BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
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]
URL: https://www.wjgnet.com/1948-5182/full/v19/i18/2740.htm
Number Citing Articles
1
Markéta Veverková, Jakub Pecl, Tereza Pinkasová, Zdeňka Čermáková, Petr Jabandžiev. Macro-AST as a cause of isolated increase of aspartate aminotransferase in an asymptomatic patientPediatrie pro praxi 2021; 22(1): 59 doi: 10.36290/ped.2021.010
2
Sagar Mehta, Tomisin John, Jordan J. Feld, Hemant Shah, Nisa Mullaithilaga, Aaron Campigotto, Karen Leung, Binita M. Kamath, Simon C. Ling, Michelle Science, Vicky L. Ng. Severe acute hepatitis of unknown etiology in a large cohort of childrenHepatology Communications 2023; 7(10) doi: 10.1097/HC9.0000000000000272
3
Marta Alonso‐Peña, Ricardo Espinosa‐Escudero, Elisa Herraez, Oscar Briz, Maria Luisa Cagigal, Jesus M. Gonzalez‐Santiago, Aida Ortega‐Alonso, Conrado Fernandez‐Rodriguez, Luis Bujanda, Marta Calvo Sanchez, Delia D´Avola, Maria‐Carlota Londoño, Moises Diago, Jose C. Fernandez‐Checa, Carmen Garcia‐Ruiz, Raul J. Andrade, Frank Lammert, Jesus Prieto, Javier Crespo, Javier Juamperez, Alvaro Diaz‐Gonzalez, Maria J. Monte, Jose J. G. Marin. Beneficial effect of ursodeoxycholic acid in patients with acyl‐CoA oxidase 2 (ACOX2) deficiency–associated hypertransaminasemiaHepatology 2022; 76(5): 1259 doi: 10.1002/hep.32517
4
Jacopo Troisi, Federica Belmonte, Antonella Bisogno, Luca Pierri, Angelo Colucci, Giovanni Scala, Pierpaolo Cavallo, Claudia Mandato, Antonella Di Nuzzi, Laura Di Michele, Anna Delli Bovi, Salvatore Guercio Nuzio, Pietro Vajro. Metabolomic Salivary Signature of Pediatric Obesity Related Liver Disease and Metabolic SyndromeNutrients 2019; 11(2): 274 doi: 10.3390/nu11020274
5
Naouel Guirat Dhouib, Monia Ben Khaled, Monia Ouederni, Habib Besbes, Fethi Mellouli, Mohamed Bejaoui. Hypertransaminasemia revealing a clinically silent muscular dystrophy in a child with sickle cell diseaseAnnals of Hematology 2018; 97(11): 2261 doi: 10.1007/s00277-018-3360-3
6
Pietro Vajro. Transaminases and Pediatric Nonalcoholic Fatty Liver Disease DiagnosisJournal of Pediatric Gastroenterology and Nutrition 2017; 65(5) doi: 10.1097/MPG.0000000000001668
7
Denisa Pilic. Praktisches Vorgehen zur Abklärung erhöhter LeberwertePädiatrie 2022; 34(2): 36 doi: 10.1007/s15014-022-3980-x
8
Víctor Fernández Ventureira, Ignacio Ros Arnal, Gerardo Rodríguez Martínez, Beatriz García Rodríguez, Ruth García Romero, Eduardo Ubalde Sainz. Evaluation of liver function tests in the paediatric patientAnales de Pediatría (English Edition) 2021; 94(6): 359 doi: 10.1016/j.anpede.2020.06.014
9
Linnea Aitokari, Pauliina Hiltunen, Heini Huhtala, Kalle Kurppa, Laura Kivelä. Measurement practices of alanine aminotransferase in children: Temporal changes and etiology for increased valuesJournal of Pediatric Gastroenterology and Nutrition 2024;  doi: 10.1002/jpn3.12167
10
Sarah Bussler, Mandy Vogel, Diana Pietzner, Kristian Harms, Theresa Buzek, Melanie Penke, Norman Händel, Antje Körner, Ulrich Baumann, Wieland Kiess, Gunter Flemming. New pediatric percentiles of liver enzyme serum levels (alanine aminotransferase, aspartate aminotransferase, γ‐glutamyltransferase): Effects of age, sex, body mass index, and pubertal stageHepatology 2018; 68(4): 1319 doi: 10.1002/hep.29542
11
Yu.M. Stepanov, N.Yu. Zavhorodnia, O.Yu. Zavhorodnia. 1GASTROENTEROLOGY 2021; 55(1): 42 doi: 10.22141/2308-2097.55.1.2021.229435
12
Aslıhan SANRI, Ceyda TUNA KIRSAÇLIOĞLU, Emre SANRI, Tülin Revide ŞAYLI. Etiological evaluation of the elevated transaminases in childrenCumhuriyet Medical Journal 2020;  doi: 10.7197/cmj.vi.593477
13
Dieter Furthner, Daniel Weghuber, Christopher Dalus, Andreas Lukas, Hannah N. Stundner-Ladenhauf, Harald Mangge, Thomas Pixner. Nonalcoholic Fatty Liver Disease in Children with Obesity: Narrative Review and Research GapsHormone Research in Paediatrics 2022; 95(2): 167 doi: 10.1159/000518595
14
ELAINE S. XIE, NIKHIL PAI, MICHELLE BATTHISH. Limited GPA and Alpha-1 Antitrypsin Deficiency in a Pediatric PatientThe Journal of Rheumatology 2019; 46(5): 543 doi: 10.3899/jrheum.180979
15
Ignacio Ros Arnal, Joaquín Reyes Andrade, María Mercadal Hally, Luis Carlos Blesa Baviera, Diana García Tirado, Samuel Héctor Campuzano Martín, Estela de la Calle Navarro, Ana María Vegas Álvarez. 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; 96(5): 448.e1 doi: 10.1016/j.anpede.2022.04.009
16
Resthie R. Putri, Thomas Casswall, Emilia Hagman. Prevalence of increased transaminases and its association with sex, age, and metabolic parameters in children and adolescents with obesity – a nationwide cross-sectional cohort studyBMC Pediatrics 2021; 21(1) doi: 10.1186/s12887-021-02747-4
17
Mario Giordano, Onofrio Iacoviello, Luisa Santangelo, Marida Martino, Diletta Torres, Vincenza Carbone, Gaia Scavia, Daniela Loconsole, Maria Chironna, Fernanda Cristofori, Ruggiero Francavilla. Gastrointestinal involvement in STEC-associated hemolytic uremic syndrome: 10 years in a pediatric centerPediatric Nephrology 2024;  doi: 10.1007/s00467-023-06258-5
18
Ignacio Ros Arnal, Joaquín Reyes Andrade, María Mercadal Hally, Luis Carlos Blesa Baviera, Diana García Tirado, Samuel Héctor Campuzano Martín, Estela de la Calle Navarro, Ana María Vegas Álvarez. Actuación diagnóstica ante hipertransaminasemia en pediatría: documento de consenso de Sociedad Española de Gastroenterología, Hepatología y Nutrición Pediátrica (SEGHNP), Asociación Española de Pediatría de Atención Primaria (AEPap) y Sociedad Española de Pediatría de Atención Primaria (SEPEAP)Anales de Pediatría 2022; 96(5): 448.e1 doi: 10.1016/j.anpedi.2022.04.002
19
Zhisheng Wei, Yeqing Huang, Aiqun Liu, Shengpeng Diao, Qingyun Yu, Zhongxing Peng, Mingfan Hong. Mutational characterization of ATP7B gene in 103 Wilson’s disease patients from Southern ChinaNeuroReport 2014; 25(14): 1075 doi: 10.1097/WNR.0000000000000216
20
Víctor Fernández Ventureira, Ignacio Ros Arnal, Gerardo Rodríguez Martínez, Beatriz García Rodríguez, Ruth García Romero, Eduardo Ubalde Sainz. Evaluación del seguimiento de niños con hallazgo de hipertransaminasemiaAnales de Pediatría 2021; 94(6): 359 doi: 10.1016/j.anpedi.2020.06.019
21
Franco Curci, Mariangela Stinco, Simona Carrera, Chiara Rubino, Giuseppe Indolfi. Diagnostic approach for children with increased serum concentrations of aminotransferasesGlobal Pediatrics 2024; 7: 100118 doi: 10.1016/j.gpeds.2023.100118
22
Christine Yang, Brandon Perumpail, Eric Yoo, Aijaz Ahmed, John Kerner Jr.. Nutritional Needs and Support for Children with Chronic Liver DiseaseNutrients 2017; 9(10): 1127 doi: 10.3390/nu9101127
23
Priyanka Udawat, Shambhavi -, S Sitaraman. Clinico-etiological profile of raised aminotransferases in hospitalized children with liver disease and correlation with their severity levelIndian Journal of Child Health 2017; 4(3): 359 doi: 10.32677/IJCH.2017.v04.i03.020
24
Le Anh Tuan Pham, Trong Tue Nguyen, Hoang Bich Nga Le, Dat Quoc Tran, Cam Tu Ho, Thinh Huy Tran, Van Thanh Ta, The Hung Bui, Van Khanh Tran. Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7BJournal of Genetics 2017; 96(6): 933 doi: 10.1007/s12041-017-0857-9
25
Taoufik Ben Houmich, Brahim Admou. Celiac disease: Understandings in diagnostic, nutritional, and medicinal aspectsInternational Journal of Immunopathology and Pharmacology 2021; 35: 205873842110087 doi: 10.1177/20587384211008709
26
Henrik Arnell, Björn Fischler. Pediatric Hepatology and Liver Transplantation2019; : 57 doi: 10.1007/978-3-319-96400-3_4
27
Claudio Veropalumbo, Angelo Campanozzi, Fabiola De Gregorio, Antonio Correra, Valeria Raia, Pietro Vajro. Shwachman-Diamond syndrome with autoimmune-like liver disease and enteropathy mimicking celiac diseaseClinics and Research in Hepatology and Gastroenterology 2015; 39(1): e1 doi: 10.1016/j.clinre.2014.06.017
28
Piotr Socha, Pietro Vajro, Dirk Lefeber, Maciej Adamowicz, Stuart Tanner. Search for rare liver diseases: The case of glycosylation defects mimicking Wilson Disease ->Clinics and Research in Hepatology and Gastroenterology 2014; 38(4): 403 doi: 10.1016/j.clinre.2014.04.012
29
Maria Anna Siano, Claudia Mandato, Lucia Nazzaro, Gennaro Iannicelli, Gian Paolo Ciccarelli, Ferdinando Barretta, Cristina Mazzaccara, Margherita Ruoppolo, Giulia Frisso, Carlo Baldi, Salvatore Tartaglione, Francesco Di Salle, Daniela Melis, Pietro Vajro. Hepatic Presentation of Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Case Report and Systematic ReviewFrontiers in Pediatrics 2021; 9 doi: 10.3389/fped.2021.672004
30
Diletta Valentini, Anna Alisi, Chiara di Camillo, Maria Rita Sartorelli, Annalisa Crudele, Andrea Bartuli, Valerio Nobili, Alberto Villani. Nonalcoholic Fatty Liver Disease in Italian Children with Down Syndrome: Prevalence and Correlation with Obesity-Related FeaturesThe Journal of Pediatrics 2017; 189: 92 doi: 10.1016/j.jpeds.2017.05.077
31
J.I. Fortea, C. Rodríguez de Lope, S. Álvarez, J. Crespo Gracía. Protocolo diagnóstico de la elevación aguda de las transaminasas en el paciente inmunocompetenteMedicine - Programa de Formación Médica Continuada Acreditado 2016; 12(9): 529 doi: 10.1016/j.med.2016.04.007
32
Carolyne Ghobrial, Nehal Abdelhamid, Hanaa El-Karaksy. Incidental hypertransaminasemia in children: Potential delay in diagnosis of muscle diseaseEgyptian Pediatric Association Gazette 2018; 66(4): 112 doi: 10.1016/j.epag.2018.09.002
33
Joana Meneses Costa, Sara Martins Pinto, Ermelinda Santos-Silva, Helena Moreira-Silva. Incidental hypertransaminasemia in children—a stepwise approach in primary careEuropean Journal of Pediatrics 2023; 182(4): 1601 doi: 10.1007/s00431-023-04825-4
34
Luca Pierri, Pasquale Saggese, Salvatore Guercio Nuzio, Jacopo Troisi, Martina Di Stasi, Marco Poeta, Riccardo Savastano, Giovanna Marchese, Roberta Tarallo, Grazia Massa, Vincenzo Ciccone, Doreen Ziegenhardt, Pierpaolo Cavallo, Ina Bergheim, Alessandro Weisz, Pietro Vajro. Relations of gut liver axis components and gut microbiota in obese children with fatty liver: A pilot studyClinics and Research in Hepatology and Gastroenterology 2018; 42(4): 387 doi: 10.1016/j.clinre.2018.03.015
35
Brahim Admou, Wissal Zkhiri, Morad Guennouni, Raja Hazime. Maladie cœliaque : une pathologie au carrefour de la médecine, de la diététique et de la pharmaceutiqueLa Presse Médicale Formation 2021; 2(6): 580 doi: 10.1016/j.lpmfor.2021.10.005
36
Valeria Casotti, Lorenzo D’Antiga. Pediatric Hepatology and Liver Transplantation2019; : 3 doi: 10.1007/978-3-319-96400-3_1
37
Naoki Tanaka, Takefumi Kimura, Naoyuki Fujimori, Yasuyuki Ichise, Kenji Sano, Akira Horiuchi. Non-alcoholic fatty liver disease later diagnosed as myotonic dystrophyWorld Journal of Hepatology 2020; 12(9): 685-692 doi: 10.4254/wjh.v12.i9.685
38
Meryem KEÇELİ BAŞARAN, Tuba ÇİÇEK. Causes of hypertransaminasemia in children, single-center experienceFamily Practice and Palliative Care 2021; 6(1): 56 doi: 10.22391/fppc.787707
39
Annarita BONGIOVANNI, Massimo SPINA, Maria PAPALE, Ilaria BRAMBILLA, Amelia LICARI, Giuseppe F. PARISI, Salvatore LEONARDI. Hypertransaminasemia in children is not always as simple as it seemsMinerva Pediatrics 2021; 73(3) doi: 10.23736/S2724-5276.19.05514-2
40
Sophia Gunzer, Andreas Kraus, Inka Buchroth, Marianne Grüneberg, Cordula Westermann, Saskia Biskup, Janine Reunert, Inga Grünewald, Thorsten Marquardt. Hypertransaminasemia and liver fibrosis associated with haptoglobin retention and anhaptoglobinemia in a paediatric patientLiver International 2021; 41(10): 2427 doi: 10.1111/liv.15029
41
Claudia Mandato, Pietro Vajro. Isolated aspartate aminotransferase elevation: Is it liver disease or what else?Acta Paediatrica 2022; 111(3): 459 doi: 10.1111/apa.16213
42
Diane Hsu, Rohit Josyabhatla, Iona M. Monteiro. Case 3: Persistent Elevated Transaminase Levels in a 9-year-old BoyPediatrics in Review 2019; 40(12): 643 doi: 10.1542/pir.2018-0022
43
Pamela Paglia, Lucia Nazzaro, Anna Giulia Elena De Anseris, Milena Lettieri, Rossella Colantuono, Maria Chiara Rocco, Maria Anna Siano, Nicola Biffaro, Pietro VAJRO. Atypically Protracted Course of Liver Involvement in Kawasaki Disease. Case Report and Literature ReviewPediatric Reports 2021; 13(3): 357 doi: 10.3390/pediatric13030044
44
Thierry Lamireau, Valérie McLin, Valério Nobili, Pietro Vajro. A practical approach to the child with abnormal liver testsClinics and Research in Hepatology and Gastroenterology 2014; 38(3): 259 doi: 10.1016/j.clinre.2014.02.010
45
Magnus J Johansen, Julie Gade, Stefan Stender, Christine Frithioff-Bøjsøe, Morten A V Lund, Elizaveta Chabanova, Henrik S Thomsen, Oluf Pedersen, Cilius E Fonvig, Torben Hansen, Jens-Christian Holm. The Effect of Overweight and Obesity on Liver Biochemical Markers in Children and AdolescentsThe Journal of Clinical Endocrinology & Metabolism 2020; 105(2): 430 doi: 10.1210/clinem/dgz010
46
Renata Alfani, Edoardo Vassallo, Anna De Anseris, Lucia Nazzaro, Ida D'Acunzo, Carolina Porfito, Claudia Mandato, Pietro Vajro. Pediatric Fatty Liver and Obesity: Not Always Justa Matter of Non-Alcoholic Fatty Liver DiseaseChildren 2018; 5(12): 169 doi: 10.3390/children5120169
47
Yoon Lee, Dae Yong Yi, Yoo Min Lee, So Yoon Choi, You Jin Choi, Kyung Jae Lee. A Multicenter Study of Real-world Practice for Management of Abnormal Liver Function Tests in Children with Acute Infectious DiseasesJournal of Korean Medical Science 2021; 36(47) doi: 10.3346/jkms.2021.36.e310
48
Seracettin Eğin, Kurtuluş Açıksarı, Gülçin Ercan, Fatih A. Aydın, Esra Aycan Üstyol, Mediha Eser, Gamze Tanrıverdi, Hakan Teoman Yanar. Effects of pentoxifylline on oxidative stress in rats with abdominal compartment syndrome modelInternational Journal of Surgery Open 2016; 5: 5 doi: 10.1016/j.ijso.2016.09.001
49
Ruchi Mantri, S. B. Bavdekar, Sushma U. Save. Congenital Hypothyroidism: An Unusual Combination of Biochemical AbnormalitiesCase Reports in Pediatrics 2016; 2016: 1 doi: 10.1155/2016/2678578
50
Wolfgang Kamin, Ortwin Adams, Peter Kardos, Heinrich Matthys, Norbert Meister, Christian P. Strassburg. Liver Involvement in Acute Respiratory Infections in Children and Adolescents – Results of a Non-interventional StudyFrontiers in Pediatrics 2022; 10 doi: 10.3389/fped.2022.840008
51
Angelo Colucci, Maria Chiara Rocco, Anna Giulia Elena De Anseris, Lucia Nazzaro, Pietro Vajro, Claudia Mandato. Pediatric vs. adult NAFLD to MAFLD transition: a welcome but tangled pathExploration of Medicine 2021;  doi: 10.37349/emed.2021.00051
52
Maria Grazia Clemente, Claudia Mandato, Marco Poeta, Pietro Vajro. Pediatric non-alcoholic fatty liver disease: Recent solutions, unresolved issues, and future research directionsWorld Journal of Gastroenterology 2016; 22(36): 8078-8093 doi: 10.3748/wjg.v22.i36.8078
53
Karen Van Hoeve, Djalila Mekahli, Eva Morava, Elena Levtchenko, Peter Witters. Liver involvement in kidney disease and vice versaPediatric Nephrology 2018; 33(6): 957 doi: 10.1007/s00467-017-3715-3
54
Yunfei Luo, Hui Lin. Inflammation initiates a vicious cycle between obesity and nonalcoholic fatty liver diseaseImmunity, Inflammation and Disease 2021; 9(1): 59 doi: 10.1002/iid3.391
55
U. Baumann. Differenzialdiagnostik bei persistierender Erhöhung der TransaminasenkonzentrationenMonatsschrift Kinderheilkunde 2015; 163(2): 167 doi: 10.1007/s00112-014-3267-6
56
Pietro Vajro, Katarzyna Zielinska, Bobby G. Ng, Marco Maccarana, Per Bengtson, Marco Poeta, Claudia Mandato, Elisa D’Acunto, Hudson H. Freeze, Erik A. Eklund. Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylationOrphanet Journal of Rare Diseases 2018; 13(1) doi: 10.1186/s13023-017-0757-3