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:
Systemic corticosteroids for the treatment of acute episodes of rhabdomyolysis in lipin‐1‐deficient patients
Caroline Tuchmann‐Durand, Célina Roda, Perrine Renard, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 46, Iss. 4, pp. 649-661
Open Access | Times Cited: 6
Caroline Tuchmann‐Durand, Célina Roda, Perrine Renard, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 46, Iss. 4, pp. 649-661
Open Access | Times Cited: 6
Showing 6 citing articles:
Emergency Management of Intoxication‐Type Inherited Metabolic Disorders
James Dexter Tarr, Andrew A. M. Morris
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
James Dexter Tarr, Andrew A. M. Morris
Journal of Inherited Metabolic Disease (2025) Vol. 48, Iss. 2
Open Access
Muscle Diseases of Metabolic and Endocrine Derivation
Bruce M. Rothschild
Rheumato (2025) Vol. 5, Iss. 1, pp. 2-2
Open Access
Bruce M. Rothschild
Rheumato (2025) Vol. 5, Iss. 1, pp. 2-2
Open Access
Metabolic Myopathies in the Era of Next-Generation Sequencing
Jon Andoni Urtizberea, Gianmarco Severa, Edoardo Malfatti
Genes (2023) Vol. 14, Iss. 5, pp. 954-954
Open Access | Times Cited: 11
Jon Andoni Urtizberea, Gianmarco Severa, Edoardo Malfatti
Genes (2023) Vol. 14, Iss. 5, pp. 954-954
Open Access | Times Cited: 11
Hydroxychloroquine sulfate: A novel treatment for lipin-1 deficiency?
Perrine Renard, Laure Caccavelli, Antoine Legendre, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 163, pp. 114813-114813
Open Access | Times Cited: 5
Perrine Renard, Laure Caccavelli, Antoine Legendre, et al.
Biomedicine & Pharmacotherapy (2023) Vol. 163, pp. 114813-114813
Open Access | Times Cited: 5
Cellular mechanisms of acute rhabdomyolysis in inherited metabolic diseases
Hortense de Calbiac, Apolline Imbard, Pascale de Lonlay
Journal of Inherited Metabolic Disease (2024) Vol. 48, Iss. 1
Closed Access | Times Cited: 1
Hortense de Calbiac, Apolline Imbard, Pascale de Lonlay
Journal of Inherited Metabolic Disease (2024) Vol. 48, Iss. 1
Closed Access | Times Cited: 1
Use of dexamethasone in acute rhabdomyolysis in LPIN1 deficiency
Mehdi Yeganeh, Kaitlin March, Catherine Jones, et al.
Molecular Genetics and Metabolism Reports (2023) Vol. 35, pp. 100961-100961
Open Access | Times Cited: 1
Mehdi Yeganeh, Kaitlin March, Catherine Jones, et al.
Molecular Genetics and Metabolism Reports (2023) Vol. 35, pp. 100961-100961
Open Access | Times Cited: 1
Telbivudine-induced rhabdomyolysis in a patient undergoing haemodialysis: A case report and review of literature
Keping Wu, Xiaochang Xu, Leidan Huang, et al.
Journal of International Medical Research (2023) Vol. 51, Iss. 12
Open Access | Times Cited: 1
Keping Wu, Xiaochang Xu, Leidan Huang, et al.
Journal of International Medical Research (2023) Vol. 51, Iss. 12
Open Access | Times Cited: 1
