Xue-Rong Chen
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Explore the profile of Xue-Rong Chen including associated specialties, affiliations and a list of published articles.
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Articles
25
Citations
161
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Recent Articles
1.
Wang Z, Liang F, Chen X, Wu P, Wu W
Se Pu
. 2024 Feb;
42(2):194-202.
PMID: 38374600
Perfluoroalkyl and polyfluoroalkyl substances (PFASs) have been extensively used as synthetic fluorine-containing compounds in various consumer products, including surfactants, cookware, lubricants, clothing, and food packaging, since the 1950s. Evidence has...
2.
Bai H, Meng Z, Ying B, Chen X
World J Clin Cases
. 2021 Jun;
9(17):4400-4407.
PMID: 34141807
Background: Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by the accumulation of phospholipoproteinaceous material in the alveoli. Cases of PAP complicated with tuberculosis are much more complex...
3.
Liu C, Liang X, Niu Z, Jin Q, Zeng X, Wang W, et al.
EBioMedicine
. 2019 Nov;
49:354-363.
PMID: 31685443
Background: Mothers are the primary source of bacteria for newborns, but it is unclear whether mother-to-newborn transmission occurs prior to, during or after birth. Similarly, the effect of the delivery...
4.
Chang X, Gu Y, Dai S, Chen X, Zhang C, Zhao H, et al.
Mutagenesis
. 2018 Jan;
32(6):599-606.
PMID: 29346610
Autosomal recessive woolly hair/hypotrichosis (ARWH/HT: OMIM #278150/604379) is a rare hereditary hair disease characterized by tightly curled hair at birth which can lead to sparse hair later in life. The...
5.
Gan Y, Jin J, Qiu Z, Chen X
Chin Med J (Engl)
. 2017 Nov;
130(22):2757-2758.
PMID: 29133769
No abstract available.
6.
Liu L, Chen X, Huang D, Zou H, Li Y, Yu X, et al.
Clin Exp Obstet Gynecol
. 2015 Apr;
41(5):578-80.
PMID: 25864264
A middle-aged woman with rheumatic heart disease, mitral valve prolapse and incompletely closed mitral valve medium, patent foramen ovale, merge multiple uterine fibroids, and moderate blood loss anemia underwent mitral...
7.
Ye Z, Nan X, Zhao H, Chen X, Song Q
Chin Med J (Engl)
. 2013 Aug;
126(16):3103-6.
PMID: 23981620
Background: Monilethrix is an autosomal dominant hair disorder characterized clinically by alopecia and follicular papules. In this study, we collected a Han monilethrix family to detect the mutations in patients...
8.
Nan X, Dai S, Li C, Chen X, Zhao H, Zhang F, et al.
Gene
. 2013 Mar;
523(1):88-91.
PMID: 23510776
Tricho-rhino-phalangeal syndrome (TRPS) is a rare autosomal dominant disorder. Deletion or mutation of the TRPS1 gene leads to the tricho-rhino-phalangeal syndromes type I or type III. In this article, we...
9.
Xiao J, Wang K, Feng Y, Chen X, Xu D, Zhang M
Chin Med J (Engl)
. 2011 Nov;
124(20):3327-33.
PMID: 22088530
Background: Airway mucus hypersecretion is an important pathophysiological feature of chronic obstructive pulmonary disease, which is closely associated with cigarette smoking. However, the signal transduction pathway from the cell surface...
10.
Wang W, Li L, Huang E, Zhang Q, Sun T, Song Q, et al.
Eur J Dermatol
. 2011 Nov;
22(1):29-33.
PMID: 22062952
Primary localized cutaneous amyloidosis (PLCA) is a chronic itching skin disease with amyloid material deposited in the upper dermis. PLCA is more common in Southeast Asia and South America, where...