Sichi Liu Selected Research

Carnitine-Acylcarnitine Translocase Deficiency

8/2021

Screening for neonatal inherited metabolic disorders by tandem mass spectrometry in Guangzhou.

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Sichi Liu Research Topics

Disease

2	GM1 Gangliosidosis (Gangliosidosis GM1) 01/2022 - 01/2021
2	Gaucher Disease (Gaucher's Disease) 01/2021 - 07/2020
1	Phenylketonurias (Phenylketonuria) 08/2021
1	Maple Syrup Urine Disease 08/2021
1	Methylmalonic acidemia 08/2021
1	Lysosomal Storage Diseases (Lysosomal Storage Disease) 01/2021
1	Thrombocytopenia (Thrombopenia) 07/2020
1	Splenomegaly 07/2020
1	Congenital Adrenal Hyperplasia (Hyperplasia, Congenital Adrenal) 11/2019
1	Birth Weight (Birth Weights) 11/2019
1	Hypophosphatasia 11/2019

Drug/Important Bio-Agent (IBA)

2	EnzymesIBA 01/2022 - 07/2020
1	G(M1) GangliosideIBA 01/2022
1	beta-Galactosidase (Lactaid)IBA 01/2022
1	AcidsIBA 08/2021
1	Systemic carnitine deficiencyIBA 08/2021
1	Carnitine-Acylcarnitine Translocase DeficiencyIBA 08/2021
1	sphingosyl beta-glucosideIBA 01/2021
1	GalactosidasesIBA 01/2021
1	GlucosidasesIBA 01/2021
1	Glucosylceramides (Glucocerebrosides)IBA 01/2021
1	Glucosylceramidase (Glucocerebrosidase)IBA 07/2020
1	17-alpha-Hydroxyprogesterone (17 Hydroxyprogesterone)IBA 11/2019
1	N- (4'- fluorobutyrophenone)- 4- (4- chlorophenyl)pyridinium (HPP(+))IBA 11/2019
1	Alkaline PhosphataseIBA 11/2019

Therapy/Procedure

1	Therapeutics 01/2021