Lili J. Liang

1665 KongJiang Road
Shanghai, 200092, China

Last Updated: 09/26/2026

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Found 83 publications

Ethical challenges and prospective strategies in orthopedic robotic-assisted surgery

Ethical challenges and prospective strategies in orthopedic robotic-assisted surgery

Journal: Zhonghua wai ke za zhi [Chinese journal of surgery]

Published: May 27, 2026

Hydroxocobalamin monotherapy in patients with cblC deficiency: Biochemical analysis and clinical observations.

Hydroxocobalamin monotherapy in patients with cblC deficiency: Biochemical analysis and clinical observations.

Journal: Molecular genetics and metabolism

Published: February 12, 2026

Clinical and genetic analyses of 17 Chinese patients with glycogen storage disease type IXc.

Clinical and genetic analyses of 17 Chinese patients with glycogen storage disease type IXc.

Journal: Orphanet journal of rare diseases

Published: August 05, 2025

Analysis of hydroxocobalamin dosage in patients with CblC deficiency.

Analysis of hydroxocobalamin dosage in patients with CblC deficiency.

Journal: Orphanet journal of rare diseases

Published: April 22, 2025

Clinical, biochemical and genetic characteristics of patients with argininosuccinate lyase deficiency from a single center cohort in China.

Clinical, biochemical and genetic characteristics of patients with argininosuccinate lyase deficiency from a single center cohort in China.

Journal: Orphanet journal of rare diseases

Published: April 16, 2025

Assessment and Application of Acylcarnitines Summations as Auxiliary Quantization Indicator for Primary Carnitine Deficiency.

Assessment and Application of Acylcarnitines Summations as Auxiliary Quantization Indicator for Primary Carnitine Deficiency.

Journal: International journal of neonatal screening

Published: April 11, 2025

Variable phenotypes and outcomes associated with the MMACHC c.1A>G variant in Chinese patients with combined methylmalonic acidemia and homocystinuria cblC type.

Variable phenotypes and outcomes associated with the MMACHC c.1A>G variant in Chinese patients with combined methylmalonic acidemia and homocystinuria cblC type.

Journal: Molecular genetics and metabolism

Published: March 25, 2025

Multi-omics analyses of the gut microbiota and metabolites in children with metabolic dysfunction-associated steatotic liver disease.

Multi-omics analyses of the gut microbiota and metabolites in children with metabolic dysfunction-associated steatotic liver disease.

Journal: mSystems

Published: March 14, 2025

Blood RNA-seq in rare disease diagnostics: a comparative study of cases with and without candidate variants.

Blood RNA-seq in rare disease diagnostics: a comparative study of cases with and without candidate variants.

Journal: Journal of translational medicine

Published: March 14, 2025

Genetic Variants and Clinical Features of Patients With Glycogen Storage Disease Type Ib.

Genetic Variants and Clinical Features of Patients With Glycogen Storage Disease Type Ib.

Journal: JAMA network open

Published: February 26, 2025

Analysis of the regional distribution differences of common variations of the MMACHC gene in cblC methylmalonic acidemia patients

Analysis of the regional distribution differences of common variations of the MMACHC gene in cblC methylmalonic acidemia patients

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: October 21, 2024

A case series of the efficacy and tolerability of ketogenic diet in children with drug-resistant epilepsy due to neonatal hypoglycemia.

A case series of the efficacy and tolerability of ketogenic diet in children with drug-resistant epilepsy due to neonatal hypoglycemia.

Journal: Epilepsy & behavior : E&B

Published: July 24, 2024

Showing 1-12 of 83

Last Updated: 09/26/2026