BPG is committed to discovery and dissemination of knowledge
Cited by in CrossRef
Number Cited Articles
1
Jessica L. Schneller, Ciaran M. Lee, Gang Bao, Charles P. Venditti. Genome editing for inborn errors of metabolism: advancing towards the clinicBMC Medicine 2017; 15(1) doi: 10.1186/s12916-017-0798-4
2
L.D. Smith, U. Garg. Biomarkers in Inborn Errors of Metabolism2017; : 103 doi: 10.1016/B978-0-12-802896-4.00004-3
3
Patrick C Lee, Brian Truong, Agustin Vega-Crespo, W Blake Gilmore, Kip Hermann, Stephanie AK Angarita, Jonathan K Tang, Katherine M Chang, Austin E Wininger, Alex K Lam, Benjamen E Schoenberg, Stephen D Cederbaum, April D Pyle, James A Byrne, Gerald S Lipshutz. Restoring Ureagenesis in Hepatocytes by CRISPR/Cas9-mediated Genomic Addition to Arginase-deficient Induced Pluripotent Stem CellsMolecular Therapy - Nucleic Acids 2016; 5: e394 doi: 10.1038/mtna.2016.98
4
Susan E. Waisbren, Arianna K. Stefanatos, Teresa M. Y. Kok, Burcu Ozturk‐Hismi. Neuropsychological attributes of urea cycle disorders: A systematic review of the literatureJournal of Inherited Metabolic Disease 2019;  doi: 10.1002/jimd.12146
5
Ernie Zuraida Ali, Yuslina Zakaria, Mohd Amran Mohd Radzi, Lock Hock Ngu, Siti Azma Jusoh. Mutation Study of Malaysian Patients with Ornithine Transcarbamylase Deficiency: Clinical, Molecular, and Bioinformatics Analyses of Two Novel Missense Mutations of the OTC GeneBioMed Research International 2018; 2018: 1 doi: 10.1155/2018/4320831
6
Hussein Algahtani, Seham Alameer, Yousef Marzouk, Bader Shirah. Urea cycle disorder misdiagnosed as multiple sclerosis: a case report and review of the literatureThe Neuroradiology Journal 2018; 31(2): 213 doi: 10.1177/1971400917715880
7
Alireza Shamsaeefar, Saman Nikeghbalian, Seyed Mohsen Dehghani, Kourosh Kazemi, Nasrin Motazedian, Bita Geramizadeh, Seyed Ali Malekhosseini. Curative Treatment of Ornithine Transcarbamylase Deficiency With a Liver Transplant: A Case ReportExperimental and Clinical Transplantation 2019; 17(1): 119 doi: 10.6002/ect.2016.0052