Wu WJ - Search Results

1

Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan.

Shen MC, Wu WJ, Cheng PJ, Ma GC, Li WC, Liou JD, Chang CS, Lin WH, Chen M. Shen MC, et al. Among authors: wu wj. Thromb J. 2016 Oct 28;14:44. doi: 10.1186/s12959-016-0118-9. eCollection 2016. Thromb J. 2016. PMID: 27799851 Free PMC article.

2

Complete resolution of hydrops by placement of double basket catheter in a case of macrocystic type multilocular pulmonary sequestration.

Wu WJ, Shih JC, Sago H, Chen M. Wu WJ, et al. Taiwan J Obstet Gynecol. 2017 Jun;56(3):402-405. doi: 10.1016/j.tjog.2017.04.027. Taiwan J Obstet Gynecol. 2017. PMID: 28600060 Free article.

3

A Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucleated Red Blood Cells.

Ma GC, Lin WH, Huang CE, Chang TY, Liu JY, Yang YJ, Lee MH, Wu WJ, Chang YS, Chen M. Ma GC, et al. Among authors: wu wj. Micromachines (Basel). 2019 Feb 17;10(2):132. doi: 10.3390/mi10020132. Micromachines (Basel). 2019. PMID: 30781548 Free PMC article.

4

Prenatal Diagnosis of Autosomal Recessive Renal Tubular Dysgenesis with Anhydramnios Caused by a Mutation in the AGT Gene.

Ma GC, Chen YC, Wu WJ, Chang SP, Chang TY, Lin WH, Chen M. Ma GC, et al. Among authors: wu wj. Diagnostics (Basel). 2019 Nov 11;9(4):185. doi: 10.3390/diagnostics9040185. Diagnostics (Basel). 2019. PMID: 31718018 Free PMC article.

5

Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis.

Chen YC, Wu WJ, Chang SP, Ma GC, Chen M. Chen YC, et al. Among authors: wu wj. Taiwan J Obstet Gynecol. 2020 Jan;59(1):157-161. doi: 10.1016/j.tjog.2019.11.027. Taiwan J Obstet Gynecol. 2020. PMID: 32039787 Free article.

6

Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.

Chang TY, Chung IF, Wu WJ, Chang SP, Lin WH, Ginsberg NA, Ma GC, Chen M. Chang TY, et al. Among authors: wu wj. Diagnostics (Basel). 2020 May 7;10(5):286. doi: 10.3390/diagnostics10050286. Diagnostics (Basel). 2020. PMID: 32392875 Free PMC article.

7

Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to Trio Analyses.

Chen M, Wu WJ, Lee MH, Ku TH, Ma GC. Chen M, et al. Among authors: wu wj. Genes (Basel). 2020 Aug 22;11(9):979. doi: 10.3390/genes11090979. Genes (Basel). 2020. PMID: 32842633 Free PMC article.

8

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray.

Yao TY, Wu WJ, Law KS, Lee MH, Chang SP, Lee DJ, Lin WH, Chen M, Ma GC. Yao TY, et al. Among authors: wu wj. Diagnostics (Basel). 2021 Aug 12;11(8):1457. doi: 10.3390/diagnostics11081457. Diagnostics (Basel). 2021. PMID: 34441391 Free PMC article.

9

Comparison of One-Stage and Two-Stage Intraoperative Uterine Artery Embolization during Cesarean Delivery for Placenta Accreta: Report of Two Clinical Cases at a Tertiary Referral Medical Center.

Lim ZW, Lee WY, Huang YC, Wu WJ, Chen M. Lim ZW, et al. Among authors: wu wj. Healthcare (Basel). 2022 Apr 22;10(5):774. doi: 10.3390/healthcare10050774. Healthcare (Basel). 2022. PMID: 35627911 Free PMC article.

10

Polyhydramnios as a sole ultrasonographic finding for detecting fetal hemolytic anemia caused by anti-c alloimmunization.

Wang SC, Wu YC, Wu WJ, Lee MH, Lin WH, Ma GC, Chen M. Wang SC, et al. Among authors: wu wj, wu yc. Taiwan J Obstet Gynecol. 2022 Jul;61(4):722-725. doi: 10.1016/j.tjog.2022.04.006. Taiwan J Obstet Gynecol. 2022. PMID: 35779930 Free article.

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