PublisherDOIYearVolumeIssuePageTitleAuthor(s)Link
Precision and Future Medicine10.23838/pfm.2019.00086201933135-138Intrafamilial variability and clinical heterogeneity in a family with PLA2G6-associated neurodegenerationJong Kyu Park, Jinyoung Youn, Jin Whan Chohttp://pfmjournal.org/upload/pdf/pfm-2019-00086.pdf, http://pfmjournal.org/journal/view.php?doi=10.23838/pfm.2019.00086, http://pfmjournal.org/upload/pdf/pfm-2019-00086.pdf
Parkinsonism & Related Disorders10.1016/j.parkreldis.2015.01.0102015214402-406Neuroimaging studies and whole exome sequencing of PLA2G6-associated neurodegeneration in a family with intrafamilial phenotypic heterogeneityYun Joong Kim, Chul Hyoung Lyoo, Sangkyoon Hong, Nan Young Kim, Myung Sik Leehttps://api.elsevier.com/content/article/PII:S1353802015000309?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1353802015000309?httpAccept=text/plain
Frontiers in Neurology10.3389/fneur.2018.0110020189PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and GenotypesYu-pei Guo, Bei-sha Tang, Ji-feng Guohttps://www.frontiersin.org/article/10.3389/fneur.2018.01100/full
Parkinsonism & Related Disorders10.1016/j.parkreldis.2019.04.002201965159-164Identification of a novel mutation in PLA2G6 gene and phenotypic heterogeneity analysis of PLA2G6-related neurodegenerationYan Ji, Yusheng Li, Changhe Shi, Yuan Gao, Jing Yang, Dongyi Liang, Zhihua Yang, Yuming Xuhttps://api.elsevier.com/content/article/PII:S1353802019301968?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1353802019301968?httpAccept=text/plain
Frontiers in Neurology10.3389/fneur.2022.922528202213Novel PLA2G6 Pathogenic Variants in Chinese Patients With PLA2G6-Associated NeurodegenerationYalan Wan, Yanyan Jiang, Zhiying Xie, Chen Ling, Kang Du, Ran Li, Yun Yuan, Zhaoxia Wang, Wei Sun, Haiqiang Jinhttps://www.frontiersin.org/articles/10.3389/fneur.2022.922528/full
Parkinsonism & Related Disorders10.1016/j.parkreldis.2018.02.01020184988-94Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegenerationYi-Jun Chen, Yu-Chao Chen, Hai-Lin Dong, Li-Xi Li, Wang Ni, Hong-Fu Li, Zhi-Ying Wuhttps://api.elsevier.com/content/article/PII:S1353802018300464?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1353802018300464?httpAccept=text/plain
Journal of Clinical Neurology10.3988/jcn.2021.17.2.3192021172319A Case of PLA2G6-Associated Neurodegeneration with Frequent Myoclonus And Generalized Onset Tonic-Clonic Seizures: Successful Treatment with ZonisamideHongchul Ahn, Hye-Jin Moon, Beomseok Jeonhttps://thejcn.com/pdf/10.3988/jcn.2021.17.2.319, https://thejcn.com/DOIx.php?id=10.3988/jcn.2021.17.2.319, https://thejcn.com/DOIx.php?id=10.3988/jcn.2021.17.2.319
Clinical Psychology Review10.1016/0272-7358(95)00025-k1995155443-456Family variables associated with the onset and impact of intrafamilial childhood sexual abuseJan Faust, Melissa K. Runyon, Maureen C. Kennyhttps://api.elsevier.com/content/article/PII:027273589500025K?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:027273589500025K?httpAccept=text/plain
Parkinsonism & Related Disorders10.1016/j.parkreldis.2020.06.127202079e29Genotype-phenotype correlations of adult-onset PLA2G6-associated neurodegenerationC.-H. Lin, Y.-T. Chu, H.-Y. Lin, P.-L. Chenhttps://api.elsevier.com/content/article/PII:S1353802020303047?httpAccept=text/xml, https://api.elsevier.com/content/article/PII:S1353802020303047?httpAccept=text/plain
Movement Disorders Clinical Practice10.1002/mdc3.12805201966479-482A Novel SGCE Nonsense Variant Associated With Marked Intrafamilial Variability in a Turkish Family With Myoclonus‐DystoniaMurat Gultekin, Neha Prakash, Christos Ganos, Meral Mirza, Ruslan Bayramov, Kailash P. Bhatia, Niccolò E. Mencaccihttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmdc3.12805, https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.12805, https://onlinelibrary.wiley.com/doi/full-xml/10.1002/mdc3.12805, https://onlinelibrary.wiley.com/doi/pdf/10.1002/mdc3.12805