OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias
Liedewei Van de Vondel, Jonathan De Winter, Vincent Timmerman, et al.
Trends in Neurosciences (2024) Vol. 47, Iss. 3, pp. 227-238
Closed Access | Times Cited: 6
Liedewei Van de Vondel, Jonathan De Winter, Vincent Timmerman, et al.
Trends in Neurosciences (2024) Vol. 47, Iss. 3, pp. 227-238
Closed Access | Times Cited: 6
Showing 6 citing articles:
The molecular landscape of hereditary ataxia: a single-center study
Elisa Bregant, Elena Betto, Chiara Dal Secco, et al.
Human Genetics (2025)
Open Access
Elisa Bregant, Elena Betto, Chiara Dal Secco, et al.
Human Genetics (2025)
Open Access
Editorial: Translational research in hereditary spastic paraplegias: filling the diagnosis gap and therapeutic perspectives
Andrea Martinuzzi, Craig Blackstone, Giovanni Stévanin
Frontiers in Neuroscience (2025) Vol. 19
Open Access
Andrea Martinuzzi, Craig Blackstone, Giovanni Stévanin
Frontiers in Neuroscience (2025) Vol. 19
Open Access
Genetic and Clinical Features of 10 Families With Hereditary Sensory Neuropathies
Ke Xu, Zhong‐Zheng Li, Mengli Wang, et al.
Journal of the Peripheral Nervous System (2025) Vol. 30, Iss. 2
Closed Access
Ke Xu, Zhong‐Zheng Li, Mengli Wang, et al.
Journal of the Peripheral Nervous System (2025) Vol. 30, Iss. 2
Closed Access
Heterozygous loss-of-function variants in SPTAN1 cause a novel early childhood onset distal myopathy with chronic neurogenic features
Jonathan De Winter, Liedewei Van de Vondel, Biljana Ermanoska, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
Jonathan De Winter, Liedewei Van de Vondel, Biljana Ermanoska, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Closed Access | Times Cited: 1
Spectrinopathies in rare neurological and neuromuscular diseases : large-scale efforts towards the identification of novel molecular causes
Liedewei Van de Vondel
(2024)
Open Access
Liedewei Van de Vondel
(2024)
Open Access
Metabolite profile in hereditary spastic paraplegia analyzed using magnetic resonance spectroscopy: a cross-sectional analysis in a longitudinal study
D. Montanaro, Marinela Vavla, Francesca Frijia, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access
D. Montanaro, Marinela Vavla, Francesca Frijia, et al.
Frontiers in Neuroscience (2024) Vol. 18
Open Access
