Tilman Esser
Overview
Explore the profile of Tilman Esser including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
40
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0
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Recent Articles
1.
Vergarajauregui S, Becker R, Steffen U, Sharkova M, Esser T, Petzold J, et al.
Elife
. 2020 Dec;
9.
PMID: 33295871
The switch from centrosomal microtubule-organizing centers (MTOCs) to non-centrosomal MTOCs during differentiation is poorly understood. Here, we identify AKAP6 as key component of the nuclear envelope MTOC. In rat cardiomyocytes,...
2.
Grill F, Behr A, Rau A, Ritschl L, Roth M, Bauer F, et al.
J Craniomaxillofac Surg
. 2019 Mar;
47(7):1077-1082.
PMID: 30885526
Objectives: The aim of this prospective study was to investigate normal fetal maxillary development with volume ultrasound during the prenatal phase, for a better estimation of maxillary growth processes. Methods:...
3.
Khalil A, Chaoui R, Lebek H, Esser T, Entezami M, Toms J, et al.
Am J Obstet Gynecol
. 2015 Oct;
214(2):291-292.
PMID: 26450406
No abstract available.
4.
Kalache K, Bamberg C, Proquitte H, Sarioglu N, Lebek H, Esser T
J Ultrasound Med
. 2006 Jul;
25(8):1041-9.
PMID: 16870897
Objectives: The purpose of this study was to describe the use and potential of Multi-Slice View 3-dimensional (3D) ultrasonographic software (Medison Co, Ltd, Seoul, Korea) in showing fetal congenital anomalies....
5.
Kalache K, Eder K, Esser T, Proquitte H, Stoltenburg-Didinger G, Hartung J, et al.
J Ultrasound Med
. 2006 Mar;
25(4):509-14.
PMID: 16567440
Objectives: The purpose of this study was to evaluate the potential of 3-dimensional ultrasonographic planar and nonplanar reslicing techniques. Methods: Fetuses with severe brain anomalies diagnosed by means of 2-dimensional...
6.
Esser T, Rogalla P, Bamberg C, Kalache K
Am J Obstet Gynecol
. 2005 Nov;
193(5):1743-5.
PMID: 16260220
Apert syndrome is a rare disorder characterized by coronal craniosynostosis, syndactyly, brachycephaly, midfacial hypoplasia, and central nervous system anomalies, among other malformations. We present a case of Apert syndrome examined...