More than a co-incidence? Comment on: Amyotrophic lateral sclerosis is over‐represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotro... by Bakels, Hannah S., Feleus, Stephanie, van Dis, Vera, de Bot, Susanne T.

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Juvenile‐Onset Huntington Disease Pathophysiology and Neurodevelopment: A Review by Bakels, Hannah S., Roos, Raymund A.C., Roon‐Mom, Willeke M.C., Bot, Susanne T.

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Post‐mortem 7T MR imaging and neuropathology in middle stage juvenile‐onset Huntington disease: A case report by Bakels, Hannah S., Duinen, Sjoerd G., Bresser, Jeroen, Roon‐Mom, Willeke M. C., Weerd, Louise, Bot, Susanne T.

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GLUT-1 changes in paediatric Huntington disease brain cortex and fibroblasts: an observational case-control study by Tramutola, Antonella, Bakels, Hannah S., Perrone, Federica, Di Nottia, Michela, Mazza, Tommaso, Abruzzese, Maria Pia, Zoccola, Martina, Pagnotta, Sara, Carrozzo, Rosalba, de Bot, Susanne T., Perluigi, Marzia, van Roon-Mom, Willeke M.C., Squitieri, Ferdinando

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The cavernous sinus in cluster headache – a quantitative structural magnetic resonance imaging study by Arkink, Enrico B, Schoonman, Guus G, van Vliet, Jorine A, Bakels, Hannah S, Sneeboer, Marjolein AM, Haan, Joost, van Buchem, Mark A, Ferrari, Michel D, Kruit, Mark C

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Interferon‐α and the calcifying microangiopathy in Aicardi–Goutières syndrome by Klok, Melanie D., Bakels, Hannah S., Postma, Nienke L., Spaendonk, Rosalina M. L., Knaap, Marjo S., Bugiani, Marianna

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GLUT-1 changes in paediatric Huntington disease brain cortex and fibroblasts: an observational case-control studyResearch in context by Antonella Tramutola, Hannah S. Bakels, Federica Perrone, Michela Di Nottia, Tommaso Mazza, Maria Pia Abruzzese, Martina Zoccola, Sara Pagnotta, Rosalba Carrozzo, Susanne T. de Bot, Marzia Perluigi, Willeke M.C. van Roon-Mom, Ferdinando Squitieri

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Exploring the Aggregation Propensity of PHF6 Peptide Segments of the Tau Protein Using Ion Mobility Mass Spectrometry Techniques by Stroganova, Iuliia, Willenberg, Hannah, Tente, Thaleia, Depraz Depland, Agathe, Bakels, Sjors, Rijs, Anouk M.

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TERT promoter mutations and BRAF mutations are rare in sporadic, and TERT promoter mutations are absent in NF1-related malignant peripheral nerve sheath tumors by Dubbink, Hendrikus J., Bakels, Hannah, Post, Edward, Zwarthoff, Ellen C., Verdijk, Robert M.

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