Akshata Moghe
Overview
Explore the profile of Akshata Moghe including associated specialties, affiliations and a list of published articles.
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32
Citations
1071
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Recent Articles
1.
Levy C, Naik H, Overbey J, Hedstrom K, Wang K, McDonough C, et al.
Hepatol Commun
. 2025 Feb;
9(3).
PMID: 39969427
Background: Erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP) are characterized by the accumulation of protoporphyrin in the marrow, erythrocytes, plasma, skin, and liver, and present clinically with painful cutaneous phototoxicity....
2.
Ramanujam V, Moghe A, Huda R, Turner S, Anderson K
Curr Protoc
. 2025 Feb;
5(2):e70092.
PMID: 39927625
Porphyrins and porphyrin precursors are normally detected in small amounts in healthy individuals but are found in large quantities in the urine, feces, blood, plasma, bone marrow, and liver in...
3.
Johnson J, Engebretsen T, Mujtaba M, Stevenson H, Kulkarni R, Lea A, et al.
Surg Pract Sci
. 2025 Jan;
16():100236.
PMID: 39845340
Introduction: In renal transplantation, donor hepatitis C virus (HCV) status is crucial to consider when selecting a recipient given the high likelihood of transmission. We analyzed the effect of donor...
4.
Mushtaq M, Colletier K, Moghe A
ACG Case Rep J
. 2024 Jun;
11(7):e01397.
PMID: 38939351
Coronavirus disease 2019 (COVID-19) has been associated with liver injury incidence reported between 15% and 53%. Viral binding to ACE2 receptors in hepatobiliary cells is believed to cause liver inflammation....
5.
Arefan D, DArdenne N, Iranpour N, Catania R, Yousef J, Chupetlovska K, et al.
Abdom Radiol (NY)
. 2024 May;
49(7):2220-2230.
PMID: 38782785
Purpose: Gain-of-function mutations in CTNNB1, gene encoding for β-catenin, are observed in 25-30% of hepatocellular carcinomas (HCCs). Recent studies have shown β-catenin activation to have distinct roles in HCC susceptibility...
6.
Gosnell J, Golovko G, Arroyave E, Moghe A, Kueht M, Saldarriaga O, et al.
World J Diabetes
. 2024 May;
15(5):886-897.
PMID: 38766421
Background: Metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH) are a growing health burden across a significant portion of the global patient population. However, these conditions seem...
7.
Moghe A, McGuire B, Levy C
Hepatology
. 2024 Apr;
PMID: 38607698
The acute hepatic porphyrias (AHPs) are a group of rare, inherited disorders of the heme biosynthesis pathway, usually manifesting with attacks of acute abdominal pain and other neurovisceral symptoms, with...
8.
Saldarriaga O, Wanninger T, Arroyave E, Gosnell J, Krishnan S, Oneka M, et al.
JHEP Rep
. 2024 Jan;
6(1):100958.
PMID: 38162144
Background & Aims: Clinical trials for reducing fibrosis in steatotic liver disease (SLD) have targeted macrophages with variable results. We evaluated intrahepatic macrophages in patients with SLD to determine if...
9.
Malone J, Zamora E, Gosnell J, Stevenson H, Moghe A
Cureus
. 2023 Dec;
15(11):e48224.
PMID: 38050504
Acute hepatitis A virus infection is routinely identified through a thorough patient history in conjunction with liver chemistries and viral serologies. The diagnosis has the potential to be delayed when...
10.
Moghe A, Dickey A, Erwin A, Leaf R, OBrien A, Quigley J, et al.
Mol Genet Metab
. 2023 Aug;
140(3):107670.
PMID: 37542766
Acute hepatic porphyria (AHP) is a group of four rare inherited diseases, each resulting from a deficiency in a distinct enzyme in the heme biosynthetic pathway. Characterized by acute neurovisceral...