Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Lisa Leth Maroun"'
Autor:
Christen Rune Stensvold, Lone Storgaard, Lisa Leth Maroun, Jørgen Anders Lindholm Kurtzhals, Henrik Vedel Nielsen
Publikováno v:
Parasite Epidemiology and Control, Vol 19, Iss , Pp e00279- (2022)
Severe granulomatous chronic villitis with focal remnants of Toxoplasma was confirmed by immunohistochemistry and DNA-based methods in the placenta from a child that died four days after birth. The immunocompetent mother was seronegative for Toxoplas
Externí odkaz:
https://doaj.org/article/0d2ff5c75e1f425db7ba478418bf76fc
Publikováno v:
Case Reports in Medicine, Vol 2010 (2010)
Background. Intraplacental choriocarcinoma is a rare but highly malignant trophoblastic neoplasm. When found near term the risk of maternal metastasis is high because of the late diagnosis. Case. We describe a case of an intraplacental choriocarcinom
Externí odkaz:
https://doaj.org/article/a5d68edd32104c0982fcf13c5d8963e3
Publikováno v:
Human Reproduction. 37:718-724
Conjoined twins are estimated to occur in 1:50 000 pregnancies. Eighteen cases of pregnancies achieved by ART have been published of which three were achieved after single embryo transfer, allowing discussion of embryo characteristics. We report, to
Autor:
Bente Utoft Andreassen, Lise Aunsholt, Elsebet Østergaard, Jakob Ek, Lisa Leth Maroun, Marianne Hørby Jørgensen
Publikováno v:
JPGN Reports. 4:e309
Autor:
Morten Bo Soendergaard Svendsen, Joergen Thorup, Nikolaj Nerup, Kristine Bach Korsholm Knudsen, Torsten Lauritsen, Per T. Sangild, Michael Patrick Achiam, Thomas Thymann, Lisa Leth Maroun, Inge Boetker Rasmussen Ifaoui, Lars Bo Svendsen
Publikováno v:
Journal of pediatric surgery. 57(4)
Reduced intestinal perfusion is thought to be a part of the pathogenesis in necrotizing enterocolitis (NEC). This study aims to evaluate the intestinal perfusion assessment in NEC-lesions by quantitative fluorescence angiography with indocyanine gree
Publikováno v:
Case Reports in Genetics, Vol 2021 (2021)
Case Reports in Genetics
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, 5539855 . https://doi.org/10.1155/2021/5539855
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, pp. 5539855 . https://doi.org/10.1155/2021/5539855
Case Reports in Genetics
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, 5539855 . https://doi.org/10.1155/2021/5539855
Faurschou, S, Lildballe, D L, Maroun, L L, Helvind, M & Rasmussen, M 2021, ' Total Anomalous Pulmonary Venous Connection in Mother and Son with a Central 22q11.2 Microdeletion ', Case Reports in Genetics, vol. 2021, pp. 5539855 . https://doi.org/10.1155/2021/5539855
In this clinical report, we describe a male infant and his mother, who had similar congenital heart defects. They were both diagnosed neonatally with total anomalous pulmonary venous connection (TAPVC) in combination with other heart defects. Neither
Autor:
Rikke Beck Jensen, John E. Nielsen, Malene Boas, Torben Larsen, Anders Juul, Anne Jørgensen, Katharina M. Main, Lisa Leth Maroun
Publikováno v:
Growth hormoneIGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society. 55
Background A common growth hormone receptor polymorphism with deletion of exon 3 (d3-GHR) has previously been linked to increased postnatal growth on the one hand and decreased fetal growth on the other. Regulation of fetal growth is positively depen
Publikováno v:
Case Reports in Pediatrics
Complications due to spontaneous septostomy of the dividing membrane in monochorionic diamniotic pregnancies are rarely described. Herein, we report the case of a preterm female neonate from a monochorionic diamniotic twin pregnancy delivered by caes
Autor:
Iben Bache, Arthur van den Wijngaard, Crool Velter, Ingrid P.C. Krapels, Kristiina Avela, Sonja Chocron, Florence H J van Tienen, Bálint Nagy, Godelieve R.F. Claes, Aimee D C Paulussen, Lisa Leth Maroun, Irene Valenzuela, Anja Steyls, Jeroen Bakkers, Jo Vanoevelen, Hubert J.M. Smeets, Catarina Lundin, Han G. Brunner, Gita M. B. Tan-Sindhunata
Publikováno v:
European Journal of Human Genetics, 24(12), 1783-1791. Nature Publishing Group
European Journal of Human Genetics, 24(12), 1783. Nature Publishing Group
Paulussen, A D C, Steyls, A, Vanoevelen, J, van Tienen, F H J, Krapels, I P C, Claes, G R F, Chocron, S, Velter, C, Tan-Sindhunata, G M, Lundin, C, Valenzuela, I, Nagy, B, Bache, I, Maroun, L L, Avela, K, Brunner, H G, Smeets, H J M, Bakkers, J & van den Wijngaard, A 2016, ' Rare novel variants in the ZIC3 gene cause X-linked heterotaxy ', European Journal of Human Genetics, vol. 24, no. 12, pp. 1783-1791 . https://doi.org/10.1038/ejhg.2016.91
European Journal of Human Genetics. Nature Publishing Group
European Journal of Human Genetics, 24, 1783-1791
European Journal of Human Genetics, 24, 12, pp. 1783-1791
European Journal of Human Genetics, 24(12), 1783. Nature Publishing Group
Paulussen, A D C, Steyls, A, Vanoevelen, J, van Tienen, F H J, Krapels, I P C, Claes, G R F, Chocron, S, Velter, C, Tan-Sindhunata, G M, Lundin, C, Valenzuela, I, Nagy, B, Bache, I, Maroun, L L, Avela, K, Brunner, H G, Smeets, H J M, Bakkers, J & van den Wijngaard, A 2016, ' Rare novel variants in the ZIC3 gene cause X-linked heterotaxy ', European Journal of Human Genetics, vol. 24, no. 12, pp. 1783-1791 . https://doi.org/10.1038/ejhg.2016.91
European Journal of Human Genetics. Nature Publishing Group
European Journal of Human Genetics, 24, 1783-1791
European Journal of Human Genetics, 24, 12, pp. 1783-1791
Contains fulltext : 168089.pdf (Publisher’s version ) (Open Access) Variants in the ZIC3 gene are rare, but have demonstrated their profound clinical significance in X-linked heterotaxy, affecting in particular male patients with abnormal arrangeme
Autor:
Anette Hessellund, Helle Zingenberg, Lisa Leth Maroun, Anne Cathrine Shalmi, Connie Jørgensen, Ditte S. Jørgensen, Finn Stener Jørgensen, Niels Vejlstrup, Torben Larsen, Charlotte Kvist Ekelund, Jesper Steensberg, Lillian Skibsted, Ann Tabor
Publikováno v:
Prenatal Diagnosis. 35:325-330
Objectives The prenatal detection rate of congenital heart disease (CHD) is low compared with other fetal malformations. Our aim was to evaluate the prenatal detection of CHD in Eastern Denmark. Methods Fetuses and infants diagnosed with CHD in the p