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OpenAlex Citation Counts

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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:

Spectrum of movement disorders in mitochondrial diseases
Olimpia Musumeci, Rosaria Oteri, António Toscano
Journal of Translational Genetics and Genomics (2020)
Open Access | Times Cited: 11

Showing 11 citing articles:

Polycystic Ovary Syndrome and Oxidative Stress—From Bench to Bedside
Natalia Żeber‐Lubecka, Michał Ciebiera, Ewa E. Hennig
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 18, pp. 14126-14126
Open Access | Times Cited: 46
Variants in ATP5F1B are associated with dominantly inherited dystonia
Alessia Nasca, Niccolò E. Mencacci, Federica Invernizzi, et al.
Brain (2023) Vol. 146, Iss. 7, pp. 2730-2738
Open Access | Times Cited: 12
Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity
Piervito Lopriore, Valentina Ricciarini, Gabriele Siciliano, et al.
Neurology International (2022) Vol. 14, Iss. 2, pp. 337-356
Open Access | Times Cited: 18
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network
Vincenzo Montano, Daniele Orsucci, Valério Carelli, et al.
Journal of Neurology (2021) Vol. 269, Iss. 3, pp. 1413-1421
Open Access | Times Cited: 18
Movement Disorders in Children with a Mitochondrial Disease: A Cross-Sectional Survey from the Nationwide Italian Collaborative Network of Mitochondrial Diseases
Chiara Ticci, Daniele Orsucci, Anna Ardissone, et al.
Journal of Clinical Medicine (2021) Vol. 10, Iss. 10, pp. 2063-2063
Open Access | Times Cited: 16
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant
Jonna Komulainen‐Ebrahim, Salla M. Kangas, Estrella López‐Martín, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 6, pp. 708-715
Open Access | Times Cited: 2
Mitochondrial Parkinsonism: A Practical Guide to Genes and Clinical Diagnosis
Piervito Lopriore, Giovanni Palermo, Adriana Meli, et al.
Movement Disorders Clinical Practice (2024) Vol. 11, Iss. 8, pp. 948-965
Closed Access | Times Cited: 1
TANGO2 Mutation: A Genetic Cause of Multifocal Combined Dystonia
Jessica Frey, Matthew R. Burns, Shannon Chiu, et al.
Movement Disorders Clinical Practice (2021) Vol. 9, Iss. 3, pp. 380-382
Open Access | Times Cited: 5
Movement disorders associated with neuromuscular and mitochondrial disorders
Jinyoung Youn, Woo Young Jang, Eungseok Oh, et al.
International review of movement disorders (2024), pp. 63-101
Closed Access
Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders
Giuditta Pellino, Raffaella Faggioli, Anna Galuppi, et al.
Mitochondrion (2021) Vol. 61, pp. 159-164
Closed Access | Times Cited: 3
Dystonia, spastic tetraplegia, and ataxia due to a novel mutation in the dynamin domain of OPA1
Yuzhi Shi, Kang Zhang, Gehong Dong, et al.
Annals of Clinical and Translational Neurology (2023) Vol. 11, Iss. 3, pp. 800-805
Open Access
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