Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Blindne"'
Autor:
Rocchini, Duccio, Nowosad, Jakub, D’Introno, Rossella, Chieffallo, Ludovico, Bacaro, Giovanni, Gatti, Roberto Cazzolla, Foody, Giles M, Furrer, Reinhard, Gábor, Lukáš, Malavasi, Marco, Marcantonio, Matteo, Marchetto, Elisa, Moudrý, Vítězslav, Ricotta, Carlo, Šímová, Petra, Torresani, Michele, Thouverai, Elisa
Maps represent powerful tools to show the spatial variation of a variable in a straightforward manner. A crucial aspect in map rendering for its interpretation by users is the gamut of colours used for displaying data. One part of this problem is lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9fb6fc17da31c02aa7456bfb7cd601b
https://doi.org/10.5167/uzh-232999
https://doi.org/10.5167/uzh-232999
Autor:
Elisabet Lopez-Soley, Irene Pulido-Valdeolivas, Alvino Bisecco, Albert Saiz, Irati Zubizarreta, Salut Alba-Arbalat, Elena H. Martinez-Lapiscina, Pablo Villoslada, Magi Andorra, Antonio Gallo, Luisa M. Villar, Sara Llufriu, Maria Sepúlveda, Carmen Montejo, Yolanda Blanco, Nuria Sola-Valls, Elisabeth Solana, Eloy Martinez-Heras, Jose Ignacio Fernández-Velasco, Rocco Capuano
Publikováno v:
Multiple Sclerosis Journal. 27:1706-1716
Background:Prognostic markers are needed to guide multiple sclerosis (MS) management in the context of large availability of disease-modifying drugs (DMDs).Objective:To investigate the role of cerebrospinal fluid (CSF) markers to inform long-term MS
Autor:
Miguel A. Teus, Daniele Tognetto, Boris Malyugin, Antoine P. Brézin, Arthur B. Cummings, Sandrine Zweifel, Mario Damiano Toro, Isabel Prieto, Omid Kermani, Dominique Bremond-Gignac, Ozlem Evren Kemer, Robert Rejdak
The most common cause of vision impairment in children is amblyopia. It is defined as impaired visual acuity in one or both eyes that is present with no demonstrable abnormality of the visual pathway and is not immediately resolved by wearing glasses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39892395e2cb0d2f45d2b810144a72bf
http://hdl.handle.net/11588/892705
http://hdl.handle.net/11588/892705
Autor:
Irene M. Häfliger, Emma Marchionatti, Michele Stengård, Sonja Wolf-Hofstetter, Julia M. Paris, Joana G. P. Jacinto, Christine Watté, Katrin Voelter, Laurence M. Occelli, András M. Komáromy, Anna Oevermann, Christine Goepfert, Angelica Borgo, Raphaël Roduit, Mirjam Spengeler, Franz R. Seefried, Cord Drögemüller
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 22
International journal of molecular sciences, vol. 22, no. 22, pp. 12440
Häfliger, Irene M.; Marchionatti, Emma; Stengard, Michele; Wolf-Hofstetter, Sonja; Paris, Julia M.; Jacinto, Joana G. P.; Watté, Christine; Voelter, Katrin; Occelli, Laurence M.; Komáromy, András M.; Oevermann, Anna; Goepfert, Christine; Borgo, Angelica; Roduit, Raphaël; Spengeler, Mirjam; Seefried, Franz R.; Drögemüller, Cord (2021). CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. International journal of molecular sciences, 22(22), p. 12440. MDPI 10.3390/ijms222212440
International Journal of Molecular Sciences, Vol 22, Iss 12440, p 12440 (2021)
Volume 22
Issue 22
International journal of molecular sciences, vol. 22, no. 22, pp. 12440
Häfliger, Irene M.; Marchionatti, Emma; Stengard, Michele; Wolf-Hofstetter, Sonja; Paris, Julia M.; Jacinto, Joana G. P.; Watté, Christine; Voelter, Katrin; Occelli, Laurence M.; Komáromy, András M.; Oevermann, Anna; Goepfert, Christine; Borgo, Angelica; Roduit, Raphaël; Spengeler, Mirjam; Seefried, Franz R.; Drögemüller, Cord (2021). CNGB3 Missense Variant Causes Recessive Achromatopsia in Original Braunvieh Cattle. International journal of molecular sciences, 22(22), p. 12440. MDPI 10.3390/ijms222212440
International Journal of Molecular Sciences, Vol 22, Iss 12440, p 12440 (2021)
Sporadic occurrence of inherited eye disorders has been reported in cattle but so far pathogenic variants were found only for rare forms of cataract but not for retinopathies. The aim of this study was to characterize the phenotype and the genetic ae
Autor:
Cheng C. -Y., Wang N., Wong T. Y., Congdon N., He M., Wang Y. X., Braithwaite T., Casson R. J., Cicinelli M. V., Das A., Flaxman S. R., Jonas J. B., Keeffe J. E., Kempen J. H., Leasher J., Limburg H., Naidoo K., Pesudovs K., Resnikoff S., Silvester A. J., Tahhan N., Taylor H. R., Bourne R. R. A., Vision Loss Expert Group of the Global Burden of Disease Study, Battaglia Parodi M.
Publikováno v:
British Journal of Ophthalmology. 104:616-622
BackgroundTo determine the prevalence and causes of blindness and vision impairment (VI) in East Asia in 2015 and to forecast the trend to 2020.MethodsThrough a systematic literature review and meta-analysis, we estimated prevalence of blindness (pre
Autor:
Liv Andrés-Jensen, Andishe Attarbaschi, Edit Bardi, Shlomit Barzilai-Birenboim, Deepa Bhojwani, Melanie M Hagleitner, Christina Halsey, Arja Harila-Saari, Raphaele R L van Litsenburg, Melissa M Hudson, Sima Jeha, Motohiro Kato, Leontien Kremer, Wojciech Mlynarski, Anja Möricke, Rob Pieters, Caroline Piette, Elizabeth Raetz, Leila Ronceray, Claudia Toro, Maria Grazia Valsecchi, Lynda M Vrooman, Sigal Weinreb, Naomi Winick, Kjeld Schmiegelow, Madeline R Adams, Liv Andres-Jensen, Katja Baust, Tineke Boesten, Gabriele Calaminus, Rachel Conyers, Anne-Sophie Darlington, Maëlle de Ville, Gabriele Escherich, Melanie Hagleitner, Jen-Yin Hou, Ting-Huan Huang, Melissa Hudson, Meriel Jenney, Maryna Krawczuk-Rybak, Leontine Kremer, Melchior Lautem, Hse-Che Liu, Elixabet Lopez Lopez, Marion Mateos, Katarzyna Muszynska-Roslan, Riitta Niinimaki, Toby Trahair, Inge van der Sluis, Raphaële van Litsenburg, Lynda Vrooman, Andreas Wiener, Michihiro Yano, Ting-Chi Yeh, Ester Zapotocka
Publikováno v:
The Lancet. Haematology. 8(7)
5-year overall survival rates have surpassed 90% for childhood acute lymphocytic leukaemia, but survivors are at risk for permanent health sequelae. Although event-free survival appropriately represents the outcome for cancers with poor overall survi
Autor:
Tomasz Chorągiewicz, Chiara Posarelli, Miguel A. Teus, Riikka Törnblom, Ozlem Evren Kemer, Boris Malyugin, Michael A. Burdon, Robert Rejdak, Daniele Tognetto, Antoine P. Brézin, Arthur B. Cummings, Mario Damiano Toro, Isabel Prieto
The recent outbreak of coronavirus disease 2019 (COVID-19) has been declared a public health emergency worldwide. The scientific community has put in much effort and published studies that described COVID-19’s biology, transmission, clinical diagno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3d4ad9c0b888e9da9406e48cadf37a8
http://hdl.handle.net/11368/2979963
http://hdl.handle.net/11368/2979963
Autor:
Francesco Santangelo, D Cereda, Claudia Balducci, Ildebrando Appollonio, Benedetta Storti, Carlo Ferrarese
Publikováno v:
Neurological Sciences
Background Selective bilateral lesions of the parietal–occipital lobes can lead to an uncommon and incompletely understood clinical entity, Balint’ syndrome, which consists of simultanagnosia, oculomotor apraxia, optic ataxia and difficulty in pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8f4fa96927de5249e43afc1b9d187e
http://hdl.handle.net/10281/298938
http://hdl.handle.net/10281/298938
Autor:
Francesco Seidita, Luigi Califano, Paola Bonavolontà, Umberto Committeri, Luca D'Andrea, Vincenzo Abbate, Giovanni Dell'Aversana Orabona, Piero Donna
Publikováno v:
Chirurgia. 33
Orbital cellulitis can be caused by distant infective foci, local spread and surgical procedures. Typical symptoms and signs are conjunctival chemosis, pain, extraocular muscles dysfunction, proptosis and visual impairment; systemic symptoms are feve
Publikováno v:
Brain Sciences, Vol 10, Iss 662, p 662 (2020)
Brain Sciences
Brain Sciences
The human cerebral cortex is asymmetrically organized with hemispheric lateralization pervading nearly all neural systems of the brain. Whether the lack of normal visual development affects hemispheric specialization subserving the deployment of visu