BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Vajro P, Maddaluno S, Veropalumbo C. Persistent hypertransaminasemia in asymptomatic children: A stepwise approach. World J Gastroenterol 2013; 19(18): 2740-2751 [PMID: 23687411 DOI: 10.3748/wjg.v19.i18.2740] [Cited by in CrossRef: 41] [Cited by in F6Publishing: 29] [Article Influence: 4.6] [Reference Citation Analysis]
Number Citing Articles
1 Hsu D, Josyabhatla R, Monteiro IM. Case 3: Persistent Elevated Transaminase Levels in a 9-year-old Boy. Pediatr Rev 2019;40:643-6. [PMID: 31792049 DOI: 10.1542/pir.2018-0022] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Fernández Ventureira V, Ros Arnal I, Rodríguez Martínez G, García Rodríguez B, García Romero R, Ubalde Sainz E. Evaluation of liver function tests in the paediatric patient. An Pediatr (Engl Ed) 2021;94:359-65. [PMID: 34090632 DOI: 10.1016/j.anpede.2020.06.014] [Reference Citation Analysis]
3 Valentini D, Alisi A, di Camillo C, Sartorelli MR, Crudele A, Bartuli A, Nobili V, Villani A. Nonalcoholic Fatty Liver Disease in Italian Children with Down Syndrome: Prevalence and Correlation with Obesity-Related Features. J Pediatr 2017;189:92-97.e1. [PMID: 28662945 DOI: 10.1016/j.jpeds.2017.05.077] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 2.8] [Reference Citation Analysis]
4 Putri RR, Casswall T, Hagman E. Prevalence of increased transaminases and its association with sex, age, and metabolic parameters in children and adolescents with obesity - a nationwide cross-sectional cohort study. BMC Pediatr 2021;21:271. [PMID: 34107897 DOI: 10.1186/s12887-021-02747-4] [Reference Citation Analysis]
5 Lee Y, Yi DY, Lee YM, Choi SY, Choi YJ, Lee KJ. A Multicenter Study of Real-world Practice for Management of Abnormal Liver Function Tests in Children with Acute Infectious Diseases. J Korean Med Sci 2021;36:e310. [PMID: 34873882 DOI: 10.3346/jkms.2021.36.e310] [Reference Citation Analysis]
6 Veropalumbo C, Campanozzi A, De Gregorio F, Correra A, Raia V, Vajro P. Shwachman-Diamond syndrome with autoimmune-like liver disease and enteropathy mimicking celiac disease. Clinics and Research in Hepatology and Gastroenterology 2015;39:e1-4. [DOI: 10.1016/j.clinre.2014.06.017] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
7 Colucci A, Rocco MC, De Anseris AGE, Nazzaro L, Vajro P, Mandato C. Pediatric vs. adult NAFLD to MAFLD transition: a welcome but tangled path. Exploration of Medicine. [DOI: 10.37349/emed.2021.00051] [Reference Citation Analysis]
8 Mandato C, Vajro P. Isolated aspartate aminotransferase elevation: Is it liver disease or what else? Acta Paediatr 2022;111:459-61. [PMID: 34935200 DOI: 10.1111/apa.16213] [Reference Citation Analysis]
9 Luo Y, Lin H. Inflammation initiates a vicious cycle between obesity and nonalcoholic fatty liver disease. Immun Inflamm Dis 2021;9:59-73. [PMID: 33332766 DOI: 10.1002/iid3.391] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
10 Kamin W, Adams O, Kardos P, Matthys H, Meister N, Strassburg CP. Liver Involvement in Acute Respiratory Infections in Children and Adolescents – Results of a Non-interventional Study. Front Pediatr 2022;10:840008. [DOI: 10.3389/fped.2022.840008] [Reference Citation Analysis]
11 Troisi J, Belmonte F, Bisogno A, Pierri L, Colucci A, Scala G, Cavallo P, Mandato C, Di Nuzzi A, Di Michele L, Delli Bovi AP, Guercio Nuzio S, Vajro P. Metabolomic Salivary Signature of Pediatric Obesity Related Liver Disease and Metabolic Syndrome. Nutrients 2019;11:E274. [PMID: 30691143 DOI: 10.3390/nu11020274] [Cited by in Crossref: 19] [Cited by in F6Publishing: 17] [Article Influence: 6.3] [Reference Citation Analysis]
12 Johansen MJ, Gade J, Stender S, Frithioff-bøjsøe C, Lund MAV, Chabanova E, Thomsen HS, Pedersen O, Fonvig CE, Hansen T, Holm J. The Effect of Overweight and Obesity on Liver Biochemical Markers in Children and Adolescents. The Journal of Clinical Endocrinology & Metabolism 2020;105:430-42. [DOI: 10.1210/clinem/dgz010] [Cited by in Crossref: 6] [Cited by in F6Publishing: 8] [Article Influence: 2.0] [Reference Citation Analysis]
13 Ghobrial C, Abdelhamid N, El-karaksy H. Incidental hypertransaminasemia in children: Potential delay in diagnosis of muscle disease. Egyptian Pediatric Association Gazette 2018;66:112-4. [DOI: 10.1016/j.epag.2018.09.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
14 Tanaka N, Kimura T, Fujimori N, Ichise Y, Sano K, Horiuchi A. Non-alcoholic fatty liver disease later diagnosed as myotonic dystrophy. World J Hepatol 2020; 12(9): 685-692 [PMID: 33033573 DOI: 10.4254/wjh.v12.i9.685] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Clemente MG, Mandato C, Poeta M, Vajro P. Pediatric non-alcoholic fatty liver disease: Recent solutions, unresolved issues, and future research directions. World J Gastroenterol 2016; 22(36): 8078-8093 [PMID: 27688650 DOI: 10.3748/wjg.v22.i36.8078] [Cited by in CrossRef: 82] [Cited by in F6Publishing: 72] [Article Influence: 13.7] [Reference Citation Analysis]
16 Bussler S, Vogel M, Pietzner D, Harms K, Buzek T, Penke M, Händel N, Körner A, Baumann U, Kiess W, Flemming G. New pediatric percentiles of liver enzyme serum levels (alanine aminotransferase, aspartate aminotransferase, γ-glutamyltransferase): Effects of age, sex, body mass index, and pubertal stage. Hepatology 2018;68:1319-30. [PMID: 28926121 DOI: 10.1002/hep.29542] [Cited by in Crossref: 64] [Cited by in F6Publishing: 52] [Article Influence: 16.0] [Reference Citation Analysis]
17 Bongiovanni A, Spina M, Papale M, Brambilla I, Licari A, Parisi GF, Leonardi S. Hypertransaminasemia in children is not always as simple as it seems. Minerva Pediatr (Torino) 2021;73:281-3. [PMID: 34047150 DOI: 10.23736/S2724-5276.19.05514-2] [Reference Citation Analysis]
18 Eğin S, Açıksarı K, Ercan G, Aydın AF, Üstyol EA, Eser M, Tanrıverdi G, Yanar HT. Effects of pentoxifylline on oxidative stress in rats with abdominal compartment syndrome model. International Journal of Surgery Open 2016;5:5-10. [DOI: 10.1016/j.ijso.2016.09.001] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
19 Paglia P, Nazzaro L, De Anseris AGE, Lettieri M, Colantuono R, Rocco MC, Siano MA, Biffaro N, Vajro P. Atypically Protracted Course of Liver Involvement in Kawasaki Disease. Case Report and Literature Review. Pediatr Rep 2021;13:357-62. [PMID: 34287369 DOI: 10.3390/pediatric13030044] [Reference Citation Analysis]
20 Fernández Ventureira V, Ros Arnal I, Rodríguez Martínez G, García Rodríguez B, García Romero R, Ubalde Sainz E. Evaluación del seguimiento de niños con hallazgo de hipertransaminasemia. Anales de Pediatría 2021;94:359-65. [DOI: 10.1016/j.anpedi.2020.06.019] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Alfani R, Vassallo E, De Anseris AG, Nazzaro L, D'Acunzo I, Porfito C, Mandato C, Vajro P. Pediatric Fatty Liver and Obesity: Not Always Justa Matter of Non-Alcoholic Fatty Liver Disease. Children (Basel) 2018;5:E169. [PMID: 30551665 DOI: 10.3390/children5120169] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
22 Ben Houmich T, Admou B. Celiac disease: Understandings in diagnostic, nutritional, and medicinal aspects. Int J Immunopathol Pharmacol 2021;35:20587384211008709. [PMID: 33878915 DOI: 10.1177/20587384211008709] [Reference Citation Analysis]
23 Pham LAT, Nguyen TT, Nga Le HB, Tran DQ, Ho CT, Tran TH, Ta VT, Bui TH, Tran VK. Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B. J Genet 2017;96:933-9. [DOI: 10.1007/s12041-017-0857-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.4] [Reference Citation Analysis]
24 Wei Z, Huang Y, Liu A, Diao S, Yu Q, Peng Z, Hong M. Mutational characterization of ATP7B gene in 103 Wilson's disease patients from Southern China: identification of three novel mutations. Neuroreport. 2014;25:1075-1080. [PMID: 25089800 DOI: 10.1097/wnr.0000000000000216] [Cited by in Crossref: 12] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
25 Socha P, Vajro P, Lefeber D, Adamowicz M, Tanner S. Search for rare liver diseases: the case of glycosylation defects mimicking Wilson Disease. Clin Res Hepatol Gastroenterol. 2014;38:403-406. [PMID: 24972800 DOI: 10.1016/j.clinre.2014.04.012] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
26 Lamireau T, Mclin V, Nobili V, Vajro P. A practical approach to the child with abnormal liver tests. Clinics and Research in Hepatology and Gastroenterology 2014;38:259-62. [DOI: 10.1016/j.clinre.2014.02.010] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 0.9] [Reference Citation Analysis]
27 Serdaroğlu F, Koca T, Dereci S, Akçam M. The etiology of hypertransaminasemia in Turkish children. Bosn J Basic Med Sci 2016;16:151-6. [PMID: 26894285 DOI: 10.17305/bjbms.2016.982] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 0.5] [Reference Citation Analysis]
28 Pierri L, Saggese P, Guercio Nuzio S, Troisi J, Di Stasi M, Poeta M, Savastano R, Marchese G, Tarallo R, Massa G, Ciccone V, Ziegenhardt D, Cavallo P, Bergheim I, Weisz A, Vajro P. Relations of gut liver axis components and gut microbiota in obese children with fatty liver: A pilot study. Clin Res Hepatol Gastroenterol 2018;42:387-90. [PMID: 29773420 DOI: 10.1016/j.clinre.2018.03.015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
29 Gunzer S, Kraus A, Buchroth I, Grüneberg M, Westermann C, Biskup S, Reunert J, Grünewald I, Marquardt T. Hypertransaminasemia and liver fibrosis associated with haptoglobin retention and anhaptoglobinemia in a paediatric patient. Liver Int 2021. [PMID: 34358398 DOI: 10.1111/liv.15029] [Reference Citation Analysis]
30 Guirat Dhouib N, Khaled MB, Ouederni M, Besbes H, Mellouli F, Bejaoui M. Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell disease. Ann Hematol 2018;97:2261-2. [PMID: 29754272 DOI: 10.1007/s00277-018-3360-3] [Reference Citation Analysis]
31 Ku MC, Kok VC, Lee MY, Hsu SM, Lee PY, Chang CW, Tyan YS, Juan CW. Clinical analysis of contributors to the delayed gallbladder opacification following the use of water-soluble contrast medium.Ther Clin Risk Manag. 2016;12:1357-1364. [PMID: 27660453 DOI: 10.2147/TCRM.S116899] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
32 Vajro P, Zielinska K, Ng BG, Maccarana M, Bengtson P, Poeta M, Mandato C, D'Acunto E, Freeze HH, Eklund EA. Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation. Orphanet J Rare Dis 2018;13:4. [PMID: 29321044 DOI: 10.1186/s13023-017-0757-3] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
33 Arnal IR, Andrade JR, Hally MM, Baviera LCB, Tirado DG, Martín SHC, de la Calle Navarro E, Álvarez AMV. Diagnostic action against hypertransaminasemia in paediatrics: Consensus document of Sociedad Española de Gastroenterología, Hepatología y Nutrición Pediátrica (SEGHNP), Asociación Española de Pediatría de Atención Primaria (AEPap) and Sociedad Española de Pediatría de Atención Primaria (SEPEAP). Anales de Pediatría (English Edition) 2022. [DOI: 10.1016/j.anpede.2022.04.009] [Reference Citation Analysis]
34 Van Hoeve K, Mekahli D, Morava E, Levtchenko E, Witters P. Liver involvement in kidney disease and vice versa. Pediatr Nephrol 2018;33:957-71. [DOI: 10.1007/s00467-017-3715-3] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]
35 Yang CH, Perumpail BJ, Yoo ER, Ahmed A, Kerner JA Jr. Nutritional Needs and Support for Children with Chronic Liver Disease. Nutrients 2017;9:E1127. [PMID: 29035331 DOI: 10.3390/nu9101127] [Cited by in Crossref: 22] [Cited by in F6Publishing: 13] [Article Influence: 4.4] [Reference Citation Analysis]
36 Mantri R, Bavdekar SB, Save SU. Congenital Hypothyroidism: An Unusual Combination of Biochemical Abnormalities. Case Rep Pediatr 2016;2016:2678578. [PMID: 27994903 DOI: 10.1155/2016/2678578] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
37 Siano MA, Mandato C, Nazzaro L, Iannicelli G, Ciccarelli GP, Barretta F, Mazzaccara C, Ruoppolo M, Frisso G, Baldi C, Tartaglione S, Di Salle F, Melis D, Vajro P. Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic Review. Front Pediatr 2021;9:672004. [PMID: 34041209 DOI: 10.3389/fped.2021.672004] [Reference Citation Analysis]
38 Vajro P. Transaminases and Pediatric Nonalcoholic Fatty Liver Disease Diagnosis. J Pediatr Gastroenterol Nutr 2017;65:e114. [PMID: 29064931 DOI: 10.1097/MPG.0000000000001668] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]