For: | Gümüş E, Özen H. Glycogen storage diseases: An update. World J Gastroenterol 2023; 29(25): 3932-3963 [PMID: 37476587 DOI: 10.3748/wjg.v29.i25.3932] |
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URL: | https://www.wjgnet.com/1007-9327/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
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2 |
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
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3 |
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
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4 |
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
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5 |
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
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6 |
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
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7 |
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
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8 |
Moyra Smith. Genetic Disease Discovery and Therapeutics. 2025; : 81 doi: 10.1016/B978-0-443-23648-8.00004-8
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9 |
Kumudesh Mishra, Or Kakhlon. Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs). Biomolecules 2024; 14(9): 1096 doi: 10.3390/biom14091096
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10 |
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
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11 |
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
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12 |
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
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13 |
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
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14 |
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
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15 |
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
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16 |
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
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17 |
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
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