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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 24185902

  • 1. Unexplained right atrial enlargement may be a sign of Holt-Oram syndrome in the fetus.
    Paladini D, Tiesi M, Buffi D, Tuo G, Marasini M.
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):475-6. PubMed ID: 24185902
    [Abstract] [Full Text] [Related]

  • 2. Holt-Oram syndrome.
    Goldfarb CA, Wall LB.
    J Hand Surg Am; 2014 Aug; 39(8):1646-8. PubMed ID: 24656395
    [No Abstract] [Full Text] [Related]

  • 3. Clinical expression of Holt-Oram syndrome on the basis of own clinical experience considering prenatal diagnosis.
    Walencka Z, Jamsheer A, Surmiak P, Baumert M, Jezela-Stanek A, Witek A, Materna-Kiryluk A, Latos-Bieleńska A, Socha M, Sowińska-Seidler A.
    Ginekol Pol; 2016 Aug; 87(10):706-710. PubMed ID: 27958623
    [Abstract] [Full Text] [Related]

  • 4. Holt-Oram syndrome: a case report.
    Chin J, Pereira S, Camacho A, Pessoa B, Bento D, Amado J, Pereira J, de Jesus I.
    Rev Port Cardiol; 2014 Nov; 33(11):737.e1-5. PubMed ID: 25455949
    [Abstract] [Full Text] [Related]

  • 5. Rare cardiac defect in Holt-Oram syndrome.
    Sinha R, Nema C.
    Cardiovasc J Afr; 2012 Mar 12; 23(2):e3-4. PubMed ID: 22447508
    [Abstract] [Full Text] [Related]

  • 6. Holt-Oram syndrome because of the novel TBX5 mutation c.481A>C.
    Koçak Eker H, Altunoglu U, Toksoy G, Kayserili H.
    Clin Dysmorphol; 2016 Oct 12; 25(4):192-4. PubMed ID: 27552067
    [No Abstract] [Full Text] [Related]

  • 7. [Holt-Oram syndrome--the importance of early diagnosis and interdisciplinary approach. A case report].
    Zakanj Z.
    Lijec Vjesn; 2013 Oct 12; 135(1-2):12-4. PubMed ID: 23607171
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.
    Stipoljev F, Miric-Tesanic D, Hafner T, Barbalic M, Logara M, Lasan-Trcic R, Vicic A, Gjergja-Juraski R.
    Eur J Med Genet; 2017 Nov 12; 60(11):589-594. PubMed ID: 28807863
    [Abstract] [Full Text] [Related]

  • 9. Atrial septal defect type II and upper limb malformation in 40-year-old male as a manifestation of Holt-Oram syndrome.
    Szymczyk E, Wejner-Mik P, Lipiec P, Michalski B, Kasprzak JD.
    Cardiol J; 2019 Nov 12; 26(3):302-303. PubMed ID: 31246270
    [No Abstract] [Full Text] [Related]

  • 10. A new mutation in the TBX5 gene in Holt-Oram syndrome: two cases in the same family and prenatal diagnosis.
    Atik T, Dervisoglu H, Onay H, Ozkinay F, Cogulu O.
    J Trop Pediatr; 2014 Jun 12; 60(3):257-9. PubMed ID: 24408148
    [Abstract] [Full Text] [Related]

  • 11. Holt-Oram syndrome with aortopulmonary window--a rare association.
    Srinivas SK, Balekundri VI, Manjunath CN.
    Cardiol Young; 2014 Oct 12; 24(5):947-9. PubMed ID: 24124729
    [Abstract] [Full Text] [Related]

  • 12. 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]

  • 13. Holt Oram syndrome: a registry-based study in Europe.
    Barisic I, Boban L, Greenlees R, Garne E, Wellesley D, Calzolari E, Addor MC, Arriola L, Bergman JE, Braz P, Budd JL, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, McDonnell B, Nelen V, Pierini A, Queisser-Wahrendorf A, Rankin J, Rissmann A, Rounding C, Tucker D, Verellen-Dumoulin C, Dolk H.
    Orphanet J Rare Dis; 2014 Oct 25; 9():156. PubMed ID: 25344219
    [Abstract] [Full Text] [Related]

  • 14. Novel compound heterozygous TBX5 variants may induce hypoplastic left heart syndrome.
    Miyao N, Hirono K, Hata Y, Yoshimura N, Ichida F.
    Pediatr Int; 2019 Jun 25; 61(6):607-609. PubMed ID: 31215120
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations.
    Jhang WK, Lee BH, Kim GH, Lee JO, Yoo HW.
    Cardiol Young; 2015 Aug 10; 25(6):1093-8. PubMed ID: 25216260
    [Abstract] [Full Text] [Related]

  • 17. [The "heart-hand" syndrome in a 8-year-old-boy with short stature].
    Petriczko E, Horodnicka-Józwa A, Prowans P, Biczysko-Mokosa A, Szmit-Domagalska J, Dawid G, Walczak M, Zajaczek S.
    Wiad Lek; 2011 Aug 10; 64(1):15-21. PubMed ID: 21812358
    [Abstract] [Full Text] [Related]

  • 18. Tetralogy of Fallot with Holt-Oram syndrome.
    Kumar V, Agrawal V, Jain D, Shankar O.
    Indian Heart J; 2012 Aug 10; 64(1):95-8. PubMed ID: 22572437
    [Abstract] [Full Text] [Related]

  • 19. A rare case of isolated right atrial enlargement and TBX5 mutation associated with Holt-Oram syndrome.
    Kikano SD, Belay W, Kavanaugh-McHugh A.
    Prenat Diagn; 2023 Jul 10; 43(8):1088-1091. PubMed ID: 37340539
    [Abstract] [Full Text] [Related]

  • 20. 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 10; 23(7):983-7. PubMed ID: 15292570
    [No Abstract] [Full Text] [Related]

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