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:
Molecular diagnosis of epileptic encephalopathy of the first year of life applying a customized gene panel in a group of Argentinean patients
Matías Juanes, Gabriel Veneruzzo, Mariana Loos, et al.
Epilepsy & Behavior (2020) Vol. 111, pp. 107322-107322
Closed Access | Times Cited: 7
Matías Juanes, Gabriel Veneruzzo, Mariana Loos, et al.
Epilepsy & Behavior (2020) Vol. 111, pp. 107322-107322
Closed Access | Times Cited: 7
Showing 7 citing articles:
Genetic testing for the epilepsies: A systematic review
Beth Rosen Sheidley, Jennifer Malinowski, Amanda Bergner, et al.
Epilepsia (2021) Vol. 63, Iss. 2, pp. 375-387
Closed Access | Times Cited: 91
Beth Rosen Sheidley, Jennifer Malinowski, Amanda Bergner, et al.
Epilepsia (2021) Vol. 63, Iss. 2, pp. 375-387
Closed Access | Times Cited: 91
The clinical, economic, and humanistic burden of Dravet syndrome – A systematic literature review
Joseph Sullivan, Alison Deighton, Maria Candida Vila, et al.
Epilepsy & Behavior (2022) Vol. 130, pp. 108661-108661
Open Access | Times Cited: 43
Joseph Sullivan, Alison Deighton, Maria Candida Vila, et al.
Epilepsy & Behavior (2022) Vol. 130, pp. 108661-108661
Open Access | Times Cited: 43
INFANTILE EPILEPTIC SPASMS SYNDROME: UNVEILING CLINICAL AND GENETIC VARIABILITY IN A CASE SERIES FROM ARGENTINA
Eugenia Fernández Martín, Lenin Intriago, Mariana Loos, et al.
Seizure (2025)
Closed Access
Eugenia Fernández Martín, Lenin Intriago, Mariana Loos, et al.
Seizure (2025)
Closed Access
A Wide Spectrum of Genetic Disorders Causing Severe Childhood Epilepsy in Taiwan: A Case Series of Ultrarare Genetic Cause and Novel Mutation Analysis in a Pilot Study
Syuan‐Yu Hong, Jiann‐Jou Yang, Shuan‐Yow Li, et al.
Journal of Personalized Medicine (2020) Vol. 10, Iss. 4, pp. 281-281
Open Access | Times Cited: 24
Syuan‐Yu Hong, Jiann‐Jou Yang, Shuan‐Yow Li, et al.
Journal of Personalized Medicine (2020) Vol. 10, Iss. 4, pp. 281-281
Open Access | Times Cited: 24
Dravet Syndrome: An Electroclinical, Genetic, Treatment, and Outcome Study of 35 Patients in Argentina
Roberto Caraballo, Gabriel Veneruzzo, Mariana Loos, et al.
Journal of Pediatric Epilepsy (2024) Vol. 13, Iss. 02, pp. 031-039
Closed Access
Roberto Caraballo, Gabriel Veneruzzo, Mariana Loos, et al.
Journal of Pediatric Epilepsy (2024) Vol. 13, Iss. 02, pp. 031-039
Closed Access
Two familial cases of infantile epileptic spasms syndrome associated with UDP‐glucose‐6‐dehydrogenase deficiency
Caroll Suyo Suyo-Suyo, Gabriela Reyes Valenzuela, Sara Melgarejo, et al.
Epileptic Disorders (2024)
Open Access
Caroll Suyo Suyo-Suyo, Gabriela Reyes Valenzuela, Sara Melgarejo, et al.
Epileptic Disorders (2024)
Open Access
SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families
Diana M. Cornejo-Sanchez, Anushree Acharya, Thashi Bharadwaj, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 754-754
Open Access | Times Cited: 2
Diana M. Cornejo-Sanchez, Anushree Acharya, Thashi Bharadwaj, et al.
Genes (2022) Vol. 13, Iss. 5, pp. 754-754
Open Access | Times Cited: 2
