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Year Number of Results
1996 1
1998 1
2005 2
2008 2
2009 4
2010 8
2011 5
2012 3
2013 5
2014 5
2015 3
2016 3
2017 11
2018 7
2019 6
2020 10
2021 5
2022 12
2023 8
2024 1

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Page 1
FLT3 inhibitors as MRD-guided salvage treatment for molecular failure in FLT3 mutated AML.
Othman J, Potter N, Mokretar K, Taussig D, Khan A, Krishnamurthy P, Latif AL, Cahalin P, Aries J, Amer M, Belsham E, Conneally E, Craddock C, Culligan D, Dennis M, Duncan C, Freeman SD, Furness C, Gilkes A, Gkreka P, Hodgson K, Ingram W, Jain M, King A, Knapper S, Kottaridis P, McMullin MF, Mohite U, Ngu L, O'Nions J, Patrick K, Rider T, Roberts W, Severinsen MT, Storrar N, Taylor T, Russell NH, Dillon R. Othman J, et al. Among authors: ngu l. Leukemia. 2023 Oct;37(10):2066-2072. doi: 10.1038/s41375-023-01994-x. Epub 2023 Aug 9. Leukemia. 2023. PMID: 37558736 Free PMC article.
Correction: Rare disease in Malaysia: Challenges and solutions.
Shafie AA, Supian A, Hassali MAA, Ngu LH, Thong MK, Ayob H, Chaiyakunapruk N. Shafie AA, et al. Among authors: ngu lh. PLoS One. 2022 Aug 26;17(8):e0273939. doi: 10.1371/journal.pone.0273939. eCollection 2022. PLoS One. 2022. PMID: 36018891 Free PMC article.
Venetoclax-based low intensity therapy in molecular failure of NPM1-mutated AML.
Jimenez-Chillon C, Othman J, Taussig D, Jimenez-Vicente C, Martinez-Roca A, Tiong IS, Jain M, Aries J, Cakmak S, Knapper S, Kristensen DT, Murthy V, Galani JZ, Kallmeyer C, Ngu L, Veale D, Bolam S, Orfali N, Parker A, Manson C, Parker J, Erblich T, Richardson D, Mokretar K, Potter N, Overgaard UM, Roug AS, Wei AH, Esteve J, Jädersten M, Russell N, Dillon R. Jimenez-Chillon C, et al. Among authors: ngu l. Blood Adv. 2024 Jan 23;8(2):343-352. doi: 10.1182/bloodadvances.2023011106. Blood Adv. 2024. PMID: 38039513 Free PMC article.
Myoclonus-Ataxia Syndrome Associated with Hyperprolinemia Type I.
Ong TL, Lau YH, Ngu LH, Hadi D, Lau KM, Mawardi AS. Ong TL, et al. Among authors: ngu lh. Mov Disord Clin Pract. 2023 Aug 24;10(Suppl 3):S38-S40. doi: 10.1002/mdc3.13780. eCollection 2023 Aug. Mov Disord Clin Pract. 2023. PMID: 37636236 No abstract available.
Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Himmelreich N, Bertoldi M, Alfadhel M, Alghamdi MA, Anikster Y, Bao X, Bashiri FA, Zeev BB, Bisello G, Ceylan AC, Chien YH, Choy YS, Elsea SH, Flint L, García-Cazorla À, Gijavanekar C, Gümüş EY, Hamad MH, Hişmi B, Honzik T, Hübschmann OK, Hwu WL, Ibáñez-Micó S, Jeltsch K, Juliá-Palacios N, Kasapkara ÇS, Kurian MA, Kusmierska K, Liu N, Ngu LH, Odom JD, Ong WP, Opladen T, Oppeboen M, Pearl PL, Pérez B, Pons R, Rygiel AM, Shien TE, Spaull R, Sykut-Cegielska J, Tabarki B, Tangeraas T, Thöny B, Wassenberg T, Wen Y, Yakob Y, Yin JGC, Zeman J, Blau N. Himmelreich N, et al. Among authors: ngu lh. Mol Genet Metab. 2023 Jul;139(3):107624. doi: 10.1016/j.ymgme.2023.107624. Epub 2023 Jun 2. Mol Genet Metab. 2023. PMID: 37348148 Free article.
Rare disease in Malaysia: Challenges and solutions.
Shafie AA, Supian A, Ahmad Hassali MA, Ngu LH, Thong MK, Ayob H, Chaiyakunapruk N. Shafie AA, et al. Among authors: ngu lh. PLoS One. 2020 Apr 2;15(4):e0230850. doi: 10.1371/journal.pone.0230850. eCollection 2020. PLoS One. 2020. PMID: 32240232 Free PMC article.
Joint ACPGBI and The Duke's Club statement on colonoscopy training.
Vaughan-Shaw P, D'Souza N, Ngu LW, Ferguson H, Harji D, Mills SC, Cripps NP, Docherty J, Brown S, Hancock L, Davis M; Prepared on behalf of the ACPGBI, the Dukes’ Club of the ACPGBI. Vaughan-Shaw P, et al. Among authors: ngu lw. Colorectal Dis. 2021 Feb 14. doi: 10.1111/codi.15584. Online ahead of print. Colorectal Dis. 2021. PMID: 33583109
90 results