Wong LJ - Search Results

1

FBXL4 defects are common in patients with congenital lactic acidemia and encephalomyopathic mitochondrial DNA depletion syndrome.

Dai H, Zhang VW, El-Hattab AW, Ficicioglu C, Shinawi M, Lines M, Schulze A, McNutt M, Gotway G, Tian X, Chen S, Wang J, Craigen WJ, Wong LJ. Dai H, et al. Among authors: wong lj. Clin Genet. 2017 Apr;91(4):634-639. doi: 10.1111/cge.12894. Epub 2017 Jan 5. Clin Genet. 2017. PMID: 27743463

2

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

Dimmock DP, Zhang Q, Dionisi-Vici C, Carrozzo R, Shieh J, Tang LY, Truong C, Schmitt E, Sifry-Platt M, Lucioli S, Santorelli FM, Ficicioglu CH, Rodriguez M, Wierenga K, Enns GM, Longo N, Lipson MH, Vallance H, Craigen WJ, Scaglia F, Wong LJ. Dimmock DP, et al. Among authors: wong lj. Hum Mutat. 2008 Feb;29(2):330-1. doi: 10.1002/humu.9519. Hum Mutat. 2008. PMID: 18205204

3

Infantile cardiomyopathy caused by a mutation in the overlapping region of mitochondrial ATPase 6 and 8 genes.

Ware SM, El-Hassan N, Kahler SG, Zhang Q, Ma YW, Miller E, Wong B, Spicer RL, Craigen WJ, Kozel BA, Grange DK, Wong LJ. Ware SM, et al. Among authors: wong lj, wong b. J Med Genet. 2009 May;46(5):308-14. doi: 10.1136/jmg.2008.063149. Epub 2009 Feb 2. J Med Genet. 2009. PMID: 19188198

4

Next-generation sequencing for disorders of low and high bone mineral density.

Sule G, Campeau PM, Zhang VW, Nagamani SC, Dawson BC, Grover M, Bacino CA, Sutton VR, Brunetti-Pierri N, Lu JT, Lemire E, Gibbs RA, Cohn DH, Cui H, Wong LJ, Lee BH. Sule G, et al. Among authors: wong lj. Osteoporos Int. 2013 Aug;24(8):2253-9. doi: 10.1007/s00198-013-2290-0. Epub 2013 Feb 27. Osteoporos Int. 2013. PMID: 23443412 Free PMC article.

5

Rapidly progressive neurological deterioration in a child with Alpers syndrome exhibiting a previously unremarkable brain MRI.

Brunetti-Pierri N, Selby K, O'Sullivan M, Hendson G, Truong C, Waters PJ, Wong LJ. Brunetti-Pierri N, et al. Among authors: wong lj. Neuropediatrics. 2008 Jun;39(3):179-83. doi: 10.1055/s-0028-1093334. Epub 2008 Nov 7. Neuropediatrics. 2008. PMID: 18991199

6

A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy.

Mobley BC, Enns GM, Wong LJ, Vogel H. Mobley BC, et al. Among authors: wong lj. Clin Neuropathol. 2009 Mar-Apr;28(2):143-9. doi: 10.5414/npp28143. Clin Neuropathol. 2009. PMID: 19353847

7

Strongly correlated multielectron bunches from interaction with quantum light.

Kumar S, Lim J, Rivera N, Wong W, Ang YS, Ang LK, Wong LJ. Kumar S, et al. Among authors: wong lj. Sci Adv. 2024 May 10;10(19):eadm9563. doi: 10.1126/sciadv.adm9563. Epub 2024 May 8. Sci Adv. 2024. PMID: 38718122 Free PMC article.

8

Free-electron crystals for enhanced X-ray radiation.

Wong LWW, Shi X, Karnieli A, Lim J, Kumar S, Carbajo S, Kaminer I, Wong LJ. Wong LWW, et al. Among authors: wong lj. Light Sci Appl. 2024 Jan 24;13(1):29. doi: 10.1038/s41377-023-01363-4. Light Sci Appl. 2024. PMID: 38267427 Free PMC article.

9

The Nanoplasmonic Purcell Effect in Ultrafast and High-Light-Yield Perovskite Scintillators.

Ye W, Yong Z, Go M, Kowal D, Maddalena F, Tjahjana L, Wang H, Arramel A, Dujardin C, Birowosuto MD, Wong LJ. Ye W, et al. Among authors: wong lj. Adv Mater. 2024 Jan 18:e2309410. doi: 10.1002/adma.202309410. Online ahead of print. Adv Mater. 2024. PMID: 38235521

10

Multicolor x-rays from free electron-driven van der Waals heterostructures.

Huang S, Duan R, Pramanik N, Go M, Boothroyd C, Liu Z, Wong LJ. Huang S, et al. Among authors: wong lj. Sci Adv. 2023 Dec;9(48):eadj8584. doi: 10.1126/sciadv.adj8584. Epub 2023 Dec 1. Sci Adv. 2023. PMID: 38039369 Free PMC article.

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