
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:
A case of early-onset Parkinson’s disease in a patient with KBG syndrome
Luca Magistrelli, Elena Contaldi, Fjorilda Caushi, et al.
Neurological Sciences (2023) Vol. 44, Iss. 12, pp. 4537-4539
Closed Access | Times Cited: 3
Luca Magistrelli, Elena Contaldi, Fjorilda Caushi, et al.
Neurological Sciences (2023) Vol. 44, Iss. 12, pp. 4537-4539
Closed Access | Times Cited: 3
Showing 3 citing articles:
Early-Onset Parkinson’s Disease in a Patient With a De Novo Frameshift Variant of the ANKRD11 Gene and KBG Syndrome
Maria-Ioanna Stefanou, Vasileios K. Katsaros, Georgia Pepe, et al.
Journal of Clinical Neurology (2025) Vol. 21, Iss. 2, pp. 153-153
Open Access
Maria-Ioanna Stefanou, Vasileios K. Katsaros, Georgia Pepe, et al.
Journal of Clinical Neurology (2025) Vol. 21, Iss. 2, pp. 153-153
Open Access
Natural history of adults with KBG syndrome: A physician-reported experience
Allan Bayat, Hannah Grimes, Elke de Boer, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101170-101170
Closed Access | Times Cited: 2
Allan Bayat, Hannah Grimes, Elke de Boer, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 8, pp. 101170-101170
Closed Access | Times Cited: 2
Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search
Dongye He, Mei Zhang, Yanying Li, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 1
Dongye He, Mei Zhang, Yanying Li, et al.
Orphanet Journal of Rare Diseases (2024) Vol. 19, Iss. 1
Open Access | Times Cited: 1