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Cited by in CrossRef
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/1007-9327/full/v29/i25/3932.htm
Number Citing Articles
1
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;  doi: 10.1002/jimd.12741
2
Rafael de Marchi, Tatiele Nalin, Fernanda Sperb-Ludwig, Franciele Cabral Pinheiro, Ida Vanessa Doederlein Schwartz, Carlos Eduardo Steiner. Glycogen Storage Disease: Expert Opinion on Clinical Diagnosis Revisited after Molecular TestingGenes 2023; 14(12): 2219 doi: 10.3390/genes14122219
3
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 2024;  doi: 10.1007/s10528-024-10787-5
4
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