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Pengqiu Li Selected Research

Osteopetrosis with renal tubular acidosis

1/2021A novel homozygous nonsense mutation in the CA2 gene (c.368G>A, p.W123X) linked to carbonic anhydrase II deficiency syndrome in a Chinese family.

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Pengqiu Li Research Topics

Disease

2Type 2 Diabetes Mellitus (MODY)
03/2016 - 01/2014
1Osteopetrosis with renal tubular acidosis
01/2021
1Insulin Resistance
03/2016
1Diabetic Ketoacidosis (Ketoacidosis, Diabetic)
01/2014
1Drug-Related Side Effects and Adverse Reactions
01/2014
1Hyperglycemia
01/2014
1Hypoglycemia (Reactive Hypoglycemia)
01/2014

Drug/Important Bio-Agent (IBA)

3Glucose (Dextrose)FDA LinkGeneric
03/2016 - 01/2014
1Nonsense Codon (Nonsense Mutation)IBA
01/2021
1hydroxide ionIBA
03/2016
1Calcifediol (Calcidiol)FDA Link
03/2016
1insulin aspart protamine drug combination 30:70 insulin aspartIBA
01/2014
1AcidsIBA
01/2014
1Insulin (Novolin)FDA Link
01/2014
1KetonesIBA
01/2014

Therapy/Procedure

1Therapeutics
01/2021
1Glycemic Control
01/2014