Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Ricardo Palma-Dias"'
Autor:
Angela Guzys, Susan M. Reid, Christie Bolch, Dinah S. Reddihough, Mark Teoh, Ricardo Palma-Dias, Alison Fung, Stephen Cole, Ryan Hodges, Michael Fahey, Susan P. Walker
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Fetoscopic laser coagulation of placental anastomoses reverses the pathological process in twin-to-twin transfusion syndrome, thereby increasing survival, but there are a paucity of studies addressing long-term neurodevelopmental
Externí odkaz:
https://doaj.org/article/7b9334eca4e542cab8a2612a5b78efa4
Autor:
Christie Bolch, Michael Fahey, Dinah Reddihough, Katrina Williams, Susan Reid, Angela Guzys, Stephen Cole, Andrew Edwards, Alison Fung, Ryan Hodges, Ricardo Palma-Dias, Mark Teoh, Susan Walker
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background Twin-to-twin transfusion syndrome (TTTS) is a serious complication of 10–15% of twin or triplet pregnancies in which multiple fetuses share a single placenta. Communicating placental vessels allow one fetus (the donor) to pump b
Externí odkaz:
https://doaj.org/article/0985fefc0dfb40a9922e6754a1c9b6bb
Publikováno v:
Ultrasound. 30:284-291
Introduction The right subclavian artery normally arises as the first vessel from the brachiocephalic trunk. An aberrant right subclavian artery (ARSA) arises directly from the aortic arch and crosses behind the trachea towards the right arm. This va
Autor:
T.-M. Ko, Elisa Bevilacqua, E.-K. A. Suk, K. J. Jones, Renee Stokowski, Jacques Jani, Maximilian Schmid, Ricardo Palma-Dias, S. L. Warsof, F. R. Grati, R. Chaoui
Publikováno v:
Ultrasound in Obstetrics & Gynecology
Objective 22q11.2 deletion is more common than trisomies 18 and 13 combined, yet no routine approach to prenatal screening for this microdeletion has been established. This study evaluated the clinical sensitivity and specificity of a targeted cell
Autor:
B. Hutchinson, J Harraway, E Kluckow, Mark D. Pertile, Ricardo Palma-Dias, A Poulton, Debbie Nisbet, Anthea Lindquist, Melody Menezes, R. McCoy, Jane Halliday, Zeffie Poulakis, L. Bonacquisto, A Howden, Nicole Martin, L. Gugasyan, A Kulkarni, Lisa Hui, F. da Silva Costa, Michael T. Bethune
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 56:215-224
OBJECTIVES: To perform individual record linkage of women undergoing screening with cell-free DNA (cfDNA), combined first-trimester screening (CFTS), second-trimester serum screening (STSS), and/or prenatal and postnatal cytogenetic testing with the
Publikováno v:
Journal of Minimally Invasive Gynecology. 26:919-927
STUDY OBJECTIVE To describe the incidence, management, and complications of cesarean scar pregnancy (CSP) and define risk factors for conversion from medical to surgical treatment of CSP. DESIGN Retrospective clinical study (Canadian Task Force class
Autor:
Christine Fenton, Ricardo Palma-Dias, Stephen Cole, Marina Demyanenko, Karen Reidy, Mark P. Umstad
Publikováno v:
Fetal Diagnosis and Therapy. 46:193-199
Background: Detection of a single yolk sac on early first trimester ultrasound was previously thought to be a reliable diagnostic feature of monochorionic monoamniotic (MCMA) twin pregnancies. Objectives: To determine the frequency of two yolk sacs i
Publikováno v:
American Journal of Obstetrics and Gynecology. 225:464-465
Li & Li have highlighted an important message from our recent publication: that an isolated increased nuchal translucency (NT) measurement does not perform well as standalone screening test for atypical chromosome conditions. We did not claim otherwi
Autor:
Ricardo Palma-Dias, J Harraway, Debbie Nisbet, Michael T. Bethune, E Kluckow, Mark D. Pertile, Fiona Norris, L Bonacquisto, Anthea Lindquist, B. Hutchinson, R. McCoy, Cecilia Pynaker, Melody Menezes, Fabricio da Silva Costa, A Poulton, Lisa Hui, L. Gugasyan, A Kulkarni, Jane Halliday, A Howden, Zeffie Poulakis, Nicole Martin
Publikováno v:
American Journal of Obstetrics and Gynecology. 225:527.e1-527.e12
The American College of Obstetricians and Gynecologists and the Society for Maternal-Fetal Medicine recently recommended offering genetic counseling and diagnostic testing for enlarged nuchal translucency at ≥3.0 mm, regardless of previous negative
Autor:
E.-K. A. Suk, K. J. Jones, T.-M. Ko, R. Chaoui, Jacques Jani, Ricardo Palma-Dias, S. Warsof, F. R. Grati, Elisa Bevilacqua, Renee Stokowski
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 58:16-16