Carla Lloyd
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Explore the profile of Carla Lloyd including associated specialties, affiliations and a list of published articles.
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Articles
32
Citations
178
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Recent Articles
11.
Jeyaraj R, Bounford K, Ruth N, Lloyd C, MacDonald F, Hendriksz C, et al.
Genes (Basel)
. 2021 Nov;
12(11).
PMID: 34828443
Many inherited conditions cause cholestasis in the neonate or infant. Next-generation sequencing methods can facilitate a prompt diagnosis in some of these cases; application of these methods in patients with...
12.
Lloyd C, Arshad A, Jara P, Burdelski M, Gridelli B, Manzanares J, et al.
Transplant Direct
. 2021 Sep;
7(10):e765.
PMID: 34557582
Methods: One hundred fifty-six patients who had taken part in a multicenter, randomized, open, parallel study of Tac and corticosteroids versus cyclosporine A microemulsion (CyA-ME), corticosteroids, and azathioprine. Patients were...
13.
Ruth N, Sharif K, Legarda M, Smith M, Lewis P, Lloyd C, et al.
Pediatr Transplant
. 2020 Jul;
24(7):e13782.
PMID: 32678500
LT is a successful treatment for end-stage liver disease. The long-term outcome of patients transplanted in childhood has not previously been widely reported. This project assessed the long-term impact of...
14.
Modin L, Arshad A, Wilkes B, Benselin J, Lloyd C, Irving W, et al.
J Hepatol
. 2018 Nov;
70(3):371-378.
PMID: 30496763
Background & Aims: Chronic hepatitis C virus (HCV) infection is a global health burden. Although HCV infection rarely contributes to morbidity during childhood, most HCV-infected children develop chronic HCV with...
15.
Ranawaka R, Lloyd C, McKiernan P, Hulton S, Sharif K, Milford D
Pediatr Nephrol
. 2016 Apr;
31(9):1539-43.
PMID: 27105881
Background: Combined liver-kidney transplantation (CLKT) is the accepted treatment for patients with both liver failure and progressive renal insufficiency. Long-term outcome data for CLKT in children is sparse and controversy...
16.
Bartlett D, Lloyd C, McKiernan P, Newsome P
J Inherit Metab Dis
. 2014 Feb;
37(5):745-52.
PMID: 24515874
Background: Tyrosinaemia type 1 (HT1) is a rare disorder of tyrosine metabolism leading to liver failure and hepatocellular carcinoma. Treatment previously consisted of dietary restriction and orthotopic liver transplantation (OLT)...
17.
Trocello J, El Balkhi S, Woimant F, Girardot-Tinant N, Chappuis P, Lloyd C, et al.
Mov Disord
. 2013 Dec;
29(4):558-62.
PMID: 24375554
Background: Family screening is a main step for the diagnosis in Wilson disease. This study was undertaken to evaluate the value of relative exchangeable copper for family screening. Methods: Data...
18.
Legarda M, Gordon G, Lloyd C, Baumann U, Kelly D, Shaw N, et al.
Pediatr Transplant
. 2013 Aug;
17(7):631-7.
PMID: 23962009
Vitamin D deficiency and insufficiency are increasingly recognized in the general population, including healthy children. There is also an increasing emphasis on the importance of vitamin D status following pediatric...
19.
Beath S, Davies P, Mukherjee A, Lloyd C, Sharif K, McKiernan P, et al.
Clin Res Hepatol Gastroenterol
. 2013 Jul;
38(1):32-9.
PMID: 23856636
Background And Aims: To evaluate risk of mortality in children with intestinal failure associated liver disease (IFALD) compared with other liver disease using two validated scores. Methods: Sixty-seven children listed...
20.
Rawat D, Kelly D, Milford D, Sharif K, Lloyd C, McKiernan P
J Pediatr Gastroenterol Nutr
. 2013 Mar;
57(2):161-6.
PMID: 23518487
Background And Objective: Congenital hepatic fibrosis (CHF) and Caroli syndrome are frequently associated with renal cystic diseases. They have a variable clinical course, and the natural history is not well...