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:
Clinical features and genetics in non-5q spinal muscular atrophy caused by acid ceramidase deficiency
Mihaela Axente, Elena-Silvia Shelby, Andrada Mirea, et al.
Journal of Medicine and Life (2021) Vol. 14, Iss. 3, pp. 424-428
Open Access | Times Cited: 8
Mihaela Axente, Elena-Silvia Shelby, Andrada Mirea, et al.
Journal of Medicine and Life (2021) Vol. 14, Iss. 3, pp. 424-428
Open Access | Times Cited: 8
Showing 8 citing articles:
Acid Ceramidase Deficiency: Bridging Gaps between Clinical Presentation, Mouse Models, and Future Therapeutic Interventions
Annie Kleynerman, Jitka Rybová, Mary L. Faber, et al.
Biomolecules (2023) Vol. 13, Iss. 2, pp. 274-274
Open Access | Times Cited: 13
Annie Kleynerman, Jitka Rybová, Mary L. Faber, et al.
Biomolecules (2023) Vol. 13, Iss. 2, pp. 274-274
Open Access | Times Cited: 13
Acid Ceramidase Deficiency
Silvestre Cuinat, Paul Rollier, Katheryn Grand, et al.
Neurology Genetics (2025) Vol. 11, Iss. 2
Closed Access
Silvestre Cuinat, Paul Rollier, Katheryn Grand, et al.
Neurology Genetics (2025) Vol. 11, Iss. 2
Closed Access
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME): three new cases and review of the mutational spectrum
Ali Najafi, Behnoosh Tasharrofi, Farshid Zandsalimi, et al.
The Italian Journal of Pediatrics/Italian journal of pediatrics (2023) Vol. 49, Iss. 1
Open Access | Times Cited: 6
Ali Najafi, Behnoosh Tasharrofi, Farshid Zandsalimi, et al.
The Italian Journal of Pediatrics/Italian journal of pediatrics (2023) Vol. 49, Iss. 1
Open Access | Times Cited: 6
Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutations
Dian Kesumapramudya Nurputra, Jessica Sofian, Kristy Iskandar, et al.
Neurological Sciences (2024) Vol. 45, Iss. 9, pp. 4583-4588
Closed Access | Times Cited: 2
Dian Kesumapramudya Nurputra, Jessica Sofian, Kristy Iskandar, et al.
Neurological Sciences (2024) Vol. 45, Iss. 9, pp. 4583-4588
Closed Access | Times Cited: 2
Five patients with spinal muscular atrophy-progressive myoclonic epilepsy (SMA-PME): a novel pathogenic variant, treatment and review of the literature
Parvaneh Karimzadeh, Hossein Najmabadi, Hanns Lochmüller, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 10, pp. 806-810
Closed Access | Times Cited: 9
Parvaneh Karimzadeh, Hossein Najmabadi, Hanns Lochmüller, et al.
Neuromuscular Disorders (2022) Vol. 32, Iss. 10, pp. 806-810
Closed Access | Times Cited: 9
The clinical spectrum of SMA‐PME and in vitro normalization of its cellular ceramide profile
Michelle M. Lee, Graeme S. V. McDowell, Darryl C. De Vivo, et al.
Annals of Clinical and Translational Neurology (2022) Vol. 9, Iss. 12, pp. 1941-1952
Open Access | Times Cited: 8
Michelle M. Lee, Graeme S. V. McDowell, Darryl C. De Vivo, et al.
Annals of Clinical and Translational Neurology (2022) Vol. 9, Iss. 12, pp. 1941-1952
Open Access | Times Cited: 8
Current and emerging targeted therapies for spinal muscular atrophy
Yuliya Lakhina, Nicholas M. Boulis, Anthony Donsante
Expert Review of Neurotherapeutics (2023) Vol. 23, Iss. 12, pp. 1189-1199
Closed Access | Times Cited: 2
Yuliya Lakhina, Nicholas M. Boulis, Anthony Donsante
Expert Review of Neurotherapeutics (2023) Vol. 23, Iss. 12, pp. 1189-1199
Closed Access | Times Cited: 2
Acid ceramidase deficiency: Farber lipogranulomatosis, spinal muscular atrophy associated with progressive myoclonic epilepsy and peripheral osteolysis
Eugen Mengel, Michael Beck, Hugo W. Moser, et al.
Elsevier eBooks (2024), pp. 665-675
Closed Access
Eugen Mengel, Michael Beck, Hugo W. Moser, et al.
Elsevier eBooks (2024), pp. 665-675
Closed Access
