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Year Number of Results
1988 1
2009 1
2010 1
2012 1
2013 1
2014 1
2015 2
2016 1
2017 1
2018 1
2024 0

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Page 1
Isolated dextrogastria in a newborn.
Docx MK, Steylemans A, Govaert P. Docx MK, et al. Arch Dis Child Fetal Neonatal Ed. 2015 Nov;100(6):F513. doi: 10.1136/archdischild-2014-307615. Epub 2015 Jun 25. Arch Dis Child Fetal Neonatal Ed. 2015. PMID: 26112270 No abstract available.
Diagnosis of Sjögren's syndrome in children.
Deprettere AJ, Van Acker KJ, De Clerck LS, Docx MK, Stevens WJ, Van Bever HP. Deprettere AJ, et al. Among authors: docx mk. Am J Dis Child. 1988 Nov;142(11):1185-7. doi: 10.1001/archpedi.1988.02150110063020. Am J Dis Child. 1988. PMID: 3052034 Review.
Intermittent Brugada syndrome in an anorexic adolescent girl.
Docx MKF, Loeys B, Simons A, Gewillig M, Proost D, Van Laer L, Mertens L. Docx MKF, et al. J Cardiol Cases. 2014 Jul 22;10(3):81-84. doi: 10.1016/j.jccase.2014.03.012. eCollection 2014 Sep. J Cardiol Cases. 2014. PMID: 30546512 Free PMC article.
Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity.
Iida A, Xing W, Docx MK, Nakashima T, Wang Z, Kimizuka M, Van Hul W, Rating D, Spranger J, Ohashi H, Miyake N, Matsumoto N, Mohan S, Nishimura G, Mortier G, Ikegawa S. Iida A, et al. Among authors: docx mk. J Med Genet. 2016 Aug;53(8):568-74. doi: 10.1136/jmedgenet-2016-103756. Epub 2016 Apr 7. J Med Genet. 2016. PMID: 27055475 Free PMC article.