Andrew Wehrman
Overview
Explore the profile of Andrew Wehrman including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
45
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0
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Recent Articles
1.
Kennedy J, Vargas S, Fishman M, Alesi N, Baek S, Khabibillin D, et al.
Med
. 2025 Feb;
:100607.
PMID: 40020677
Background: Childhood interstitial and diffuse lung diseases are a collection of rare disorders with significant associated morbidity. Only a small subset of these diseases have precise diagnostic or therapeutic options...
2.
McCullagh K, Yeoh L, Holmes B, Sacharow S, Wehrman A, Kritzer A, et al.
Pediatrics
. 2024 Sep;
154(4).
PMID: 39290186
Acute liver failure is rare in the neonatal and infant population; however, when encountered, it requires timely diagnosis, management, and identification of the underlying etiology to provide the best clinical...
3.
Hartjes K, Koo D, Al-Ibraheemi A, Sweeny K, Wehrman A, Elisofon S, et al.
Pediatr Transplant
. 2024 Jun;
28(5):e14818.
PMID: 38940480
Introduction: Allograft dysfunction within the first week posttransplant is an uncommon but known complication following liver transplantation. Seventh-Day Syndrome (7DS) is a rare complication of allograft dysfunction following liver transplantation...
4.
Ovchinsky N, Aumar M, Baker A, Baumann U, Bufler P, Cananzi M, et al.
Lancet Gastroenterol Hepatol
. 2024 Apr;
9(7):632-645.
PMID: 38670135
Background: In patients with Alagille syndrome, cholestasis-associated clinical features can include high serum bile acids and severe pruritus that can necessitate liver transplantation. We aimed to evaluate the efficacy and...
5.
Chiu M, Cuenca A, Koo D, Hartjes K, Wehrman A, Kim H, et al.
Pediatr Transplant
. 2024 Feb;
28(1):e14693.
PMID: 38317339
Background: Pulmonary calcification (PC) is a rare clinical entity observed following liver transplantation (LT). Most often identified in adults or in patients with concomitant renal failure, PC is rarely reported...
6.
Gumm A, Perez-Atayde A, Wehrman A
Clin Liver Dis (Hoboken)
. 2022 Oct;
20(4):130-135.
PMID: 36245678
No abstract available.
7.
Wehrman A, Lee C
Curr Opin Pediatr
. 2022 Aug;
34(5):491-495.
PMID: 35942658
Purpose Of Review: Cholestasis in infants can indicate a serious hepatobiliary disease and requires timely assessment, diagnosis and intervention to prevent progression to serious liver decompensation. This report aims to...
8.
Wehrman A, Waisbourd-Zinman O, Rand E
J Pediatr
. 2019 Apr;
210:243-244.
PMID: 31005277
No abstract available.
9.
Agawu A, Wehrman A, Pogoriler J, Terry N, Lin H
BMC Pediatr
. 2019 Mar;
19(1):72.
PMID: 30849955
Background: Total parenteral nutrition (TPN) and biliary atresia (BA) are common causes of cholestasis in infancy. The diagnosis of BA is time sensitive due to an inverse correlation between age...
10.
Wehrman A, Waisbourd-Zinman O, Wells R
F1000Res
. 2019 Mar;
8.
PMID: 30828434
Biliary atresia (BA) is a neonatal liver disease characterized by progressive obstruction and fibrosis of the extrahepatic biliary tree as well as fibrosis and inflammation of the liver parenchyma. Recent...