BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Sen Sarma M, Tripathi PR. Natural history and management of liver dysfunction in lysosomal storage disorders. World J Hepatol 2022; 14(10): 1844-1861 [PMID: 36340750 DOI: 10.4254/wjh.v14.i10.1844]
URL: https://www.wjgnet.com/1948-5182/full/v14/i10/1844.htm
Number Citing Articles
1
Pasquale Piccolo, Nicola Brunetti-Pierri. Current and Emerging Issues in Adeno-Associated Virus Vector-Mediated Liver-Directed Gene TherapyHuman Gene Therapy 2025; 36(3-4) doi: 10.1089/hum.2024.179
2
Nato D. Vashakmadze, Nataliya V. Zhurkova. Niemann-Pick Disease: Seven Questions about itCurrent Pediatrics 2024; 22(6) doi: 10.15690/vsp.v22i6.2702
3
N. N. Martynovich, A. N. Kolchina. Clinical polymorphism of storage diseases: A diferential diagnostic algorithmMeditsinskiy sovet = Medical Council 2025; (11) doi: 10.21518/ms2025-217
4
Yan Zhou, Juan Putra. Practical Liver PathologyPractical Anatomic Pathology 2025;  doi: 10.1007/978-3-031-97506-6_2
5
Ana Lancho Muñoz, Paula Iglesias Conejero, María Ángeles López Garrido, Patricia Becerra Massare, Eduardo Redondo Cerezo. The role of lysosomal acid lipase deficiency in dyslipidemia and liver disordersRevista Española de Enfermedades Digestivas 2025;  doi: 10.17235/reed.2025.11007/2024
6
Hsu‐Heng Lin, Hui‐An Chen, Shyh‐Jer Lin, Rai‐Hseng Hsu, Ni‐Chung Lee, Wuh‐Liang Hwu, Yen‐Hsuan Ni, Yen‐Yin Chou, Pao‐Chin Chiu, Steven Shinn‐Forng Peng, Yin‐Hsiu Chien. Pathogenic Variants and Olipudase Alfa Treatment of Patients With Acid Sphingomyelinase Deficiency in TaiwanMolecular Genetics & Genomic Medicine 2026; 14(2) doi: 10.1002/mgg3.70204
7
Trinh Van Le, Nhung Hai Truong, Ai Xuan L. Holterman. Autophagy modulates physiologic and adaptive response in the liverLiver Research 2023; 7(4) doi: 10.1016/j.livres.2023.12.001
8
Patryk Lipiński, Anna Tylki-Szymańska. The Liver and Lysosomal Storage Diseases: From Pathophysiology to Clinical Presentation, Diagnostics, and TreatmentDiagnostics 2024; 14(12) doi: 10.3390/diagnostics14121299
9
Nataliya V. Zhurkova, Nato V. Vashakmadze, Andrey N. Surkov, Tatiana V. Turti, Kristina V. Bogdanova, Yuliya Yu. Kotalevskaya, Ekaterina Yu. Zakharova, Leyla S. Namazova-Baranova. Niemann-Pick Disease, Type A: Clinical Case of 5 Months Old PatientCurrent Pediatrics 2024; 23(3) doi: 10.15690/vsp.v23i3.2762
10
Moinak Sen Sarma, Arghya Samanta. Approach to a Child with Massive HepatomegalyAnnals of Pediatric Gastroenterology and Hepatology ISPGHAN 2024; 5(4) doi: 10.5005/jp-journals-11009-0147
11
Raluca Maria Vlad, Ruxandra Dobritoiu, Daniela Pacurar. From Genes to Treatment: Literature Review and Perspectives on Acid Sphingomyelinase Deficiency in ChildrenDiagnostics 2025; 15(7) doi: 10.3390/diagnostics15070804
12
Tarekegn Hiwot, Forbes D. Porter, Tatiana Bremova‐Ertl, Uma Ramaswami, Caroline Hastings, Bénédicte Héron, Justin Hopkin, Joella Melville, Hernan Amartino, Mireia del Toro, Federica Deodato, Fatih Ezgü, Paul Gissen, James B. Gibson, Can Ficicioglu, Roberto Giugliani, Orna Staretz‐Chacham, Frances Platt, Nathalie Guffon, Kristina Julich, Nikola Kresojević, Anna Lehman, Yann Nadjar, Susanne A. Schneider, Simon Jones, Eugen Mengel, Michel Tchan, Mark Walterfang, Ozlem Goker‐Alpan, Charlotte Dawson, Sandra Cowie, Toni Mathieson, Elizabeth Berry‐Kravis, Marc C. Patterson. 2025 Consensus Clinical Management Guidelines for Niemann‐Pick Disease Type CJournal of Inherited Metabolic Disease 2026; 49(3) doi: 10.1002/jimd.70185
13
Nadezhda N. Kotova, Vladimir A. Shcherbak, Natalia M. Shcherbak. Modern concepts about lysosomal acid lipase deficiency (review)Pediatrician (St. Petersburg) 2024; 15(2) doi: 10.17816/PED15263-70
14
G.V. Volynets, G.B. Movsisyan, A.S. Potapov, A.I. Khavkin, A.V. Nikitin, T.A. Skvortsova, E.A. Morozova, V.M. Rogozhina. Liver involvement in Gaucher disease in children: A literature review and clinical observationsRussian Journal of Evidence-Based Gastroenterology 2025; 14(2) doi: 10.17116/dokgastro20251402178
15
Kiri Koshu, Kazuhiro Muramatsu, Tomomi Maru, Yoshie Kurokawa, Yoshitaka Mizobe, Hirokazu Yamagishi, Daisuke Matsubara, Koji Yokoyama, Eriko Jimbo, Hideki Kumagai, Yukihiro Sanada, Yasunaru Sakuma, Noriyoshi Fukushima, Aya Narita, Takanori Yamagata, Hitoshi Osaka. Neonatal onset of Niemann-Pick disease type C in a patient with cholesterol re-accumulation in the transplanted liver and inflammatory bowel diseaseBrain and Development 2023; 45(9) doi: 10.1016/j.braindev.2023.06.006
16
Reza Heidari. Genetic Syndromes2023;  doi: 10.1007/978-3-319-66816-1_1776-1