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Roland Axt-Fliedner

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 5, 2025
Non-Invasive Prenatal Testing by Cell-Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants-Prenatal Findings and Postnatal OutcomesIvonne Bedei, Johanna Bruder, Ida C B Lund, et al.
Archives of Gynecology and Obstetrics|May 30, 2019
Application of the INTERGROWTH-21st chart compared to customized growth charts in fetuses with left heart obstruction: late trimester biometry, cerebroplacental hemodynamics and perinatal outcomeOliver Graupner, Franziska Helfrich, Eva Ostermayer, et al.
Orphanet Journal of Rare Diseases|March 13, 2024
Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one caseMateja Pfeifer, Helga Rehder, Maria Gerykova Bujalkova, et al.
Archives of Gynecology and Obstetrics|February 15, 2021
Natural history of pulmonary atresia with intact ventricular septum (PAIVS) and critical pulmonary stenosis (CPS) and prediction of outcomeAline Wolter, Natalia Markert, Jan Sebastian Wolter, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 30, 2020
Prenatal Diagnosis and Outcome of Congenital Corrected Transposition of the Great Arteries - A Multicenter Report of 69 CasesCarina Nina Vorisek, Christian Enzensberger, Steven Willomeit, et al.
Prenatal Diagnosis|June 17, 2017
Absent pulmonary valve syndrome - diagnosis, associations, and outcome in 71 prenatally diagnosed casesRoland Axt-Fliedner, Andrii Kurkevych, Maciej Slodki, et al.
Journal of Clinical Medicine|August 12, 2023
Implementation and Assessment of a Laparotomy-Assisted Three-Port Fetoscopic Spina Bifida Repair ProgramCorinna Keil, Siegmund Köhler, Benjamin Sass, et al.
Prenatal Diagnosis|February 2, 2023
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsIvonne Bedei, Tascha Gehrke, Karl-Philipp Gloning, et al.
Prenatal Diagnosis|January 5, 2023
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomeIvonne Bedei, Karl-Philipp Gloning, Luc Joyeux, et al.
Journal of Clinical Medicine|August 12, 2022
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 5, 2025
Non-Invasive Prenatal Testing by Cell-Free DNA (cfNIPT) for Detecting Turner Syndrome With Mosaicism and Structural Variants-Prenatal Findings and Postnatal OutcomesIvonne Bedei, Johanna Bruder, Ida C B Lund, et al.
Archives of Gynecology and Obstetrics|May 30, 2019
Application of the INTERGROWTH-21st chart compared to customized growth charts in fetuses with left heart obstruction: late trimester biometry, cerebroplacental hemodynamics and perinatal outcomeOliver Graupner, Franziska Helfrich, Eva Ostermayer, et al.
Orphanet Journal of Rare Diseases|March 13, 2024
Tracheal agenesis versus tracheal atresia: anatomical conditions, pathomechanisms and causes with a possible link to a novel MAPK11 variant in one caseMateja Pfeifer, Helga Rehder, Maria Gerykova Bujalkova, et al.
Archives of Gynecology and Obstetrics|February 15, 2021
Natural history of pulmonary atresia with intact ventricular septum (PAIVS) and critical pulmonary stenosis (CPS) and prediction of outcomeAline Wolter, Natalia Markert, Jan Sebastian Wolter, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 30, 2020
Prenatal Diagnosis and Outcome of Congenital Corrected Transposition of the Great Arteries - A Multicenter Report of 69 CasesCarina Nina Vorisek, Christian Enzensberger, Steven Willomeit, et al.
Prenatal Diagnosis|June 17, 2017
Absent pulmonary valve syndrome - diagnosis, associations, and outcome in 71 prenatally diagnosed casesRoland Axt-Fliedner, Andrii Kurkevych, Maciej Slodki, et al.
Journal of Clinical Medicine|August 12, 2023
Implementation and Assessment of a Laparotomy-Assisted Three-Port Fetoscopic Spina Bifida Repair ProgramCorinna Keil, Siegmund Köhler, Benjamin Sass, et al.
Prenatal Diagnosis|February 2, 2023
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsIvonne Bedei, Tascha Gehrke, Karl-Philipp Gloning, et al.
Prenatal Diagnosis|January 5, 2023
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomeIvonne Bedei, Karl-Philipp Gloning, Luc Joyeux, et al.
Journal of Clinical Medicine|August 12, 2022
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, et al.
Pageof 10