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Yi-Ning Su

Showing results (1-10 of 250) with videos related to

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Journal of Medical Ultrasound|August 2, 2018
Early Screening and Prevention of PreeclampsiaTzu Hung Lin, Yi Ning Su
Taiwanese Journal of Obstetrics & Gynecology|August 7, 2013
Lethal fetal stroke in uteroTzu-Hung Lin, Chien-Nan Lee, Yi-Ning Su
Pediatrics and Neonatology|April 20, 2013
PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndromeTzu-Chiang Wang, Yi-Ning Su, Ming-Chi Lai
Journal of the American Academy of Dermatology|August 25, 2009
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA syndrome): report of a sporadic case without an identifiable mutation in the CD2BP1 geneJin-Bon Hong, Yi-Ning Su, Hsien-Ching Chiu
Journal of Child Neurology|July 22, 2010
Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosisYi-Pei Lin, Yi-Ning Su, Wen-Chin Weng, et al.
Prenatal Diagnosis|July 27, 2012
Maternal ascites after thoracoamniotic shuntingTzu-Hung Lin, Jin-Chung Shih, Yi-Ning Su, et al.
Obstetrics and Gynecology|July 9, 2014
Prenatal diagnosis of true diphallia and associated anomaliesYi-An Tu, Yi-Ning Su, Po-Kai Yang, et al.
Pediatrics and Neonatology|April 20, 2013
Pelizaeus-Merzbacher disease, easily misdiagnosed as cerebral palsy: a report of a three-generation familyYen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, et al.
Prenatal Diagnosis|February 16, 2005
Asymmetrical terminal limb defects in a hydropic infant with homozygous alpha-thalassemia-1Chih-Ping Chen, Yi-Ning Su, Jian-Pei Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 28, 2011
Prenatal diagnosis of microvillus inclusion diseaseChih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, et al.
Pageof 25

Showing results (1-10 of 250) with videos related to

Sort By:
Pageof 25
Journal of Medical Ultrasound|August 2, 2018
Early Screening and Prevention of PreeclampsiaTzu Hung Lin, Yi Ning Su
Taiwanese Journal of Obstetrics & Gynecology|August 7, 2013
Lethal fetal stroke in uteroTzu-Hung Lin, Chien-Nan Lee, Yi-Ning Su
Pediatrics and Neonatology|April 20, 2013
PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndromeTzu-Chiang Wang, Yi-Ning Su, Ming-Chi Lai
Journal of the American Academy of Dermatology|August 25, 2009
Pyogenic arthritis, pyoderma gangrenosum, and acne syndrome (PAPA syndrome): report of a sporadic case without an identifiable mutation in the CD2BP1 geneJin-Bon Hong, Yi-Ning Su, Hsien-Ching Chiu
Journal of Child Neurology|July 22, 2010
Novel neurotrophic tyrosine kinase receptor type 1 gene mutation associated with congenital insensitivity to pain with anhidrosisYi-Pei Lin, Yi-Ning Su, Wen-Chin Weng, et al.
Prenatal Diagnosis|July 27, 2012
Maternal ascites after thoracoamniotic shuntingTzu-Hung Lin, Jin-Chung Shih, Yi-Ning Su, et al.
Obstetrics and Gynecology|July 9, 2014
Prenatal diagnosis of true diphallia and associated anomaliesYi-An Tu, Yi-Ning Su, Po-Kai Yang, et al.
Pediatrics and Neonatology|April 20, 2013
Pelizaeus-Merzbacher disease, easily misdiagnosed as cerebral palsy: a report of a three-generation familyYen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, et al.
Prenatal Diagnosis|February 16, 2005
Asymmetrical terminal limb defects in a hydropic infant with homozygous alpha-thalassemia-1Chih-Ping Chen, Yi-Ning Su, Jian-Pei Huang, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 28, 2011
Prenatal diagnosis of microvillus inclusion diseaseChih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, et al.
Pageof 25