Yu-peng Liu

Hsinchu, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 24 publications

Predicting complications and morbidities in PAD patients through lower extremity compositions with dual-energy CT and material decomposition: a 2-year follow-up observational study.

Predicting complications and morbidities in PAD patients through lower extremity compositions with dual-energy CT and material decomposition: a 2-year follow-up observational study.

Journal: BMC cardiovascular disorders

Published: December 14, 2023

Lower-extremity muscle wasting in patients with peripheral arterial disease: quantitative measurement and evaluation with CT.

Lower-extremity muscle wasting in patients with peripheral arterial disease: quantitative measurement and evaluation with CT.

Journal: European radiology

Published: September 07, 2022

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

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

Journal: Orphanet journal of rare diseases

Published: February 10, 2022

Prenatal diagnosis of abdominal lymphatic malformations.

Prenatal diagnosis of abdominal lymphatic malformations.

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 15, 2020

Magnetic Resonance Imaging Features of Pediatric Coxsackievirus Encephalitis.

Magnetic Resonance Imaging Features of Pediatric Coxsackievirus Encephalitis.

Journal: Journal of the Belgian Society of Radiology

Published: January 15, 2019

Prenatal diagnosis of congenital lobar fluid overload.

Prenatal diagnosis of congenital lobar fluid overload.

Journal: Taiwanese journal of obstetrics & gynecology

Published: May 03, 2017

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

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

Journal: Taiwanese journal of obstetrics & gynecology

Published: March 30, 2017

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.

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.

Journal: Taiwanese journal of obstetrics & gynecology

Published: August 30, 2016

A Congenital Intercostal Arteriovenous Fistula.

A Congenital Intercostal Arteriovenous Fistula.

Journal: The Journal of pediatrics

Published: March 27, 2015

Suppressive function of low-dose deguelin on the invasion of oral cancer cells by downregulating tumor necrosis factor alpha-induced nuclear factor-kappa B signaling.

Suppressive function of low-dose deguelin on the invasion of oral cancer cells by downregulating tumor necrosis factor alpha-induced nuclear factor-kappa B signaling.

Journal: Head & neck

Published: March 05, 2015

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.

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.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 05, 2014

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

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

Journal: Taiwanese journal of obstetrics & gynecology

Published: October 29, 2014

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Last Updated: 09/26/2026