Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Elisabeth Smet"'
Publikováno v:
Fetal Diagnosis and Therapy. 50:29-36
Early identification of fetal sex is possible due to both improved ultrasound resolution and the incorporation of cell-free DNA testing into routine prenatal screening services. While ultrasound assessment of the external genitalia generally suffices
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a899b988303e5011ed784c781dfb137c
https://doi.org/10.1159/000529505
https://doi.org/10.1159/000529505
Autor:
Stefaan Pacquee, Dean H Conrad, Tal D Saar, David Rosen, Gregory Cario, Danny Chou, Maria-Elisabeth Smet
Publikováno v:
Gynecology and Minimally Invasive Therapy, Vol 7, Iss 3, Pp 127-129 (2018)
We herein describe the operative approach of a postmenopausal woman with a history of surgically corrected congenital bladder exstrophy-epispadias who presented with long-standing complete procidentia. The patient was initially treated by laparoscopi
Externí odkaz:
https://doaj.org/article/893dcfcc6f9b4ea08590be137b472b35
Bladder exstrophy (BE) is a congenital genito-urinary malformation where there is a defect in the abdominal wall resulting in a protruding open bladder with exposed mucosa [1]. Several reconstructive procedures are required to correct the anomalies r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9d6fb964ab187684c8e1ad714b525e6
https://doi.org/10.21203/rs.3.rs-2679626/v1
https://doi.org/10.21203/rs.3.rs-2679626/v1
Autor:
Christine Thuy-Trang Tran, Maria-Elisabeth Smet, Jonathan Forsey, Andreas Zankl, Roshini Nayyar
Publikováno v:
Fetal Diagnosis and Therapy. 49:479-485
Introduction: Bruck syndrome is a rare autosomal recessive disease characterized by multiple joint contractures, bone fragility, and fractures. Two genes have been associated with Bruck syndrome, FKBP10 and PLOD2, though they are phenotypically indis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::565f9bf19bf4128ee4f7d38b01c622d5
https://doi.org/10.1159/000527594
https://doi.org/10.1159/000527594
Autor:
Fergus Scott, Biao Li, Andrew McLennan, Edwin P. Kirk, Maria-Elisabeth Smet, Tristan Hardy, Louise Carey, Michael Friedlander, Samantha Leigh Sundercombe
Publikováno v:
Prenatal Diagnosis. 41:1273-1276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d63ef62ff00105ef66185f97bf3b1be4
https://doi.org/10.1002/pd.6020
https://doi.org/10.1002/pd.6020
Publikováno v:
Journal of Ultrasound in Medicine. 40:1743-1748
We report on a rare case of a prenatally diagnosed isolated facial teratoma, presenting as an avascular elongated ossified lesion arising from the inferior lateral rim of the orbit. There was no evidence of fetal compromise throughout the course of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e25726cf1680c3d6516a2caabcec2590
https://doi.org/10.1002/jum.15564
https://doi.org/10.1002/jum.15564
Autor:
Susan Heath, Maria-Elisabeth Smet, Jennifer Curnow, Christine Wu, Thushari I. Alahakoon, Jacob George, Ming-Wei Lin
Publikováno v:
Journal of Obstetrics and Gynaecology Research. 47:822-826
Sodium taurocholate co-transporting polypeptide deficiency is a rare metabolic autosomal recessive condition resulting in critically elevated plasma bile acid levels. Hypercholanaemia in similar conditions such as intrahepatic cholestasis of pregnanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43a5be81047a883c6dabed18c12054e4
https://doi.org/10.1111/jog.14568
https://doi.org/10.1111/jog.14568
Autor:
Andrew McLennan, Maria-Elisabeth Smet
Publikováno v:
Australas J Ultrasound Med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e2dc119e35f843f68034414ceb49879
https://pubmed.ncbi.nlm.nih.gov/34760503
https://pubmed.ncbi.nlm.nih.gov/34760503
Autor:
Tristan Hardy, T. Fullston, Melody Menezes, Daniel L. Rolnik, Andrew McLennan, K. Carey, Maria-Elisabeth Smet, Fergus Scott
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and GynecologyREFERENCES. 59(1)
Cell-free DNA (cfDNA) screening assesses both maternal and placental cfDNA. Fibroids are common and release cfDNA into maternal serum. Genetic abnormality is seen in 50% of fibroids. We aimed to assess the impact of fibroids on the accuracy of genome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13de231d5eef6fb1b1055c7d6f54fb93
https://pubmed.ncbi.nlm.nih.gov/34985817
https://pubmed.ncbi.nlm.nih.gov/34985817
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