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2021 | 1 |
2024 | 3 |
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Characteristics and phenotype heterogeneity in late-onset Behçet's syndrome: a cohort from a referral center in China.
Clin Rheumatol. 2021 Jun;40(6):2319-2326. doi: 10.1007/s10067-020-05536-z. Epub 2021 Jan 7.
Clin Rheumatol. 2021.
PMID: 33411142
Clinical phenotypes of adult-onset Behçet's syndrome: a comprehensive cross-sectional study in China.
She CH, Hu D, Zou J, Bao HF, Shen Y, Cai JF, Ye JF, Luo D, Jian LL, Ma HF, Hou CC, Chen Y, Guan JL.
She CH, et al.
Clin Rheumatol. 2024 May 10. doi: 10.1007/s10067-024-06995-4. Online ahead of print.
Clin Rheumatol. 2024.
PMID: 38724819
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PLK1-activating IFI16-STING-TBK1 pathway induces apoptosis of intestinal epithelial cells in patients with intestinal Behçet's syndrome.
Bao HF, She CH, Hou CC, Ji DN, Hu D, Zou J, Shen Y, Jian LL, Cai JF, Ye JF, Luo D, Ma HF, Guan JL.
Bao HF, et al.
FEBS J. 2024 Apr 27. doi: 10.1111/febs.17147. Online ahead of print.
FEBS J. 2024.
PMID: 38676954
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Clinical heterogeneity and five phenotypes identified in pediatric Behçet's syndrome: a cohort study from Shanghai Behçet's syndrome database.
Hu D, She CH, Bao HF, Zou J, Cai JF, Ye JF, Shen Y, Ma HF, Luo D, Guan JL.
Hu D, et al.
World J Pediatr. 2024 Feb 5. doi: 10.1007/s12519-023-00785-9. Online ahead of print.
World J Pediatr. 2024.
PMID: 38315355
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