| For: | Li JQ, Gong JY, Knisely AS, Zhang MH, Wang JS. Recurrent acute liver failure associated with novel SCYL1 mutation: A case report. World J Clin Cases 2019; 7(4): 494-499 [PMID: 30842961 DOI: 10.12998/wjcc.v7.i4.494] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i4/494.htm |
| Number | Citing Articles |
| 1 |
Engin Demir, Ümmühan Öncül, Merve Havan, Ceyda Tuna Kirsaçlioğlu, Fatma Tuba Eminoğlu, Tanil Kendirli, Zarife Kuloğlu, Aydan Kansu. Coexistence of spinocerebellar ataxia autosomal recessive type 21 and Ehlers-Danlos syndrome spondylodysplastic type 3 in a patient. Clinical Dysmorphology 2023; 32(1) doi: 10.1097/MCD.0000000000000435
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| 2 |
D. Tetik, P. Bingöl Kızıltunç, H. Atilla. Early optic nerve changes in CALFAN syndrome – OCT and OCTA findings. Journal Français d'Ophtalmologie 2026; 49(4) doi: 10.1016/j.jfo.2026.104804
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| 3 |
Genki Amano, Shinsuke Matsuzaki, Yasutake Mori, Ko Miyoshi, Sarina Han, Sho Shikada, Hironori Takamura, Takeshi Yoshimura, Taiichi Katayama, Kozo Kaibuchi. SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. Molecular Biology of the Cell 2020; 31(18) doi: 10.1091/mbc.E20-02-0100
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| 4 |
Infantile Liver Failure as the Initial Manifestation of SCYL1-Related CALFAN Syndrome: A Case Report and Literature Review. Archives of Pediatric Gastroenterology, Hepatology, and Nutrition 2026; 5(2) doi: 10.58427/apghn.5.2.2026.86-97
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| 5 |
Bianca Peters, Tal Dattner, Lea D. Schlieben, Tian Sun, Christian Staufner, Dominic Lenz. Disorders of vesicular trafficking presenting with recurrent acute liver failure: NBAS, RINT1, and SCYL1 deficiency. Journal of Inherited Metabolic Disease 2025; 48(1) doi: 10.1002/jimd.12707
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| 6 |
Sanghoon Lee, Jung Nyeo Chun, Hae-Jeung Lee, Hyun Ho Park, Insuk So, Ju-Hong Jeon, Eun-Jung Park. Transcriptome Analysis of the Anti-TGFβ Effect of Schisandra chinensis Fruit Extract and Schisandrin B in A7r5 Vascular Smooth Muscle Cells. Life 2021; 11(2) doi: 10.3390/life11020163
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| 7 |
Stanley Kwong, Cherise Meyerson, Wei Zheng, Ari Kassardjian, Nicholas Stanzione, Kuixing Zhang, Hanlin L. Wang. Acute hepatitis and acute liver failure: Pathologic diagnosis and differential diagnosis. Seminars in Diagnostic Pathology 2019; 36(6) doi: 10.1053/j.semdp.2019.07.005
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| 8 |
Vanda McNiven, Daniela Gattini, Iram Siddiqui, Stephane Pelletier, Herbert Brill, Yaron Avitzur, Saadet Mercimek‐Andrews. SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1. American Journal of Medical Genetics Part A 2021; 185(4) doi: 10.1002/ajmg.a.62079
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| 9 |
John Hellicar, Tal Dattner, Tian Sun, Lily Percival, Ruby Chrisp, Andrea Pietrobattista, Tomasz Witkos, Aleksander Mironov, Lina Leghlam, Carolin Jentsch, Stefan Koelker, Georg F. Hoffmann, Christian Staufner, Wanjin Hong, Dominic Lenz, Martin Lowe. SCYL1 deficiency in CALFAN syndrome is associated with ER stress and cell death. Disease Models & Mechanisms 2025; 18(11) doi: 10.1242/dmm.052371
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| 10 |
Alisha Babbar, Raghav Lal, Suvradeep Mitra, Chennakeshava Thunga, Sadhna Lal. Recurrent Liver Failure due to SCYL1 Deficiency: A Report of 2 Cases and a Review of the Literature. Journal of Clinical and Experimental Hepatology 2026; 16(4) doi: 10.1016/j.jceh.2026.103558
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| 11 |
Yanfei Cui, Fawudan Abudu, Yipaguli Simijiang. Recurrent fever-associated acute liver failure and cranial dysmorphism in children caused by RINT1 gene mutations: a rare case report. Frontiers in Pediatrics 2025; 13 doi: 10.3389/fped.2025.1698931
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| 12 |
Long-Gang Niu, Ping Liu, Zhao-Wen Wang, Bojun Chen. Slo2 potassium channel function depends on RNA editing-regulated expression of a SCYL1 protein. eLife 2020; 9 doi: 10.7554/eLife.53986
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| 13 |
J. Chavany, A. Cano, B. Roquelaure, P. Bourgeois, J. Boubnova, P. Gaignard, C. Hoebeke, R. Reynaud, B. Rhomer, A. Slama, C. Badens, B. Chabrol, A. Fabre. Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review. Archives de Pédiatrie 2020; 27(3) doi: 10.1016/j.arcped.2020.01.003
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| 14 |
Laila Kazem, Wafaa Al-Qabandi, Buthaina Albash, Reem Elshafie, Miao He, Hind Alsharhan. SCYL1 deficiency and intrafamilial variability: Two cases from Kuwait. Molecular Genetics and Metabolism Reports 2025; 45 doi: 10.1016/j.ymgmr.2025.101269
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| 15 |
Mariam Youssef, Katherine L. Mascia, Brendan McGuire, Chirag R. Patel, Sameer Al Diffalha, Deepti Dhall, Goo Lee, Mauro Vigano. CALFAN (Low γ-Glutamyl Transpeptidase (GGT) Cholestasis, Acute Liver Failure, and Neurodegeneration) Syndrome: A Case Report with 3-Year Follow-Up after Liver Transplantation in Early Adulthood. Case Reports in Hepatology 2023; 2023 doi: 10.1155/2023/3010131
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| 16 |
Stéphanie Kaeser-Pebernard, Christine Vionnet, Muriel Mari, Devanarayanan Siva Sankar, Zehan Hu, Carole Roubaty, Esther Martínez-Martínez, Huiyuan Zhao, Miguel Spuch-Calvar, Alke Petri-Fink, Gregor Rainer, Florian Steinberg, Fulvio Reggiori, Jörn Dengjel. mTORC1 controls Golgi architecture and vesicle secretion by phosphorylation of SCYL1. Nature Communications 2022; 13(1) doi: 10.1038/s41467-022-32487-7
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| 17 |
Hasan M Isa, Jawaher F Alkaabi, Wasan H Alhammadi, Khadija A Marjan. Recurrent Acute Liver Failure in a Bahraini Child With a Novel Mutation of Spinocerebellar Ataxia-21. Cureus 2023; doi: 10.7759/cureus.36249
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| 18 |
Barath Jagadisan, Anil Dhawan. Emergencies in paediatric hepatology. Journal of Hepatology 2022; 76(5) doi: 10.1016/j.jhep.2021.12.027
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| 19 |
Bingxin Jiang, Fangfei Xiao, Xiaolu Li, Yongmei Xiao, Yizhong Wang, Ting Zhang. Case Report: Pediatric Recurrent Acute Liver Failure Caused by Neuroblastoma Amplified Sequence (NBAS) Gene Mutations. Frontiers in Pediatrics 2021; 8 doi: 10.3389/fped.2020.607005
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| 20 |
Narges Zare, Hosein Saneian, Majid Khademian. A Rare Case of Spinocerebellar Ataxia Autosomal Recessive 21 Presented with Liver Disease. Advanced Biomedical Research 2023; 12(1) doi: 10.4103/abr.abr_139_22
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