OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource
Rebecca L. Koch, Claudia Soler‐Alfonso, Bridget T. Kiely, et al.
Molecular Genetics and Metabolism (2023) Vol. 138, Iss. 3, pp. 107525-107525
Closed Access | Times Cited: 25
Rebecca L. Koch, Claudia Soler‐Alfonso, Bridget T. Kiely, et al.
Molecular Genetics and Metabolism (2023) Vol. 138, Iss. 3, pp. 107525-107525
Closed Access | Times Cited: 25
Showing 25 citing articles:
Glycogen storage diseases
William B. Hannah, Terry G. J. Derks, Mitchell L. Drumm, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Closed Access | Times Cited: 40
William B. Hannah, Terry G. J. Derks, Mitchell L. Drumm, et al.
Nature Reviews Disease Primers (2023) Vol. 9, Iss. 1
Closed Access | Times Cited: 40
Gene therapy for glycogen storage diseases
Dwight D. Koeberl, Rebecca L. Koch, Jeong‐A Lim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 93-118
Closed Access | Times Cited: 19
Dwight D. Koeberl, Rebecca L. Koch, Jeong‐A Lim, et al.
Journal of Inherited Metabolic Disease (2023) Vol. 47, Iss. 1, pp. 93-118
Closed Access | Times Cited: 19
A 61-Year-Old Man With Weakness and Gait Dysfunction
Felipe J.S. Jones, Christyn Edmundson, Jennifer Orthmann‐Murphy
JAMA Neurology (2025)
Closed Access
Felipe J.S. Jones, Christyn Edmundson, Jennifer Orthmann‐Murphy
JAMA Neurology (2025)
Closed Access
Brain Glycogen—Its Metabolic Role in Neuronal Health and Neurological Disorders—An Extensive Narrative Review
Ana Isabel Beltrán-Velasco
Metabolites (2025) Vol. 15, Iss. 2, pp. 128-128
Open Access
Ana Isabel Beltrán-Velasco
Metabolites (2025) Vol. 15, Iss. 2, pp. 128-128
Open Access
Clinical genetic analysis of an adult polyglucosan body disease (APBD) family caused by the compound heterozygous variant of GBE1 p.R156C and deletion exon 3-7
Juan Zhu, Hongping Yu, Jing Zou, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Juan Zhu, Hongping Yu, Jing Zou, et al.
Frontiers in Genetics (2025) Vol. 16
Open Access
Nutritional management and geno-phenotyping of clinical nutrition in patients with glycogen storage diseases type VI and IX
Sema Kalkan Uçar, Alperen Elek, Havva Yazıcı, et al.
European Journal of Clinical Nutrition (2025)
Open Access
Sema Kalkan Uçar, Alperen Elek, Havva Yazıcı, et al.
European Journal of Clinical Nutrition (2025)
Open Access
GBE1 alleviates MPTP-induced PD symptoms in mice by enhancing glycolysis and oxidative phosphorylation
Hongyan Chen, Hao Ding, Dongya Huang, et al.
Brain Research (2025), pp. 149663-149663
Closed Access
Hongyan Chen, Hao Ding, Dongya Huang, et al.
Brain Research (2025), pp. 149663-149663
Closed Access
Induced pluripotent stem cell (iPSC) modeling validates reduced GBE1 enzyme activity due to a novel variant, p.Ile694Asn, found in a patient with suspected glycogen storage disease IV
C Naito, Karis Kosar, Eriko Kishimoto, et al.
Molecular Genetics and Metabolism Reports (2024) Vol. 39, pp. 101069-101069
Open Access | Times Cited: 1
C Naito, Karis Kosar, Eriko Kishimoto, et al.
Molecular Genetics and Metabolism Reports (2024) Vol. 39, pp. 101069-101069
Open Access | Times Cited: 1
Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care
Alessandro Rossi, Chiara Simeoli, Rosario Pivonello, et al.
Reviews in Endocrine and Metabolic Disorders (2024) Vol. 25, Iss. 4, pp. 707-725
Open Access | Times Cited: 1
Alessandro Rossi, Chiara Simeoli, Rosario Pivonello, et al.
Reviews in Endocrine and Metabolic Disorders (2024) Vol. 25, Iss. 4, pp. 707-725
Open Access | Times Cited: 1
Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs)
Kumudesh Mishra, Or Kakhlon
(2024)
Open Access | Times Cited: 1
Kumudesh Mishra, Or Kakhlon
(2024)
Open Access | Times Cited: 1
Mitochondrial Dysfunction in Glycogen Storage Disorders (GSDs)
Kumudesh Mishra, Or Kakhlon
Biomolecules (2024) Vol. 14, Iss. 9, pp. 1096-1096
Open Access | Times Cited: 1
Kumudesh Mishra, Or Kakhlon
Biomolecules (2024) Vol. 14, Iss. 9, pp. 1096-1096
Open Access | Times Cited: 1
Continuous glucose monitoring in patients with inherited metabolic disorders at risk for Hypoglycemia and Nutritional implications
Giorgia Gugelmo, Evelina Maines, Federico Boscari, et al.
Reviews in Endocrine and Metabolic Disorders (2024)
Open Access | Times Cited: 1
Giorgia Gugelmo, Evelina Maines, Federico Boscari, et al.
Reviews in Endocrine and Metabolic Disorders (2024)
Open Access | Times Cited: 1
Thésaurismoses adultes et pédiatriques : maladies de surcharge lysosomale, surcharges lipidiques et glycogénoses
Sophie Collardeau‐Frachon
Annales de Pathologie (2024)
Closed Access | Times Cited: 1
Sophie Collardeau‐Frachon
Annales de Pathologie (2024)
Closed Access | Times Cited: 1
Case report: Expanding the understanding of the adult polyglucosan body disease continuum: novel presentations, diagnostic pitfalls, and clinical pearls
Matthew M. Gayed, Paulo Sgobbi, Wladimir Bocca Vieira de Rezende Pinto, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
Matthew M. Gayed, Paulo Sgobbi, Wladimir Bocca Vieira de Rezende Pinto, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 3
Natural history study of hepatic glycogen storage disease type IV and comparison to Gbe1ys/ys model
Rebecca L. Koch, Bridget T. Kiely, Su Jin Choi, et al.
JCI Insight (2024) Vol. 9, Iss. 12
Open Access
Rebecca L. Koch, Bridget T. Kiely, Su Jin Choi, et al.
JCI Insight (2024) Vol. 9, Iss. 12
Open Access
Development of the APBD-SQ, a novel patient-reported outcome for health-related quality of life in adult polyglucosan body disease
Genevieve E. Wilson, Deberah S. Goldman, Harriet Saxe, et al.
Journal of the Neurological Sciences (2024) Vol. 464, pp. 123168-123168
Closed Access
Genevieve E. Wilson, Deberah S. Goldman, Harriet Saxe, et al.
Journal of the Neurological Sciences (2024) Vol. 464, pp. 123168-123168
Closed Access
РЕДКАЯ ФОРМА ГЛИКОГЕНОВОЙ БОЛЕЗНИ IV ТИПА: КЛИНИЧЕСКОЕ НАБЛЮДЕНИЕ
R.O. Bəylərov, N.C. Rəhimova
Azerbajdžanskij medicinskij žurnal (2024), Iss. 1, pp. 164-169
Closed Access
R.O. Bəylərov, N.C. Rəhimova
Azerbajdžanskij medicinskij žurnal (2024), Iss. 1, pp. 164-169
Closed Access
Neuro-Ophthalmic Manifestations of Adult Polyglucosan Body Disease
Andrew Dugue, Nicolas J. Abreu, Cinthi Pillai, et al.
Journal of Neuro-Ophthalmology (2024)
Closed Access
Andrew Dugue, Nicolas J. Abreu, Cinthi Pillai, et al.
Journal of Neuro-Ophthalmology (2024)
Closed Access
Metabolic Liver Diseases presenting as Pediatric onset Hypoglycemia: A Hepatologist’s Primer
Snigdha Verma, Vikrant Sood, Bikrant Bihari Lal, et al.
Journal of Clinical and Experimental Hepatology (2024) Vol. 15, Iss. 1, pp. 102425-102425
Closed Access
Snigdha Verma, Vikrant Sood, Bikrant Bihari Lal, et al.
Journal of Clinical and Experimental Hepatology (2024) Vol. 15, Iss. 1, pp. 102425-102425
Closed Access
Glycogen and polyglucosan storage diseases
Salvatore DiMauro, Hasan O. Akman
Elsevier eBooks (2024), pp. 733-743
Closed Access
Salvatore DiMauro, Hasan O. Akman
Elsevier eBooks (2024), pp. 733-743
Closed Access
Molecular profiles and long-term outcomes of Thai children with hepatic glycogen storage disease in Thailand
Jaravee Vanduangden, Rungnapa Ittiwut, Chupong Ittiwut, et al.
World Journal of Clinical Pediatrics (2024) Vol. 13, Iss. 4
Closed Access
Jaravee Vanduangden, Rungnapa Ittiwut, Chupong Ittiwut, et al.
World Journal of Clinical Pediatrics (2024) Vol. 13, Iss. 4
Closed Access
Glycogen storage disease type IV without detectable polyglucosan bodies: importance of broad gene panels
Agata Oliwa, Gavin Langlands, Anna Sárközy, et al.
Neuromuscular Disorders (2023) Vol. 33, Iss. 9, pp. 98-105
Closed Access | Times Cited: 1
Agata Oliwa, Gavin Langlands, Anna Sárközy, et al.
Neuromuscular Disorders (2023) Vol. 33, Iss. 9, pp. 98-105
Closed Access | Times Cited: 1
An Unusual Case of Neonatal Hypotonia and Femur Fracture: Neuromuscular Variant of Glycogen Storage Disease Type IV
Handan Bezirganoğlu, Kübra Adanur Sağlam
Children (2023) Vol. 10, Iss. 8, pp. 1375-1375
Open Access
Handan Bezirganoğlu, Kübra Adanur Sağlam
Children (2023) Vol. 10, Iss. 8, pp. 1375-1375
Open Access
A Rare Cause of Cirrhosis in a Toddler
Jasna Nizar Raseena, Prasanth KN Sobhan, Ajith K Ananda Krishnan Sarasam
Annals of Pediatric Gastroenterology and Hepatology ISPGHAN (2023) Vol. 5, Iss. 3, pp. 45-46
Closed Access
Jasna Nizar Raseena, Prasanth KN Sobhan, Ajith K Ananda Krishnan Sarasam
Annals of Pediatric Gastroenterology and Hepatology ISPGHAN (2023) Vol. 5, Iss. 3, pp. 45-46
Closed Access
