Janssen MCH - Search Results

1

Cognitive functioning and mental health in mitochondrial disease: A systematic scoping review.

Klein IL, van de Loo KFE, Smeitink JAM, Janssen MCH, Kessels RPC, van Karnebeek CD, van der Veer E, Custers JAE, Verhaak CM. Klein IL, et al. Among authors: janssen mch. Neurosci Biobehav Rev. 2021 Jun;125:57-77. doi: 10.1016/j.neubiorev.2021.02.004. Epub 2021 Feb 11. Neurosci Biobehav Rev. 2021. PMID: 33582231 Free article. Review.

2

Risk factors and prognosis of young stroke. The FUTURE study: a prospective cohort study. Study rationale and protocol.

Rutten-Jacobs LC, Maaijwee NA, Arntz RM, Van Alebeek ME, Schaapsmeerders P, Schoonderwaldt HC, Dorresteijn LD, Overeem S, Drost G, Janssen MC, van Heerde WL, Kessels RP, Zwiers MP, Norris DG, van der Vlugt MJ, van Dijk EJ, de Leeuw FE. Rutten-Jacobs LC, et al. BMC Neurol. 2011 Sep 20;11:109. doi: 10.1186/1471-2377-11-109. BMC Neurol. 2011. PMID: 21933424 Free PMC article.

3

Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.

de Laat P, Koene S, van den Heuvel LP, Rodenburg RJ, Janssen MC, Smeitink JA. de Laat P, et al. J Inherit Metab Dis. 2012 Nov;35(6):1059-69. doi: 10.1007/s10545-012-9465-2. Epub 2012 Mar 9. J Inherit Metab Dis. 2012. PMID: 22403016 Free PMC article.

4

Inheritance of the m.3243A>G mutation.

de Laat P, Koene S, Heuvel LP, Rodenburg RJ, Janssen MC, Smeitink JA. de Laat P, et al. JIMD Rep. 2013;8:47-50. doi: 10.1007/8904_2012_159. Epub 2012 Jul 6. JIMD Rep. 2013. PMID: 23430519 Free PMC article.

5

Mitochondrial retinal dystrophy associated with the m.3243A>G mutation.

de Laat P, Smeitink JAM, Janssen MCH, Keunen JEE, Boon CJF. de Laat P, et al. Among authors: janssen mch. Ophthalmology. 2013 Dec;120(12):2684-2696. doi: 10.1016/j.ophtha.2013.05.013. Epub 2013 Jun 24. Ophthalmology. 2013. PMID: 23806424

6

Serum FGF21 levels in adult m.3243A>G carriers: clinical implications.

Koene S, de Laat P, van Tienoven DH, Vriens D, Brandt AM, Sweep FC, Rodenburg RJ, Donders AR, Janssen MC, Smeitink JA. Koene S, et al. Neurology. 2014 Jul 8;83(2):125-33. doi: 10.1212/WNL.0000000000000578. Epub 2014 Jun 6. Neurology. 2014. PMID: 24907231

7

High prevalence of complementary and alternative medicine use in patients with genetically proven mitochondrial disorders.

Franik S, Huidekoper HH, Visser G, de Vries M, de Boer L, Hermans-Peters M, Rodenburg R, Verhaak C, Vlieger AM, Smeitink JA, Janssen MC, Wortmann SB. Franik S, et al. J Inherit Metab Dis. 2015 May;38(3):477-82. doi: 10.1007/s10545-014-9773-9. Epub 2014 Oct 11. J Inherit Metab Dis. 2015. PMID: 25303853

8

Serum GDF15 Levels Correlate to Mitochondrial Disease Severity and Myocardial Strain, but Not to Disease Progression in Adult m.3243A>G Carriers.

Koene S, de Laat P, van Tienoven DH, Weijers G, Vriens D, Sweep FC, Timmermans J, Kapusta L, Janssen MC, Smeitink JA. Koene S, et al. JIMD Rep. 2015;24:69-81. doi: 10.1007/8904_2015_436. Epub 2015 May 13. JIMD Rep. 2015. PMID: 25967227 Free PMC article.

9

Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome.

de Laat P, Fleuren LH, Bekker MN, Smeitink JA, Janssen MC. de Laat P, et al. Mitochondrion. 2015 Nov;25:98-103. doi: 10.1016/j.mito.2015.10.005. Epub 2015 Oct 9. Mitochondrion. 2015. PMID: 26455484

10

International Paediatric Mitochondrial Disease Scale.

Koene S, Hendriks JCM, Dirks I, de Boer L, de Vries MC, Janssen MCH, Smuts I, Fung CW, Wong VCN, de Coo IRFM, Vill K, Stendel C, Klopstock T, Falk MJ, McCormick EM, McFarland R, de Groot IJM, Smeitink JAM. Koene S, et al. Among authors: janssen mch. J Inherit Metab Dis. 2016 Sep;39(5):705-712. doi: 10.1007/s10545-016-9948-7. Epub 2016 Jun 9. J Inherit Metab Dis. 2016. PMID: 27277220 Free PMC article.

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