Academic Content and Language Evaluation of This Article
CrossCheck and Google Search of This Article
Academic Rules and Norms of This Article
Citation of this article
Corresponding Author of This Article
Research Domain of This Article
Article-Type of This Article
Open-Access Policy of This Article
Times Cited Counts in Google of This Article
Number of Hits and Downloads for This Article
- Total Article Views (17430)
All Articles published online
|
Featured Article
|
Publishing Process of This Article
|
Jul 7, 2023 (publication date) through Feb 24, 2025
Times Cited of This Article
Journal Information of This Article
Publication Name
World Journal of Gastroenterology
ISSN
1007-9327
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Gümüş E, Özen H. Glycogen storage diseases: An update. World J Gastroenterol 2023; 29(25): 3932-3963 [PMID: PMC10354582 DOI: 10.3748/wjg.v29.i25.3932] |
|---|---|
| URL: | https://www.wjgnet.com/2307-8960/full/v29/i25/3932.htm |
| Number | Citing Articles |
| 1 |
Matthieu Colpaert, Pankaj K. Singh, Katherine J. Donohue, Natacha T. Pires, David D. Fuller, Manuela Corti, Barry J. Byrne, Ramon C. Sun, Craig W. Vander Kooi, Matthew S. Gentry. Neurological glycogen storage diseases and emerging therapeutics. Neurotherapeutics 2024; 21(5): e00446 doi: 10.1016/j.neurot.2024.e00446
|
| 2 |
Sema Kalkan Uçar, Yasemin Atik Altınok, Yelda Mansuroglu, Ebru Canda, Havva Yazıcı, Merve Yoldaş Çelik, Fehime Erdem, Ayşe Yüksel Yanbolu, Zülal Ülger, Mahmut Çoker. Long‐term personalized high‐protein, high‐fat diet in pediatric patients with glycogen storage disease type IIIa: Evaluation of myopathy, metabolic control, physical activity, growth, and dietary compliance. Journal of Inherited Metabolic Disease 2024; 47(5): 1001 doi: 10.1002/jimd.12741
|
| 3 |
Snigdha Verma, Vikrant Sood, Bikrant B. Lal, Rajeev Khanna, Seema Alam. Metabolic Liver Diseases Presenting as Pediatric Onset Hypoglycemia: A Hepatologist's Primer. Journal of Clinical and Experimental Hepatology 2025; 15(1): 102425 doi: 10.1016/j.jceh.2024.102425
|
| 4 |
Andrey N. Surkov, Leyla S. Namazova-Baranova, Anna L. Arakelyan, Evgeny E. Bessonov, Natalia V. Zhurkova. Sodium-Dependent Glucose Transporter Type 2 Inhibitors as a Breakthrough in Neutropenia and Neutrophil Dysfunction Management in Patients with Glycogen Storage Disease Type Ib. Current Pediatrics 2024; 23(3): 162 doi: 10.15690/vsp.v23i3.2761
|
| 5 |
Xiaotang Du, Hanlin L. Wang. Rare Liver Diseases With Near-Normal Histology: A Review Focusing on Metabolic, Storage, and Inclusion Disorders. Advances in Anatomic Pathology 2025; doi: 10.1097/PAP.0000000000000488
|
| 6 |
Hülya Gözde Önal, Hülya Nalçacıoğlu, Işıl Özer, Demet Tekcan Karalı. The Efficacy and Outcomes of Renal Replacement Therapy in Pediatric Metabolic Disorders. Journal of Clinical Medicine 2024; 13(21): 6452 doi: 10.3390/jcm13216452
|
| 7 |
Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel. Neuromuscular Disorders. 2024; : 465 doi: 10.1007/978-981-97-9010-4_31
|
| 8 |
Motoaki YUHI, Tomokazu TANAKA, Hiro MATSUURA, Kotaro ITO, Takao IDE, Hirokazu NOSHIRO. Laparoscopic Liver Resection for Hepatocellular Carcinoma Associated with Hepatic Glycogen Storage Disease—A Case Report—. Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association) 2024; 85(7): 945 doi: 10.3919/jjsa.85.945
|
| 9 |
Rafael de Marchi, Tatiele Nalin, Fernanda Sperb-Ludwig, Franciele Pinheiro, Ida Schwartz, Carlos Steiner. Glycogen Storage Disease: Expert Opinion on Clinical Diagnosis Revisited after Molecular Testing. Genes 2023; 14(12): 2219 doi: 10.3390/genes14122219
|
| 10 |
Giorgia Gugelmo, Evelina Maines, Federico Boscari, Livia Lenzini, Gian Paolo Fadini, Alberto Burlina, Angelo Avogaro, Nicola Vitturi. Continuous glucose monitoring in patients with inherited metabolic disorders at risk for Hypoglycemia and Nutritional implications. Reviews in Endocrine and Metabolic Disorders 2024; 25(5): 897 doi: 10.1007/s11154-024-09903-y
|
| 11 |
Marina Parezanovic, Nina Stevanovic, Marina Andjelkovic, Milena Ugrin, Sonja Pavlovic, Maja Stojiljkovic, Anita Skakic. Phenylbutyric Acid Modulates Apoptosis and ER Stress‐Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model. Molecular Genetics & Genomic Medicine 2025; 13(1) doi: 10.1002/mgg3.70054
|
| 12 |
Ana Isabel Beltran-Velasco. Brain Glycogen—Its Metabolic Role in Neuronal Health and Neurological Disorders—An Extensive Narrative Review. Metabolites 2025; 15(2): 128 doi: 10.3390/metabo15020128
|
| 13 |
Sara J. Edmund, Beth Ann Heuer. Metabolic myopathies series part 1: What we need to know. Journal of the American Association of Nurse Practitioners 2025; 37(2): 85 doi: 10.1097/JXX.0000000000001103
|
| 14 |
I. F. Fedoseeva, T. V. Poponnikova, O. S. Pinevich. Myopathy in glycogen storage disease type IV: case report of a family. Bulletin of Siberian Medicine 2024; 23(3): 172 doi: 10.20538/1682-0363-2024-3-172-177
|
| 15 |
Naiyu Chen, Shulei Wang, Yajie Yin, Guoling Ren, Yiting Zhang, Lina Qu, Lei Ling. Genome-wide identification of the AAAP gene family and expression analysis under tissue-specific expression in five legumes. BMC Genomics 2025; 26(1) doi: 10.1186/s12864-025-11224-6
|
| 16 |
Parinaz Moghimi, Farzad Hashemi-Gorji, Sanaz Jamshidi, Sahand Tehrani Fateh, Shadab Salehpour, Hossein Sadeghi, Fatemeh Norouzi Rostami, Reza Mirfakhraie, Mohammad Miryounesi, Mohammad-Reza Ghasemi. Broadening the Phenotype and Genotype Spectrum of Glycogen Storage Disease by Unraveling Novel Variants in an Iranian Patient Cohort. Biochemical Genetics 2024; doi: 10.1007/s10528-024-10787-5
|
| 17 |
Chandrashekar Yashaswini, Neelakanta Sarvashiva Kiran, Ankita Chatterjee. Zebrafish navigating the metabolic maze: insights into human disease – assets, challenges and future implications. Journal of Diabetes & Metabolic Disorders 2024; 24(1) doi: 10.1007/s40200-024-01539-8
|
| 18 |
Moyra Smith. Genetic Disease Discovery and Therapeutics. 2025; : 81 doi: 10.1016/B978-0-443-23648-8.00004-8
|
| 19 |
Urszula Krekora, Akash Mathavan, Akshay Mathavan, Ali Ataya. Glycogen storage disease type V: delayed diagnosis of a cause of exercise intolerance in a patient with hereditary haemorrhagic telangiectasia. BMJ Case Reports 2025; 18(2): e263586 doi: 10.1136/bcr-2024-263586
|
| 20 |
Kumudesh Mishra, Or Kakhlon. Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs). Biomolecules 2024; 14(9): 1096 doi: 10.3390/biom14091096
|
| 21 |
Tamer A. Addissouky. Polyploidy-mediated resilience in hepatic aging: molecular mechanisms and functional implication. Egyptian Liver Journal 2024; 14(1) doi: 10.1186/s43066-024-00391-y
|
| 22 |
Ewa Stefanik, Magda Dubińska-Magiera, Damian Lewandowski, Małgorzata Daczewska, Marta Migocka-Patrzałek. Metabolic aspects of glycogenolysis with special attention to McArdle disease. Molecular Genetics and Metabolism 2024; 142(4): 108532 doi: 10.1016/j.ymgme.2024.108532
|
| 23 |
Riya Patel, Smriti Nair, Hassaam Choudhry, Mustafa Jaffry, Mohammad Dastjerdi. Ocular manifestations of liver disease: an important diagnostic aid. International Ophthalmology 2024; 44(1) doi: 10.1007/s10792-024-03103-y
|
| 24 |
Ayesha Abid, Eman Nasir, Hassaan Mehboob Awan. In silico analysis of point mutation (c.687dupC; p. Met230Hisfs∗6) in PGAM2 gene that causes Glycogen Storage Disease (GSD) Type X. Kuwait Journal of Science 2025; 52(1): 100344 doi: 10.1016/j.kjs.2024.100344
|
| 25 |
Silvia Vai, Alberto Falchetti, Sabrina Corbetta, Maria Luisa Bianchi, Chiara Alberio, Silvia Carrara, Serena Gasperini, Roberta Pretese, Loredana Parisi, Anna Teti, Antonio Maurizi. Glycogen Storage Disease Type I and Bone: Clinical and Cellular Characterization. Calcified Tissue International 2024; 115(5): 661 doi: 10.1007/s00223-024-01302-4
|
| 26 |
Arne S. Schaefer, Luigi Nibali, Noha Zoheir, Niki M. Moutsopoulos, Bruno G. Loos. Genetic risk variants implicate impaired maintenance and repair of periodontal tissues as causal for periodontitis—A synthesis of recent findings. Periodontology 2000 2025; doi: 10.1111/prd.12622
|
| 27 |
Colin Walsh, Sha Jin. Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage Diseases. Cells 2024; 13(12): 1052 doi: 10.3390/cells13121052
|
| 28 |
Nethika R. Ariyasinghe, Divya Gupta, Sean Escopete, Deepika Rai, Aleksandr Stotland, Niveda Sundararaman, Benjamin Ngu, Kruttika Dabke, Liam McCarthy, Roberta S. Santos, Megan L. McCain, Dhruv Sareen, Sarah J. Parker. Identification of Disease-Relevant, Sex-Based Proteomic Differences in iPSC-Derived Vascular Smooth Muscle Cells. International Journal of Molecular Sciences 2024; 26(1): 187 doi: 10.3390/ijms26010187
|