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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 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.
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