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Journal of Hypertension|February 8, 2022
Higher SBP in female patients with mitochondrial diseaseDaan H H M Viering, Marjolein D van Borselen, Jaap Deinum, et al.Journal of Inherited Metabolic Disease|March 10, 2012
Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutationPaul de Laat, Saskia Koene, Lambert P W J van den Heuvel, et al.Nederlands Tijdschrift Voor Geneeskunde|July 5, 2012
[Erythrocytapheresis for hereditary haemochromatosis]Eva Rombout-Sestrienkova, Cees Th B M van Deursen, Mirian C H Janssen, et al.JIMD Reports|July 5, 2023
Increased prevalence of Parkinson's disease in alkaptonuriaLakshminarayan Ranganath, Milad Khedr, Anna M Milan, et al.Clinical Pharmacology and Therapeutics|July 31, 2018
The KHENERGY Study: Safety and Efficacy of KH176 in Mitochondrial m.3243A>G Spectrum DisordersMirian C H Janssen, Saskia Koene, Paul de Laat, et al.Orphanet Journal of Rare Diseases|March 27, 2020
Psychological functioning in children suspected for mitochondrial disease: the need for careKim F E van de Loo, José A E Custers, Saskia Koene, et al.Journal of Vascular Surgery|June 4, 2002
The development of postthrombotic syndrome in relationship to venous reflux and calf muscle pump dysfunction at 2 years after the onset of deep venous thrombosisJosé H Haenen, Mirian C H Janssen, Hub Wollersheim, et al.Journal of Inherited Metabolic Disease|April 25, 2024
Impact of theta transcranial alternating current stimulation on language production in adult classic galactosemia patientsBritt Derks, Varsha Shashi Kumar, Sai Yadnik, et al.Orphanet Journal of Rare Diseases|October 1, 2022
Cognitive functioning and mental health in children with a primary mitochondrial diseaseKim F E van de Loo, José A E Custers, Lonneke de Boer, et al.Molecular Genetics and Metabolism|July 22, 2026
Gut microbiota alterations in individuals with mitochondrial disease caused by the m.3243A >G mutationDave G J de Bruijn, Alem Gusinac, Thomas H A Ederveen, et al.Pageof 12