N. Sarioglu
Charité
28 Papers
67 Citations
N. Sarioglu is an academic researcher from Charité. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 9, co-authored 18 publications.
Chat about Author
Papers
Mirror syndrome: a systematic review of fetal associated conditions, maternal presentation and perinatal outcome.
Thorsten Braun,Martin Brauer,I. Fuchs,Christoph Czernik,Joachim W. Dudenhausen,Wolfgang Henrich,N. Sarioglu +6 more
TL;DR: A case report in association with fetal Ebstein anomaly is described, a systematic review on the fetal associated conditions, maternal presentation and perinatal outcome reported for mirror syndrome, and a substantial increase in fetal mortality and maternal morbidity are provided.
Abnormal vascular architecture at the placental-maternal interface in placenta increta.
Frédéric Chantraine,Silvia Blacher,Sarah Berndt,José M. Palacios-Jaraquemada,N. Sarioglu,Michelle Nisolle,Thorsten Braun,Carine Munaut,Jean-Michel Foidart +8 more
TL;DR: The size and spatial organization of the placenta-increta vascular architecture at the placental-maternal interface differed from normal and might partially explain the severe hemorrhage observed during placentas increta deliveries.
65
Molecular cytogenetic characterisation of an interstitial deletion 12p detected by prenatal diagnosis
Markus Stumm,Eva Klopocki,Adam Gasiorek-Wiens,Ute Knoll,Deni Wirjadi,N. Sarioglu,Rolf-Dieter Wegner,Holger Tönnies +7 more
TL;DR: This work reports on the first case detected by prenatal diagnosis of interstitial deletions in the short arm of chromosome 12, indicated by fetal abnormalities detected by ultrasound examination.
14
Three-dimensional ultrasonographic demonstration of agenesis of the 12th rib in a fetus with trisomy 21.
TL;DR: A correct prenatal diagnosis of Uhl’s anomaly can be useful for selecting patients who need more attention, especially in the first months of postnatal life, to improve ventricular function, reduce complications and increase the chances of survival.
14
Fetal akinesia caused by a novel actin filament aggregate myopathy skeletal muscle actin gene (ACTA1) mutation.
Werner Stenzel,Stefan Prokop,Wolfram Kress,Stephanie Huppmann,Andrea Loui,N. Sarioglu,Nigel G. Laing,John C. Sparrow,Frank L. Heppner,Hans H. Goebel,Hans H. Goebel +10 more
TL;DR: Analysis of the location of the mutated amino-acid in the actin molecule suggests the mutation most likely causes abnormal nucleotide binding, and consequent pathological actin polymerization.
13