Zobrazeno 1 - 10
of 2 246
pro vyhledávání: '"G Bartsch"'
Publikováno v:
Indian Journal of Urology, Vol 24, Iss 3, Pp 309-312 (2008)
During the 10 th week of gestation human prostate development is about to start. Androgens are the crucial factors to stimulate the initial interactions between the epithelium and mesenchyme. One of the key events in androgen metabolism is the transf
Externí odkaz:
https://doaj.org/article/fe85884cd7a940809392bc9d3b2fa3f3
Autor:
Yiqian Wang, Carlo Galang, William R. Freeman, Alexandra Warter, Anna Heinke, Dirk-Uwe G. Bartsch, Truong Q. Nguyen, Cheolhong An
Publikováno v:
IEEE Access, Vol 11, Pp 103319-103332 (2023)
Optical Coherence Tomography (OCT) is a widely used 3D imaging technology in ophthalmology. Segmentation of retinal layers in OCT is important for diagnosis and evaluation of various retinal and systemic diseases. While 2D segmentation algorithms hav
Externí odkaz:
https://doaj.org/article/f6944bee0bd746c09dcb124721bf88df
Autor:
Alexa L. Li, MD, Moira Feng, MS, Zixi Wang, MS, Sally L. Baxter, MD, MSc, Lingling Huang, MD, PhD, Justin Arnett, MD, Dirk-Uwe G. Bartsch, PhD, David E. Kuo, MD, Bharanidharan Radha Saseendrakumar, MS, Joy Guo, MS, Eric Nudleman, MD, PhD
Publikováno v:
Ophthalmology Science, Vol 3, Iss 2, Pp 100254- (2023)
Objective: To develop automated algorithms for the detection of posterior vitreous detachment (PVD) using OCT imaging. Design: Evaluation of a diagnostic test or technology. Subjects: Overall, 42 385 consecutive OCT images (865 volumetric OCT scans)
Externí odkaz:
https://doaj.org/article/27778efe41174d80b28fcecd46f05f36
Autor:
Varsha Alex, Tahmineh Motevasseli, William R. Freeman, Jefy A. Jayamon, Dirk-Uwe G. Bartsch, Shyamanga Borooah
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Comparing automated retinal layer segmentation using proprietary software (Heidelberg Spectralis HRA + OCT) and cross-platform Optical Coherence Tomography (OCT) segmentation software (Orion). Image segmentations of normal and diseased (iAMD
Externí odkaz:
https://doaj.org/article/a055deeebdab41cda94b64eb0e243df8
Autor:
Yiqian Wang, Junkang Zhang, Melina Cavichini, Dirk-Uwe G. Bartsch, William R. Freeman, Truong Q. Nguyen, Cheolhong An
Publikováno v:
IEEE Access, Vol 8, Pp 190897-190905 (2020)
Retinal imaging is crucial in diagnosing and treating retinal diseases, and multimodal retinal image registration constitutes a major advance in understanding retinal diseases. Despite the fact that many methods have been proposed for the registratio
Externí odkaz:
https://doaj.org/article/f4c9b5c3194c4e4aae426837409ea15d
Autor:
Melina Cavichini, Dirk-Uwe G. Bartsch, Alexandra Warter, Sumit Singh, Cheolhong An, Yiqian Wang, Junkang Zhang, Truong Nguyen, William R. Freeman
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 54:108-113
Background and Objective: The purpose of this study was to evaluate the accuracy and the time to find a lesion, taken in different platforms, color fundus photographs and infrared scanning laser ophthalmoscope images, using the traditional side-by-si
Autor:
Shaden H. Yassin, Yiqian Wang, William R. Freeman, Anna Heinke, Evan Walker, Truong Nguyen, Dirk‐Uwe G. Bartsch, Cheolhong An, Shyamanga Borooah
Publikováno v:
Clinical & Experimental Ophthalmology.
Autor:
Junkang Zhang, Yiqian Wang, Ji Dai, Melina Cavichini, Dirk-Uwe G. Bartsch, William R. Freeman, Truong Q. Nguyen, Cheolhong An
Publikováno v:
IEEE Trans Image Process
Multi-modal retinal image registration plays an important role in the ophthalmological diagnosis process. The conventional methods lack robustness in aligning multi-modal images of various imaging qualities. Deep-learning methods have not been widely
Publikováno v:
2022 10th International Conference on Systems and Control (ICSC).
Autor:
Pooja Biswas, Anne Marie Berry, Qais Zawaydeh, Dirk-Uwe G. Bartsch, Pongali B. Raghavendra, J. Fielding Hejtmancik, Naheed W. Khan, S. Amer Riazuddin, Radha Ayyagari
Publikováno v:
Genes; Volume 13; Issue 8; Pages: 1461
Genes, vol 13, iss 8
Genes, vol 13, iss 8
We previously identified a homozygous G178R mutation in human ASRGL1 (hASRGL1) through whole-exome analysis responsible for early onset retinal degeneration (RD) in patients with cone–rod dystrophy. The mutant G178R ASRGL1 expressed in Cos-7 cells