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Iron Deficiency in Anemic Children Surviving Critical Illness: Post Hoc Analysis of a Single-Center Prospective Cohort in Canada, 2019-2022.
Pediatr Crit Care Med. 2024 Apr 1;25(4):344-353. doi: 10.1097/PCC.0000000000003442. Epub 2024 Feb 15.
Pediatr Crit Care Med. 2024.
PMID: 38358779
Early effects of very early cochlear implant activation on tinnitus.
Chau IY, Li SY, Shiao AS, Islam AS, Coelho DH.
Chau IY, et al.
J Chin Med Assoc. 2023 Sep 1;86(9):850-853. doi: 10.1097/JCMA.0000000000000968. Epub 2023 Jul 23.
J Chin Med Assoc. 2023.
PMID: 37481759
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The effects of mindfulness-based stress reduction on depression, anxiety, and stress in older adults: A systematic review and meta-analysis.
Li SYH, Bressington D.
Li SYH, et al.
Int J Ment Health Nurs. 2019 Jun;28(3):635-656. doi: 10.1111/inm.12568. Epub 2019 Jan 17.
Int J Ment Health Nurs. 2019.
PMID: 30656813
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Identification of novel FBN1 and TGFBR2 mutations in 65 probands with Marfan syndrome or Marfan-like phenotypes.
Chung BH, Lam ST, Tong TM, Li SY, Lun KS, Chan DH, Fok SF, Or JS, Smith DK, Yang W, Lau YL.
Chung BH, et al.
Am J Med Genet A. 2009 Jul;149A(7):1452-9. doi: 10.1002/ajmg.a.32918.
Am J Med Genet A. 2009.
PMID: 19533785
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Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.
Wong VC, Li SY.
Wong VC, et al.
J Child Neurol. 2007 Dec;22(12):1397-400. doi: 10.1177/0883073807307091.
J Child Neurol. 2007.
PMID: 18174559
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Exon 3 polymorphisms of dopamine D4 receptor (DRD4) gene and attention deficit hyperactivity disorder in Chinese children.
Cheuk DK, Li SY, Wong V.
Cheuk DK, et al.
Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):907-11. doi: 10.1002/ajmg.b.30397.
Am J Med Genet B Neuropsychiatr Genet. 2006.
PMID: 16917940
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No association between VNTR polymorphisms of dopamine transporter gene and attention deficit hyperactivity disorder in Chinese children.
Cheuk DK, Li SY, Wong V.
Cheuk DK, et al.
Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):123-5. doi: 10.1002/ajmg.b.30280.
Am J Med Genet B Neuropsychiatr Genet. 2006.
PMID: 16402340
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