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» Authors » S Tercanli

S Tercanli

Explore the profile of S Tercanli including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 74
Citations 185
Followers 0
Related Specialties
Gynecology & Obstetrics
General Medicine
Genetics
Top 10 Co-Authors
W Holzgreve
P Miny
I Hosli
E Merz
H Steiner
C Batukan
O Lapaire
J Horst
B J Hackeloer
R Schloo
Published In
Ultraschall Med
Ultrasound Obstet Gynecol
Praxis (Bern 1994)
Ther Umsch
Prenat Diagn
Affiliations
Soon will be listed here.
Recent Articles
1.
The Fetal Medicine Foundation (FMF) Germany after 20 Years - Quality Assurance of Ultrasound Examinations during First Trimester Screening
Merz E, Thode C, Hackeloer B, Eiben B, Faber R, Tercanli S, et al.
Ultraschall Med . 2022 Apr; 43(2):115-119. PMID: 35381614
No abstract available.
2.
Fetal Neurosonogaphy: Ultrasound and Magnetic Resonance Imaging in Competition
Tercanli S, Prufer F
Ultraschall Med . 2016 Dec; 37(6):555-557. PMID: 27978593
Both in routine diagnostics and detailed, highly specialized workups, major advances have been observed in many areas of ultrasound due to an increase in expertise and improved technology in recent...
3.
Neurocutaneous Melanosis Associated with Prenatally Diagnosed Arachnoid Cyst
Tercanli S, Itin P, Weber P
Ultraschall Med . 2016 Dec; 37(6):551-554. PMID: 27978592
No abstract available.
4.
Quality Requirements for the early Fetal Ultrasound Assessment at 11-13+6 Weeks of Gestation (DEGUM Levels II and III)
von Kaisenberg C, Chaoui R, Hausler M, Kagan K, Kozlowski P, Merz E, et al.
Ultraschall Med . 2016 Apr; 37(3):297-302. PMID: 27093520
The early fetal ultrasound assessment at 11 - 13(+6) weeks of gestation remains the cornerstone of care despite the progress in diagnosing fetal chromosomal defects using cell-free fetal DNA (cffDNA)...
5.
Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)
Schmid M, Klaritsch P, Arzt W, Burkhardt T, Duba H, Hausler M, et al.
Ultraschall Med . 2015 Oct; 36(5):507-10. PMID: 26468773
No abstract available.
6.
An Appeal for Ultrasound and Current Guidelines
Tercanli S, Filges I
Ultraschall Med . 2015 Oct; 36(5):424-6. PMID: 26468769
No abstract available.
7.
Prenatal diagnosis of an isolated coronary arterial fistula
Tercanli S, Gunthard J
Ultraschall Med . 2014 Oct; 35(4):295-7. PMID: 25268023
No abstract available.
8.
Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype
Filges I, Nosova E, Bruder E, Tercanli S, Townsend K, Gibson W, et al.
Clin Genet . 2013 Oct; 86(3):220-8. PMID: 24128419
Gene discovery using massively parallel sequencing has focused on phenotypes diagnosed postnatally such as well-characterized syndromes or intellectual disability, but is rarely reported for fetal disorders. We used family-based whole-exome...
9.
Non-invasive chromosome test raises new questions in prenatal diagnosis about the significance of ultrasound and questions about new screening strategies
Tercanli S, Vial Y, Merz E
Ultraschall Med . 2013 Oct; 34(5):417-20. PMID: 24127381
No abstract available.
10.
Is ultrasound training in specialized qualified prenatal diagnosis in German-speaking countries still sufficient?
Merz E, Tercanli S, Steiner H
Ultraschall Med . 2013 Apr; 34(2):111-2. PMID: 23558395
No abstract available.