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May 16, 2023 (publication date) through Feb 11, 2026
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| Ding L, Huang TT, Ying GH, Wang SY, Xu HF, Qian H, Rahman F, Lu XP, Guo H, Zheng G, Zhang G. De novo mutation of NAXE (APOAIBP)-related early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy-1: A case report. World J Clin Cases 2023; 11(14): 3340-3350 [PMID: 37274027 DOI: 10.12998/wjcc.v11.i14.3340] |
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| ©2004-2026 Baishideng Publishing Group Inc. All rights reserved. 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA | |
| For: | Ding L, Huang TT, Ying GH, Wang SY, Xu HF, Qian H, Rahman F, Lu XP, Guo H, Zheng G, Zhang G. De novo mutation of NAXE (APOAIBP)-related early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy-1: A case report. World J Clin Cases 2023; 11(14): 3340-3350 [PMID: 37274027 DOI: 10.12998/wjcc.v11.i14.3340] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v11/i14/3340.htm |
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| 2 |
Zijian Zhang, Yingjun Wang, Hao Yang, Yanhong Jiang, Guyuan Wang, Renfang Mao. Apolipoprotein A‐I Binding Protein: Functions, Mechanisms, and Therapeutic Targets in Neurological Disorders. Advanced Biology 2025; 9(9) doi: 10.1002/adbi.202500012
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Yanjie Zhu, Peifeng He, Rong Luo, Xiaolu Chen. Progressive encephalopathy associated with novel compound heterozygous NAXE mutations in a Chinese patient: case report and literature review. Frontiers in Pediatrics 2026; 14 doi: 10.3389/fped.2026.1766864
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| 4 |
Boraan Abdulkarim, Setu Mittal, Hassan Vahidnezhad, Dawn Marie Davis, Michael J. Camilleri, Nessa Aghazadeh Mohandesi. Cutaneous Manifestations of NAXD or NAXE Deficiency: A Literature Review for the Dermatologist. Pediatric Dermatology 2025; 42(2): 233 doi: 10.1111/pde.15868
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Kokoro Ozaki, Yukiko Yatsuka, Yoshinobu Oyazato, Atsushi Nishiyama, Kazuhiro R. Nitta, Yoshihito Kishita, Takuya Fushimi, Masaru Shimura, Shohei Noma, Yohei Sugiyama, Michihira Tagami, Moe Fukunaga, Hiroko Kinoshita, Tomoko Hirata, Wataru Suda, Yasuhiro Murakawa, Piero Carninci, Akira Ohtake, Kei Murayama, Yasushi Okazaki. Biallelic GGGCC repeat expansion leading to NAXE-related mitochondrial encephalopathy. npj Genomic Medicine 2024; 9(1) doi: 10.1038/s41525-024-00429-5
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