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Archana M Agarwal

Explore the profile of Archana M Agarwal including associated specialties, affiliations and a list of published articles. Areas
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Articles 67
Citations 935
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Recent Articles
11.
Meznarich J, Rets A, Agarwal A, Christensen R, Reading N, Kuypers F, et al.
Am J Hematol . 2021 Sep; 96(12):E448-E450. PMID: 34553403
No abstract available.
12.
Agarwal A, Rets A
Int J Lab Hematol . 2021 Jul; 43 Suppl 1:65-70. PMID: 34288450
Anemia is a global health problem in all age groups. According to World Health Organization (WHO), approximately 40% of pregnant women are anemic. Iron deficiency anemia (IDA) due to nutritional...
13.
Cowman S, Fuja D, Liu X, Slack Tidwell R, Kandula N, Sirohi D, et al.
Clin Cancer Res . 2021 Jun; 27(11):3265. PMID: 34074655
No abstract available.
14.
Bahr T, Knudsen M, Lozano-Chinga M, Agarwal A, Meznarich J, Ohls R, et al.
Biomed Hub . 2021 May; 5(3):227-234. PMID: 34055814
Infantile pyknocytosis is a rare, self-limited, hemolytic condition of unknown pathogenesis. It is diagnosed when a neonate with Coombs-negative hemolytic anemia has abundant pyknocytes and a characteristic clinical course after...
15.
Kim S, Song J, Reading N, Lautersztain J, Kutlar A, Agarwal A, et al.
Am J Hematol . 2021 Feb; 96(5):E150-E154. PMID: 33556202
No abstract available.
16.
Cardenas F, Agarwal A, Vagher J, Maese L, Fluchel M, Afify Z
J Pediatr Hematol Oncol . 2021 Jan; 43(8):e1210-e1213. PMID: 33448720
X-linked lymphoproliferative disease type 1 (XLP1) is a primary immunodeficiency disorder caused by pathogenic variants in the SH2D1A gene (SH2 domain containing protein 1A). Patients with XLP1 may present acutely...
17.
Lozano-Chinga M, Draper L, George T, Agarwal A, Dansie D, Maese L
Pediatr Blood Cancer . 2020 Dec; 68(3):e28806. PMID: 33314722
Bone marrow necrosis (BMN) is a rare pathologic finding, but when encountered is most often associated with malignancy. In adults, its presence correlates with an inferior prognosis, however in children...
18.
Rets A, Reading N, Agarwal A
Hemoglobin . 2020 Oct; 44(6):438-441. PMID: 33054450
High prevalence of hemoglobin (Hb) disorders mandates national programs for screening and genetic counseling in many countries. Increased Hb A levels are commonly associated with β-thalassemias, however, various disorders including...
19.
Bahr T, Lozano-Chinga M, Agarwal A, Meznarich J, Yost C, Li P, et al.
Neonatology . 2020 Sep; 117(4):532-535. PMID: 32987391
We report a novel glucose-6-phosphate dehydrogenase (G6PD) variant (c.1375C>G) discovered in a 3-day-old Hispanic male child from Salt Lake City, UT, USA. This newborn presented with severe hyperbilirubinemia (29.8 mg/dL...
20.
Bahr T, Agarwal A, Christensen R
J Perinatol . 2020 Sep; 41(4):658-660. PMID: 32958836
No abstract available.