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Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Rao J, Liu X, Mao J, Tang X, Shen Q, Li G, Sun L, Bi Y, Wang X, Qian Y, Wu B, Wang H, Zhou W, Ma D, Zheng B, Shen Y, Chen Z, Luan J, Wang X, Wang M, Dang X, Wang Y, Wu Y, Hou L, Sun S, Li Q, Liu X, Bai H, Yang Y, Shao X, Li Y, Zheng S, Han M, Liu C, Cao G, Zhao L, Qiu S, Dong Y, Zhu Y, Wang F, Zhang D, Li Y, Zhao L, Yang C, Luo X, Chen L, Jiang X, Zhang A, Xu H; for “Internet Plus” Nephrology Alliance of National Center for Children's Care. Rao J, et al. Among authors: luan j. Clin Genet. 2019 Nov;96(5):402-410. doi: 10.1111/cge.13606. Epub 2019 Jul 25. Clin Genet. 2019. PMID: 31328266
IPDN-China promotes the development of pediatric dialysis in China.
Zhai Y, Liu X, Yang Q, Dang X, Sun S, Shao X, Liu X, Wu Y, Bai H, Mao J, Dong Y, Ma Q, Kang G, Huang W, Zhu H, Fu R, Zhang A, Xu R, Sun Q, Jiang X, Lai L, Huang J, Luan J, Xia Z, Cui J, Zhao M, Wu X, Zhang Q, Li Y, Liu C, Wang M, Wang F, Tao Y, Huang Z, Zhang D, Zhao B, Chen C, Huang C, Gao X, Shen Q, Shen Y, Xu H; IPDN-China investigators. Zhai Y, et al. Among authors: luan j. Pediatr Nephrol. 2020 Nov;35(11):2163-2171. doi: 10.1007/s00467-020-04630-3. Epub 2020 Jun 11. Pediatr Nephrol. 2020. PMID: 32529322
Integrating Population Variants and Protein Structural Analysis to Improve Clinical Genetic Diagnosis and Treatment in Nephrogenic Diabetes Insipidus.
Liao P, Xiang T, Li H, Fang Y, Fang X, Zhang Z, Cao Q, Zhai Y, Chen J, Xu L, Liu J, Tang X, Liu X, Wang X, Luan J, Shen Q, Chen L, Jiang X, Ma D, Xu H, Rao J. Liao P, et al. Among authors: luan j. Front Pediatr. 2021 Apr 29;9:566524. doi: 10.3389/fped.2021.566524. eCollection 2021. Front Pediatr. 2021. PMID: 33996673 Free PMC article.
Evaluation of a new frequency-volume chart for children with primary monosymptomatic nocturnal enuresis: a prospective, comparative study.
Wang JJ, Wang DJ, Fu HD, Wang DX, Yang Q, Peng XJ, Fu R, Yang HD, Zhang RF, Wang XW, Luan JW, Zhao F, Chen QX, Liang FF, Cao L, Zhang JJ, Li YJ, Dong Y, Huang HM, Bao Y, Shen XY, Zhou W, Cao GH, Liu CH, Jin YY, Ma ML, Jiang L, Shen Q, Xu H, Mao JH. Wang JJ, et al. World J Pediatr. 2021 Dec;17(6):643-652. doi: 10.1007/s12519-021-00474-5. Epub 2021 Oct 30. World J Pediatr. 2021. PMID: 34716893 Clinical Trial.
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy.
Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Ziętkiewicz S, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schijvens AM, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Deng F, Rousset-Rouviere C, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; mitoNET Consortium; CCGKDD Consortium; Schaefer F. Drovandi S, et al. Kidney Int. 2022 Sep;102(3):592-603. doi: 10.1016/j.kint.2022.02.040. Epub 2022 Apr 26. Kidney Int. 2022. PMID: 35483523 Free article.
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency.
Drovandi S, Lipska-Ziętkiewicz BS, Ozaltin F, Emma F, Gulhan B, Boyer O, Trautmann A, Xu H, Shen Q, Rao J, Riedhammer KM, Heemann U, Hoefele J, Stenton SL, Tsygin AN, Ng KH, Fomina S, Benetti E, Aurelle M, Prikhodina L, Schreuder MF, Tabatabaeifar M, Jankowski M, Baiko S, Mao J, Feng C, Liu C, Sun S, Deng F, Wang X, Clavé S, Stańczyk M, Bałasz-Chmielewska I, Fila M, Durkan AM, Levart TK, Dursun I, Esfandiar N, Haas D, Bjerre A, Anarat A, Benz MR, Talebi S, Hooman N, Ariceta G; PodoNet Consortium; mitoNET Consortium; CCGKDD Consortium; Schaefer F. Drovandi S, et al. Kidney Int. 2022 Sep;102(3):604-612. doi: 10.1016/j.kint.2022.04.029. Epub 2022 May 25. Kidney Int. 2022. PMID: 35643375 Free article.
1,402 results