Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Van der Knaap, Marjo S  [Clear All Filters]
2024
Al-Saady ML, Galabova H, Schoenmakers DH, Beerepoot S, Lindemans C, van Hasselt PM, Van der Knaap MS, Wolf NI, Pouwels PJW. Longitudinal volumetric analysis of gray matter atrophy in metachromatic leukodystrophy. J Inherit Metab Dis. 2024.
Beerepoot S, Boelens JJan, Lindemans C, de Witte MA, Nierkens S, Vrancken AFJE, Van der Knaap MS, Bugiani M, Wolf NI. Progressive demyelinating polyneuropathy after hematopoietic cell transplantation in metachromatic leukodystrophy: a case series. J Neurol. 2024.
2022
Hillen AEJ, Leferink PS, Breeuwsma NB, Dooves S, Bergaglio T, Van der Knaap MS, Heine VM. Therapeutic potential of human stem cell transplantations for Vanishing White Matter: A quest for the Goldilocks graft. CNS Neurosci Ther. 2022.
2021
Beerepoot S, Heijst H, Roos B, Wamelink MMC, Boelens JJan, Lindemans CA, van Hasselt PM, Jacobs EH, Van der Knaap MS, Teunissen CE, et al. Neurofilament light chain and glial fibrillary acidic protein levels in metachromatic leukodystrophy. Brain. 2021.
2020
Wolf NI, Breur M, Plug B, Beerepoot S, Westerveld ASR, van Rappard DF, de Vries SI, Kole MHP, Vanderver A, Van der Knaap MS, et al. Metachromatic leukodystrophy and transplantation: remyelination, no cross-correction. Ann Clin Transl Neurol. 2020.
2019
Leferink PS, Dooves S, Hillen AEJ, Watanabe K, Jacobs G, Gasparotto L, Cornelissen-Steijger P, Van der Knaap MS, Heine VM. Astrocyte subtype vulnerability in stem cell models of Vanishing White Matter. Ann Neurol. 2019.
2018
Gurgel-Giannetti J, Lynch DS, de Paiva ARodrigues, Lucato LTavares, Yamamoto G, Thomsen C, Basu S, Freua F, Giannetti AVarella, de Assis BDella Ripa, et al. A novel complex neurological phenotype due to a homozygous mutation in FDX2. Brain. 2018.