132 related articles for article (PubMed ID: 37243436)
1. Arginase deficiency-An unheralded cause of developmental epileptic encephalopathy.
Pavuluri H; Jose M; Fasaludeen A; Sundaram S; Radhakrishnan A; Banerjee M; Menon RN
Epileptic Disord; 2023 Aug; 25(4):556-561. PubMed ID: 37243436
[TBL] [Abstract][Full Text] [Related]
2. Arginase I deficiency: severe infantile presentation with hyperammonemia: more common than reported?
Jain-Ghai S; Nagamani SC; Blaser S; Siriwardena K; Feigenbaum A
Mol Genet Metab; 2011; 104(1-2):107-11. PubMed ID: 21802329
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A Delayed Presentation of Arginase Deficiency Presenting with Status Epilepticus.
Olgac A; Yildiz E; Yilmaz A; Kasapkara CS; Ceylaner S; Alioglu B
J Coll Physicians Surg Pak; 2022 Dec; 32(12):1629-1631. PubMed ID: 36474391
[TBL] [Abstract][Full Text] [Related]
5. Hyperargininemic Encephalopathy with Unique Clinical Presentation and Novel Genetic Mutations.
Nagarjunakonda S; Daggumati R; Amalakanti S
J Coll Physicians Surg Pak; 2020 May; 30(5):535-536. PubMed ID: 32580855
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Clinical effect and safety profile of pegzilarginase in patients with arginase 1 deficiency.
Diaz GA; Schulze A; McNutt MC; Leão-Teles E; Merritt JL; Enns GM; Batzios S; Bannick A; Zori RT; Sloan LS; Potts SL; Bubb G; Quinn AG
J Inherit Metab Dis; 2021 Jul; 44(4):847-856. PubMed ID: 33325055
[TBL] [Abstract][Full Text] [Related]
8. Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency.
Burrage LC; Sun Q; Elsea SH; Jiang MM; Nagamani SC; Frankel AE; Stone E; Alters SE; Johnson DE; Rowlinson SW; Georgiou G; ; Lee BH
Hum Mol Genet; 2015 Nov; 24(22):6417-27. PubMed ID: 26358771
[TBL] [Abstract][Full Text] [Related]
9. Epilepsia partialis continua and generalized nonconvulsive status epilepticus during the course of argininemia: a report on two cases.
Grioni D; Furlan F; Canonico F; Parini R
Neuropediatrics; 2014 Apr; 45(2):123-8. PubMed ID: 24258525
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. 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]
13. Phenotypic Pleiotropy in Arginase Deficiency: A Single Center Cohort.
Bharathi NK; Thomas MM; Yoganathan S; Chandran M; Aaron R; Danda S
Ann Indian Acad Neurol; 2022; 25(6):1104-1108. PubMed ID: 36911443
[TBL] [Abstract][Full Text] [Related]
14. The molecular and phenotypic spectrum of IQSEC2-related epilepsy.
Zerem A; Haginoya K; Lev D; Blumkin L; Kivity S; Linder I; Shoubridge C; Palmer EE; Field M; Boyle J; Chitayat D; Gaillard WD; Kossoff EH; Willems M; Geneviève D; Tran-Mau-Them F; Epstein O; Heyman E; Dugan S; Masurel-Paulet A; Piton A; Kleefstra T; Pfundt R; Sato R; Tzschach A; Matsumoto N; Saitsu H; Leshinsky-Silver E; Lerman-Sagie T
Epilepsia; 2016 Nov; 57(11):1858-1869. PubMed ID: 27665735
[TBL] [Abstract][Full Text] [Related]
15. Diagnosis of Lennox-Gastaut syndrome and strategies for early recognition.
Pujar S; Cross JH
Expert Rev Neurother; 2024 Apr; 24(4):383-389. PubMed ID: 38415629
[TBL] [Abstract][Full Text] [Related]
16. Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency.
Truong B; Allegri G; Liu XB; Burke KE; Zhu X; Cederbaum SD; Häberle J; Martini PGV; Lipshutz GS
Proc Natl Acad Sci U S A; 2019 Oct; 116(42):21150-21159. PubMed ID: 31501335
[TBL] [Abstract][Full Text] [Related]
17. Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia.
Huang Y; Sharma R; Feigenbaum A; Lee C; Sahai I; Sanchez Russo R; Neira J; Brooks SS; Jackson KE; Wong D; Cederbaum S; Lacbawan FL; Rowland CM; Tanpaiboon P; Salazar D
Mol Genet Metab Rep; 2021 Jun; 27():100735. PubMed ID: 33732618
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
