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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1982 1
1985 1
1992 2
1993 1
1994 1
1995 2
1996 3
1999 1
2001 1
2003 1
2005 1
2008 1
2010 1
2011 1
2012 5
2013 3
2014 1
2015 1
2016 3
2017 2
2018 5
2019 3
2024 0

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37 results

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Page 1
A case report on endarteritis in a child with coarctation of aorta.
Gnanam D, Bartelds B, van Leeuwen WJ, Frohn-Mulder IM, Koopman LP. Gnanam D, et al. Among authors: frohn mulder im. Echocardiography. 2019 Jul;36(7):1427-1430. doi: 10.1111/echo.14418. Epub 2019 Jun 25. Echocardiography. 2019. PMID: 31237036 Free PMC article.
Outcomes of Contemporary Family Screening in Hypertrophic Cardiomyopathy.
van Velzen HG, Schinkel AFL, Baart SJ, Oldenburg RA, Frohn-Mulder IME, van Slegtenhorst MA, Michels M. van Velzen HG, et al. Among authors: frohn mulder ime. Circ Genom Precis Med. 2018 Apr;11(4):e001896. doi: 10.1161/CIRCGEN.117.001896. Circ Genom Precis Med. 2018. PMID: 29661763
Aspects of the aetiology of congenital heart disease.
Buskens E, Grobbee DE, Frohn-Mulder IM, Wladimiroff JW, Hess J. Buskens E, et al. Among authors: frohn mulder im. Eur Heart J. 1995 May;16(5):584-7. doi: 10.1093/oxfordjournals.eurheartj.a060960. Eur Heart J. 1995. PMID: 7588888 Review.
Endocarditis of a congenital coronary fistula in a child.
Krasemann T, van Beynum IM, Frohn-Mulder IME, Dalinghaus M. Krasemann T, et al. Among authors: frohn mulder ime. Cardiol Young. 2018 Feb;28(2):334-337. doi: 10.1017/S1047951117001846. Epub 2017 Sep 11. Cardiol Young. 2018. PMID: 28889830
Biallelic Truncating Mutations in ALPK3 Cause Severe Pediatric Cardiomyopathy.
Almomani R, Verhagen JM, Herkert JC, Brosens E, van Spaendonck-Zwarts KY, Asimaki A, van der Zwaag PA, Frohn-Mulder IM, Bertoli-Avella AM, Boven LG, van Slegtenhorst MA, van der Smagt JJ, van IJcken WF, Timmer B, van Stuijvenberg M, Verdijk RM, Saffitz JE, du Plessis FA, Michels M, Hofstra RM, Sinke RJ, van Tintelen JP, Wessels MW, Jongbloed JD, van de Laar IM. Almomani R, et al. Among authors: frohn mulder im. J Am Coll Cardiol. 2016 Feb 9;67(5):515-25. doi: 10.1016/j.jacc.2015.10.093. J Am Coll Cardiol. 2016. PMID: 26846950 Free article.
Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndrome.
van de Laar IM, van der Linde D, Oei EH, Bos PK, Bessems JH, Bierma-Zeinstra SM, van Meer BL, Pals G, Oldenburg RA, Bekkers JA, Moelker A, de Graaf BM, Matyas G, Frohn-Mulder IM, Timmermans J, Hilhorst-Hofstee Y, Cobben JM, Bruggenwirth HT, van Laer L, Loeys B, De Backer J, Coucke PJ, Dietz HC, Willems PJ, Oostra BA, De Paepe A, Roos-Hesselink JW, Bertoli-Avella AM, Wessels MW. van de Laar IM, et al. Among authors: frohn mulder im. J Med Genet. 2012 Jan;49(1):47-57. doi: 10.1136/jmedgenet-2011-100382. J Med Genet. 2012. PMID: 22167769
Homozygous Truncating Variant in PKP2 Causes Hypoplastic Left Heart Syndrome.
Verhagen JMA, van den Born M, Kurul S, Asimaki A, van de Laar IMBH, Frohn-Mulder IME, Kammeraad JAE, Yap SC, Bartelings MM, van Slegtenhorst MA, von der Thüsen JH, Wessels MW. Verhagen JMA, et al. Among authors: frohn mulder ime. Circ Genom Precis Med. 2018 Dec;11(12):e002397. doi: 10.1161/CIRCGEN.118.002397. Circ Genom Precis Med. 2018. PMID: 30562116 No abstract available.
Delayed Diagnosis of Danon Disease in Patients Presenting With Isolated Cardiomyopathy.
Demirdas S, van Slegtenhorst MA, Verdijk RM, Lee M, van den Hout HMP, Wessels MW, Frohn-Mulder IME, Gardeitchik T, van der Ploeg AT, Schaaf GJ. Demirdas S, et al. Among authors: frohn mulder ime. Circ Genom Precis Med. 2019 Mar;12(3):e002395. doi: 10.1161/CIRCGEN.118.002395. Circ Genom Precis Med. 2019. PMID: 30919683 No abstract available.
Fluorinated steroids do not improve outcome of isolated atrioventricular block.
Van den Berg NW, Slieker MG, van Beynum IM, Bilardo CM, de Bruijn D, Clur SA, Cornette JM, Frohn-Mulder IM, Haak MC, van Loo-Maurus KE, Manten GT, Rackowitz AB, Rammeloo LA, Reimer A, Rijlaarsdam ME, Freund MW. Van den Berg NW, et al. Among authors: frohn mulder im. Int J Cardiol. 2016 Dec 15;225:167-171. doi: 10.1016/j.ijcard.2016.09.119. Epub 2016 Sep 30. Int J Cardiol. 2016. PMID: 27728859
NPHP4 variants are associated with pleiotropic heart malformations.
French VM, van de Laar IM, Wessels MW, Rohe C, Roos-Hesselink JW, Wang G, Frohn-Mulder IM, Severijnen LA, de Graaf BM, Schot R, Breedveld G, Mientjes E, van Tienhoven M, Jadot E, Jiang Z, Verkerk A, Swagemakers S, Venselaar H, Rahimi Z, Najmabadi H, Meijers-Heijboer H, de Graaff E, Helbing WA, Willemsen R, Devriendt K, Belmont JW, Oostra BA, Amack JD, Bertoli-Avella AM. French VM, et al. Among authors: frohn mulder im. Circ Res. 2012 Jun 8;110(12):1564-74. doi: 10.1161/CIRCRESAHA.112.269795. Epub 2012 May 1. Circ Res. 2012. PMID: 22550138 Free PMC article.
37 results