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:
Early recognition of patients with leukodystrophies
Nicholson Modesti, Sarah Helen Evans, Nicole Jaffe, et al.
Current problems in pediatric and adolescent health care (2022) Vol. 52, Iss. 12, pp. 101311-101311
Open Access | Times Cited: 7
Nicholson Modesti, Sarah Helen Evans, Nicole Jaffe, et al.
Current problems in pediatric and adolescent health care (2022) Vol. 52, Iss. 12, pp. 101311-101311
Open Access | Times Cited: 7
Showing 7 citing articles:
Nucleotide metabolism, leukodystrophies, and CNS pathology
Francesco Gavazzi, Carlos Dominguez Gonzalez, Kaley Arnold, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 860-875
Closed Access | Times Cited: 7
Francesco Gavazzi, Carlos Dominguez Gonzalez, Kaley Arnold, et al.
Journal of Inherited Metabolic Disease (2024) Vol. 47, Iss. 5, pp. 860-875
Closed Access | Times Cited: 7
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individuals
Dana E. Layo-Carris, Emily E. Lubin, Annabel K. Sangree, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 928-937
Open Access | Times Cited: 4
Dana E. Layo-Carris, Emily E. Lubin, Annabel K. Sangree, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 928-937
Open Access | Times Cited: 4
Advancing CNS Therapeutics: Enhancing Neurological Disorders with Nanoparticle-Based Gene and Enzyme Replacement Therapies
Shuhan Liu, Haisong Li, Shiwen Xi, et al.
International Journal of Nanomedicine (2025) Vol. Volume 20, pp. 1443-1490
Open Access
Shuhan Liu, Haisong Li, Shiwen Xi, et al.
International Journal of Nanomedicine (2025) Vol. Volume 20, pp. 1443-1490
Open Access
Adult-onset cerebral X-linked adrenoleukodystrophy presenting with frontal lobe syndrome caused by a de novo ABCD1 mutation (c.1415_1416delAG, p.Gln472fs*83).
Ritwik Ghosh, Moisés León‐Ruiz, Arup Jana, et al.
Neurology Perspectives (2025), pp. 100186-100186
Open Access
Ritwik Ghosh, Moisés León‐Ruiz, Arup Jana, et al.
Neurology Perspectives (2025), pp. 100186-100186
Open Access
Leukodystrophy with Macrocephaly, Refractory Epilepsy, and Severe Hyponatremia—The Neonatal Type of Alexander Disease
Justyna Paprocka, Magdalena Nowak, Magdalena Machnikowska-Sokołowska, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 350-350
Open Access | Times Cited: 2
Justyna Paprocka, Magdalena Nowak, Magdalena Machnikowska-Sokołowska, et al.
Genes (2024) Vol. 15, Iss. 3, pp. 350-350
Open Access | Times Cited: 2
Globoid Cell Leukodystrophy (Krabbe Disease): An Update
Azzam A. Maghazachi
ImmunoTargets and Therapy (2023) Vol. Volume 12, pp. 105-111
Open Access | Times Cited: 2
Azzam A. Maghazachi
ImmunoTargets and Therapy (2023) Vol. Volume 12, pp. 105-111
Open Access | Times Cited: 2
Foreword: Leukodystrophies in children: Early recognition, complications, and multidisciplinary care Part I
Louis M. Bell
Current problems in pediatric and adolescent health care (2022) Vol. 52, Iss. 12, pp. 101314-101314
Closed Access
Louis M. Bell
Current problems in pediatric and adolescent health care (2022) Vol. 52, Iss. 12, pp. 101314-101314
Closed Access
