Zobrazeno 1 - 10
of 154
pro vyhledávání: '"misrouting"'
Publikováno v:
Clinical Ophthalmology, Vol Volume 16, Pp 1569-1587 (2022)
Magella M Neveu,1,2 Srikanta Kumar Padhy,3 Srishti Ramamurthy,4 Brijesh Takkar,4 Subhadra Jalali,4 Deepika CP,4 Tapas Ranjan Padhi,3 Anthony G Robson1,2 1Department Electrophysiology, Moorfields Eye Hospital, London, EC1V 2PD, UK; 2Institute of Ophth
Externí odkaz:
https://doaj.org/article/6f25facf5299413d9411a0899ae917f4
Publikováno v:
Emitter: International Journal of Engineering Technology, Vol 10, Iss 2 (2022)
Today's Multiprocessor System-on-Chip (MPSoC) contains many cores and integrated circuits. Due to the current requirements of communication, we make use of Network-on-Chip (NoC) to obtain high throughput and low latency. NoC is a communication archit
Externí odkaz:
https://doaj.org/article/34846dcf9b9e47f2847eb6327583df67
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Convolutional neural network (CNN) models are of great promise to aid the segmentation and analysis of brain structures. Here, we tested whether CNN trained to segment normal optic chiasms from the T1w magnetic resonance imaging (MRI) image can be al
Externí odkaz:
https://doaj.org/article/e44b15a235484fe3bcc45b0fddd7c419
Autor:
Karina Juarez-Navarro, Victor M. Ayala-Garcia, Estela Ruiz-Baca, Ivan Meneses-Morales, Jose Luis Rios-Banuelos, Angelica Lopez-Rodriguez
Publikováno v:
Biomolecules, Vol 10, Iss 5, p 728 (2020)
An extensive catalog of plasma membrane (PM) protein mutations related to phenotypic diseases is associated with incorrect protein folding and/or localization. These impairments, in addition to dysfunction, frequently promote protein aggregation, whi
Externí odkaz:
https://doaj.org/article/bbdb419517974f68abe5262b504d5496
Autor:
Puźniak, Robert, Pestilli, Franco
We describe a collection of T1-, diffusion- and functional T2*-weighted magnetic resonance imaging data from human individuals with albinism and achiasma. This repository can be used as a test-bed to develop and validate tractography methods like dif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cddb6a9e816306531aec7c73b4cba785
Autor:
Camilla Rocca, Lucia Tiberi, Sara Bargiacchi, Viviana Palazzo, Samuela Landini, Elisa Marziali, Roberto Caputo, Francesca Tinelli, Viviana Marchi, Alessandro Benedetto, Angelica Pagliazzi, Giacomo Maria Bacci
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 14; Pages: 7825
Oculocutaneous albinism is an autosomal recessive disorder characterized by the presence of typical ocular features, such as foveal hypoplasia, iris translucency, hypopigmented fundus oculi and reduced pigmentation of skin and hair. Albino patients c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3e42cb836f57c3065b4668624bc0d4c
Akademický článek
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Publikováno v:
Documenta Ophthalmologica. Advances in Ophthalmology
Purpose To describe the trans-occipital asymmetries of pattern and flash visual evoked potentials (VEPs), in an infant with MRI findings of unilateral optic nerve aplasia and hemi-chiasm dysplasia. Methods A child with suspected left cystic microphth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d468c3b0ea959627f5181a02723b97
http://europepmc.org/articles/PMC7943516
http://europepmc.org/articles/PMC7943516
Autor:
Charlotte C. Kruijt, Libe Gradstein, Arthur A. Bergen, Ralph J. Florijn, Benoit Arveiler, Eulalie Lasseaux, Xavier Zanlonghi, Laura Bagdonaite-Bejarano, Anne B. Fulton, Claudia Yahalom, Anat Blumenfeld, Yonatan Perez, Ohad S. Birk, Gerard C. de Wit, Nicoline E. Schalij-Delfos, Maria M. van Genderen
Publikováno v:
Kruijt, C C, Gradstein, L, Bergen, A A, Florijn, R J, Arveiler, B, Lasseaux, E, Zanlonghi, X, Bagdonaite-Bejaran, L, Fulton, A B, Yahalom, C, Blumenfeld, A, Perez, Y, Birk, O S, de Wit, G C, Schalij-Delfos, N E & van Genderen, M M 2022, ' The Phenotypic and Mutational Spectrum of the FHONDA Syndrome and Oculocutaneous Albinism : Similarities and Differences ', Investigative Ophthalmology and Visual Science, vol. 63, no. 1, 19 . https://doi.org/10.1167/iovs.63.1.19
Investigative Ophthalmology & Visual Science, 63(1). ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Investigative Ophthalmology and Visual Science, 63(1):19. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, 63(1). Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology and Visual Science, 63(1):19
Investigative Ophthalmology & Visual Science, 63(1). ASSOC RESEARCH VISION OPHTHALMOLOGY INC
Investigative Ophthalmology and Visual Science, 63(1):19. Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology & Visual Science
Investigative Ophthalmology & Visual Science, 63(1). Association for Research in Vision and Ophthalmology Inc.
Investigative Ophthalmology and Visual Science, 63(1):19
PURPOSE. The purpose of this study was to further expand the mutational spectrum of the Foveal Hypoplasia, Optic Nerve Decussation defect, and Anterior segment abnormalities (FHONDA syndrome), to describe the phenotypic spectrum, and to compare it to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325324e4b89613cc2a8007ac34b667ab
https://hdl.handle.net/1887/3485320
https://hdl.handle.net/1887/3485320
Autor:
Karamese, Hacer
Multistage adaptive testing (MST) has become popular in the testing industry because the research has shown that it combines the advantages of both linear tests and item-level computer adaptive testing (CAT). The previous research efforts primarily f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd7bcffbc1f65ba1111a6ac6660e83a3