Robert H Squires
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Explore the profile of Robert H Squires including associated specialties, affiliations and a list of published articles.
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94
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1583
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Recent Articles
11.
Zellos A, Debray D, Indolfi G, Czubkowski P, Samyn M, Hadzic N, et al.
J Pediatr Gastroenterol Nutr
. 2022 Feb;
74(3):338-347.
PMID: 35226644
Objectives: The Hepatology Committee of the European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) aims to educate pediatric gastroenterologists, members of ESPGHAN and professionals from other specialties promoting an...
12.
Zellos A, Debray D, Indolfi G, Czubkowski P, Samyn M, Hadzic N, et al.
J Pediatr Gastroenterol Nutr
. 2022 Feb;
74(3):e45-e56.
PMID: 35226643
Objectives: The Hepatology Committee of the European Society for Pediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN) aims to educate pediatric gastroenterologists, members of ESPGHAN and professionals from other specialties promoting an...
13.
Squires J, McKiernan P, Squires R
Pediatrics
. 2021 Dec;
149(1 Suppl 1):S59-S65.
PMID: 34970684
Context: Develop evidence-based criteria for individual organ dysfunction. Objectives: Evaluate current evidence and develop contemporary consensus criteria for acute liver dysfunction with associated outcomes in critically ill children. Data Sources:...
14.
Bembea M, Agus M, Akcan-Arikan A, Alexander P, Basu R, Bennett T, et al.
Pediatrics
. 2021 Dec;
149(1 Suppl 1):S1-S12.
PMID: 34970673
Prior criteria for organ dysfunction in critically ill children were based mainly on expert opinion. We convened the Pediatric Organ Dysfunction Information Update Mandate (PODIUM) expert panel to summarize data...
15.
Leung D, Sorensen L, Ye W, Hawthorne K, Ng V, Loomes K, et al.
J Pediatr Gastroenterol Nutr
. 2021 Oct;
74(1):96-103.
PMID: 34694263
Objective: To evaluate neurodevelopmental status among children with inherited cholestatic liver diseases with native liver and variables predictive of impairment. Methods: Participants with Alagille syndrome (ALGS), progressive familial intrahepatic cholestasis...
16.
Squires J, Alonso E, Ibrahim S, Kasper V, Kehar M, Martinez M, et al.
J Pediatr Gastroenterol Nutr
. 2021 Aug;
74(1):138-158.
PMID: 34347674
Pediatric acute liver failure (PALF) is a rare, rapidly progressive clinical syndrome with significant morbidity and mortality. The phenotype of PALF manifests as abrupt onset liver dysfunction, which can be...
17.
Henkel S, Salgado C, Reyes-Mugica M, Soltys K, Strauss K, Mazariegos G, et al.
Pediatr Transplant
. 2021 Aug;
25(8):e14108.
PMID: 34339082
Background: Progressive familial intrahepatic cholestasis type 1 (PFIC1) arises from biallelic variants in the ATP8B1 gene that annul FIC1 activity, resulting in progressive liver disease. Liver transplant (LT) is indicated...
18.
Ewing C, Soltys K, Strauss K, Sindhi R, Vockley J, McKiernan P, et al.
J Pediatr
. 2021 Jun;
237:59-64.e1.
PMID: 34153280
Objectives: To assess outcomes following liver transplantation for maple syrup urine disease by determining attainment and sustainability of metabolic control and apply an "ideal" outcome composite in long-term survivors. Study...
19.
Hertel P, Bull L, Thompson R, Goodrich N, Ye W, Magee J, et al.
J Pediatr Gastroenterol Nutr
. 2021 May;
73(2):169-177.
PMID: 34016879
Objectives: To advance our understanding of monogenic forms of intrahepatic cholestasis. Methods: Analyses included participants with pathogenic biallelic mutations in adenosine triphosphate (ATP)-binding cassette subfamily B member 11 (ABCB11) (bile...
20.
Squires R, Monga S
J Pediatr Gastroenterol Nutr
. 2021 Mar;
72(5):641-643.
PMID: 33661247
No abstract available.