Bruton's Tyrosine Kinase and Phospholipase Cγ2 Mediate Chemokine-Controlled B Cell Migration and Homing von de Gorter, David J.J., Beuling, Esther A., Kersseboom, Rogier, Middendorp, Sabine, van Gils, Janine M., Hendriks, Rudolf W., Pals, Steven T., Spaargaren, Marcel

Volltext

Tumor suppressor function of Bruton tyrosine kinase is independent of its catalytic activity von Middendorp, Sabine, Zijlstra, Esther A.J., Kersseboom, Rogier, Dingjan, Gemma M., Jumaa, Hassan, Hendriks, Rudolf W.

Volltext

Somatic thrombopoietin (THPO) gene mutations in childhood myeloid leukemias von Houwing, Maite E., Koopman-Coenen, Eva A., Kersseboom, Rogier, Gooskens, Saskia, Appel, Inge M., Arentsen-Peters, Susan T. C. J. M., de Vries, Andrica C. H., Reinhardt, Dirk, Stary, Jan, Baruchel, André, de Haas, Valerie, Blink, Marjolein, Lopes Cardozo, Rob H., Pieters, Rob, Michel Zwaan, C., van den Heuvel-Eibrink, Marry M.

Volltext

ANKRD26-related thrombocytopenia and myeloid malignancies von Noris, Patrizia, Favier, Remi, Alessi, Marie-Christine, Geddis, Amy E., Kunishima, Shinji, Heller, Paula G., Giordano, Paola, Niederhoffer, Karen Y., Bussel, James B., Podda, Gian Marco, Vianelli, Nicola, Kersseboom, Rogier, Pecci, Alessandro, Gnan, Chiara, Marconi, Caterina, Auvrignon, Anne, Cohen, William, Yu, Jennifer C., Iguchi, Akihiro, Miller Imahiyerobo, Allison, Boehlen, Francoise, Ghalloussi, Dorsaf, De Rocco, Daniela, Magini, Pamela, Civaschi, Elisa, Biino, Ginevra, Seri, Marco, Savoia, Anna, Balduini, Carlo L.

Volltext

Missed Diagnoses and Health Problems in Adults With Prader-Willi Syndrome: Recommendations for Screening and Treatment von Pellikaan, Karlijn, Rosenberg, Anna G W, Kattentidt-Mouravieva, Anja A, Kersseboom, Rogier, Bos-Roubos, Anja G, Veen-Roelofs, José M C, van Wieringen, Nina, Hoekstra, Franciska M E, van den Berg, Sjoerd A A, van der Lely, Aart Jan, de Graaff, Laura C G

Volltext

MYH9-Related Disease: A Novel Prognostic Model to Predict the Clinical Evolution of the Disease Based on Genotype-Phenotype Correlations von Pecci, Alessandro, Klersy, Catherine, Gresele, Paolo, Lee, Kieran J.D., De Rocco, Daniela, Bozzi, Valeria, Russo, Giovanna, Heller, Paula G., Loffredo, Giuseppe, Ballmaier, Matthias, Fabris, Fabrizio, Beggiato, Eloise, Kahr, Walter H.A., Pujol-Moix, Nuria, Platokouki, Helen, Van Geet, Christel, Noris, Patrizia, Yerram, Preethi, Hermans, Cedric, Gerber, Bernhard, Economou, Marina, De Groot, Marco, Zieger, Barbara, De Candia, Erica, Fraticelli, Vincenzo, Kersseboom, Rogier, Piccoli, Giorgina B., Zimmermann, Stefanie, Fierro, Tiziana, Glembotsky, Ana C., Vianello, Fabrizio, Zaninetti, Carlo, Nicchia, Elena, Güthner, Christiane, Baronci, Carlo, Seri, Marco, Knight, Peter J., Balduini, Carlo L., Savoia, Anna

Volltext

Brutons Tyrosine Kinase and Phospholipase C gamma 2 Mediate Chemokine-Controlled B Cell Migration and Homing von De Gorter, David JJ, Beuling, Esther A, Kersseboom, Rogier, Middendorp, Sabine, Van Gils, Janine M, Hendriks, Rudolf W, Pals, Steven T, Spaargaren, Marcel

Volltext

Educational paper: Syndromic forms of primary immunodeficiency von Kersseboom, Rogier, Brooks, Alice, Weemaes, Corry

Volltext

Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles von Bassani, Sissy, Chrast, Jacqueline, Ambrosini, Giovanna, Voisin, Norine, Schütz, Frédéric, Brusco, Alfredo, Sirchia, Fabio, Turban, Lydia, Schubert, Susanna, Abou Jamra, Rami, Schlump, Jan-Ulrich, DeMille, Desiree, Bayrak-Toydemir, Pinar, Nelson, Gary Rex, Wong, Kristen Nicole, Duncanson, Laura, Mosera, Mackenzie, Gilissen, Christian, Vissers, Lisenka E L M, Pfundt, Rolph, Kersseboom, Rogier, Yttervik, Hilde, Hansen, Geir Åsmund Myge, Smeland, Marie Falkenberg, Butler, Kameryn M, Lyons, Michael J, Carvalho, Claudia M B, Zhang, Chaofan, Lupski, James R, Potocki, Lorraine

Volltext

Educational paper von Kersseboom, Rogier, Brooks, Alice, Weemaes, Corry

Volltext

Hematopoietic Stem Cell Transplantation in a Patient With ICF2 Syndrome Presenting With EBV-Induced Hemophagocytic Lymphohystiocytosis von Harnisch, Esther, Buddingh, Emilie P, Thijssen, Peter E, Brooks, Alice S, Driessen, Gertjan J, Kersseboom, Rogier, Lankester, Arjan C

Volltext

Sex steroids influence pancreatic islet hypertrophy and subsequent autoimmune infiltration in nonobese diabetic (NOD) and NODscid mice von ROSMALEN, Judith G. M, PIGMANS, Marieke J. G, KERSSEBOOM, Rogier, DREXHAGE, Hemmo A, LEENEN, Pieter J. M, HOMO-DELARCHE, Francoise

Volltext

Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin-10 Receptor von Veenbergen, Sharon, van Leeuwen, Marieke A, Driessen, Gertjan J, Kersseboom, Rogier, de Ruiter, Lilian F, Raatgeep, Rolien H C, Lindenbergh-Kortleve, Dicky J, Simons-Oosterhuis, Ytje, Biermann, Katharina, Halley, Dicky J J, de Ridder, Lissy, Escher, Johanna C, Samsom, Janneke N

Volltext

Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin‐10 Receptor von Veenbergen, Sharon, Leeuwen, Marieke A., Driessen, Gertjan J., Kersseboom, Rogier, Ruiter, Lilian F., Raatgeep, Rolien (H.)C., Lindenbergh‐Kortleve, Dicky J., Simons‐Oosterhuis, Ytje, Biermann, Katharina, Halley, Dicky J.J., Ridder, Lissy, Escher, Johanna C., Samsom, Janneke N.

Volltext

Syndromic forms of primary immunodeficiency von KERSSEBOOM, Rogier, BROOKS, Alice, WEEMAES, Corry

Volltext

Constitutive activation of Bruton's tyrosine kinase induces the formation of autoreactive IgM plasma cells von Kersseboom, Rogier, Kil, Laurens, Flierman, Roelof, van der Zee, Marten, Dingjan, Gemma M, Middendorp, Sabine, Maas, Alex, Hendriks, Rudi W

Volltext

Effects of Childhood Multidisciplinary Care and Growth Hormone Treatment on Health Problems in Adults with Prader-Willi Syndrome von Pellikaan, Karlijn, Rosenberg, Anna G. W., Davidse, Kirsten, Kattentidt-Mouravieva, Anja A., Kersseboom, Rogier, Bos-Roubos, Anja G., Grootjen, Lionne N., Damen, Layla, van den Berg, Sjoerd A. A., van der Lely, Aart J., Hokken-Koelega, Anita C. S., de Graaff, Laura C. G.

Volltext

What Every Internist-Endocrinologist Should Know about Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five Years of 'I... von Rosenberg, Anna G. W., Pater, Minke R. A., Pellikaan, Karlijn, Davidse, Kirsten, Kattentidt-Mouravieva, Anja A., Kersseboom, Rogier, Bos-Roubos, Anja G., van Eeghen, Agnies, Veen, Jose M. C., van der Meulen, Jiske J., Van Aalst-van Wieringen, Nina, Hoekstra, Franciska M. E., van der Lely, Aart J., de Graaff, Laura C. G.

Volltext

What Every Internist Should Know About Rare Genetic Syndromes in Order to Prevent Needless Diagnostics, Missed Diagnoses and Medical Complications: Five-Year Experience of Internal... von Rosenberg, Anna G W, Pater, Minke R A, Davidse, Kirsten, Kattentidt-Mouravieva, Anja A, Kersseboom, Rogier, Bos-Roubos, Anja G, van Eeghen, Agnies, van der Meulen, Jiske J, Veen, José M C, van Aalst, Nina, Hoekstra, Franciska M E, Van der Lely, Aart J, de Graaff, Laura C G

Volltext