070912
    [Abstract] [Full Text] [Related]

  • 33. Holt-Oram syndrome: novel TBX5 mutation and associated anomalous right coronary artery.
    Vianna CB, Miura N, Pereira AC, Jatene MB.
    Cardiol Young; 2011 Jun 13; 21(3):351-3. PubMed ID: 21272410
    [Abstract] [Full Text] [Related]

  • 34. Holt-Oram: when the key to a broken heart is in the hand.
    Naderi N, McCurdy MT, Reed RM.
    BMJ Case Rep; 2014 Apr 10; 2014():. PubMed ID: 24722718
    [No Abstract] [Full Text] [Related]

  • 35. Molecular basis of the clinical features of Holt-Oram syndrome resulting from missense and extended protein mutations of the TBX5 gene as well as TBX5 intragenic duplications.
    Al-Qattan MM, Abou Al-Shaar H.
    Gene; 2015 Apr 15; 560(2):129-36. PubMed ID: 25680289
    [Abstract] [Full Text] [Related]

  • 36. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.
    Guo DF, Li RG, Yuan F, Shi HY, Hou XM, Qu XK, Xu YJ, Zhang M, Liu X, Jiang JQ, Yang YQ, Qiu XB.
    Mol Med Rep; 2016 May 15; 13(5):4349-56. PubMed ID: 27035640
    [Abstract] [Full Text] [Related]

  • 37. TBX5 mutations in non-Holt-Oram syndrome (HOS) malformed hearts.
    Reamon-Buettner SM, Borlak J.
    Hum Mutat; 2004 Jul 15; 24(1):104. PubMed ID: 15221798
    [Abstract] [Full Text] [Related]

  • 38. Holt-Oram Syndrome in a Patient with Crohn's Disease: a Rare Case Report and Literature Review.
    Arkoumanis PT, Gklavas A, Karageorgou M, Gourzi P, Mantzaris G, Pantou M, Papaconstantinou I.
    Med Arch; 2018 Oct 15; 72(4):292-294. PubMed ID: 30514998
    [Abstract] [Full Text] [Related]

  • 39. Tetralogy of Fallot with Holt-Oram syndrome: case report and review.
    Tidake A, Gangurde P, Shaikh Z, Mahajan A.
    Clin Res Cardiol; 2015 Sep 15; 104(9):790-3. PubMed ID: 25903110
    [No Abstract] [Full Text] [Related]

  • 40. Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variants.
    Vanlerberghe C, Jourdain AS, Ghoumid J, Frenois F, Mezel A, Vaksmann G, Lenne B, Delobel B, Porchet N, Cormier-Daire V, Smol T, Escande F, Manouvrier-Hanu S, Petit F.
    Eur J Hum Genet; 2019 Mar 15; 27(3):360-368. PubMed ID: 30552424
    [Abstract] [Full Text] [Related]

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