S. Tercanli

发表

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)

P. Klaritsch, E. Merz, M. Schmid, 2015, Ultraschall in der Medizin.

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype

W. Wasserman, Judith G Hall, J. Friedman, 2014, Clinical genetics.

Influence of Volume Preloading on Uteroplacental and Fetal Circulation during Spinal Anaesthesia for Caesarean Section in Uncomplicated Singleton Pregnancies

W. Holzgreve, I. Hösli, S. Tercanli, 2002, Fetal Diagnosis and Therapy.

Ten reasons why we should not abandon a detailed first trimester anomaly scan

K. Kagan, M. Hoopmann, S. Tercanli, 2021, Ultraschall in der Medizin - European Journal of Ultrasound.

Preeclampsia in Fetal Medicine

S. Tercanli, C. Birdir, 2017, Ultraschall in der Medizin - European Journal of Ultrasound.

Reproductive Biology and Endocrinology Open Access Potential Markers of Preeclampsia – a Review

W. Holzgreve, R. Zanetti-Dällenbach, S. Grill, 2022 .

Differentiation and management of endometrium abnormalities and leiomyomas by hydrosonography.

W. Holzgreve, G. Feichter, O. Köchli, 2000, Contributions to gynecology and obstetrics.

Sirenomelia, the mermaid syndrome—detection in the first trimester

W. Holzgreve, O. Lapaire, S. Tercanli, 2003, Prenatal diagnosis.

Multiple gestations: pregnancy evaluation by ultrasonography

W. Holzgreve, R. Zanetti-Dällenbach, I. Hösli, 2006 .

Cervical length assessment by ultrasound as a predictor of preterm labour—is there a role for routine screening?

W. Holzgreve, S. Tercanli, I. Hoesli, 2003, BJOG : an international journal of obstetrics and gynaecology.

Expanding the spectrum of SMAD3‐related phenotypes to agnathia‐otocephaly

P. Miny, S. Tercanli, E. Bruder, 2020, Molecular genetics & genomic medicine.

Cell-free foetal DNA in maternal plasma does not appear to be derived from the rich pool of cell-free foetal DNA in amniotic fluid

W. Holzgreve, X. Zhong, S. Hahn, 2005, Archives of Gynecology and Obstetrics.

Fetal arthrogryposis: Challenges and perspectives for prenatal detection and management

S. Tercanli, I. Filges, J. Hall, 2019, American journal of medical genetics. Part C, Seminars in medical genetics.

Bedside estimation of Down syndrome risk during first‐trimester ultrasound screening

W. Holzgreve, S. Tercanli, E. Dreazen, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Umbilical cord edema associated with patent urachus

W. Holzgreve, O. Lapaire, S. Tercanli, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester Screening.

S. Wellek, C. Thode, E. Merz, 2022, Ultraschall in der Medizin.

Two case reports of rare fetal tumors: an indication for surface rendering?

W. Holzgreve, I. Hösli, S. Tercanli, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Genetic communication between fetus and mother: short- and long-term consequences.

W. Holzgreve, X. Zhong, I. Hösli, 2007, American journal of obstetrics and gynecology.

How genomics is changing the practice of prenatal testing

W. Holzgreve, P. Miny, S. Tercanli, 2021, Journal of perinatal medicine.

Dual independent genetic etiologies in a lethal complex malformation phenotype.

F. Prüfer, N. Deigendesch, S. Tercanli, 2020, Ultraschall in der Medizin.

Transabdominal first trimester embryofetoscopy as a potential approach to early in utero stem cell transplantation and gene therapy

W. Holzgreve, S. Tercanli, D. Surbek, 2000, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Prenatal diagnosis of a highly undifferentiated brain tumour—a case report and review of the literature

W. Holzgreve, M. Dören, S. Tercanli, 1997, Prenatal diagnosis.

Is a routine ultrasound in the third trimester justified? Additional fetal anomalies diagnosed after two previous unremarkable ultrasound examinations.

S. Tercanli, G. Manegold, A. Kang, 2011, Ultraschall in der Medizin.

Quality management of nuchal translucency measurement in residents.

W. Holzgreve, S. Tercanli, C. Troeger, 2007, Ultraschall in der Medizin.

Large Placental Chorioangioma as a Cause of Sudden Intrauterine Fetal Death

W. Holzgreve, I. Hösli, S. Tercanli, 2001, Fetal Diagnosis and Therapy.

[Pregnant women's assessment and level of knowledge of prenatal counseling].

W. Holzgreve, S. Tschudin, J. Bitzer, 2008, Ultraschall in der Medizin.

Increased Nuchal Translucency in a Case of Long-Chain 3-Hydroxyacyl- Coenzyme A Dehydrogenase Deficiency

W. Holzgreve, I. Hösli, S. Tercanli, 2000, Fetal Diagnosis and Therapy.

A simpler technique for umbilical-cord blockade of an acardiac twin.

G. Schuierer, W. Holzgreve, S. Tercanli, 1994, The New England journal of medicine.

Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally.

W. Holzgreve, H. Rehder, B. Dworniczak, 1995, American journal of medical genetics.

Fetal Polydactyly

J. Hench, P. Miny, S. Tercanli, 2011, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?

P. Miny, S. Tercanli, F. Wenzel, 2013, Microarrays.

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

K. Heinimann, P. Miny, S. Tercanli, 2012, Molecular Cytogenetics.

Prenatal diagnosis of a partial trisomy 19q

W. Holzgreve, I. Hösli, S. Tercanli, 2000, Prenatal diagnosis.

Chromosomale und nicht-chromosomale Syndrome

P. Miny, S. Tercanli, 2013 .

Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villus sampling and placental biopsies

W. Holzgreve, P. Miny, J. Horst, 1991, Prenatal diagnosis.

aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis

K. Heinimann, P. Miny, S. Tercanli, 2011, Prenatal diagnosis.

Charts for cervical length in singleton pregnancy

W. Holzgreve, S. Tercanli, I. Hoesli, 2003, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Prenatal karyotyping: when, how and whom?

W. Holzgreve, P. Miny, S. Tercanli, 1992, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Cystic hygrolma as an early first‐trimester ultrasound marker for recurrent Fryns' syndrome

W. Holzgreve, H. Rehder, I. Hösli, 1997, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Spontaneous fetal loss rates in a non-selected population.

W. Holzgreve, S. Tercanli, I. Hoesli, 2001, American journal of medical genetics.

Prenatal diagnosis of an infratentorial subdural hemorrhage: case report

W. Holzgreve, E. Radü, S. Tercanli, 2002, Ultrasound in Obstetrics and Gynecology.

Complications of lost needle after suture of vaginal tear following delivery

W. Holzgreve, I. Hösli, S. Tercanli, 2000, Archives of Gynecology and Obstetrics.

Approximately half of the erythroblasts in maternal blood are of fetal origin.

R. Burgemeister, W. Holzgreve, X. Zhong, 1999, Molecular human reproduction.

12th Fetal Cell Workshop

P. Hufnagl, J. Foidart, M. Dietel, 2001, Fetal Diagnosis and Therapy.

Developments in laboratory techniques for prenatal diagnosis

W. Holzgreve, P. Miny, S. Tercanli, 2002, Current opinion in obstetrics & gynecology.

Improved Detection Rate of Ovarian Cancer Using a 2-Step Triage Model of the Risk of Malignancy Index and Expert Sonography in an Outpatient Screening Setting

N. Hacker, A. Schoetzau, O. Lapaire, 2016, International Journal of Gynecologic Cancer.

Quality Requirements for the early Fetal Ultrasound Assessment at 11–13+6 Weeks of Gestation (DEGUM Levels II and III)

K. Kagan, A. Rempen, R. Chaoui, 2016, Ultraschall in der Medizin.

TRPS1 codon 952 constitutes a mutational hot spot in trichorhinophalangeal syndrome type I and could be associated with intellectual disability

A. Huber, J. Sidler, G. Ramelli, 2012, Clinical dysmorphology.

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

R. Chaoui, J. Hench, S. Hoeller, 2019, European Journal of Human Genetics.

Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF

M. Schubach, S. Hoeller, S. Schulzke, 2016, Human Mutation.

Prenatal diagnosis of a case of ectrodactyly in 2D and 3D ultrasound.

W. Holzgreve, S. Tercanli, E. Bruder, 2009, Ultraschall in der Medizin.

Fetal cells in maternal blood: diagnostic and clinical aspects

W. Holzgreve, R. Zanetti-Dällenbach, I. Hösli, 2006 .

Prenatal sonographic diagnosis of a vein of Galen aneurysm: relevance of associated malformations for timing and mode of delivery

W. Holzgreve, M. Dören, S. Tercanli, 1995, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Screening for trisomy 21 by fetal nuchal translucency and maternal age: a multicenter project in Germany, Austria and Switzerland

P. Kuhn, F. Bahlmann, P. Kozlowski, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Myomectomy during the first trimester associated with fetal limb anomalies and hydrocephalus in a twin pregnancy

W. Holzgreve, P. Miny, S. Tercanli, 2001, Prenatal diagnosis.

Noninvasive Prenatal Test Raises Concern Over Screening Strategies and the Role of Ultrasound

E. Merz, Y. Vial, S. Tercanli, 2013, Ultraschall in der Medizin - European Journal of Ultrasound.

Non-invasive chromosome test raises new questions in prenatal diagnosis about the significance of ultrasound and questions about new screening strategies.

E. Merz, Y. Vial, S. Tercanli, 2013, Ultraschall in der Medizin.

Lost intrauterine devices during pregnancy: maternal and fetal outcome after ultrasound‐guided extraction. An analysis of 82 cases

W. Holzgreve, O. Lapaire, S. Tercanli, 2004, Ultrasound in Obstetrics and Gynecology.

[Use of 3-dimensional ultrasound for assessment of intrauterine device position].

W. Holzgreve, I. Hösli, S. Tercanli, 2001, Ultraschall in der Medizin.

Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?

I. Hösli, O. Lapaire, S. Hahn, 2011, Expert Reviews in Molecular Medicine.

Split hand and foot malformation: ultrasound detection in the first trimester

W. Holzgreve, O. Lapaire, S. Tercanli, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The special role of ultrasound for screening, staging and surveillance of malignant ovarian tumors: distinction from other methods of diagnostic imaging

O. Lapaire, V. Heinzelmann-Schwarz, S. Tercanli, 2014, Archives of Gynecology and Obstetrics.

The fetus with ventriculomegaly: prenatal diagnosis, associated malformations, pathophysiology and prognostic factors

S. Kupesic, W. Holzgreve, S. Tercanli, 2001 .

Numerous erythroblasts in maternal blood are impervious to fluorescent in situ hybridization analysis, a feature related to a dense compact nucleus with apoptotic character.

W. Holzgreve, S. Mergenthaler, S. Hahn, 2005, Haematologica.

Fetal Neurosonogaphy: Ultrasound and Magnetic Resonance Imaging in Competition

F. Prüfer, S. Tercanli, 2016, Ultraschall in der Medizin - European Journal of Ultrasound.

[Screening for aneuploidy by first trimester nuchal translucency measurement: results from a prospective trial including 1980 cases in a single center in Switzerland].

W. Holzgreve, P. Miny, S. Tercanli, 2002, Ultraschall in der Medizin.

Two- versus three-dimensional ultrasound in the second and third trimester of pregnancy: impact on recognition and maternal–fetal bonding. A prospective pilot study

W. Holzgreve, O. Lapaire, S. Tercanli, 2007, Archives of Gynecology and Obstetrics.

Comparison of pregnancy outcome of euploid fetuses with increased nuchal translucency (NT) expressed in NT MoM or delta‐NT

W. Holzgreve, A. Herman, S. Tercanli, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Fanconi anemia associated with increased nuchal translucency detected by first‐trimester ultrasound

W. Holzgreve, I. Hösli, P. Miny, 2001, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Three dimensional volume measurement of the cervix during pregnancy compared to conventional 2D‐sonography

W. Holzgreve, S. Tercanli, D. Surbek, 1999, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Noninvasive Prenatal Diagnosis Strategy for a Clinical Trial

W. Holzgreve, P. Miny, S. Tercanli, 1994, Annals of the New York Academy of Sciences.

[Manifestations and prognosis of congenital diaphragmatic hernia].

R. Hentschel, G. Hülskamp, S. Tercanli, 1994, Zeitschrift fur Geburtshilfe und Perinatologie.

Neurocutaneous Melanosis Associated with Prenatally Diagnosed Arachnoid Cyst

P. Itin, S. Tercanli, P. Weber, 2016, Ultraschall in der Medizin - European Journal of Ultrasound.

Fetal arthrogryposis—what do we tell the prospective parents?

S. Tercanli, E. Viehweger, I. Filges, 2023, Prenatal diagnosis.

In vitro volume measurement by three‐dimensional ultrasound: comparison of two different systems

W. Holzgreve, I. Hösli, S. Tercanli, 1998, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The role of ultrasound in first-trimester screening after the introduction of NIPT as a service of public health insurance – a consensus statement of the Fetal Medicine Foundation (FMF) Germany

C. Thode, S. Tercanli, B. Eiben, 2023, Ultraschall in der Medizin - European Journal of Ultrasound.

Exome sequencing of fetal anomaly syndromes: novel phenotype–genotype discoveries

R. Chaoui, J. Hench, S. Hoeller, 2019, European Journal of Human Genetics.

Neurocutaneous Melanosis Associated with Prenatally Diagnosed Arachnoid Cyst

P. Itin, S. Tercanli, P. Weber, 2016, Ultraschall in der Medizin - European Journal of Ultrasound.

[Prenatal diagnosis of diastematomyelia and tethered cord - a case report and review of the literature].

W. Holzgreve, S. Tercanli, E. Visca, 2007, Ultraschall in der Medizin.

Quantitative Proteomics Analysis of Maternal Plasma in Down Syndrome Pregnancies Using Isobaric Tagging Reagent (iTRAQ)

Mahesh Choolani, M. Choolani, P. Jenö, 2009, Journal of biomedicine & biotechnology.

[DEGUM Level III recommendation for "follow-up" ultrasound examination (= DEGUM Level II) in the 11 -- 14 week period of pregnancy].

A. Staudach, E. Merz, J. Deutinger, 2004, Ultraschall in der Medizin.

POCUS – Chance or Risk?

S. Tercanli, J. Osterwalder, 2018, Ultraschall in der Medizin - European Journal of Ultrasound.

DEGUM, ÖGUM, SGUM and FMF Germany Recommendations for the Implementation of First-Trimester Screening, Detailed Ultrasound, Cell-Free DNA Screening and Diagnostic Procedures.

S. Tercanli, Constantin von Kaisenberg, Horst Steiner, 2018, Ultraschall in der Medizin.

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice : Austrian-German-Swiss Recommendations for non-invasive prenatal tests ( NIPT ) Drei

P. Klaritsch, E. Merz, M. Schmid, 2015 .