Pengqiu Li Selected Research

Osteopetrosis with renal tubular acidosis

1/2021

A 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

2	Type 2 Diabetes Mellitus (MODY) 03/2016 - 01/2014
1	Dizziness (Lightheadedness) 01/2022
1	Arthralgia (Joint Pain) 01/2022
1	Osteoporosis 01/2022
1	Hypercalcemia (Milk Alkali Syndrome) 01/2022
1	Osteopetrosis with renal tubular acidosis 01/2021
1	Insulin Resistance 03/2016
1	Drug-Related Side Effects and Adverse Reactions 01/2014
1	Hyperglycemia 01/2014
1	Hypoglycemia (Reactive Hypoglycemia) 01/2014
1	Diabetic Ketoacidosis (Ketoacidosis, Diabetic) 01/2014

Drug/Important Bio-Agent (IBA)

3	Glucose (Dextrose)FDA LinkGeneric 03/2016 - 01/2014
1	Teriparatide (Parathar)FDA Link 01/2022
1	Alendronate (Alendronate Sodium)FDA LinkGeneric 01/2022
1	Parathyroid Hormone (Parathormone)IBA 01/2022
1	Alkaline PhosphataseIBA 01/2022
1	Nonsense Codon (Nonsense Mutation)IBA 01/2021
1	Calcifediol (Calcidiol)FDA Link 03/2016
1	hydroxide ionIBA 03/2016
1	insulin aspart protamine drug combination 30:70 insulin aspartIBA 01/2014
1	AcidsIBA 01/2014
1	Insulin (Novolin)FDA Link 01/2014
1	KetonesIBA 01/2014

Therapy/Procedure

1	Therapeutics 01/2021
1	Glycemic Control 01/2014