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

Year Number of Results
1986 1
1987 1
1988 1
1991 1
1992 1
1999 2
2007 1
2009 1
2010 2
2011 1
2013 1
2023 1
2024 1

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15 results

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Page 1
Circulating biomarkers of cardiovascular disease are related to aneurysm volume in abdominal aortic aneurysm.
Bouwens E, Vanmaele A, Hoeks SE, Verhagen HJ, Fioole B, Moelker A, Ten Raa S, Hussain B, Oliveira-Pinto J, Bastos Gonçalves F, Ijpma AS, Hoefer IE, van Lier F, Akkerhuis KM, Majoor-Krakauer DF, Boersma E, Kardys I. Bouwens E, et al. Among authors: majoor krakauer df. Vasc Med. 2023 Oct;28(5):433-442. doi: 10.1177/1358863X231181159. Epub 2023 Jul 3. Vasc Med. 2023. PMID: 37395286 Free PMC article.
Genetic analysis of von Hippel-Lindau disease.
Nordstrom-O'Brien M, van der Luijt RB, van Rooijen E, van den Ouweland AM, Majoor-Krakauer DF, Lolkema MP, van Brussel A, Voest EE, Giles RH. Nordstrom-O'Brien M, et al. Among authors: majoor krakauer df. Hum Mutat. 2010 May;31(5):521-37. doi: 10.1002/humu.21219. Hum Mutat. 2010. PMID: 20151405
Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.
Hoedemaekers YM, Cohen-Overbeek TE, Frohn-Mulder IM, Dooijes D, Majoor-Krakauer DF. Hoedemaekers YM, et al. Among authors: majoor krakauer df. Ultrasound Obstet Gynecol. 2013 Mar;41(3):336-9. doi: 10.1002/uog.12279. Ultrasound Obstet Gynecol. 2013. PMID: 22859017 Free article.
Twin vessels in von Hippel-Lindau disease.
de Jong PT, Verkaart RJ, van de Vooren MJ, Majoor-Krakauer DF, Wiegel AR. de Jong PT, et al. Among authors: majoor krakauer df. Am J Ophthalmol. 1988 Feb 15;105(2):165-9. doi: 10.1016/0002-9394(88)90181-x. Am J Ophthalmol. 1988. PMID: 3341434
Targeted proteomics and metabolomics for biomarker discovery in abdominal aortic aneurysm and post-EVAR sac volume.
Vanmaele A, Bouwens E, Hoeks SE, Kindt A, Lamont L, Fioole B, Moelker A, Ten Raa S, Hussain B, Oliveira-Pinto J, Ijpma AS, van Lier F, Akkerhuis KM, Majoor-Krakauer DF, Hankemeier T, de Rijke Y, Verhagen HJ, Boersma E, Kardys I. Vanmaele A, et al. Among authors: majoor krakauer df. Clin Chim Acta. 2024 Feb 1;554:117786. doi: 10.1016/j.cca.2024.117786. Epub 2024 Jan 20. Clin Chim Acta. 2024. PMID: 38246209 Free article.
Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.
Hoogerwaard EM, van der Wouw PA, Wilde AA, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, van Essen AJ, Leschot NJ, de Visser M. Hoogerwaard EM, et al. Among authors: majoor krakauer df. Neuromuscul Disord. 1999 Jul;9(5):347-51. doi: 10.1016/s0960-8966(99)00018-8. Neuromuscul Disord. 1999. PMID: 10407858
The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.
Hoedemaekers YM, Caliskan K, Michels M, Frohn-Mulder I, van der Smagt JJ, Phefferkorn JE, Wessels MW, ten Cate FJ, Sijbrands EJ, Dooijes D, Majoor-Krakauer DF. Hoedemaekers YM, et al. Among authors: majoor krakauer df. Circ Cardiovasc Genet. 2010 Jun;3(3):232-9. doi: 10.1161/CIRCGENETICS.109.903898. Epub 2010 Jun 8. Circ Cardiovasc Genet. 2010. PMID: 20530761
Autosomal dominant inheritance of cardiac valves anomalies in two families: extended spectrum of left-ventricular outflow tract obstruction.
Wessels MW, van de Laar IM, Roos-Hesselink J, Strikwerda S, Majoor-Krakauer DF, de Vries BB, Kerstjens-Frederikse WS, Vos YJ, de Graaf BM, Bertoli-Avella AM, Willems PJ. Wessels MW, et al. Among authors: majoor krakauer df. Am J Med Genet A. 2009 Feb;149A(2):216-25. doi: 10.1002/ajmg.a.32594. Am J Med Genet A. 2009. PMID: 19161153
Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification.
Hes FJ, van der Luijt RB, Janssen AL, Zewald RA, de Jong GJ, Lenders JW, Links TP, Luyten GP, Sijmons RH, Eussen HJ, Halley DJ, Lips CJ, Pearson PL, van den Ouweland AM, Majoor-Krakauer DF. Hes FJ, et al. Among authors: majoor krakauer df. Clin Genet. 2007 Aug;72(2):122-9. doi: 10.1111/j.1399-0004.2007.00827.x. Clin Genet. 2007. PMID: 17661816
Intragenic probe used for diagnostics in fragile X families.
Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Among authors: majoor krakauer df. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192
15 results