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1دورية أكاديمية
المؤلفون: Zhuhui Ge, Jianhua Mao, Huijun Shen, Yu Xu, Haidong Fu, Weiwei Zhang, Dongyan Li
المصدر: BMC Pediatrics, Vol 21, Iss 1, Pp 1-7 (2021)
مصطلحات موضوعية: Mucopolysaccharidosis IVA, Neurogenic bladder, Pathogenesis, Comorbidity, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/1471-2431Test
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2دورية أكاديمية
المؤلفون: Xue He, Huijun Shen, Haidong Fu, Chunyue Feng, Zhixia Liu, Yanyan Jin, Jianhua Mao
المصدر: BMC Pediatrics, Vol 20, Iss 1, Pp 1-6 (2020)
مصطلحات موضوعية: 13q deletion syndrome, 13q33–34 deletion, Chromosome 13, Renal hypoplasia, Congenital heart disease, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s12887-020-02205-7Test; https://doaj.org/toc/1471-2431Test
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3دورية أكاديمية
المؤلفون: Lingxia Zhang, Ke Huang, Shugang Wang, Haidong Fu, Jingjing Wang, Huijun Shen, Zhihong Lu, Junyi Chen, Yu Bao, Chunyue Feng, Guanping Dong, Jianhua Mao
المصدر: Frontiers in Pediatrics, Vol 9 (2021)
مصطلحات موضوعية: Gitelman's syndrome, congenital tubulopathy, genotype, mutation-genetics, phenotype [mesh], Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2021.544925/fullTest; https://doaj.org/toc/2296-2360Test
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4دورية أكاديمية
المؤلفون: Xue He, Yueling Zhu, Haidong Fu, Chunyue Feng, Zhixia Liu, Weizhong Gu, Yanyan Jin, Binbin Yang, Huijun Shen
المصدر: Frontiers in Pediatrics, Vol 9 (2021)
مصطلحات موضوعية: Abernethy malformation, congenital extrahepatic portosystemic shunt, membranoproliferative glomerulonephritis, arachnoid cyst, focal nodular hyperplasia, Pediatrics, RJ1-570
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/articles/10.3389/fped.2021.647364/fullTest; https://doaj.org/toc/2296-2360Test
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5دورية أكاديمية
المؤلفون: Ting Li, Zhihong Lu, Jingjing Wang, Junyi Chen, Haidong Fu, Jianhua Mao
المصدر: Children, Vol 8, Iss 10, p 887 (2021)
مصطلحات موضوعية: mitochondrial DNA, 4977-bp deletion, Fanconi syndrome, growth retardation, children, Pediatrics, RJ1-570
وصف الملف: electronic resource
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6
المؤلفون: Zhihong Lu, Haidong Fu, Jianhua Mao, Jingjing Wang, Ting Li, Junyi Chen
المصدر: Children
Children, Vol 8, Iss 887, p 887 (2021)مصطلحات موضوعية: Glycosuria, medicine.medical_specialty, Mitochondrial DNA, Proteinuria, business.industry, Mitochondrial disease, Fanconi syndrome, growth retardation, Metabolic acidosis, Case Report, mitochondrial DNA, medicine.disease, Pediatrics, RJ1-570, Levocarnitine, 4977-bp deletion, Endocrinology, children, Internal medicine, Pediatrics, Perinatology and Child Health, medicine, medicine.symptom, business, Hypophosphatemia
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b78e8026359595f9811571d957829318Test
http://europepmc.org/articles/PMC8535084Test