These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
130 related articles for article (PubMed ID: 35236361)
1. Arginase 1 Deficiency: using genetic databases as a tool to establish global prevalence. Catsburg C; Anderson S; Upadhyaya N; Bechter M Orphanet J Rare Dis; 2022 Mar; 17(1):94. PubMed ID: 35236361 [TBL] [Abstract][Full Text] [Related]
2. Epidemiology, methods of diagnosis, and clinical management of patients with arginase 1 deficiency (ARG1-D): A systematic review. Bin Sawad A; Jackimiec J; Bechter M; Trucillo A; Lindsley K; Bhagat A; Uyei J; Diaz GA Mol Genet Metab; 2022; 137(1-2):153-163. PubMed ID: 36049366 [TBL] [Abstract][Full Text] [Related]
3. The global prevalence and genetic spectrum of lysosomal acid lipase deficiency: A rare condition that mimics NAFLD. Carter A; Brackley SM; Gao J; Mann JP J Hepatol; 2019 Jan; 70(1):142-150. PubMed ID: 30315827 [TBL] [Abstract][Full Text] [Related]
4. Arginase deficiency in Bulgaria: first cases and potential endemic region for the disorder. Atemin S; Todorov T; Tourtourikov I; Ivanova MB; Chamova T; Avdjieva-Tzavella D; Kathom H; Georgieva B; Guergueltcheva V; Savov IBA; Tournev I; Mitev V; Todorova A J Genet; 2023; 102():. PubMed ID: 36722221 [TBL] [Abstract][Full Text] [Related]
5. The global prevalence of Wilson disease from next-generation sequencing data. Gao J; Brackley S; Mann JP Genet Med; 2019 May; 21(5):1155-1163. PubMed ID: 30254379 [TBL] [Abstract][Full Text] [Related]
6. Three novel mutations of ARG1 identified in Chinese patients with argininemia detected by newborn screening. Zhang T; Yang J; Yin X; Yu P; Mooney R; Huang X; Qi M Clin Chim Acta; 2017 Mar; 466():68-71. PubMed ID: 28089752 [TBL] [Abstract][Full Text] [Related]
7. Analysis of novel ARG1 mutations causing hyperargininemia and correlation with arginase I activity in erythrocytes. Carvalho DR; Brand GD; Brum JM; Takata RI; Speck-Martins CE; Pratesi R Gene; 2012 Nov; 509(1):124-30. PubMed ID: 22959135 [TBL] [Abstract][Full Text] [Related]
8. Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia. Mohseni J; Boon Hock C; Abdul Razak C; Othman SN; Hayati F; Peitee WO; Haniffa M; Zilfalil BA; Mohd Rawi R; Ngu LH; Sasongko TH Gene; 2014 Jan; 533(1):240-5. PubMed ID: 24103480 [TBL] [Abstract][Full Text] [Related]
9. Estimated birth prevalence of Menkes disease and ATP7A-related disorders based on the Genome Aggregation Database (gnomAD). Kaler SG; Ferreira CR; Yam LS Mol Genet Metab Rep; 2020 Sep; 24():100602. PubMed ID: 32528851 [TBL] [Abstract][Full Text] [Related]
10. The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis. Hannah WB; Seifert BA; Truty R; Zariwala MA; Ameel K; Zhao Y; Nykamp K; Gaston B Lancet Respir Med; 2022 May; 10(5):459-468. PubMed ID: 35051411 [TBL] [Abstract][Full Text] [Related]
11. Inducible arginase 1 deficiency in mice leads to hyperargininemia and altered amino acid metabolism. Sin YY; Ballantyne LL; Mukherjee K; St Amand T; Kyriakopoulou L; Schulze A; Funk CD PLoS One; 2013; 8(11):e80001. PubMed ID: 24224027 [TBL] [Abstract][Full Text] [Related]
12. Arginase-1 deficiency. Sin YY; Baron G; Schulze A; Funk CD J Mol Med (Berl); 2015 Dec; 93(12):1287-96. PubMed ID: 26467175 [TBL] [Abstract][Full Text] [Related]
13. Natural history of arginase 1 deficiency and the unmet needs of patients: A systematic review of case reports. Bin Sawad A; Pothukuchy A; Badeaux M; Hodson V; Bubb G; Lindsley K; Uyei J; Diaz GA JIMD Rep; 2022 Jul; 63(4):330-340. PubMed ID: 35822089 [TBL] [Abstract][Full Text] [Related]
14. Current status of surviving patients with arginase 1 deficiency in Japan. Kido J; Matsumoto S; Takeshita E; Hayasaka C; Yamada K; Kagawa J; Nakajima Y; Ito T; Iijima H; Endo F; Nakamura K Mol Genet Metab Rep; 2021 Dec; 29():100805. PubMed ID: 34646736 [TBL] [Abstract][Full Text] [Related]
15. Two Japanese siblings with arginase-1 deficiency identified using a novel frameshift mutation of Nakajima H; Fukuhara S J Pediatr Endocrinol Metab; 2022 Jan; 35(1):125-129. PubMed ID: 34653322 [TBL] [Abstract][Full Text] [Related]
16. The role and control of arginine levels in arginase 1 deficiency. Diaz GA; Bechter M; Cederbaum SD J Inherit Metab Dis; 2023 Jan; 46(1):3-14. PubMed ID: 36175366 [TBL] [Abstract][Full Text] [Related]
18. A novel mutation in ARG1 gene is responsible for arginase deficiency in an Asian family. Hertecant JL; Al-Gazali LI; Karuvantevida NS; Ali BR Saudi Med J; 2009 Dec; 30(12):1601-3. PubMed ID: 19936428 [TBL] [Abstract][Full Text] [Related]
19. Molecular basis of phenotypic variation in patients with argininemia. Uchino T; Snyderman SE; Lambert M; Qureshi IA; Shapira SK; Sansaricq C; Smit LM; Jakobs C; Matsuda I Hum Genet; 1995 Sep; 96(3):255-60. PubMed ID: 7649538 [TBL] [Abstract][Full Text] [Related]
20. Five novel mutations in ARG1 gene in Chinese patients of argininemia. Wu TF; Liu YP; Li XY; Wang Q; Ding Y; Ma YY; Song JQ; Yang YL Pediatr Neurol; 2013 Aug; 49(2):119-23. PubMed ID: 23859858 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]