Archana M Agarwal
Overview
Explore the profile of Archana M Agarwal including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
67
Citations
935
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Balciuniene J, Yilmaz S, Chonat S, Grace R, Soff G, Ravindranath Y, et al.
Br J Haematol
. 2025 Mar;
PMID: 40058880
Data from a large cohort of individuals referred for NGS testing evaluate the utility of next-generation sequencing in clinical practice for diagnosing hereditary haemolytic anaemias.
2.
3.
Dadelahi A, Jackson T, Agarwal A, Lin L, Rets A, Ng D
Clin Lab Med
. 2024 Aug;
44(3):495-509.
PMID: 39089754
Clinical flow cytometry plays a vital role in the diagnosis and monitoring of various red blood cell disorders. The high throughput, precision, and automation potential of this technique allows for...
4.
Agarwal A, Rets A
Clin Lab Med
. 2024 Aug;
44(3):441-453.
PMID: 39089750
Hemoglobin (Hb) disorders are among the most prevalent inherited diseases. Despite a limited number of involved genes, these conditions represent a broad clinical and prognostic spectrum. The menu of laboratory...
5.
Agarwal A, Rets A
Int J Lab Hematol
. 2023 Jun;
45 Suppl 2:79-86.
PMID: 37290893
Hereditary hemolytic anemia (HHA) is a heterogeneous group of disorders due to genetically caused defects in red blood cell membrane structure, enzymes, heme and globin synthesis, erythroid proliferation, and differentiation....
6.
Agarwal A, McMurty V, Clayton A, Bolia A, Reading N, Mani C, et al.
Eur J Haematol
. 2023 Feb;
110(6):688-695.
PMID: 36825813
Introduction: Hereditary hemolytic anemias (HHA) comprise a heterogeneous group of disorders resulting from defective red blood cell (RBC) cytoskeleton, RBC enzyme deficiencies, and hemoglobin (Hb) synthesis disorders such as thalassemia...
7.
Lin Y, Agarwal A, Anderson L, Marshall A
J Mass Spectrom Adv Clin Lab
. 2023 Feb;
28:20-26.
PMID: 36814695
β-thalassemia is a quantitative hemoglobin (Hb) disorder resulting in reduced production of Hb A and increased levels of Hb A. Diagnosis of β-thalassemia can be problematic when combined with other...
8.
Montgomery H, Agarwal A, Lim M
Int J Lab Hematol
. 2022 Jul;
44(6):1015-1016.
PMID: 35799500
Azathioprine (AZA) is an immunosuppressant that is widely used to treat many disease states including rheumatoid arthritis. We present a patient who was treated with AZA for rheumatoid arthritis and...
9.
Lin Y, Agarwal A, Marshall A, Anderson L
J Am Soc Mass Spectrom
. 2021 Dec;
33(1):123-130.
PMID: 34955023
Hemoglobinopathies are one of the most prevalent genetic disorders, affecting millions throughout the world. These are caused by pathogenic variants in genes that control the production of hemoglobin (Hb) subunits....
10.
Bahr T, Agarwal A, Meznarich J, Prince W, Wait T, Prchal J, et al.
Blood Cells Mol Dis
. 2021 Nov;
92:102625.
PMID: 34773909
In North America, jaundiced neonates are not usually tested for G6PD deficiency if the family is of European ancestry. However, we describe such a family where ≥35 males have had...