Luk HM - Search Results

1

Patient-Initiated Follow-Up in Ovarian Cancer.

Luk HM, Ngu SF, Lau LSK, Tse KY, Chu MMY, Kwok ST, Ngan HYS, Chan KKL. Luk HM, et al. Curr Oncol. 2023 Mar 26;30(4):3627-3636. doi: 10.3390/curroncol30040276. Curr Oncol. 2023. PMID: 37185389 Free PMC article.

2

Applications and Safety of Sentinel Lymph Node Biopsy in Endometrial Cancer.

Chiu WK, Kwok ST, Wang Y, Luk HM, Chan AHY, Tse KY. Chiu WK, et al. Among authors: luk hm. J Clin Med. 2022 Oct 31;11(21):6462. doi: 10.3390/jcm11216462. J Clin Med. 2022. PMID: 36362690 Free PMC article. Review.

3

Expression and clinical significance of Gal-3 and NFκB pathway-related factors in epithelial ovarian carcinoma.

Luk HM, Wang DY, Xie LL, Liu XY, Xu GC, Lu HW. Luk HM, et al. Int J Clin Exp Pathol. 2020 May 1;13(5):1197-1205. eCollection 2020. Int J Clin Exp Pathol. 2020. PMID: 32509095 Free PMC article.

4

Improving Diagnostic Classification of Stillbirths and Neonatal Deaths Using ICD-PM (International Classification of Diseases for Perinatal Mortality) Codes: Validation Study.

Luk HM, Allanson E, Ming WK, Leung WC. Luk HM, et al. JMIR Med Inform. 2020 Aug 3;8(8):e20071. doi: 10.2196/20071. JMIR Med Inform. 2020. PMID: 32744510 Free PMC article.

5

A de novo pathogenic variant in neuronal differentiation factor 2 in a Chinese patient with early infantile epileptic encephalopathy.

Poon JYY, Mok MTS, Ho SKL, Cheng SSW, Lo IFM, Luk HM. Poon JYY, et al. Among authors: luk hm. Clin Dysmorphol. 2024 Jul 1;33(3):128-133. doi: 10.1097/MCD.0000000000000498. Epub 2024 Apr 17. Clin Dysmorphol. 2024. PMID: 38818821 No abstract available.

6

Natural history of adults with KBG syndrome: a physician-reported experience.

Bayat A, Grimes H, de Boer E, Herlin MK, Dahl RS, Lund ICB, Bayat M, Skjelmose Bolund AC, Gjerulfsen CE, Gregersen PA, Zilmer M, Juhl S, Cebula K, Rahikkala E, Maystadt I, Peron A, Vignoli A, Alfano RM, Stanzial F, Benedicenti F, Currò A, Luk HM, Jouret G, Zurita E, Heuft L, Schnabel F, Busche A, Veenstra-Knol HE, Tkemaladze T, Vrielynck P, Lederer D, Platzer K, Ockeloen CW, Goel H, Low KJ. Bayat A, et al. Among authors: luk hm. Genet Med. 2024 May 27:101170. doi: 10.1016/j.gim.2024.101170. Online ahead of print. Genet Med. 2024. PMID: 38818797

7

Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.

Ho SKL, Ng SYL, Yung TK, Mok MTS, Yiu WC, Cheng HHY, Cheng SSW, Luk HM, Lo IFM, Kan ASY. Ho SKL, et al. Among authors: luk hm. Am J Med Genet A. 2024 May 15:e63657. doi: 10.1002/ajmg.a.63657. Online ahead of print. Am J Med Genet A. 2024. PMID: 38747677

8

A Baby With Complete Androgen Insensitivity Syndrome and the Fortuitous Discovery of 45,X/46,XY Mosaicism.

Wong WY, Wong LM, Tam YH, Luk HM. Wong WY, et al. Among authors: luk hm. Cureus. 2023 Aug 11;15(8):e43352. doi: 10.7759/cureus.43352. eCollection 2023 Aug. Cureus. 2023. PMID: 37700992 Free PMC article.

9

Public and Healthcare Provider Receptivity toward the Retention of Dried Blood Spot Cards and Their Usage for Extended Genetic Testing in Hong Kong.

Belaramani KM, Fung CW, Kwok AMK, Lee SYR, Yau EKC, Luk HM, Mak CM, Yeung MCW, Ngan OMY. Belaramani KM, et al. Among authors: luk hm. Int J Neonatal Screen. 2023 Aug 11;9(3):45. doi: 10.3390/ijns9030045. Int J Neonatal Screen. 2023. PMID: 37606482 Free PMC article.

10

Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.

Hui PW, Mok YK, Luk HM, Au SLK, Lau EYT, Chung B, Kan ASY. Hui PW, et al. Among authors: luk hm. Prenat Diagn. 2023 Sep;43(10):1366-1369. doi: 10.1002/pd.6414. Epub 2023 Aug 2. Prenat Diagn. 2023. PMID: 37529930

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