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Did you mean jingsheng ma (14 results)?
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.
Yang-Li D, Fei-Hong L, Hui-Wen Z, Ming-Sheng M, Xiao-Ping L, Li L, Yi W, Qing Z, Yong-Hui J, Chao-Chun Z; PWS Cooperation Group of Rare Diseases Branch of Chinese Pediatric Society; Zhejiang Expert Group for PWS. Yang-Li D, et al. Orphanet J Rare Dis. 2022 Jun 13;17(1):221. doi: 10.1186/s13023-022-02302-z. Orphanet J Rare Dis. 2022. PMID: 35698200 Free PMC article. Review.
Arsenic speciation analysis.
Gong Z, Lu X, Ma M, Watt C, Le XC. Gong Z, et al. Among authors: ma m. Talanta. 2002 Aug 16;58(1):77-96. doi: 10.1016/s0039-9140(02)00258-8. Talanta. 2002. PMID: 18968736
Early recombinant human growth hormone treatment improves mental development and alleviates deterioration of motor function in infants and young children with Prader-Willi syndrome.
Cheng RQ, Ying YQ, Qiu ZQ, Fu JF, Gong CX, Yang YL, Shi W, Li H, Ma MS, Wang CY, Liu M, Chen JJ, Su C, Luo XP, Luo FH, Lu W. Cheng RQ, et al. World J Pediatr. 2023 May;19(5):438-449. doi: 10.1007/s12519-022-00653-y. Epub 2022 Dec 24. World J Pediatr. 2023. PMID: 36564648 Free PMC article. Clinical Trial.
Farber disease in a patient from China.
Bao X, Ma M, Zhang Z, Xu Y, Qiu Z. Bao X, et al. Among authors: ma m. Am J Med Genet A. 2020 Sep;182(9):2184-2186. doi: 10.1002/ajmg.a.61752. Epub 2020 Jul 24. Am J Med Genet A. 2020. PMID: 32706452
48 results