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Mitochondrion|October 13, 2015
Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcomePaul de Laat, Leanne H J Fleuren, Mireille N Bekker, et al.Ophthalmology|June 29, 2013
Mitochondrial retinal dystrophy associated with the m.3243A>G mutationPaul de Laat, Jan A M Smeitink, Mirian C H Janssen, et al.Thrombosis and Haemostasis|November 8, 2005
The post-thrombotic syndrome: incidence and prognostic value of non-invasive venous examinations in a six-year follow-up studyEdith M Roumen-Klappe, Martin den Heijer, Mirian C H Janssen, et al.Clinical Rheumatology|April 25, 2014
New gout test: enhanced ex vivo cytokine production from PBMCS in common gout patients and a gout patient with Kearns-Sayre syndromeTim L Jansen, Dianne Berendsen, Tania O Crisan, et al.Journal of Inherited Metabolic Disease|September 2, 2022
Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variantInge-Lot Klein, Christianne M Verhaak, Jan A M Smeitink, et al.Orphanet Journal of Rare Diseases|July 15, 2022
A conceptual disease model for quality of life in mitochondrial diseaseKim F E van de Loo, Nander T van Zeijl, José A E Custers, et al.BBA Clinical|June 23, 2016
Three families with 'de novo' m.3243A > G mutationPaul de Laat, Mirian C H Janssen, Charlotte L Alston, et al.Nederlands Tijdschrift Voor Geneeskunde|July 17, 2025
[Inherited metabolic disorders in adults:growing patient numbers, advanced diagnostic tools and new treatment modalities]Mirjam Langeveld, Martijn C G J Brouwers, Laura van Dussen, et al.JPEN. Journal of Parenteral and Enteral Nutrition|March 20, 2020
Association of Body Composition, Physical Functioning, and Protein Intake in Adult Patients With Mitochondrial DiseasesHeidi E E Zweers, Valentine Bordier, Jeanne In 't Hulst, et al.Journal of Inherited Metabolic Disease|March 14, 2018
Quantification of gait in children with mitochondrial diseaseSaskia Koene, Niki M Stolwijk, Rob Ramakers, et al.Pageof 12