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.
158 related articles for article (PubMed ID: 29443755)
1. Argininemia as a cause of severe chronic stunting and partial growth hormone deficiency (PGHD): A case report. Cai X; Yu D; Xie Y; Zhou H Medicine (Baltimore); 2018 Feb; 97(7):e9880. PubMed ID: 29443755 [TBL] [Abstract][Full Text] [Related]
2. [Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk]. Wu T; Li X; Ding Y; Liu Y; Song J; Wang Q; Li M; Qin Y; Yang Y Zhonghua Er Ke Za Zhi; 2015 Jun; 53(6):425-30. PubMed ID: 26310552 [TBL] [Abstract][Full Text] [Related]
3. A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report. Cui D; Liu Y; Jin L; Hu L; Cao L Medicine (Baltimore); 2020 Aug; 99(32):e21634. PubMed ID: 32769929 [TBL] [Abstract][Full Text] [Related]
4. [Advances in clinical and molecular genetics studies on argininemia]. Wu TF; Yang YL Zhongguo Dang Dai Er Ke Za Zhi; 2013 Nov; 15(11):954-9. PubMed ID: 24229587 [TBL] [Abstract][Full Text] [Related]
5. Neurological Deterioration in Three Siblings: Exploring the Spectrum of Argininemia. Garg D; Bijarnia-Mahay S; Elwadhi A; Ray S; Häberle J; Sharma S Indian J Pediatr; 2021 Mar; 88(3):266-268. PubMed ID: 32770317 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Argininemia as a cause of severe chronic stunting in a low-resource developing country setting: a case report. King N; Alvizures R; García P; Wessel A; Rohloff P BMC Pediatr; 2016 Aug; 16(1):142. PubMed ID: 27549856 [TBL] [Abstract][Full Text] [Related]
8. Argininemia presenting with progressive spastic diplegia. Lee BH; Jin HY; Kim GH; Choi JH; Yoo HW Pediatr Neurol; 2011 Mar; 44(3):218-20. PubMed ID: 21310339 [TBL] [Abstract][Full Text] [Related]
9. Case series of arginase 1 deficiency: Expanding the spectrum in hyperargininemia. Dorum S; Havalı C Pediatr Int; 2022 Jan; 64(1):e14945. PubMed ID: 34343381 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review. Prasad AN; Breen JC; Ampola MG; Rosman NP J Child Neurol; 1997 Aug; 12(5):301-9. PubMed ID: 9378897 [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. Hyperargininemia: 7-month follow-up under sodium benzoate therapy in an Italian child presenting progressive spastic paraparesis, cognitive decline, and novel mutation in ARG1 gene. Baranello G; Alfei E; Martinelli D; Rizzetto M; Cazzaniga F; Dionisi-Vici C; Gellera C; Castellotti B Pediatr Neurol; 2014 Sep; 51(3):430-3. PubMed ID: 24997092 [TBL] [Abstract][Full Text] [Related]
14. 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]