Wang NL, Chen L, Lin J, Lu Y, Fang WY, Xie XB, Wang JS. Non-invasive biomarkers for identification of vanishing bile duct syndrome among children with acute cholestatic hepatitis. Transl Pediatr. 2023;12(10): 1782-1790.
王能里, 王建设. 腺病毒感染是不明原因儿童严重急性肝炎的病因? 肝脏. 2022; 27(10): 1062-1064.
王能里, 王建设. 儿童不明原因严重急性肝炎的病因与临床特征及评估和治疗策略. 西南医科大学学报. 2022; 45(6): 474-477.
Wang NL, Lin J, Chen L, Lu Y, Xie XB, Abuduxikuer K, Wang JS. Neonatal cholestasis is an early liver manifestation of children with acid sphingomyelinase deficiency. BMC Gastroenterol. 2022; 22(1):227.
王能里, 谢新宝. 儿童急性肝衰竭的肝移植治疗. 临床肝胆病杂. 2022; 38(2): 278-281.
Wang NL, Chen L, Lu Y, Xie XB, Lin J, Abuduxikuer K, Wang JS. The Presence of vacuolated Kupffer cells raises a clinical suspicion of Niemann- Pick Disease Type C in Neonatal Cholestasis. Front Genet. 2022; 13:867413.
Wang NL, Lu Y, Gong JY, Xie XB, Lin J, Abuduxikuer K, Zhang MH, Wang JS. Molecular findings in children with inherited intrahepatic cholestasis. Pediatr Res. 2020; 87(1):112-117.
Wang NL, Qiu YL, Guan WC, Li G, Lu Y, Zhang MH, Luan WS, Wang JS. Splicing analysis of rare/novel synonymous or intronic variants identified in ABCB11 heterozygotes presenting as progressive intrahepatic cholestasis with low γ-glutamyltransferase. Hepatol Res. 2018; 48(7):574-584.
Wang NL, Lu YL, Zhang P, Zhang MH, Gong JY, Lu Y, Xie XB, Qiu YL, Yan YY, Wu BB, Wang JS. A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions. PLoS One. 2016;11(10):e0164058.
Wang NL, Li LT, Wu BB, Gong JY, Abuduxikuer K, Li G, Wang JS. The Features of GGT in Patients with ATP8B1 or ABCB11 Deficiency Improve the Diagnostic Efficiency. PLoS One. 2016;11(4):e0153114.