刊物出版

Post-laparoscopic shoulder-tip pain (STP)

P.-H. Wang , S.-T. Yang and W.-L. Lee

Cervical cancer in Taiwan

S.-T. Yang , P.-H. Wang and C.-H. Lai

Is the far-advanced endometrial cancer curable?

P.-H. Wang , C.-H. Liu and W.-S. Liou

The decision for adjuvant therapy for early-stage high-risk endometrial cancer is in dilemma

P.-H. Wang , Y. Kobayashi and B.-G. Kim

Is the less the better for early-stage low-risk cervical cancer?

P.-H. Wang , W.-T. Chao and J.-W. Kim

Locally advanced cervical cancer treatment: Immunotherapy or induction dose-dense chemotherapy?

P.-H. Wang , W.-T. Chao and T.-C. Kuo

Recent advances in cervical cancer treatment: Innovations from early-stage to advanced disease

H. Lin , C.-H. Wu , H.-C. Fu and Y.-C. Ou

Molecular subtyping and the 2023 FIGO staging in endometrial cancer: Redefi ning adjuvant therapy

H. Lin , Y.-C. Ou , H.-C. Fu , S.-W. Huang , C.-H. Wu and C.-C. Changchien

Falloposcope for early screening of high-grade serous ovarian carcinoma

A.D. Burtman , J. Heusinkveld , C.-D. Hsu and R. Goyal

Postpartum readmission associated with severe maternal morbidity: A systematic review

W.-C. Huang and C.-C.C. Lin

Better pregnancy outcomes in women with day 2 or day 3 fresh embryo transfer when progesterone supplementation for luteal phase support is initiated on the day of oocyte retrieval

C.-C. Lee , K.-S. Lee , C.S.-C. Chiu , R.K.-K. Lee and M.-H. Lin

Placental mesenchymal dysplasia: A cause of intrauterine growth restriction and intrauterine death

E. Çobankent Aytekin , A. Boduro g˘ lu , C.Y. Sanhal and H.S. Toru

Abnormal methylation of ST8SIA4 in low-motility sperm: A genome-wide identifi cation approach

C.-C. Chang , L.-C. Liu , Y.-T. Chou , C.-W. Chen , C.-C. Guo , C.-C. Chan , T.-J. Lin , C.-H. Chen and M.-T. Chung

Obstetric and neonatal outcomes in pregnant women with left-sided valvular stenosis in a tertiary medical center in Taiwan

H.-L. Lee , H.-T. Liu , C.-Y. Chiang , S.-C. Chou and C.-C. Chou

PHLDA2 expression and promoter methylation in placental trophoblasts: Associations with preeclampsia development

J. Chen , Y. Zheng , L. Hang and H. Wang

Comparison of motor imagery focused pelvic floor exercises and relaxation exercises for treating dysmenorrhea: A randomized controlled study

S.Koço˘glu, Ö. ¸ Sevgin and B.D. Hosba¸

Diagnostic contribution of conventional and molecular karyotyping in congenital diaphragmatic hernia related copy number variations

G. Somayyeh Heidargholizadeh , C. Gulec , G. Bulut , I.H. Kalelioglu , R. Has , T.S. Sivrikoz , T. Kalayci , B.O. Selcuk and B. Karaman

Risk factors for failed induction of labor: A retrospective study in a single, tertiary, perinatal-care center

M. Nariai , O. Wada-Hiraike , T. Iriyama , T. Seyama , K. Kumasawa , Y. Hirota and Y. Osuga

OHVIRA syndrome: A case report treated with delayed diagnosis and multidisciplinary approaches

E. Akay and A.D. Uzun G ü l

The first report of a successful birth by preimplantation genetic testing for leukodystrophy induced by IBA57 gene

J. Wang , Z. Xu , D. Chen and H. Xiang

Plateletpheresis for treating essential thrombocythemia that developed during pregnancy: A case report

N. Masuko , K. Tanimura , K. Moriuchi , T. Kita , K. Obata , S. Suda , H. Imafuku , M. Deguchi , K. Kurata , K. Yakushijin , K. Kono , T. Kawakatsu and Y. Terai

A prenatally diagnosed Klinefelter syndrome case of 46,XX/47,XXY mosaicism with partial deletion of Y chromosome

H. Okubo , Y. Ito , T. Kawai , H. Kamura , M. Yamamura , M. Kaneko , A. Hasegawa , K. Takahashi , M. Kobayashi , H. Kawame , K. Hata , O. Samura and A. Okamoto

Recurrent cesarean scar pregnancy successfully managed by laparoscopy: Case report and current trend

J.W. Lin , H.Y. Lai , J.Y. Tseng and P.-H. Wang

Detection of mosaic 1q21.1 microdeletion in a fetus associated with megacystis and arthrogryposis of bilateral hands

C.-P. Chen

47,XYY/45,X at amniocentesis in a pregnancy associated with a favorable fetal outcome and perinatal progressive decrease of the 45,X cell line

C.-P. Chen

Low-level mosaic trisomy 12 at amniocentesis in a pregnancy associated with complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome

C.-P. Chen

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome in a pregnancy with low-level mosaic trisomy 21 at amniocentesis

C.-P. Chen

Incidental detection of a familial 361-kb 9q34.3 microduplication encompassing EHMT1 and CACNA1B without apparently phenotypic abnormality

C.-P. Chen

Prenatal diagnosis of a familial Xq27.1-q28 deletion with an asymptomatic mother carrier and no abnormality in the female fetus

C.-P. Chen

Low-level mosaicism for 45,X in 45,X/46,XY at amniocentesis associated with complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the 45,X cell line and a favorable fetal outcome

C.-P. Chen

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy with a favorable fetal outcome and a normal karyotype at birth

C.-P. Chen

Prenatal diagnosis of a familial 22q11.21 microduplication and mosaic trisomy 20 in a pregnancy with an asymptomatic father carrier and a favorable fetal outcome

C.-P. Chen

Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with an abnormal first-trimester maternal serum screening result, a favorable fetal outcome and postnatal decrease of the aneuploid cell line

C.-P. Chen

Detection of a rare maternal 6q27 microduplication in a fetus with no phenotypic abnormalities

J. Wu , W. Tian , T. Tou and S. Xu

Prenatal diagnosis and genetic counselling of a paternal inherited GLI3 frameshift deletion in a Chinese family

R. Mei , W. Tang and Y. Peng

“Armadillo” sign as a new prenatal ultrasound clue for Pierre Robin sequence

T.-Y. Yang , P.K.-T. Chen , K. Olisova , H. Ko and T.-Y. Chang

Routine transvaginal ultrasound preceding mid-pregnancy fetal anatomical screening is a feasible and valuable tool in screening for vasa previa

P.-C. Wu , C.-C. Hsia , K. Olisova , C.-C. Yeh and T.-Y. Chang

Prenatal diagnosis and genetic counseling of a de novo 18q21.2 microdeletion associated with normal phenotype

Y. Feng , R. Chang , T. Wu and W. Tang

Prenatal diagnosis and genetic counselling of monozygotic triplets with paternally inherited chromosome 15q11.2 microdeletion in a Chinese family

B. Liu , Y. Wang , S. Fei , H. Jiang and S. Li