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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]
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 therapeuticsNeurotherapeutics 2024; 21(5): e00446 doi: 10.1016/j.neurot.2024.e00446
2
Siba Shanak, Shahd Abu Naim, Beesan AlArdah, Najlaa Bassalat, Hilal Zaid. Ligand-protein docking of phytochemicals in their plausible binding to alpha-amylase and alpha-glucosidase enzymes and ligand bioavailabilityFood Chemistry Advances 2025; 8: 101051 doi: 10.1016/j.focha.2025.101051
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 complianceJournal of Inherited Metabolic Disease 2024; 47(5): 1001 doi: 10.1002/jimd.12741
4
Yang Zhang, Liping Cui, Jian Gao, Yurong Song, Yijun Fan, Min Yang. Glycogen storage disease type Ia complicated by gestational hypertriglyceridemic pancreatitis: A rare case reportBMC Pregnancy and Childbirth 2025; 25(1) doi: 10.1186/s12884-025-08067-0
5
Snigdha Verma, Vikrant Sood, Bikrant B. Lal, Rajeev Khanna, Seema Alam. Metabolic Liver Diseases Presenting as Pediatric Onset Hypoglycemia: A Hepatologist's PrimerJournal of Clinical and Experimental Hepatology 2025; 15(1): 102425 doi: 10.1016/j.jceh.2024.102425
6
Mahsa M.Amoli, Forough Taheri, Akram Goharifar, Mehri Safari, Arash Salmaninejad. Interdisciplinary Advances in Endocrinology2025; : 11 doi: 10.1007/978-981-95-2286-6_2
7
Hülya Gözde Önal, Hülya Nalçacıoğlu, Işıl Özer, Demet Tekcan Karalı. The Efficacy and Outcomes of Renal Replacement Therapy in Pediatric Metabolic DisordersJournal of Clinical Medicine 2024; 13(21): 6452 doi: 10.3390/jcm13216452
8
Satish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel. Neuromuscular Disorders2024; : 465 doi: 10.1007/978-981-97-9010-4_31
9
Yasuo Amano, Mika Ishige, Maki Amano, Naoki Shinoda, Chisato Ando, Ryo Takagi. Pictorial Review of MRI Findings of Glycogen Storage Disease from Children to Young AdultsChildren 2025; 12(3): 295 doi: 10.3390/children12030295
10
Jungyun Han, Minjy Kim, Na Yeon Lee, Yunkoo Kang. Effects of Extended-Release Cornstarch Supplementation on Glycemic Stability and Metabolic Parameters in Korean Patients with Glycogen Storage DiseaseNutrients 2026; 18(7): 1094 doi: 10.3390/nu18071094
11
Rajat Kumar Shah, Sajjad Ahmed Khan, Dikshya Devkota, Manjisha Aryal, Nishan Subedi, Basna Aryal, Binita Gurubacharya, Shamin Parajuli, Ashwini Gupta, Surya Bahadur Parajuli, Huma Kausar. Glycogen Storage Disease in Twins: When Two Lives Reflect One Silent BattleClinical Case Reports 2026; 14(1) doi: 10.1002/ccr3.71889
12
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 implicationsReviews in Endocrine and Metabolic Disorders 2024; 25(5): 897 doi: 10.1007/s11154-024-09903-y
13
Eugene Looi, Helen M. Lawler. Non-Diabetic Hypoglycemia: Evaluation and Management in AdultsJournal of Clinical Medicine 2025; 14(13): 4393 doi: 10.3390/jcm14134393
14
Rula Al-Shahrabi, Ghadeera Al Mansoori, Muna Al-Saffar, Nadia Akawi. Metabolic perturbations in cardiomyopathies: implications for early diagnosis and targeted interventionsFrontiers in Cardiovascular Medicine 2025; 12 doi: 10.3389/fcvm.2025.1616677
15
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 ModelMolecular Genetics & Genomic Medicine 2025; 13(1) doi: 10.1002/mgg3.70054
16
Deniz Kor, Fatma Derya Bulut, Burcu Köşeci, Esra Kara, Ezgi Burgaç, İrem Kaplan, Nazmiye Tüzel Gündüz, Halise Neslihan Önenli Mungan. Clinical features and rare complications in 132 patients with hepatic glycogenosisOrphanet Journal of Rare Diseases 2025; 20(1) doi: 10.1186/s13023-025-03783-4
17
Faiq I Gorial, Nabaa Ihsan Awadh, Sara S Khunda, Sajjad Ghanim Al-Badri, Ali Falah Alibrahimi. Avascular necrosis as an uncommon manifestation in glycogen storage disease type III: diagnostic and therapeutic challengesOxford Medical Case Reports 2025; 2025(8) doi: 10.1093/omcr/omaf145
18
Nanobiomaterials and Nanomedicines for Metabolic Disorders2026; : 421 doi: 10.1016/B978-0-443-28942-2.00016-8
19
Sara J. Edmund, Beth Ann Heuer. Metabolic myopathies series part 1: What we need to knowJournal of the American Association of Nurse Practitioners 2025; 37(2): 85 doi: 10.1097/JXX.0000000000001103
20
I. F. Fedoseeva, T. V. Poponnikova, O. S. Pinevich. Myopathy in glycogen storage disease type IV: case report of a familyBulletin of Siberian Medicine 2024; 23(3): 172 doi: 10.20538/1682-0363-2024-3-172-177
21
Edoardo Santamato, Gian Pio Sorice, Miriam Grazioso, Sergio Di Molfetta, Luigi Laviola, Francesco Giorgino. Anomalie genetiche del metabolismo causa di ipoglicemiaL'Endocrinologo 2026; 27(1): 83 doi: 10.1007/s40619-026-01750-0
22
Chandrashekar Yashaswini, Neelakanta Sarvashiva Kiran, Ankita Chatterjee. Zebrafish navigating the metabolic maze: insights into human disease – assets, challenges and future implicationsJournal of Diabetes & Metabolic Disorders 2024; 24(1) doi: 10.1007/s40200-024-01539-8
23
Kumudesh Mishra, Or Kakhlon. Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs)Biomolecules 2024; 14(9): 1096 doi: 10.3390/biom14091096
24
Tamer A. Addissouky. Polyploidy-mediated resilience in hepatic aging: molecular mechanisms and functional implicationEgyptian Liver Journal 2024; 14(1) doi: 10.1186/s43066-024-00391-y
25
Mateo Chvatal-Medina, Yakun Li, María Camila Trillos-Almanza, Adrian Post, Margery A. Connelly, Han Moshage, Stephan J. L. Bakker, Vincent E. de Meijer, Hans Blokzijl, Robin P. F. Dullaart. Plasma Beta-Hydroxybutyrate and All-Cause Mortality in Patients with Liver CirrhosisBiomedicines 2025; 13(5): 1120 doi: 10.3390/biomedicines13051120
26
Nikol P. Shimkova, Mariya A. Snegurenko, Eva Yunkevich, Nataliya V. Klimina, Anastasiya A. Shepina, Lyubov E. Larina. Glycogen Storage Disease Type Ib in the Compound Heterozygous State: Case ReportPediatric pharmacology 2025; 22(2): 178 doi: 10.15690/pf.v22i2.2894
27
I. O. Panchuk, O. V. Grigorieva, E. V. Kondrateva, E. V. Kurshakova, I. O. Petrova, E. S. Voronina, V. O. Pozhitnova, O. A. Shchagina, V. Yu. Tabakov, T. V. Strokova, A. V. Lavrov, S. A. Smirnikhina, S. I. Kutsev. Generation of iPSC Lines from Family with Glycogen Storage Disease Type IaRussian Journal of Developmental Biology 2025; 56(1): 57 doi: 10.1134/S1062360425700067
28
Bianca Monti, Erica Ricci, Marcello Mariani, Alessio Mesini, Carolina Saffioti, Alessia Cafaro, Annalisa Madeo, Alessandro La Rosa, Giuliana Cangemi, Elio Castagnola. The ‘double hit’ on dalbavancin pharmacokinetics: hypertriglyceridaemia and augmented renal clearance in a child with glycogen storage disease type IbJournal of Antimicrobial Chemotherapy 2026; 81(3) doi: 10.1093/jac/dkag028
29
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 CharacterizationCalcified Tissue International 2024; 115(5): 661 doi: 10.1007/s00223-024-01302-4
30
Patryk Lipiński, Anna Doroba. The Usefulness of Basic Laboratory Analyses in Diagnostics of Inherited Metabolic Diseases in ChildrenDiagnostics 2025; 15(21): 2806 doi: 10.3390/diagnostics15212806
31
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 findingsPeriodontology 2000 2025;  doi: 10.1111/prd.12622
32
Colin Walsh, Sha Jin. Induced Pluripotent Stem Cells and CRISPR-Cas9 Innovations for Treating Alpha-1 Antitrypsin Deficiency and Glycogen Storage DiseasesCells 2024; 13(12): 1052 doi: 10.3390/cells13121052
33
Arghya Samanta, Gautam Ray. Hepatic glycogen storage disease: Deciphering the genotype-phenotype conundrumWorld Journal of Clinical Pediatrics 2025; 14(3): 103415 doi: 10.5409/wjcp.v14.i3.103415
34
Cristiano Susin, Amanda Finger Stadler, Alex Haas, Jasim M. Albandar. Periodontal Manifestations of Systemic DiseasesJournal of Periodontal Research 2025;  doi: 10.1111/jre.70034
35
Li-xiao Shen, Yin-gui Wu, Mu-dan Ke. The Liver Disease-Related Hypoglycemia: An Overview of the Impact, Management Approaches, and Underlying MechanismsBritish Journal of Hospital Medicine 2025; 86(6): 1 doi: 10.12968/hmed.2025.0028
36
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 IbCurrent Pediatrics 2024; 23(3): 162 doi: 10.15690/vsp.v23i3.2761
37
Yuan Chen, Zhi-Yi Wang, Bao-Qi Chen, Yu-Juan Qi, Hai-Yan Liu, Wen-Xin Shi, Lu Guo, Zhi Liu, Li-Feng Sun. Clinical characteristics and genetic causes of unexplained pediatric liver diseaseWorld Journal of Hepatology 2025; 17(10): 109770 doi: 10.4254/wjh.v17.i10.109770
38
Sheikha Nasser AlQahtani, Sara AlGubaisi, Faisal Ahmed AlHaffaf, Rabab Jamel Makki, Eman Ali Alohali, Raneem Omran AlMadani, Haifa Mujahed AlSagiheer, Mastourah Mousa Al-Otaibi, Hossam Tawakol Mohammed. Nutrition Support Therapy for Hospitalized Children with Malnutrition: A Narrative ReviewHealthcare 2025; 13(5): 497 doi: 10.3390/healthcare13050497
39
Tomàs Pinós, Richard M. Cubbon, Alfredo Santalla, Carmen Fiuza-Luces, Alejandro Santos-Lozano, Miguel A. Martín, Joaquín Arenas, Joachim Nielsen, Niels Ørtenblad, Alejandro Lucia. Cardiovascular involvement in glycogen storage diseasesNature Reviews Cardiology 2026; 23(1): 39 doi: 10.1038/s41569-025-01171-w
40
Xiaotang Du, Hanlin L. Wang. Rare Liver Diseases With Near-Normal Histology: A Review Focusing on Metabolic, Storage, and Inclusion DisordersAdvances in Anatomic Pathology 2025; 32(6): 363 doi: 10.1097/PAP.0000000000000488
41
Ryou Ishikawa, Takeo Kondo, Sonoko Kondo, Tomohiro Kishimoto, Seiko Kagawa, Reiji Haba. Liver Biopsy-Associated Diagnosis of Glycogen Storage Disease Type IV (Andersen Disease)Pediatric and Developmental Pathology 2026;  doi: 10.1177/10935266261427156
42
Mohammed Al-Beltagi, Nermin Saeed, Adel Bediwy, Reem Elbeltagi. Navigating gastrointestinal challenges in genetic myopathies: Diagnostic insights and future directionsWorld Journal of Methodology 2025; 15(4): 102408 doi: 10.5662/wjm.v15.i4.102408
43
Büşra Akyol Yılmaz, Elvan Yılmaz Akyüz, Tanyel Zübarioğlu. Effect of Uncooked Cornstarch Treatment on Metabolic Control in Patients With Hepatic Glycogen Storage DiseasesJournal of Basic and Clinical Health Sciences 2025; 9(3): 494 doi: 10.30621/jbachs.1659440
44
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
45
Lucio Teresi, Giancarlo Trimarchi, Roberto Licordari, Davide Restelli, Giovanni Taverna, Paolo Liotta, Antonino Micari, Ignazio Smecca, Gregory Dendramis, Dario Turturiello, Alessia Chiara Latini, Giulio Falasconi, Cesare de Gregorio, Pasquale Crea, Giuseppe Dattilo, Antonio Berruezo, Antonio Micari, Gianluca Di Bella. Hypertrophic Cardiomyopathy Phenocopies: Classification, Key Features, and Differential DiagnosisBiomedicines 2025; 13(12): 3062 doi: 10.3390/biomedicines13123062
46
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 TestingGenes 2023; 14(12): 2219 doi: 10.3390/genes14122219
47
Marco Maria Dicorato, Gaia De Sario, Maria Cristina Carella, Andrea Igoren Guaricci, Marco Matteo Ciccone, Cinzia Forleo, Gabriele D’Amato, Maria Felicia Faienza. Genetic Mutations Underlying Growth Impairment and Cardiomyopathies in Children: Molecular Mechanisms, Clinical Implications and Targeted TherapiesGenes 2026; 17(3): 355 doi: 10.3390/genes17030355
48
Mohammad Shboul, Mohammed El-Khateeb, Rajaa Fathallah. Genetic diagnosis of Jordanian patients with glycogen storage diseasesOrphanet Journal of Rare Diseases 2025; 20(1) doi: 10.1186/s13023-025-03982-z
49
Ana Isabel Beltran-Velasco. Brain Glycogen—Its Metabolic Role in Neuronal Health and Neurological Disorders—An Extensive Narrative ReviewMetabolites 2025; 15(2): 128 doi: 10.3390/metabo15020128
50
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 legumesBMC Genomics 2025; 26(1) doi: 10.1186/s12864-025-11224-6
51
Dóra Kósa, Ágota Pető, Ildikó Bácskay. Pharmacological Targets in Metabolic Diseases2026; : 53 doi: 10.1016/B978-0-443-27370-4.00020-2
52
Xiaohui Wu, Yueyu Sun, Min Yang. Growth impairment in glycogen storage disease type I versus types III/VI/IX: a cross-sectional studyBMC Pediatrics 2025; 25(1) doi: 10.1186/s12887-025-06053-1
53
Maroua Jakani, Imane Assiri, Sana El Foutat, Samira Najeh, Miloud Hammoud, Abdelati Berrachid, Karima Lafhal, Es-said Sabir, Khouloud Elmazi, Mariam Lagrine, Aicha Bourrahouat, Naima Fdil. Identification of a novel nonsense mutation in the AGL gene in glycogen storage disease type IIIa: first genetically confirmed case report from MoroccoMolecular Biology Reports 2026; 53(1) doi: 10.1007/s11033-025-11345-x
54
Burcu Kumru Akin, Emine Goksoy. Low bone mineral density in rare metabolic disorders: data from a Turkish cohort of patients with glycogen storage disorders and organic acidemiasTrends in Pediatrics 2025; 6(3): 194 doi: 10.59213/TP.2025.320
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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 CohortBiochemical Genetics 2025; 63(2): 1752 doi: 10.1007/s10528-024-10787-5
56
Khulood Kayed SHATTNAWI, Raheeq Mohammad Al-Hmoud. Navigating Glycogen Storage Disease: The Spiritual and Cultural Journeys of Jordanian MothersJournal of Religion and Health 2025;  doi: 10.1007/s10943-025-02451-y
57
Tiffany Huynh, Hien Nguyen, Michelle Nguyen. Hypercholesterolemia Successfully Treated With Two Different PCSK9 Inhibitors in a Patient With Glycogen Storage Disease IXd: Phosphorylase Kinase DeficiencyJournal of Lipid and Atherosclerosis 2026; 15(1): 183 doi: 10.12997/jla.2026.15.1.183
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Ting Zhang, Yun Wang, Cuiping Shi, Ye Zi, Wei Cai, Jian Zhong. Foods for special medical purposes for the dietary therapy of rare diseases: Current status and future prospectsIntractable & Rare Diseases Research 2026; 15(1): 26 doi: 10.5582/irdr.2025.01075
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Meifen Wang, Mingying Wang, Juan Li, Rui Chen, Zhongrui Bi, Hongchao Jiang, Jiwei Li. Sodium taurocholate cotransporter polypeptide deficiency combined with novel PYGL mutations in glycogen storage disease type VI: a rare case reportClinics and Research in Hepatology and Gastroenterology 2026; 50(4): 102801 doi: 10.1016/j.clinre.2026.102801
60
Maja Ziemian, Joanna Szmydtka, Wojciech Snoch, Sandra Milner, Szymon Wojciechowski, Aleksandra Dłuszczakowska, Jakub W. Chojnowski, Zofia Pallach, Katarzyna Żamojda, Grzegorz Węgrzyn, Estera Rintz. Integrative Approaches to Myopathies and Muscular Dystrophies: Molecular Mechanisms, Diagnostics, and Future TherapiesInternational Journal of Molecular Sciences 2025; 26(16): 7972 doi: 10.3390/ijms26167972
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Jang Hoon Ru, Ji Seung Ryu, Yunkoo Kang, Sejung Yang. Continuous Glucose Monitoring–Driven Personalization of Cornstarch Therapy in Glycogen Storage Disease: A Retrospective AnalysisYonsei Medical Journal 2026; 67 doi: 10.3349/ymj.2025.0468
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Maria Evangelia Koloutsou, Maria P. Yavropoulou, Konstantinos Makrilakis. Spontaneous restoration of premature ovarian insufficiency and conception in a patient with glycogen storage disease type 1b managed with empagliflozinHormones 2025; 24(3): 891 doi: 10.1007/s42000-025-00672-0
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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 telangiectasiaBMJ Case Reports 2025; 18(2): e263586 doi: 10.1136/bcr-2024-263586
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Ziqiu Chen, Zheng Sun, Ge Li, Huaien Bu. Safety of SGLT-2 inhibitors in patients with glycogen storage disease type Ib and their efficacy in treating disease-associated digestive symptoms and disordersActa Diabetologica 2026;  doi: 10.1007/s00592-025-02627-8
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Ewa Stefanik, Magda Dubińska-Magiera, Damian Lewandowski, Małgorzata Daczewska, Marta Migocka-Patrzałek. Metabolic aspects of glycogenolysis with special attention to McArdle diseaseMolecular Genetics and Metabolism 2024; 142(4): 108532 doi: 10.1016/j.ymgme.2024.108532
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Riya Patel, Smriti Nair, Hassaam Choudhry, Mustafa Jaffry, Mohammad Dastjerdi. Ocular manifestations of liver disease: an important diagnostic aidInternational Ophthalmology 2024; 44(1) doi: 10.1007/s10792-024-03103-y
67
Loai A. Shakerdi, Halima Mshelia, Abrar Al Zaher, Rawia Debo, Sarah Connellan, Cathy Newman Thacker, Mairead O’Riordan, James J. O’Byrne, Claire M. McCarthy. Successful multidisciplinary management of pregnancy in a woman with glycogen storage disease type IIIAObstetric Medicine 2026;  doi: 10.1177/1753495X261431284
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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 XKuwait Journal of Science 2025; 52(1): 100344 doi: 10.1016/j.kjs.2024.100344
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Apoorva K. Iyengar, Xue Zou, Jian Dai, Rhodricia A. Francis, Alexias Safi, Karynne Patterson, Rebecca L. Koch, Shannon Clarke, M. Makenzie Beaman, Shruthi Mohan, Jessica X. Chong, Michael J. Bamshad, William H. Majoros, R. Catherine Rehder, Deeksha S. Bali, Andrew S. Allen, Gregory E. Crawford, Priya S. Kishnani, Timothy E. Reddy. Cell modeling and rescue of a novel noncoding genetic cause of glycogen storage disease IXGenetics in Medicine Open 2026; 4: 103474 doi: 10.1016/j.gimo.2025.103474
70
Tzu-Han Weng, Yu-Chung Pien, Ching-Jou Chen, Po-Pang Chen, Yu-Ting Tseng, Ying-Chen Chen, Wen-Po Hsiao, Ying-Ting Lee, Yi-An Chen, Yao-Chi Chen, Carmay Lim, Tzu-Han Hsu, Sung-Jan Lin, Hsin-Yung Yen, Kuo-Chiang Hsia, Su-Yi Tsai. Human glycogenins maintain glucose homeostasis by regulating glycogen metabolismNature Communications 2025; 16(1) doi: 10.1038/s41467-025-61862-3
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Yan Zhou, Juan Putra. Practical Liver PathologyPractical Anatomic Pathology 2025; : 15 doi: 10.1007/978-3-031-97506-6_2
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Maria Vinciguerra, Catiana El Kharef, Christopher Bruhn, Lucia Falbo, Chiara Milanese, Matteo Audano, Galina V. Beznoussenko, Alexander A. Mironov, Domenico Delia, Marco Foiani, Pier Giorgio Mastroberardino, Nico Mitro, Vincenzo Costanzo. Targeting the FNIP2-SERCA2b axis improves metabolic and mitochondrial defects in Ataxia TelangiectasiaCell Death & Disease 2026; 17(1) doi: 10.1038/s41419-026-08507-5
73
Alamin Alkundi, Rabiu Momoh. Hypoglycaemic Unawareness in a Glycogen Storage Disorder Patient: A Case Report and Review of the LiteratureCureus 2025;  doi: 10.7759/cureus.81805
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Aashi Gurijala, Emma Rushton, Shannon N. Leahy, Nichalas Nelson, Charles R. Tessier, Kendal Broadie. Interaction between neuromuscular junction metabolic requirements in fragile X syndrome and glycogen storage disease modelsDisease Models & Mechanisms 2025; 18(8) doi: 10.1242/dmm.052183
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G. Chalès, F. Robin, P. Guggenbuhl. Glycogénoses, hyperoxaluries, aminoacidopathies et hyperlipidémies : manifestations ostéoarticulairesEMC - Appareil locomoteur 2026; 40(1): 1 doi: 10.1016/S0246-0521(25)47869-3
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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 CellsInternational Journal of Molecular Sciences 2024; 26(1): 187 doi: 10.3390/ijms26010187