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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 3 |
2021 | 3 |
2024 | 0 |
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5 results
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Page 1
Dent disease: classification, heterogeneity and diagnosis.
World J Pediatr. 2021 Feb;17(1):52-57. doi: 10.1007/s12519-020-00357-1. Epub 2020 Apr 4.
World J Pediatr. 2021.
PMID: 32248351
Review.
[Clinical features and enzyme replacement therapy in 4 children with Fabry disease].
Lu ZH, Wang JJ, Yu L, Mao JH.
Lu ZH, et al.
Zhonghua Er Ke Za Zhi. 2021 Apr 2;59(4):322-326. doi: 10.3760/cma.j.cn112140-20200902-00842.
Zhonghua Er Ke Za Zhi. 2021.
PMID: 33775053
Chinese.
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Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1-34 deletion: case report and literature review.
He X, Shen H, Fu H, Feng C, Liu Z, Jin Y, Mao J.
He X, et al.
BMC Pediatr. 2020 Jul 2;20(1):327. doi: 10.1186/s12887-020-02205-7.
BMC Pediatr. 2020.
PMID: 32616040
Free PMC article.
Review.
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Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report.
Li T, Lu Z, Wang J, Chen J, Fu H, Mao J.
Li T, et al.
Children (Basel). 2021 Oct 4;8(10):887. doi: 10.3390/children8100887.
Children (Basel). 2021.
PMID: 34682152
Free PMC article.
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Case report: a Chinese girl with dent disease 1 and turner syndrome due to a hemizygous CLCN5 gene mutation and Isochromosome (Xq).
Ye Y, Wang J, Quan X, Xu K, Fu H, Gu W, Mao J.
Ye Y, et al.
BMC Nephrol. 2020 May 11;21(1):171. doi: 10.1186/s12882-020-01827-4.
BMC Nephrol. 2020.
PMID: 32393202
Free PMC article.
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