Xiaoxiao Mi
Overview
Explore the profile of Xiaoxiao Mi including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
56
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0
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Recent Articles
1.
Xu N, Gong L, Mi X, Yang W, Tang D
Radiologie (Heidelb)
. 2024 Jun;
64(Suppl 1):102-108.
PMID: 38829428
Purpose: Progressive familial intrahepatic cholestasis type 3 (PFIC-3) is a rare autosomal recessive cholestatic liver disorder. This study aimed to present the clinical and magnetic resonance imaging (MRI) features of...
2.
Sun J, Mi X, Ye X, ShenTu Y, Liu C, Tang D, et al.
BMC Infect Dis
. 2023 Oct;
23(1):715.
PMID: 37872485
Background: CHF (Congenital hepatic fibrosis) is a rare hereditary disease characterized by periportal fibrosis and ductal plate malformation. Little is known about the clinical presentations and outcome in CHF patients...
3.
Mi X, Song Y, Deng C, Yan J, Li Z, Li Y, et al.
Cell Mol Gastroenterol Hepatol
. 2023 Jul;
16(5):657-684.
PMID: 37406734
Background & Aims: Wilson's disease is an inherited hepatoneurologic disorder caused by mutations in the copper transporter ATP7B. Liver disease from Wilson's disease is one leading cause of cirrhosis in...
4.
Ye X, Mi X, Sun J, ShenTu Y, Fei Y, Tang D, et al.
Clin Res Hepatol Gastroenterol
. 2023 May;
47(6):102141.
PMID: 37207893
Background: Protein S (PS) is a vitamin K-dependent plasma glycoprotein, and the deficiency of PS increases the risk of venous thromboembolism (VTE). PS deficiency has been found in 1.5-7% of...
5.
Cheng J, Gong L, Mi X, Wu X, Zheng J, Yang W
Front Med (Lausanne)
. 2022 Dec;
9:962408.
PMID: 36569137
Objective: To improve the accuracy of the diagnosis of familial progressive intrahepatic cholestasis type 3 (PFIC3, https://www.omim.org/entry/602347). Materials And Methods: Between September 2019 and March 2021, we recruited four patients...
6.
Mi X, Wu Y, Yan J, Li Y, Shi J, Liu D
Ann Anat
. 2021 Oct;
239:151840.
PMID: 34716087
No abstract available.
7.
ShenTu Y, Mi X, Tang D, Jiang Y, Gao L, Ma X, et al.
Clin Chim Acta
. 2021 Aug;
521:258-263.
PMID: 34332988
Background: Alagille syndrome (ALGS) is a rare multisystem disorder caused by mutations in the JAG1 or NOTCH2 gene. However NOTCH2 gene mutations were rarely found in the Alagille patients. Little...
8.
Li J, Liu Y, Li Q, Huang X, Zhou D, Xu H, et al.
Neurosci Bull
. 2020 Dec;
37(3):311-322.
PMID: 33355901
Myoclonus dystonia syndrome (MDS) is an inherited movement disorder, and most MDS-related mutations have so far been found in the ε-sarcoglycan (SGCE) coding gene. By generating SGCE-knockout (KO) and human...
9.
Mi X, Li Z, Yan J, Li Y, Zheng J, Zhuang Z, et al.
Biochim Biophys Acta Mol Basis Dis
. 2020 May;
1866(10):165842.
PMID: 32446740
Wilson's disease is an autosomal recessive disease characterized by excess copper accumulated in the liver and brain. It is caused by mutations in the copper transporter gene ATP7B. However, based...
10.
Zhou J, Liu J, Sheng H, You N, Chen J, Mi X, et al.
Adv Ther
. 2019 Mar;
36(4):880-895.
PMID: 30820874
Introduction: Haptoglobin (Hp) genotypes were reported as an independent risk factor for metabolic diseases. This study aimed to investigate the association between Hp gene polymorphism and the severity of nonalcoholic...