Yu‐Peng Liu

发表

Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).

Chih-ping Chen, S. Chern, H. Au, 2011, Taiwanese journal of obstetrics & gynecology.

Neonatal infected subgaleal hematoma: an unusual complication of early-onset E. coli sepsis.

Hsiao-Fang Hung, H. Fu, K. Cheng, 2015, Pediatrics and neonatology.

Autosomal recessive polycystic kidney disease: appearance on fetal MRI

Sho-Jen Cheng, S. Shih, Yu‐Peng Liu, 2006, Pediatric Radiology.

A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome.

S. Ng, Chih-ping Chen, S. Chern, 2012, European journal of medical genetics.

Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Magnetic Resonance Imaging Features of Pediatric Coxsackievirus Encephalitis

Yu‐Peng Liu, Yang-Kai Fan, 2019, Journal of the Belgian Society of Radiology.

Fetal cystic lung lesions: Evaluation with magnetic resonance imaging

Chih-ping Chen, Fei-Shih Yang, S. Shih, 2010, Pediatric pulmonology.

Evaluation of arterial phase MDCT for the characterization of lower gastrointestinal bleeding in infants and children: Preliminary results.

Fei-Shih Yang, Hung-Chang Lee, Y. Tsai, 2010, AJR. American journal of roentgenology.

Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2013, Gene.

Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

OMPHALOCELE IN A MALE FETUS: PRENATAL MAGNETIC RESONANCE IMAGING FINDINGS AND LITERATURE REVIEW

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009 .

Prenatal 3‐dimensional sonographic and MRI findings in omphalocele–exstrophy–imperforate anus–spinal defects complex

Chih-ping Chen, F. Tsai, Wayseen Wang, 2008, Journal of clinical ultrasound : JCU.

Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal ultrasound demonstration of scoliosis, absence of one rib, a radial club hand, congenital heart defects and absent stomach in a fetus with VACTERL association.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1

Chih-ping Chen, C. Tzen, S. Chern, 2007, Prenatal diagnosis.

There is something in the ear: mondini dysplasia.

N. Chiu, Chien-Yu Lin, H. Chi, 2014, The Journal of pediatrics.

Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of congenital lobar fluid overload.

Chih-ping Chen, Yu‐Peng Liu, Dao-Chen Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Fetal Magnetic Resonance Imaging of Congenital Chest Malformations: A Pictorial Review

Yi-Lan Lin, Su‐Chiu Chen, Yu‐Peng Liu, 2013 .

Congenital lobar emphysema: appearance on fetal MRI

S. Shih, Yu‐Peng Liu, 2008, Pediatric Radiology.

Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2006, Prenatal diagnosis.

Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.

Chih-ping Chen, Yeou-Lih Wang, S. Chern, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of abdominal lymphatic malformations.

Chih-ping Chen, Yu‐Peng Liu, Dao-Chen Lin, 2021, Taiwanese journal of obstetrics & gynecology.

Delayed-onset Right Diaphragmatic Hernia of Newborn after Group B Streptococcal pneumonia: a case report

Fei-Shih Yang, S. Shih, Yu‐Peng Liu, 2010 .

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Apert syndrome associated with upper airway obstruction and gastroesophageal reflux inducing polyhydramnios in the third trimester.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Meconium peritonitis with intestinal atresia mimicking huge tumor in a preterm neonate.

Chien-Yu Lin, Hung-Yang Chang, Chi-Hone Lien, 2013, Jornal de Pediatria.

Mesoaortic compression of left renal vein revealed by multidetector computed tomography: nutcracker syndrome

Fei-Shih Yang, Yu‐Peng Liu, Wan-Ju Yang, 2007, Emergency Medicine Journal.

Adjunct diagnostic value of radiological findings in mucopolysaccharidosis type IVa-related thoracic spinal abnormalities: a pilot study

Kun-Shuo Huang, Yasmeen Jan, Yu‐Peng Liu, 2022, Orphanet Journal of Rare Diseases.

Fetal Magnetic Resonance Imaging of Congenital Renal Anomalies: A Pictorial Review

Su‐Chiu Chen, Yu‐Peng Liu, 2014 .

Perinatal Magnetic Resonance Imaging Demonstration of Duplication of the Right Renal Collecting System with Ipsilateral Hydronephrosis and Hydroureter, and Contralateral Renal Hypoplasia

Chih-ping Chen, Wayseen Wang, Jun-Wei Su, 2011 .

An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2013, Gene.

Acute urinary retention in a 7-year-old girl: an unusual complication of cytomegalovirus cystitis.

J. Tsai, Fei-Shih Yang, Y. Tsai, 2008, Journal of pediatric surgery.

Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Journal of the Chinese Medical Association.

Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

Fetal MRI of hydrometrocolpos with septate vagina and uterus didelphys as well as massive urinary ascites due to cloacal malformation

Chih-ping Chen, Yu‐Peng Liu, 2009, Pediatric Radiology.

Myxoinflammatory fibroblastic sarcoma of the chest wall

Pei-Wen Huang, Yu‐Peng Liu, Wun-Ke Chen, 2017 .

Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, in vitro fertilization and embryo transfer.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Magnetic resonance imaging demonstration of sirenomelia in one fetus of a dizygotic twin pregnancy conceived by intracytoplasmic sperm injection, invitro fertilization and embryo transfer

Chih-ping Chen, F. Tsai, S. Chern, 2022 .

Galloway-Mowat syndrome: prenatal ultrasound and perinatal magnetic resonance imaging findings.

Chih-ping Chen, F. Tsai, Shuan-Pei Lin, 2011, Taiwanese journal of obstetrics & gynecology.

Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome.

Chih-ping Chen, Jian-Pei Huang, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of choledochal cyst by magnetic resonance cholangiography

S. Shih, Yu‐Peng Liu, 2006, Pediatric Radiology.

Prenatal Diagnosis of Cerebral Tubers by Magnetic Resonance Imaging Following Detection of Cardiac Rhabdomyomas by Prenatal Ultrasound in a Fetus With a Nonsense Mutation in the TSC2 gene

Chih-ping Chen, Wayseen Wang, Yidi Su, 2011 .

Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas

Chih-ping Chen, N. Chiu, Wayseen Wang, 2005, Prenatal diagnosis.

Internal supravesical hernia.

K. Jeng, Ya-ting Jan, Fei-Shih Yang, 2008, American journal of surgery.

Cystic lymphatic malformation of the pelvis mimicking seminal vesicle cysts.

Kun-Shuo Huang, Nien-Lu Wang, Yu‐Peng Liu, 2010, Journal of pediatric surgery.

Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester.

Chih-ping Chen, F. Tsai, S. Weng, 2012, Taiwanese journal of obstetrics & gynecology.

Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of concomitant gallbladder hydrops and pyelectasis with spontaneous resolution.

Chih-ping Chen, Wayseen Wang, S. Chien, 2007, Taiwanese journal of obstetrics & gynecology.

Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling.

Chih-ping Chen, N. Chiu, S. Chern, 2016, Taiwanese Journal of Obstetrics & Gynecology.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene.

Fuu-Jen Tsai, Chih-ping Chen, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2009, Taiwanese journal of obstetrics & gynecology.

Fetal Magnetic Resonance Imaging of Congenital Renal Anomalies: A Pictorial Review

Su‐Chiu Chen, Yu‐Peng Liu, 2014 .

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.