Lili Liang
6PUBLICATIONS
14CO-AUTHORS
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Publications (6)
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|Aug 16, 2023
Genetic and phenotypic spectrum of non-21-hydroxylase-deficiency primary adrenal insufficiency in childhood: data from 111 Chinese patients.Ying Duan, Wanqi Zheng, Yu Xia
|Jun 14, 2023
Evaluation of the clinical, biochemical, genotype and prognosis of mut-type methylmalonic acidemia in 365 Chinese cases.Lili Liang, Shiying Ling, Yue Yu
|Feb 10, 2022
Diagnosis and follow-up of glycogen storage disease (GSD) type VI from the largest GSD center in China.Xiaomei Luo, Ying Duan, Di Fang
|Oct 20, 2021
Different mutations in the MMUT gene are associated with the effect of vitamin B12 in a cohort of 266 Chinese patients with mut-type methylmalonic acidemia: A retrospective study.Yue Yu, Ruixue Shuai, Lili Liang
|Sep 15, 2021
Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy.Sha Hong, Tianwen Zhu, Simin Zheng
|Nov 26, 2019
Examining the blood amino acid status in pretherapeutic patients with hyperphenylalaninemia.Lili Liang, Jun Ye, Lianshu Han
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