Changes of Sublingual Microcirculation during the Treatment of Severe Diabetic Ketoacidosis

by Vlasta Krausova, David Neumann, Jaroslav Skvor, Pavel Dostal
Published 2024-03-01

Neurophysiological Evidence for a Compensatory Activity during a Simple Oddball Task in Adolescents with Type 1 Diabetes Mellitus

by Tereza Vitvarová, David Neumann, Radka Šimáková, Jan Kremláček
Published 2018-01-01

Ovotesticular Disorder of Sexual Development and Non-Palpable Testis

by Radek Štichhauer, Antonín Šafus, David Neumann, Ivo Novák, Vladana Skutilová, Jan Laco
Published 2021-04-01

Risk estimation of SARS-CoV-2 transmission from bluetooth low energy measurements

by Felix Sattler, Jackie Ma, Patrick Wagner, David Neumann, Markus Wenzel, Ralf Schäfer, Wojciech Samek, Klaus-Robert Müller, Thomas Wiegand
Published 2020-10-01

Are all HCL systems the same? long term outcomes of three HCL systems in children with type 1 diabetes: real-life registry-based study

by Alzbeta Santova, Alzbeta Santova, Lukas Plachy, Vit Neuman, Marketa Pavlikova, Lenka Petruzelkova, Petra Konecna, Petra Venhacova, Jaroslav Skvor, Renata Pomahacova, David Neumann, Jan Vosahlo, Jiri Strnadel, Kamila Kocourkova, Barbora Obermannova, Stepanka Pruhova, Ondrej Cinek, Zdenek Sumnik
Published 2023-10-01

Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation

by Jürgen Klammt, David Neumann, Evelien F. Gevers, Shayne F. Andrew, I. David Schwartz, Denise Rockstroh, Roberto Colombo, Marco A. Sanchez, Doris Vokurkova, Julia Kowalczyk, Louise A. Metherell, Ron G. Rosenfeld, Roland Pfäffle, Mehul T. Dattani, Andrew Dauber, Vivian Hwa
Published 2018-05-01

Is it harder to know or to reason? Analyzing two-tier science assessment items using the Rasch measurement model

by Fulmer, G., Chu, H., Treagust, David, Neumann, K.
Published 2015

Learning to Walk in Minutes Using Massively Parallel Deep Reinforcement Learning

by Rudin, Nikita; id_orcid0000-0001-5893-0348, Hoeller, David, Reist, Philipp, Hutter, Marco; id_orcid0000-0002-4285-4990
Published 2022

Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.

by Beysen, Diane, De Jaegere, Sarah, Amor, David, Bouchard, Philippe, Christin-Maitre, Sophie, Fellous, Marc, Touraine, Philippe, Grix, Arthur W, Hennekam, Raoul, Meire, Françoise, Oyen, Nina, Wilson, Louise C, Barel, Dalit, Clayton-Smith, Jill, de Ravel, Thomy, Decock, Christian, Delbeke, Patricia, Ensenauer, Regina, Ebinger, Friedrich, Gillessen-Kaesbach, Gabriele, Hendriks, Yvonne, Kimonis, Virginia, Laframboise, Rachel, Laissue, Paul, Leppig, Kathleen, Leroy, Bart P, Miller, David T, Mowat, David, Neumann, Luitgard, Plomp, Astrid, Van Regemorter, Nicole, Wieczorek, Dagmar, Veitia, Reiner A, De Paepe, Anne, De Baere, Elfride
Published 2008