In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients von Leysen, Laura, Delbeke, Heleen, Desmet, Stefanie, Schauwvlieghe, Pieter-Paul, Maes, Piet, Blanckaert, Gauthier, Matthys, Emiel, Joossens, Marie, Casteels, Ingele

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Corrigendum to “In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients” [Clin Microbiol Infect 28(8) (2022 Aug) 1172–117... von Leysen, Laura, Delbeke, Heleen, Desmet, Stefanie, Schauwvlieghe, Pieter-Paul, Maes, Piet, Blanckaert, Gauthier, Matthys, Emiel, Joossens, Marie, Casteels, Ingele

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In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients von Leysen, Laura, Delbeke, Heleen, Desmet, Stefanie, Schauwvlieghe, Pieter-Paul, Maes, Piet, Blanckaert, Gauthier, Matthys, Emiel, Joossens, Marie, Casteels, Ingele

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In search of viable SARS-CoV-2 in the tear film: a prospective clinical study in hospitalized symptomatic patients (vol 28, pg 1172, 2022) von Leysen, Laura, Delbeke, Heleen, Desmet, Stefanie, Schauwvlieghe, Pieter-Paul, Maes, Piet, Blanckaert, Gauthier, Matthys, Emiel, Joossens, Marie, Casteels, Ingele

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Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia von Bolar, Nikhita Ajit, Golzio, Christelle, Živná, Martina, Hayot, Gaëlle, Van Hemelrijk, Christine, Schepers, Dorien, Vandeweyer, Geert, Hoischen, Alexander, Huyghe, Jeroen R., Raes, Ann, Matthys, Erve, Sys, Emiel, Azou, Myriam, Gubler, Marie-Claire, Praet, Marleen, Van Camp, Guy, McFadden, Kelsey, Pediaditakis, Igor, Přistoupilová, Anna, Hodaňová, Kateřina, Vyleťal, Petr, Hartmannová, Hana, Stránecký, Viktor, Hůlková, Helena, Barešová, Veronika, Jedličková, Ivana, Sovová, Jana, Hnízda, Aleš, Kidd, Kendrah, Bleyer, Anthony J., Spong, Richard S., Vande Walle, Johan, Mortier, Geert, Brunner, Han, Van Laer, Lut, Kmoch, Stanislav, Katsanis, Nicholas, Loeys, Bart L.

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Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease von Lenk, Guy M., Szymanska, Krystyna, Debska-Vielhaber, Grazyna, Rydzanicz, Malgorzata, Walczak, Anna, Bekiesinska-Figatowska, Monika, Vielhaber, Stefan, Hallmann, Kerstin, Stawinski, Piotr, Buehring, Sonja, Hsu, David A., Kunz, Wolfram S., Meisler, Miriam H., Ploski, Rafal

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Heterozygous loss-of-function SEC61A1 mutations cause autosomal-dominant tubulo-interstitial and glomerulocystic kidney disease with anemia von Bolar, Nikhita Ajit, Golzio, Christelle, Živná, Martina, Hayot, Gaëlle, VAN HEMELRIJK, CHRISTINE, Schepers, Dorien, Vandeweyer, Geert, Hoischen, Alexander, Huyghe, Jeroen R, Raes, Ann, Matthys, Erve, Sys, Emiel, Azou, Myriam, Gubler, Marie-Claire, Praet, Marleen, Van Camp, Guy, McFadden, Kelsey, Pediaditakis, Igor, Přistoupilová, Anna, Hodaňová, Kateřina, Vylet'al, Petr, Hartmannová, Hana, Stránecký, Viktor, Hůlková, Helena, Barešová, Veronika, Jedličková, Ivana, Sovová, Jana, Hnízda, Aleš, Kidd, Kendrah, Bleyer, Anthony J, Spong, Richard S, Vande Walle, Johan, Mortier, Geert, Brunner, Han, Van Laer, Lut, Kmoch, Stanislav, Katsanis, Nicholas, Loeys, Bart

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Enzyme activity of rat tibialis anterior muscle differs between treatment with triamcinolone and prednisolone and nutritional deprivation von LANG, E. K.-D, HESSELINK, M. K. C, DROST, M. R, VAN DER VUSSE, G. J, WOUTERS, E. F. M, SCHOLS, A. M. W. J

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