
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:
Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome
Arunan Selvarajah, Carolina Gorodetsky, Paula Marques, et al.
Neurology (2022) Vol. 98, Iss. 22
Open Access | Times Cited: 17
Arunan Selvarajah, Carolina Gorodetsky, Paula Marques, et al.
Neurology (2022) Vol. 98, Iss. 22
Open Access | Times Cited: 17
Showing 17 citing articles:
Dravet syndrome: A systematic literature review of the illness burden
Adam Strzelczyk, Lieven Lagae, Jo M. Wilmshurst, et al.
Epilepsia Open (2023) Vol. 8, Iss. 4, pp. 1256-1270
Open Access | Times Cited: 33
Adam Strzelczyk, Lieven Lagae, Jo M. Wilmshurst, et al.
Epilepsia Open (2023) Vol. 8, Iss. 4, pp. 1256-1270
Open Access | Times Cited: 33
The natural history of CDKL5 deficiency disorder into adulthood
Ángel Aledo‐Serrano, David Lewis‐Smith, Helen Leonard, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Ángel Aledo‐Serrano, David Lewis‐Smith, Helen Leonard, et al.
medRxiv (Cold Spring Harbor Laboratory) (2025)
Open Access
Dravet syndrome: From neurodevelopmental to neurodegenerative disease?
Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Epilepsia (2025)
Open Access
Arunan Selvarajah, Andrea Sabo, Carolina Gorodetsky, et al.
Epilepsia (2025)
Open Access
Variants in ATP6V0C are associated with Dravet‐like developmental and epileptic encephalopathy
Marlene Rong, Paula Marques, Quratulain Zulfiqar Ali, et al.
Epilepsia (2025)
Open Access
Marlene Rong, Paula Marques, Quratulain Zulfiqar Ali, et al.
Epilepsia (2025)
Open Access
Spotlight on mechanism of sudden unexpected death in epilepsy in Dravet syndrome
WeiHui Shao, Lu Liu, JiaXuan Gu, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
WeiHui Shao, Lu Liu, JiaXuan Gu, et al.
Translational Psychiatry (2025) Vol. 15, Iss. 1
Open Access
Case Report of Myoclonus‐Ataxia Syndrome in an Indian Patient Due to SCNA1 Gene Mutation
Anjali Chouksey
Movement Disorders Clinical Practice (2025)
Closed Access
Anjali Chouksey
Movement Disorders Clinical Practice (2025)
Closed Access
Decreased homovanillic acid and 5‐hydroxyindoleacetic acid levels in the cerebrospinal fluid of patients with Dravet syndrome with parkinsonism
Rino Sugiyama, Takashi Saito, Atsuko Katsumoto, et al.
Epilepsia Open (2025)
Open Access
Rino Sugiyama, Takashi Saito, Atsuko Katsumoto, et al.
Epilepsia Open (2025)
Open Access
Effect of levodopa on pathological gait in Dravet syndrome: A randomized crossover trial using three‐dimensional gait analysis
Takeshi Suzuki, Jun Natsume, Yuji Ito, et al.
Epilepsia (2024) Vol. 65, Iss. 5, pp. 1304-1313
Open Access | Times Cited: 3
Takeshi Suzuki, Jun Natsume, Yuji Ito, et al.
Epilepsia (2024) Vol. 65, Iss. 5, pp. 1304-1313
Open Access | Times Cited: 3
Morphometry and network-based atrophy patterns in SCN1A-related Dravet syndrome
Matteo Lenge, Simona Balestrini, Davide Mei, et al.
Cerebral Cortex (2023) Vol. 33, Iss. 16, pp. 9532-9541
Open Access | Times Cited: 6
Matteo Lenge, Simona Balestrini, Davide Mei, et al.
Cerebral Cortex (2023) Vol. 33, Iss. 16, pp. 9532-9541
Open Access | Times Cited: 6
Adult Phenotype of SYNGAP1 -DEE
Marlene Rong, Tim A. Benke, Quratulain Zulfiqar Ali, et al.
Neurology Genetics (2023) Vol. 9, Iss. 6
Open Access | Times Cited: 6
Marlene Rong, Tim A. Benke, Quratulain Zulfiqar Ali, et al.
Neurology Genetics (2023) Vol. 9, Iss. 6
Open Access | Times Cited: 6
Measuring the inch stones for progress: Gross motor function in the developmental and epileptic encephalopathies
Anne T. Berg, Aaron J. Kaat, Deborah Gaebler‐Spira
Epilepsy & Behavior (2022) Vol. 137, pp. 108953-108953
Closed Access | Times Cited: 10
Anne T. Berg, Aaron J. Kaat, Deborah Gaebler‐Spira
Epilepsy & Behavior (2022) Vol. 137, pp. 108953-108953
Closed Access | Times Cited: 10
Epilepsy genetics: a practical guide for adult neurologists
William Owen Pickrell, Andrew E. Fry
Practical Neurology (2023) Vol. 23, Iss. 2, pp. 111-119
Open Access | Times Cited: 4
William Owen Pickrell, Andrew E. Fry
Practical Neurology (2023) Vol. 23, Iss. 2, pp. 111-119
Open Access | Times Cited: 4
The Impact of Non-Seizure Symptoms in Dravet Syndrome and Lennox–Gastaut Syndrome
Eleanor Roberts
EMJ Neurology (2024), pp. 2-11
Open Access | Times Cited: 1
Eleanor Roberts
EMJ Neurology (2024), pp. 2-11
Open Access | Times Cited: 1
Medial septum parvalbumin-expressing inhibitory neurons are impaired in a mouse model of Dravet Syndrome
Limei Zhu, Yiannos Demetriou, Joseph Barden, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Limei Zhu, Yiannos Demetriou, Joseph Barden, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Epileptic seizures worsen the gait and motor abnormalities in adult patients with Dravet syndrome (with a case report and literature review)
Xiaoping Du, Shizhong Lian, Meizhen Sun, et al.
Epilepsia Open (2023) Vol. 8, Iss. 4, pp. 1576-1580
Open Access | Times Cited: 1
Xiaoping Du, Shizhong Lian, Meizhen Sun, et al.
Epilepsia Open (2023) Vol. 8, Iss. 4, pp. 1576-1580
Open Access | Times Cited: 1
Recognition of Movement Disorders in Genetic, Developmental, and Epileptic Encephalopathies
Elia M. Pestana-Knight
Neurology (2023) Vol. 101, Iss. 19, pp. 815-816
Closed Access | Times Cited: 1
Elia M. Pestana-Knight
Neurology (2023) Vol. 101, Iss. 19, pp. 815-816
Closed Access | Times Cited: 1
Broadening Neurologic Manifestations in Adult Patients With Dravet Syndrome
Shoji Tsuji
Neurology (2022) Vol. 98, Iss. 22, pp. 913-914
Closed Access | Times Cited: 1
Shoji Tsuji
Neurology (2022) Vol. 98, Iss. 22, pp. 913-914
Closed Access | Times Cited: 1