Fructose and sorbitol malabsorption in ambulatory patients with functional dyspepsia: Comparison with lactose maldigestion/malabsorption von MISHKIN, D, SABLAUSKAS, L, YALOVSKY, M, MISHKIN, S

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"H2 nonproducers" and malabsorption of carbohydrate von Mishkin, S, Sablauskas, L, Schwarcz, J

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Fructose and/or Sorbitol Intolerance in a Subgroup of Lactose Intolerant Patients von Mishkin, SR, Sablauskas, L, Mishkin, S

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De novo mutations in children born after medical assisted reproduction von Smits, R M, Xavier, M J, Oud, M S, Astuti, G D N, Meijerink, A M, de Vries, P F, Holt, G S, Alobaidi, B K S, Batty, L E, Khazeeva, G, Sablauskas, K, Vissers, L E L M, Gilissen, C, Fleischer, K, Braat, D D M, Ramos, L, Veltman, J A

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P1465Artificial intelligence in echocardiography - Steps to automatic cardiac measurements in routine practice von Karuzas, A, Sablauskas, K, Skrodenis, L, Verikas, D, Rumbinaite, E, Zaliaduonyte-Peksiene, D, Ziuteliene, K, Vaskelyte, J J, Jurkevicius, R, Plisiene, J

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Accurate prediction of left ventricular diastolic dysfunction in 2D echocardiography using ensemble of deep convolutional neural networks von Karuzas, A, Sablauskas, K, Verikas, D, Skrodenis, L, Teleisyte, E, Matuliauskas, D, Balciunas, J, Kiziela, A, Rumbinaite, E, Lapinskas, T, Ereminiene, E, Mizariene, V, Vaskelyte, J.J, Jurkevicius, R, Plisiene, J

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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1) von Töpf, Ana, Pyle, Angela, Griffin, Helen, Matalonga, Leslie, Schon, Katherine, Sickmann, Albert, Schara-Schmidt, Ulrike, Hentschel, Andreas, Chinnery, Patrick F, Kölbel, Heike, Roos, Andreas, Horvath, Rita

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544 Deep learning in segmentation and function evaluation of right ventricle in 2D echocardiography von Karuzas, A, Sablauskas, K, Verikas, D, Teleisyte, E, Skrodenis, L, Matuliauskas, D, Balciunas, J, Mileris, J, Rumbinaite, E, Zaliaduonyte-Peksiene, D, Vaskelyte, J J, Jurkevicius, R, Plisiene, J

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Automated evaluation of the right-sided heart function and geometry using deep learning von Karuzas, A, Sablauskas, K, Zvirblyte, R, Skrodenis, L, Teleisyte, E, Verikas, D, Balciunas, J, Matuliauskas, D, Kiziela, A, Rumbinaite, E, Vaskelyte, JJ, Ereminiene, E, Jurkevicius, R, Plisiene, J

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A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis von de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J H, Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E L M

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Correction: A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis (European Journal of Human Genet... von de Boer, Elke, Ockeloen, Charlotte W., Matalonga, Leslie, Horvath, Rita, Cohen, Enzo, Nelson, Isabelle, Rodenburg, Richard J., Coenen, Marieke J. H., Janssen, Mirian, Henssen, Dylan, Gilissen, Christian, Steyaert, Wouter, Paramonov, Ida, Trimouille, Aurelien, Kleefstra, Tjitske, Verloes, Alain, Vissers, Lisenka E. L. M.

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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1) von Töpf, A, Pyle, A, Griffin, H, Matalonga, L, Schon, K, Cohen, E, Cuesta, I, Danis, D, Denommé-Pichon, AS, Duffourd, Y, Gilissen, C, Johari, M, Laurie, S, Li, S, Nelson, I, Paramonov, I, Peters, S, Prasanth, S, Robinson, P, Sablauskas, K, Savarese, M, Steyaert, W, van der Velde, JK, Vitobello, A, Baets, J, Beijer, D, Bonne, G, Cossins, J, Evangelista, T, Ferlini, A, Hackman, P, Hanna, MG, Houlden, H, Lau, J, Lochmüller, H, Macken, WL, Musacchia, F, Nascimento, A, Natera-de Benito, D, Nigro, V, Piluso, G, Pini, V, Pitceathly, RDS, Polavarapu, K, Cruz, PMR, Sarkozy, A, Selvatici, R, Thompson, R, Torella, A, Udd, B, Van de Vondel, L, Vandrovcova, J, Zaharieva, I, Sickmann, A, Schara–Schmidt, U, Hentschel, A, Chinnery, PF, Kölbel, H, Roos, A, Horvath, R

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A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis von de Boer, Elke, Ockeloen, Charlotte W, Matalonga, Leslie, Horvath, Rita, Rodenburg, Richard J, Coenen, Marieke J. H, Janssen, Mirian, Henssen, Dylan, Paramonov, Ida, Trimouille, Aurélien, Kleefstra, Tjitske, Vissers, Lisenka E. L. M, Cohen, Enzo, Cuesta, Isabel, Danis, Daniel, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Gilissen, Christian, Johari, Mridul, Laurie, Steven, Li, Shuang, Nelson, Isabelle, Peters, Sophia, Prasanth, Sivakumar, Robinson, Peter, Sablauskas, Karolis, Savarese, Marco, Steyaert, Wouter, Töpf, Ana, van der Velde, Joeri K, Vitobello, Antonio, Banka, Siddharth, Benetti, Elisa, Casari, Giorgio, Ciolfi, Andrea, Clayton-Smith, Jill, Dallapiccola, Bruno, Faivre, Laurence, Haack, Tobias B, Hammarsjö, Anna, Havlovicova, Marketa, Hoischen, Alexander, Hugon, Anne, Jackson, Adam, Lindstrand, Anna, López-Martín, Estrella, Macek, Milan, Jr, Nigro, Vicenzo, Nordgren, Ann, Pettersson, Maria, Pinelli, Michele, Pizzi, Simone, Posada, Manuel, Radio, Francesca Clementina, Renieri, Alessandra, Rooryck, Caroline, Ryba, Lukas, Schwarz, Martin, Tartaglia, Marco, Thauvin, Christel, Torella, Annalaura, Verloes, Alain, Vissers, Lisenka, Vyshka, Klea, Zurek, Birte

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Exome reanalysis and proteomic profiling identified TRIP4 as a novel cause of cerebellar hypoplasia and spinal muscular atrophy (PCH1) von Töpf, Ana, Pyle, Angela, Griffin, Helen, Matalonga, Leslie, Schon, Katherine, Sickmann, Albert, Schara–Schmidt, Ulrike, Hentschel, Andreas, Chinnery, Patrick F, Kölbel, Heike, Roos, Andreas, Horvath, Rita, Cohen, Enzo, Cuesta, Isabel, Danis, Daniel, Denommé-Pichon, Anne-Sophie, Duffourd, Yannis, Gilissen, Christian, Johari, Mridul, Laurie, Steven, Li, Shuang, Nelson, Isabelle, Paramonov, Ida, Peters, Sophia, Prasanth, Sivakumar, Robinson, Peter, Sablauskas, Karolis, Savarese, Marco, Steyaert, Wouter, van der Velde, Joeri K, Vitobello, Antonio, Baets, Jonathan, Beijer, Danique, Bonne, Gisèle, Cossins, Judith, Evangelista, Teresinha, Ferlini, Alessandra, Hackman, Peter, Hanna, Michael G, Houlden, Henry, Lau, Jarred, Lochmüller, Hanns, Macken, William L, Musacchia, Francesco, Nascimento, Andres, Natera-de Benito, Daniel, Nigro, Vincenzo, Piluso, Giulio, Pini, Veronica, Pitceathly, Robert D. S, Polavarapu, Kiran, Cruz, Pedro M. Rodriguez, Sarkozy, Anna, Selvatici, Rita, Thompson, Rachel, Torella, Annalaura, Udd, Bjarne, Van de Vondel, Liedewei, Vandrovcova, Jana, Zaharieva, Irina

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