نتائج البحث - Patrick Verloo

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  1. 1
    Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients

    Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients حسب Patrick Verloo, Clemens H. M. Kocken, Annemarie Voorberg-van der Wel, Ben C. Tilly, Boris M. Hogema, M. Sinaasappel, Alan W. Thomas, Hugo R. de Jonge

    منشور في 2004
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    Artigo
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  2. 2
    Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects

    Blue Native Polyacrylamide Gel Electrophoresis: A Powerful Tool in Diagnosis of Oxidative Phosphorylation Defects حسب Rudy Van Coster, Joél Smet, Edith George, Linda De Meırleır, Sara Seneca, Johan Van Hove, Guillaume Sébire, Hélène Verhelst, Jan De Bleecker, Bruno Van Vlem, Patrick Verloo, Jules G. Leroy

    منشور في 2001
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    Artigo
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  3. 3
    Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)

    Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA) حسب Nika Schuermans, Dimitri Hemelsoet, Wim Terryn, Sanne Steyaert, Rudy Van Coster, Paul Coucke, Wouter Steyaert, Bert Callewaert, Elke Bogaert, Patrick Verloo, Arnaud Vanlander, Elke Debackere, Jody Ghijsels, Pontus LeBlanc, Hannah Verdin, Leslie Naesens, Filomeen Haerynck, Steven Callens, Bart Dermaut, Bruce Poppe, Jan De Bleecker, Patrick Santens, Paul Boon, Guy Laureys, Tessa Kerre

    منشور في 2022
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    Artigo
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  4. 4
    Electrophysiological studies of malaria parasite-infected erythrocytes: Current status

    Electrophysiological studies of malaria parasite-infected erythrocytes: Current status حسب Henry M. Staines, Abdulnaser Alkhalil, Richard J. Allen, Hugo R. de Jonge, Elvira T. Derbyshire, Stéphane Égée, Hagai Ginsburg, David A. Hill, Stephan M. Huber, Kiaran Kirk, Florian Läng, Godfrey Lisk, Eugene K. Oteng, Ajay D. Pillai, Kempaiah Rayavara, Sherin J. Rouhani, Kevin J. Saliba, Crystal Shen, Tsione Solomon, Serge Thomas, Patrick Verloo, Sanjay A. Desai

    منشور في 2007
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    Revisão
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  5. 5
    A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

    A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation حسب Simon J. Tavernier, Vicki Athanasopoulos, Patrick Verloo, Gesine Behrens, Jens Staal, Debby Bogaert, Leslie Naesens, Marieke De Bruyne, Sofie Van Gassen, Eef Parthoens, Julia I. Ellyard, Jean Cappello, L. X. Morris, Hanne Van Gorp, Gert Van Isterdael, Yvan Saeys, Mohamed Lamkanfi, Petra Schelstraete, Joke Dehoorne, Victoria Bordon, Rudy Van Coster, Bart N. Lambrecht, Björn Menten, Rudi Beyaert, Carola G. Vinuesa, Vigo Heissmeyer, Mélissa Dullaers, Filomeen Haerynck

    منشور في 2019
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    Artigo
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  6. 6
    Integration of proteomics with genomics and transcriptomics increases the diagnostic rate of Mendelian disorders

    Integration of proteomics with genomics and transcriptomics increases the diagnostic rate of Mendelian disorders حسب Robert Kopajtich, Dmitrii Smirnov, Sarah L. Stenton, Stefan Loipfinger, Chen Meng, Ines F. Scheller, Peter Freisinger, Robert Baski, Riccardo Berutti, Jürgen Behr, Martina Bucher, Felix Distelmaier, Elisabeth Graf, Mirjana Gušić, Maja Hempel, Lea Kulterer, Johannes A. Mayr, Thomas Meitinger, Christian Mertes, Metodi D. Metodiev, Agnieszka Nadel, Alessia Nasca, Akira Ohtake, Yasushi Okazaki, Rikke Katrine Jentoft Olsen, Dorota Piekutowska‐Abramczuk, Agnès Rötig, René Santer, Detlev Schindler, Abdelhamid Slama, Christian Staufner, Tim M. Strom, Patrick Verloo, Jürgen‐Christoph von Kleist-Retzow, Saskia B. Wortmann, Vicente A. Yépez, Costanza Lamperti, Daniele Ghezzi, Kei Murayama, Christina Ludwig, Julien Gagneur, Holger Prokisch

    منشور في 2021
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    Pré-impressão
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  7. 7
    Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

    Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes حسب Heather C. Mefford, Andrew J. Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv Maloney, John A. Crolla, Diana Baralle, Amanda Collins, Catherine Mercer, Koen Norga, Thomy de Ravel, Koenraad Devriendt, Ernie M.H.F. Bongers, Nicole de Leeuw, William Reardon, Stefania Gimelli, Frédérique Béna, Raoul C. M. Hennekam, Alison Male, Lorraine Gaunt, Jill Clayton‐Smith, Ingrid Simonic, Soo Mi Park, Sarju Mehta, Serena Nik‐Zainal, C. Geoffrey Woods, Helen V. Firth, Georgina Parkin, Marco Fichera, S Reitano, Mariangela Lo Giudice, Kelly E. Li, Iris Casuga, Adam Broomer, Bernard Conrad, Markus Schwerzmann, Lorenz Räber, Sabina Gallati, Pasquale Striano, Antonietta Coppola, John Tolmie, Edward S. Tobias, Chris J. Lilley, Lluı́s Armengol, Yves Spysschaert, Patrick Verloo, Anja De Coene, Linde Goossens, Geert Mortier, Frank Speleman, Ellen van Binsbergen, Marcel Nelen, Ron Hochstenbach, Martin Poot, Louise Gallagher, Michael Gill, Jon McClellan, Mary‐Claire King, Regina Regan, Cindy Skinner, Roger E. Stevenson, Stylianos E. Antonarakis, Caifu Chen, Xavier Estivill, Björn Menten, Giorgio Gimelli, Susan Gribble, Stuart Schwartz, James S. Sutcliffe, Tom Walsh, Samantha J.L. Knight, Jonathan Sebat, Corrado Romano, Charles E. Schwartz, Joris A. Veltman, Bert B.A. de Vries, Joris Vermeesch, John Barber, Lionel Willatt, May Tassabehji, Evan E. Eichler

    منشور في 2008
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    Artigo
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