BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
For: Al-Haggar M. Fanconi-Bickel syndrome as an example of marked allelic heterogeneity. World J Nephrol 2012; 1(3): 63-68 [PMID: 24175243 DOI: 10.5527/wjn.v1.i3.63]
URL: https://www.wjgnet.com/2220-6124/full/v1/i3/63.htm
Number Citing Articles
1
Huseyin Demirbilek, Sonya Galcheva, Dogus Vuralli, Sara Al-Khawaga, Khalid Hussain. Ion Transporters, Channelopathies, and Glucose DisordersInternational Journal of Molecular Sciences 2019; 20(10): 2590 doi: 10.3390/ijms20102590
2
Li-Jing Xiong, Mao-Ling Jiang, Li-Na Du, Lan Yuan, Xiao-Li Xie. Fanconi-Bickel syndrome in an infant with cytomegalovirus infection: A case report and review of the literatureWorld Journal of Clinical Cases 2020; 8(21): 5467-5473 doi: 10.12998/wjcc.v8.i21.5467
3
Jennifer Pogoriler, Allison F O’Neill, Stephan D Voss, Robert C Shamberger, Antonio R Perez-Atayde. Hepatocellular Carcinoma in Fanconi-Bickel SyndromePediatric and Developmental Pathology 2018; 21(1): 84 doi: 10.1177/1093526617693540
4
Priya S. Kishnani, Yuan-Tsong Chen. Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics2021; : 105 doi: 10.1016/B978-0-12-812535-9.00004-2
5
Sanaa Sharari, Mohamad Abou-Alloul, Khalid Hussain, Faiyaz Ahmad Khan. Fanconi–Bickel Syndrome: A Review of the Mechanisms That Lead to DysglycaemiaInternational Journal of Molecular Sciences 2020; 21(17): 6286 doi: 10.3390/ijms21176286
6
Miriam Massese, Francesco Tagliaferri, Carlo Dionisi-Vici, Arianna Maiorana. Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XIOrphanet Journal of Rare Diseases 2022; 17(1) doi: 10.1186/s13023-022-02387-6
7
Joseph I. Wolfsdorf, Charles A. Stanley. Sperling Pediatric Endocrinology2021; : 904 doi: 10.1016/B978-0-323-62520-3.00023-3