A Patient with Autoimmune Pancreatitis Type 1 with Previously Known Lymphadenopathy, Both in the Context of IgG4-related Disease

Por Alidjan, Fazil M., Karim, Faiz, Verdijk, Rob M., van Esser, Joost W., van Heerde, Marianne J.
Publicado no Am J Case Rep (2015)

IgG4-related disease: a systematic review of this unrecognized disease in pediatrics

Por Karim, Faiz, Loeffen, Jan, Bramer, Wichor, Westenberg, Lauren, Verdijk, Rob, van Hagen, Martin, van Laar, Jan
Publicado no Pediatr Rheumatol Online J (2016)

Expression and inhibition of BRD4, EZH2 and TOP2A in neurofibromas and malignant peripheral nerve sheath tumors

Por Amirnasr, Azadeh, Verdijk, Rob M., van Kuijk, Patricia F., Taal, Walter, Sleijfer, Stefan, Wiemer, Erik A. C.
Publicado no PLoS One (2017)

Distinctive Cytokines as Biomarkers Predicting Fatal Outcome of Severe Staphylococcus aureus Bacteremia in Mice

Por van den Berg, Sanne, Laman, Jon D., Boon, Louis, ten Kate, Marian T., de Knegt, Gerjo J., Verdijk, Rob M., Verbrugh, Henri A., Nouwen, Jan L., Bakker-Woudenberg, Irma A. J. M.
Publicado em 2013

Fatal Balamuthia mandrillaris Meningoencephalitis in the Netherlands after Travel to The Gambia

Por van der Beek, Nadine A.M.E., van Tienen, Carla, de Haan, Jubi E., Roelfsema, Jeroen, Wismans, Pieter J., van Genderen, Perry J.J., Tanghe, Herve L., Verdijk, Rob M., Titulaer, Maarten J., van Hellemond, Jaap J.
Publicado no Emerg Infect Dis (2015)

Prognostic parameters in uveal melanoma and their association with BAP1 expression

Por van Essen, T Huibertus, van Pelt, Sake I, Versluis, Mieke, Bronkhorst, Inge HG, van Duinen, Sjoerd G, Marinkovic, Marina, Kroes, Wilma GM, Ruivenkamp, Claudia AL, Shukla, Shruti, de Klein, Annelies, Kiliç, Emine, Harbour, J William, Luyten, Gregorius PM, van der Velden, Pieter A, Verdijk, Rob M, Jager, Martine J
Publicado no Br J Ophthalmol (2014)

Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease

Por Kamps, Rick, Szklarczyk, Radek, Theunissen, Tom E., Hellebrekers, Debby M. E. I., Sallevelt, Suzanne C. E. H., Boesten, Iris B., de Koning, Bart, van den Bosch, Bianca J., Salomons, Gajja S., Simas-Mendes, Marisa, Verdijk, Rob, Schoonderwoerd, Kees, de Coo, Irenaeus F. M., Vanoevelen, Jo M., Smeets, Hubert J. M.
Publicado no Eur J Hum Genet (2018)

Novel FOXF1 mutations in sporadic and familial cases of Alveolar Capillary Dysplasia with Misaligned Pulmonary Veins imply a role for its DNA binding domain

Por Sen, Partha, Yang, Yaping, Navarro, Colby, Silva, Iris, Szafranski, Przemyslaw, Kolodziejska, Katarzyna E., Dharmadhikari, Avinash V., Mostafa, Hasnaa, Kozakewich, Harry, Kearney, Debra, Cahill, John B., Whitt, Merrissa, Bilic, Masha, Margraf, Linda, Charles, Adrian, Goldblatt, Jack, Gibson, Kathleen, Lantz, Patrick, Garvin, Julian, Petty, John, Kiblawi, Zeina, Zuppan, Craig, McConkie-Rosell, Allyn, McDonald, Marie T., Peterson-Carmichael, Stacey L., Gaede, Jane T., Shivanna, Binoy, Schady, Deborah, Friedlich, Philippe S., Hays, Stephen R., Palafoll, Irene Valenzuela, Siebers-Renelt, Ulrike, Bohring, Axel, Finn, Laura S., Siebert, Joseph R., Galambos, Csaba, Nguyen, Lananh, Riley, Melissa, Chassaing, Nicolas, Vigouroux, Adeline, Rocha, Gustavo, Fernandes, Susana, Brumbaugh, Jane, Roberts, Kari, Ho-ming, Luk, Lo, Ivan, Lam, Stephen, Gerychova, Romana, Jezova, Marta, Valaskova, Iveta, Fellmann, Florence, Afshar, Katayoun, Giannoni, Eric, Muhlethaler, Vincent, Liang, Jinlong, Beckmann, Jacques S., Lioy, Janet, Deshmukh, Hitesh, Srinivasan, Lakshmi, Swarr, Daniel T., Sloman, Melissa, Shaw-Smith, Charles, van Loon, Rosa Laura, Hagman, Cecilia, Sznajer, Yves, Barrea, Catherine, Galant, Christine, Detaille, Thierry, Wambach, Jennifer A., Cole, F. Sessions, Hamvas, Aaron, Prince, Lawrence S., Diderich, Karin E.M., Brooks, Alice S., Verdijk, Rob M., Ravindranathan, Hari, Sugo, Ella, Mowat, David, Baker, Michael L., Langston, Claire, Welty, Stephen, Stankiewicz, Pawel
Publicado em 2013