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Year | Number of Results |
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2021 | 1 |
2022 | 4 |
2023 | 2 |
2024 | 1 |
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hoang nguyen[Author]
(916 results)?
Treatment and outcomes of symptomatic hyperammonemia following asparaginase therapy in children with acute lymphoblastic leukemia.
Mol Genet Metab. 2023 Jul;139(3):107627. doi: 10.1016/j.ymgme.2023.107627. Epub 2023 Jun 7.
Mol Genet Metab. 2023.
PMID: 37327713
Outpatient Primary Care Genetic Testing Primer: What to Order and Testing Considerations.
Lee A, Neidich J, Nguyen H.
Lee A, et al. Among authors: nguyen h.
Mo Med. 2022 Jul-Aug;119(4):390-396.
Mo Med. 2022.
PMID: 36118815
Free PMC article.
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Methionine synthase deficiency: Variable clinical presentation and benefit of early diagnosis and treatment.
Kripps KA, Sremba L, Larson AA, Van Hove JLK, Nguyen H, Wright EL, Mirsky DM, Watkins D, Rosenblatt DS, Ketteridge D, Berry SA, McCandless SE, Baker PR 2nd.
Kripps KA, et al. Among authors: nguyen h.
J Inherit Metab Dis. 2022 Mar;45(2):157-168. doi: 10.1002/jimd.12448. Epub 2021 Oct 21.
J Inherit Metab Dis. 2022.
PMID: 34625984
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Case Report: A Novel EIF2B3 Pathogenic Variant in Central Nervous System Hypomyelination/Vanishing White Matter.
Wongkittichote P, Mar SS, McKinstry RC, Nguyen H.
Wongkittichote P, et al. Among authors: nguyen h.
Front Genet. 2022 Jun 17;13:893057. doi: 10.3389/fgene.2022.893057. eCollection 2022.
Front Genet. 2022.
PMID: 35783294
Free PMC article.
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D-mannose as a new therapy for fucokinase deficiency-related congenital disorder of glycosylation (FCSK-CDG).
Starosta RT, Lee AJ, Toolan ER, He M, Wongkittichote P, Daniel EJP, Radenkovic S, Budhraja R, Pandey A, Sharma J, Morava E, Nguyen H, Dickson PI.
Starosta RT, et al. Among authors: nguyen h.
Mol Genet Metab. 2024 May 9;142(2):108488. doi: 10.1016/j.ymgme.2024.108488. Online ahead of print.
Mol Genet Metab. 2024.
PMID: 38735264
Review.
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S-adenosylmethionine and nicotinamide riboside therapy in Arts syndrome: A case report and literature review.
Lee A, Knox R, Reynolds M, McRoy E, Nguyen H.
Lee A, et al. Among authors: nguyen h.
JIMD Rep. 2023 Sep 1;64(6):417-423. doi: 10.1002/jmd2.12395. eCollection 2023 Nov.
JIMD Rep. 2023.
PMID: 37927483
Free PMC article.
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Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations.
Starosta RT, Hou YC, Leestma K, Singh P, Viehl L, Manwaring L, Granadillo JL, Schroeder MC, Colombo JN, Whitehead H, Dickson PI, Hulbert ML, Nguyen HT.
Starosta RT, et al. Among authors: nguyen ht.
Front Pediatr. 2022 Sep 28;10:944178. doi: 10.3389/fped.2022.944178. eCollection 2022.
Front Pediatr. 2022.
PMID: 36245745
Free PMC article.
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