[1] |
He Xiumei, Cao Wenqi, WU Honglin, Zhou Qifeng, HE Xiyu.
Case report and literarure review of aldosterone synthase deficiency caused by CYP11B2 gene mutation
[J]. Chinese Journal of Child Health Care, 2024, 32(10): 1155-1160.
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[2] |
WANG Qiao, GONG Chunxiu.
Dietary therapy and challenges for familial chylomicronemia syndrome
[J]. Chinese Journal of Child Health Care, 2024, 32(9): 934-936.
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[3] |
CHENG Shuang, WANG Ju.
Research progress on the prevention and treatment of cow's milk protein allergy with probiotics, prebiotics, synbiotics and postbiotics
[J]. Chinese Journal of Child Health Care, 2024, 32(9): 989-993.
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[4] |
XIE Tingting, PEI Ziyi, ZHANG Yue.
Application of music therapy in children's rehabilitation
[J]. Chinese Journal of Child Health Care, 2024, 32(9): 1004-1007.
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[5] |
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[J]. Chinese Journal of Child Health Care, 2024, 32(9): 1040-1044.
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[6] |
LUO Guangyue, LU Wei, XU Deyong, QIU Zhengfei, LI Zonglong.
Effects of different feeding methods on intestinal microbiota in infants with cow's milk protein allergy
[J]. Chinese Journal of Child Health Care, 2024, 32(8): 908-913.
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[7] |
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[J]. Chinese Journal of Child Health Care, 2024, 32(8): 924-928.
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[8] |
CHEN Liyu, HU Yan, ZHANG Xuan.
Effect and mechanism of food diversity in the prevention of food allergy in infancy
[J]. Chinese Journal of Child Health Care, 2024, 32(7): 767-771.
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[9] |
XU Dan, CHEN Yao-yao, GAN Ling, CAO Tian-si, CHU Man-man, WANG Jun-ling, JIA Tian-ming, ZHANG Xiao-li.
Au-Kline syndrome caused byHNRNPK gene novel mutations:a case report and literature review
[J]. Chinese Journal of Child Health Care, 2024, 32(7): 809-812.
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[10] |
LI Sixiu, DENG Jia, WANG Yanjuan, et al.
Case report and literature review on NFIX gene variation associated overgrowth, macrocephaly and intellectual disability
[J]. Chinese Journal of Child Health Care, 2024, 32(5): 572-575.
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[11] |
FENG Xuan, ZHU Shaohua, LIN Pengwu, et al.
Genetic analysis of two cases with Smith-Magenis syndrome
[J]. Chinese Journal of Child Health Care, 2024, 32(5): 576-580.
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[12] |
ZHAO Chenyue, JIANG Jinsong, ZHANG Lixue, GUO Min, GAO Jingbo, SUN Xiayu, GUO Rong, LU Hongyong, WU Jianrui, XUE Huiqin.
Family analysis of primary microcephaly caused by complex heterozygous variants of the RTTN gene and literature review
[J]. Chinese Journal of Child Health Care, 2024, 32(2): 212-217.
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[13] |
DONG Wenxin, ZHANG Hua, LI Zailing.
Dynamic changes of platelet-related indicators in infants with cow's milk protein allergy
[J]. Chinese Journal of Child Health Care, 2024, 32(1): 93-97.
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[14] |
TAO Dongying, CHENG Shengquan, ZHANG Jingjing, ZHANG Huiqin, NIU Huanhong.
Clinical phenotype and gene variation profile in children with Noonan syndrome
[J]. Chinese Journal of Child Health Care, 2023, 31(12): 1365-1369.
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[15] |
ZULIHUMAER·Rixiati, LUO Yanfei, SUN Guanghui, MIREGULI·Maimati.
Genetic characteristics and clinical phenotype analysis of a case with 3q distal microdeletion syndrome
[J]. Chinese Journal of Child Health Care, 2023, 31(11): 1273-1276.
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