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Florence H.J. van Tienen

Maastricht University

9

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22

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Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle.

2021 Frontiers in Genetics
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Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle

2021
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Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency.

2021 European Journal of Human Genetics
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Natural history, outcome measures and trial readiness in LAMA2-related muscular dystrophy and SELENON-related myopathy in children and adults: protocol of the LAST STRONG study

2021 BMC Neurology
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MOESM1 of Healthy, mtDNA-mutationÂ free mesoangioblasts from mtDNA patients qualify for autologous therapy

2019
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Healthy, mtDNA-mutation free mesoangioblasts from mtDNA patients qualify for autologous therapy

2019 Stem Cell Research & Therapy
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Lamin A/C-Related Cardiac DiseaseCLINICAL PERSPECTIVE: Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation

2017 Circulation-cardiovascular Genetics
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Rare novel variants in the ZIC3 gene cause X-linked heterotaxy

2016 European Journal of Human Genetics
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