Sheng D. Wang
Chengdu, 610041, China
Last Updated: 09/26/2026
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Found 59 publications
Impact of PSMA PET on the management and clinical outcomes of patients with biochemical failure of prostate cancer after definitive treatment: a systematic review and meta-analysis.
Journal: International urology and nephrology
Published: January 15, 2026
Proteolytic dysregulation in the skin: insight from rare monogenic skin diseases.
Journal: Cell and tissue research
Published: November 12, 2025
Gut microbial metabolites in cancer immunomodulation.
Journal: Molecular cancer
Published: September 08, 2025
Abbreviated biparametric versus multiparametric MRI for the detection of clinically significant prostate cancer in treatment-naïve patients: a diagnostic test accuracy systematic review and meta-analysis.
Journal: International journal of surgery (London, England)
Published: April 15, 2025
Gain-of-function variant in NNT causes premature diffuse familial sebaceous hyperplasia.
Journal: The British journal of dermatology
Published: April 11, 2025
Late-Onset Nagashima-Type Palmoplantar Keratosis in a Chinese Family With a Novel Potential Causative Heterozygous M208I Variant of the SERPINB7 Gene.
Journal: The Journal of dermatology
Published: February 19, 2025
Clinical and genetic characteristics of generalized pustular psoriasis: A retrospective study based on a registry database.
Journal: Chinese medical journal
Published: December 06, 2024
Successful treatment of generalized inflammatory linear verrucous epidermal naevus with a somatic mutation in KRT10 with crisaborole 2% ointment.
Journal: Clinical and experimental dermatology
Published: November 27, 2024
Phenotypic and genotypic analysis of SERPINA12-related autosomal recessive palmoplantar keratoderma in southwestern China.
Journal: The Journal of dermatology
Published: November 03, 2024
Current status of generalized pustular psoriasis: Findings from a multicenter hospital-based survey of 127 Chinese patients.
Journal: Chinese medical journal
Published: October 16, 2024
Biallelic pathogenic variants in the LSS gene cause congenital alopecia-cataract syndrome.
Journal: The Journal of dermatology
Published: September 02, 2024
Last Updated: 09/26/2026