H. Smeets

Blood biomarkers for assessment of mitochondrial dysfunction: An expert review.

I. D. de Coo, H. Smeets, T. Gorgels, 2021, Mitochondrion.

The transmission of OXPHOS disease and methods to prevent this.

I. D. de Coo, H. Smeets, J. Geraedts, 2006, Human reproduction update.

Termination of damaged protein repair defines the occurrence of symptoms in carriers of the m.3243A>G tRNALeu mutation

I. D. de Coo, T. Ayoubi, W. Sluiter, 2008, Journal of Medical Genetics.

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

H. Smeets, J. Maassen, L. T. ’t Hart, 1997, Journal of the American Society of Nephrology : JASN.

Patients with Leber hereditary optic neuropathy fail to compensate impaired oxidative phosphorylation.

H. Smeets, W. Sluiter, A. Korsten, 2010, Biochimica et biophysica acta.

Pearson syndrome and the role of deletion dimers and duplications in the mtDNA

I. D. de Coo, H. Smeets, J. Geraedts, 2004, Journal of Inherited Metabolic Disease.

Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.

H. Smeets, V. Procaccio, G. Putet, 1999, The Journal of clinical investigation.

PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring.

I. D. de Coo, H. Smeets, P. Chinnery, 2012, Human reproduction update.