| [1] |
Dubin IN, Johnson FB. Chronic idiopathic jaundice with unidentified pigment in liver cells; a new clinicopathologic entity with a report of 12 cases[J]. Medicine (Baltimore), 1954，33(3)：155-197.
|
| [2] |
孟璐璐，邱建武，林伟霞，等. 1例Dubin-Johnson综合征婴儿的临床特征及ABCC2基因型研究[J]. 中国当代儿科杂志，2019，21(1)：64-67.
|
| [3] |
Togawa T, Sugiura T, Ito K, et al. Molecular genetic dissection and neonatal/infantile intrahepatic cholestasis using targeted next-generation sequencing[J]. J Pediatr, 2016，171: 171-177.
|
| [4] |
Buget MI, Ozkan E, Edipoglu IS, et al, Anesthetic approach for a patient with Jeune syndrome[J]. Case Rep Anesthesiol, 2015：509196.
|
| [5] |
Togawa T, Mizuochi T, Sugiura T, et al. Clinical, pathologic, and genetic features of neonatal Dubin-Johnson syndrome: a multicenter study in Japan[J]. J Pediatrics, 2018，196：161-167.
|
| [6] |
Erlinger S, Arias IM, Dhumeaux D. Inherited disorders of bilirubin transport and conjugation: new insights into molecular mechanisms and consequences[J]. Gastroenterology, 2014，146(7)：1625-1638.
|
| [7] |
Stapelbroek JM, van Erpecum KJ, Klomp LW, et al. Liver disease associated with canalicular transport defects: current and future therapies[J]. J Hepatol, 2010，52(2)：258-271.
|
| [8] |
孟祥慈，黄晓峰，韩英，等. Dubin-Johnson综合征肝细胞色素和脂褐素的超微结构特征[J]. 中国医药导报，2013，10(9)：100-101.
|
| [9] |
Jeune M, Beraud C, Carron R. Asphyxiating thoracic dystrophy with familial characteristics[J]. Arch Fr Pediatr, 1955，12(8)：886-891.
|
| [10] |
Mei L, Huang Y, Pan Q, et al. Targeted next-generation sequencing identifies novel compound heterozygous mutations of DYNC2H1 in a fetus with short rib-polydactyly syndrome, typeⅢ[J]. Clin Chim Acta, 2015，447：47-51.
|
| [11] |
Chen CP, Ko TM, Chang TY, et al. Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus[J]. Taiwan J Obstet Gynecol, 2018，57(1)：123-127.
|
| [12] |
Chen CP, Chern SR, Chang TY, et al. Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type Ⅲ(Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene[J]. Taiwan J Obstet Gynecol, 2012，51(2)：266-270.
|
| [13] |
Mistry KA, Suthar PP, Bhesania SR, et al. Antenatal diagnosis of Jeune syndrome (asphyxiating thoracic dysplasia) with micromelia and facial dysmorphism on second-trimester ultrasound[J]. Pol J Radiol, 2015，80：296-299.
|
| [14] |
沙恩波，姜久盛，刘彧，等. DYNC2H1基因复合杂合突变致短肋-胸廓发育不良综合征3型一例[J]. 中华围产医学杂志，2018，21(7)：499-501.
|
| [15] |
Yerian LM, Brady L, Hart J. Hepatic manifestations of Jeune syndrome (asphyxiating thoracic dystrophy)[J]. Semin Liver Dis, 2003，23(2)：195-200.
|
| [16] |
Kajantie E, Andersson S, Kaitila I. Familial asphyxiating thoracic dysplasia: clinical variability and impact of improved neonatal intensive care[J]. J Pediatr, 2001，139(1): 130-133.
|
| [17] |
甘雨，张鸿飞，朱世殊，等. Dubin-Johnson综合征临床特点分析[J]. 中国全科医学，2011，14(18)：2089-2090.
|
| [18] |
Xing T, Zhong L, Peng Z. Safety and effectiveness of antifungal prophylaxis in preventing fungal infection after liver transplantation: a meta-analysis of randomized clinical trials[J]. Int J Clin Pharmacol Ther, 2016，54(8)：564-571.
|
| [19] |
吕少诚，王苑，潘冰，等. 肝移植术后肺部感染的诊治及其危险因素[J]. 中华肝胆外科杂志，2018，24(6)：371-375.
|
| [20] |
Kim SI. Bacterial infection after liver transplantation[J]. World J Gastroenterol, 2014，20(20): 6211-6220.
|
| [21] |
韩环立，黄英，张明满，等. 儿童活体肝移植术后早期肺部感染临床分析[J]. 中华儿科杂志，2012，50(8): 612-616.
|