Michiel R. Fokkens

Mutations in potassium channel <i>kcnd3</i> cause spinocerebellar ataxia type 19

Anna Duarri, Justyna Jezierska, Michiel R. Fokkens et al. · Annals of Neurology · 2012 · 136 citations · Full text

Life Sciences, Genetics, Neurology +17

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia

Esther Nibbeling, Anna Duarri, Corien C. Verschuuren‐Bemelmans et al. · Brain · 2017 · 123 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Early transient presence of implanted bone marrow stem cells reduces lesion size after cerebral ischaemia in adult rats

Erik Keimpema, Michiel R. Fokkens, Zsolt Nagy et al. · Neuropathology and Applied Neurobiology · 2008 · 67 citations · Full text

Medicine, Neurobiology, Neuroscience +17

Parkinson’s disease–associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy

Kai Yu, Michiel R. Fokkens, Fulvio Reggiori et al. · Translational Neurodegeneration · 2021 · 58 citations · Full text

Life Sciences, Cell Biology, Neuroscience +17

Elevated mutant dynorphin A causes Purkinje cell loss and motor dysfunction in spinocerebellar ataxia type 23

Cleo J. L. M. Smeets, Justyna Jezierska, Hiroyuki Watanabe et al. · Brain · 2015 · 36 citations · Full text

Life Sciences, Neurology, Neuroscience +13