Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Long-Ching Kuan"'
Autor:
Po-Fan Chen, Long-Ching Kuan, Chiu-Ching Kao, Hui-Kuo Hsu, Ming Chen, Tsung-Cheng Kuo, Pao-Lin Kuo
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 170-173 (2022)
Objective: Cystic hygromas are frequently encountered in fetus with Turner syndrome (TS). Nevertheless, identification of genetic loci responsible for the cystic hygroma has been problematic. Here, we tried to elucidate the candidate gene for cystic
Externí odkaz:
https://doaj.org/article/f6d291a33cd8465ca42397b8c0fff2a2
Autor:
Yiu-Tai Li, James Ching-Hung Hsieh, Guang-Qiong Hou, Tien-Hui Chen, Yi-Chih Chu, Ta-Chin Lin, Long-Ching Kuan, Mau Lin, Hsun-Han Tang, Tsung-Cheng Kuo
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 50, Iss 1, Pp 11-14 (2011)
Objective: Simultaneous mifepristone 200 mg and vaginal misoprostol 800 μg produces a complete abortion rate of approximately 90% at up to 63 days of gestation. The aim of this study was to determine the effectiveness of concurrent administration of
Externí odkaz:
https://doaj.org/article/dc4b7eee4104489ea5b8ba742e652281
Autor:
Yiu-Tai Li, Guang-Qiong Hou, Tien-Hui Chen, Yi-Chih Chu, Ta-Chin Lin, Long-Ching Kuan, Mau Lin, Shu-Feng Huang, Fu-Min Chen, Tsung-Cheng Kuo
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 47, Iss 4, Pp 408-411 (2008)
Objective: The aim of this study was to determine the complete abortion rate for the vaginal administration of high-dose misoprostol after a failed medical abortion. Materials and Methods: When their medical abortions failed after the conventional or
Externí odkaz:
https://doaj.org/article/8b3a88cc24f9403db36d08a711de56db
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 45, Iss 3, Pp 239-243 (2006)
Objective: When a patient's chief complaint is lower abdominal pain, but physical and ultrasonic examinations and laboratory tests show no evidence of any noticeable disease, physicians may make a wrong diagnosis, such as abdominal adhesion, chronic
Externí odkaz:
https://doaj.org/article/d4c50eb10af54366a4051c5a5c32c63b
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 52, Iss 3, Pp 443-445 (2013)
Externí odkaz:
https://doaj.org/article/32ae5375ae3742b89544ffce4f25e0ed
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 43, Iss 2, Pp 120-124 (2004)
Objective: We report the treatment of a patient with persistent gestational trophoblastic disease. Case Report: A 42-year-old woman, gravida 2, para 1, was initially diagnosed with choriocarcinoma from curettage specimens. She initially responded to
Externí odkaz:
https://doaj.org/article/5c2d41e146634c649cb298192f0f9a54
Autor:
Po-Fan Chen, Long-Ching Kuan, Chiu-Ching Kao, Hui-Kuo Hsu, Ming Chen, Tsung-Cheng Kuo, Pao-Lin Kuo
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 61, Iss 1, Pp 170-173 (2022)
Objective: Cystic hygromas are frequently encountered in fetus with Turner syndrome (TS). Nevertheless, identification of genetic loci responsible for the cystic hygroma has been problematic. Here, we tried to elucidate the candidate gene for cystic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c93410c35304b2d97e661c1c75137aa
https://pubmed.ncbi.nlm.nih.gov/35181033
https://pubmed.ncbi.nlm.nih.gov/35181033
Publikováno v:
Prenatal Diagnosis. 36:492-495
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5ea78f7c7eed759dff582b1730fd888
https://doi.org/10.1002/pd.4796
https://doi.org/10.1002/pd.4796
Publikováno v:
Journal of Assisted Reproduction and Genetics. 30:1559-1562
The dicentric Y chromosomes are the most commonly found in the structural aberration of Y chromosome. If the dicentric chromosome has completely symmetric arms, it is considered an isodicentric chromosome. The sites of breakage and fusion at Yp and Y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a4d3686f681de8d23a369fd96e2b40a
https://doi.org/10.1007/s10815-013-0119-6
https://doi.org/10.1007/s10815-013-0119-6
Publikováno v:
Fertility and Sterility. 96:e29-e34
Objective To investigate genomic changes in a family with deletion of X chromosome q22.3-q25 associated with normal constitutional and reproductive phenotypes. Design Case report. Setting Academic district hospital genetic laboratory. Patient(s) A fa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a3f2bc0493df18c4ee0ce895a81f650
https://doi.org/10.1016/j.fertnstert.2011.04.061
https://doi.org/10.1016/j.fertnstert.2011.04.061