Abhilasha Sampagar Selected Research

Congenital Nonspherocytic Hemolytic Anemia (Anemia, Hemolytic Congenital, Nonspherocytic)

1/2021

Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family.

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Abhilasha Sampagar Research Topics

Disease

2	Hemolytic Anemia 02/2022 - 01/2019
1	Neonatal Jaundice 02/2022
1	Intellectual Disability (Idiocy) 02/2022
1	Neurologic Manifestations (Neurological Manifestations) 02/2022
1	Hemophagocytic Lymphohistiocytosis (Hemophagocytic Syndrome) 01/2021
1	Congenital Nonspherocytic Hemolytic Anemia (Anemia, Hemolytic Congenital, Nonspherocytic) 01/2021
1	Inflammation (Inflammations) 01/2021
1	type 2C Congenital disorder of glycosylation 01/2020
1	Inborn Genetic Diseases (Disease, Hereditary) 01/2019
1	Nervous System Diseases (Neurological Disorders) 01/2019

Drug/Important Bio-Agent (IBA)

2	IsomerasesIBA 02/2022 - 01/2019
2	Phosphates (Orthophosphate)IBA 02/2022 - 01/2019
2	Glucose (Dextrose)FDA LinkGeneric 02/2022 - 01/2019
1	Adenylate KinaseIBA 01/2021
1	CytokinesIBA 01/2021
1	Polysaccharides (Glycans)IBA 01/2020
1	Glucose-6-Phosphate Isomerase (Phosphoglucose Isomerase)IBA 01/2019

Therapy/Procedure

1	Splenectomy 02/2022