Feed-through insecticides for the control of the sand fly Phlebotomus argentipes von INGENLOFF, K., GARLAPATI, R., POCHÉ, D., SINGH, M. I., REMMERS, J. L., POCHÉ, R. M.

Volltext

Endovascular Therapy for Stroke Due to Basilar-Artery Occlusion von Langezaal, Lucianne C.M, van der Hoeven, Erik J.R.J, Mont’Alverne, Francisco J.A, de Carvalho, João J.F, Lima, Fabrício O, Dippel, Diederik W.J, van der Lugt, Aad, Lo, Rob T.H, Boiten, Jelis, Lycklama à Nijeholt, Geert J, Staals, Julie, van Zwam, Wim H, Nederkoorn, Paul J, Majoie, Charles B.L.M, Gerber, Johannes C, Mazighi, Mikael, Piotin, Michel, Zini, Andrea, Vallone, Stefano, Hofmeijer, Jeannette, Martins, Sheila O, Nolte, Christian H, Szabo, Kristina, Dias, Francisco A, Abud, Daniel G, Wermer, Marieke J.H, Remmers, Michel J.M, Schneider, Hauke, Rueckert, Christina M, de Laat, Karlijn F, Yoo, Albert J, van Doormaal, Pieter-Jan, van Es, Adriaan C.G.M, Emmer, Bart J, Michel, Patrik, Puetz, Volker, Audebert, Heinrich J, Pontes-Neto, Octavio M, Vos, Jan-Albert, Kappelle, L. Jaap, Algra, Ale, Schonewille, Wouter J

Volltext

Behçet disease-associated MHC class I residues implicate antigen binding and regulation of cell-mediated cytotoxicity von Ombrello, Michael J., Kirino, Yohei, de Bakker, Paul I. W., Gül, Ahmet, Kastner, Daniel L., Remmers, Elaine F.

Volltext

CT within 6 hours of headache onset to rule out subarachnoid hemorrhage in nonacademic hospitals von Blok, Katelijn M, Rinkel, Gabriel J.E, Majoie, Charles B.L.M, Hendrikse, Jeroen, Braaksma, Meriam, Tijssen, Cees C, Wong, Yu Yi, Hofmeijer, Jeannette, Extercatte, Jorunn, Kerklaan, Bertjan, Schreuder, Tobien H.C.M.L, ten Holter, Susanne, Verheul, Freek, Harlaar, Laurike, Pruissen, D. Martijn O, Kwa, Vincent I.H, Brouwers, Paul J, Remmers, Michel J.M, Schonewille, Wouter J, Kruyt, Nyika D, Vergouwen, Mervyn D.I

Volltext

Common genetic susceptibility loci link PFAPA syndrome, Behçet’s disease, and recurrent aphthous stomatitis von Manthiram, Kalpana, Preite, Silvia, Dedeoglu, Fatma, Demir, Selcan, Ozen, Seza, Edwards, Kathryn M., Lapidus, Sivia, Katz, Alexander E., Feder, Henry M., Lawton, Maranda, Licameli, Greg R., Wright, Peter F., Le, Julie, Barron, Karyl S., Ombrello, Amanda K., Barham, Beverly, Romeo, Tina, Jones, Anne, Srinivasalu, Hemalatha, Mudd, Pamela A., DeBiasi, Roberta L., Gül, Ahmet, Marshall, Gary S., Jones, Olcay Y., Chandrasekharappa, Settara C., Stepanovskiy, Yuriy, Ferguson, Polly J., Schwartzberg, Pamela L., Remmers, Elaine F., Kastner, Daniel L.

Volltext

Apixaban versus no anticoagulation after anticoagulation-associated intracerebral haemorrhage in patients with atrial fibrillation in the Netherlands (APACHE-AF): a randomised, ope... von Schreuder, Floris H B M, van Nieuwenhuizen, Koen M, Hofmeijer, Jeannette, Vermeer, Sarah E, Kerkhoff, Henk, Zock, Elles, Luijckx, Gert-Jan, Messchendorp, Gert P, van Tuijl, Julia, Bienfait, H Paul, Booij, Suzanne J, van den Wijngaard, Ido R, Remmers, Michel J M, Schreuder, Antonia H C M L, Dippel, Diederik W, Staals, Julie, Brouwers, Paul J A M, Wermer, Marieke J H, Coutinho, Jonathan M, Kwa, Vincent I H, van Gelder, Isabelle C, Schutgens, Roger E G, Zweedijk, Berber, Algra, Ale, van Dalen, Jan Willem, Jaap Kappelle, L, Rinkel, Gabriel J E, van der Worp, H Bart, Klijn, Catharina J M

Volltext

Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production von Brehm, Anja, Liu, Yin, Sheikh, Afzal, Marrero, Bernadette, Omoyinmi, Ebun, Zhou, Qing, Montealegre, Gina, Biancotto, Angelique, Reinhardt, Adam, Almeida de Jesus, Adriana, Pelletier, Martin, Tsai, Wanxia L, Remmers, Elaine F, Kardava, Lela, Hill, Suvimol, Kim, Hanna, Lachmann, Helen J, Megarbane, Andre, Chae, Jae Jin, Brady, Jilian, Castillo, Rhina D, Brown, Diane, Casano, Angel Vera, Gao, Ling, Chapelle, Dawn, Huang, Yan, Stone, Deborah, Chen, Yongqing, Sotzny, Franziska, Lee, Chyi-Chia Richard, Kastner, Daniel L, Torrelo, Antonio, Zlotogorski, Abraham, Moir, Susan, Gadina, Massimo, McCoy, Phil, Wesley, Robert, Rother, Kristina I, Rother, Kristina, Hildebrand, Peter W, Brogan, Paul, Krüger, Elke, Aksentijevich, Ivona, Goldbach-Mansky, Raphaela

Volltext

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B51 and ERAP1 von Kirino, Yohei, Bertsias, George, Ishigatsubo, Yoshiaki, Mizuki, Nobuhisa, Tugal-Tutkun, Ilknur, Seyahi, Emire, Ozyazgan, Yilmaz, Sacli, F Sevgi, Erer, Burak, Inoko, Hidetoshi, Emrence, Zeliha, Cakar, Atilla, Abaci, Neslihan, Ustek, Duran, Satorius, Colleen, Ueda, Atsuhisa, Takeno, Mitsuhiro, Kim, Yoonhee, Wood, Geryl M, Ombrello, Michael J, Meguro, Akira, Gül, Ahmet, Remmers, Elaine F, Kastner, Daniel L

Volltext

Clinical features and functional significance of the P369S/R408Q variant in pyrin, the familial Mediterranean fever protein von Ryan, J G, Masters, S L, Booty, M G, Habal, N, Alexander, J D, Barham, B K, Remmers, E F, Barron, K S, Kastner, D L, Aksentijevich, I

Volltext

Diagnostic yield and accuracy of CT angiography, MR angiography, and digital subtraction angiography for detection of macrovascular causes of intracerebral haemorrhage: prospective... von van Asch, Charlotte J J, Velthuis, Birgitta K, Rinkel, Gabriël J E, Algra, Ale, de Kort, Gérard A P, Witkamp, Theo D, de Ridder, Johanna C M, van Nieuwenhuizen, Koen M, de Leeuw, Frank-Erik, Schonewille, Wouter J, de Kort, Paul L M, Dippel, Diederik W, Raaymakers, Theodora W M, Hofmeijer, Jeannette, Wermer, Marieke J H, Kerkhoff, Henk, Jellema, Korné, Bronner, Irene M, Remmers, Michel J M, Bienfait, Henri Paul, Witjes, Ron J G M, Greving, Jacoba P, Klijn, Catharina J M

Volltext

Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications von Ombrello, MJ, Arthur, VL, Remmers, EF, Hinks, A, Tachmazidou, I, Grom, AA, Foell, D, Martini, A, Gattorno, M, Ozen, S

Volltext

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2 von Zhou, Qing, Yang, Dan, Ombrello, Amanda K, Zavialov, Andrey V, Toro, Camilo, Zavialov, Anton V, Stone, Deborah L, Chae, Jae Jin, Rosenzweig, Sergio D, Bishop, Kevin, Barron, Karyl S, Kuehn, Hye Sun, Hoffmann, Patrycja, Negro, Alejandra, Tsai, Wanxia L, Cowen, Edward W, Pei, Wuhong, Milner, Joshua D, Silvin, Christopher, Heller, Theo, Chin, David T, Patronas, Nicholas J, Barber, John S, Lee, Chyi-Chia R, Wood, Geryl M, Ling, Alexander, Kelly, Susan J, Kleiner, David E, Mullikin, James C, Ganson, Nancy J, Kong, Heidi H, Hambleton, Sophie, Candotti, Fabio, Quezado, Martha M, Calvo, Katherine R, Alao, Hawwa, Barham, Beverly K, Jones, Anne, Meschia, James F, Worrall, Bradford B, Kasner, Scott E, Rich, Stephen S, Goldbach-Mansky, Raphaela, Abinun, Mario, Chalom, Elizabeth, Gotte, Alisa C, Punaro, Marilynn, Pascual, Virginia, Verbsky, James W, Torgerson, Troy R, Singer, Nora G, Gershon, Timothy R, Ozen, Seza, Karadag, Omer, Fleisher, Thomas A, Remmers, Elaine F, Burgess, Shawn M, Moir, Susan L, Gadina, Massimo, Sood, Raman, Hershfield, Michael S, Boehm, Manfred, Kastner, Daniel L, Aksentijevich, Ivona

Volltext

The Preventive Antibiotics in Stroke Study (PASS): a pragmatic randomised open-label masked endpoint clinical trial von Westendorp, Willeke F, MD, Vermeij, Jan-Dirk, MD, Zock, Elles, MSc, Hooijenga, Imke J, MA, Kruyt, Nyika D, MD, Bosboom, Hans J L W, MD, Kwa, Vincent I H, MD, Weisfelt, Martijn, MD, Remmers, Michel J M, MD, ten Houten, Robert, MD, Schreuder, A H C M (Tobien), MD, Vermeer, Sarah E, MD, van Dijk, Ewout J, MD, Dippel, Diederik W J, Prof, Dijkgraaf, Marcel G W, PhD, Spanjaard, Lodewijk, MD, Vermeulen, Marinus, Prof, van der Poll, Tom, Prof, Prins, Jan M, Prof, Vermeij, Frederique H, MD, Roos, Yvo B W E M, Prof, Kleyweg, Ruud P, MD, Kerkhoff, Henk, MD, Brouwer, Matthijs C, MD, Zwinderman, Aeilko H, Prof, van de Beek, Diederik, Prof, Nederkoorn, Paul J, MD

Volltext

Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci von Zhernakova, Alexandra, Stahl, Eli A, Trynka, Gosia, Raychaudhuri, Soumya, Festen, Eleanora A, Franke, Lude, Westra, Harm-Jan, Fehrmann, Rudolf S N, Kurreeman, Fina A S, Thomson, Brian, Gupta, Namrata, Romanos, Jihane, McManus, Ross, Ryan, Anthony W, Turner, Graham, Brouwer, Elisabeth, Posthumus, Marcel D, Remmers, Elaine F, Tucci, Francesca, Toes, Rene, Grandone, Elvira, Mazzilli, Maria Cristina, Rybak, Anna, Cukrowska, Bozena, Coenen, Marieke J H, Radstake, Timothy R D J, van Riel, Piet L C M, Li, Yonghong, de Bakker, Paul I W, Gregersen, Peter K, Worthington, Jane, Siminovitch, Katherine A, Klareskog, Lars, Huizinga, Tom W J, Wijmenga, Cisca, Plenge, Robert M

Volltext

Endoplasmic reticulum-associated amino-peptidase 1 and rheumatic disease: genetics von Ombrello, Michael J, Kastner, Daniel L, Remmers, Elaine F

Volltext

Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease von Kirino, Yohei, Zhou, Qing, Ishigatsubo, Yoshiaki, Mizuki, Nobuhisa, Tugal-Tutkun, Ilknur, Seyahi, Emire, Özyazgan, Yilmaz, Ugurlu, Serdal, Erer, Burak, Abaci, Neslihan, Ustek, Duran, Meguro, Akira, Ueda, Atsuhisa, Takeno, Mitsuhiro, Inoko, Hidetoshi, Ombrello, Michael J., Satorius, Colleen L., Maskeri, Baishali, Mullikin, James C., Sun, Hong-Wei, Gutierrez-Cruz, Gustavo, Kim, Yoonhee, Wilson, Alexander F., Kastner, Daniel L., Gül, Ahmet, Remmers, Elaine F.

Volltext

Epac2 Mediates cAMP-Dependent Potentiation of Neurotransmission in the Hippocampus von Fernandes, Herman B, Riordan, Sean, Nomura, Toshihiro, Remmers, Christine L, Kraniotis, Stephen, Marshall, John J, Kukreja, Lokesh, Vassar, Robert, Contractor, Anis

Volltext

Brief Report: Deficiency of Complement 1r Subcomponent in Early‐Onset Systemic Lupus Erythematosus: The Role of Disease‐Modifying Alleles in a Monogenic Disease von Demirkaya, Erkan, Zhou, Qing, Smith, Carolyne K., Ombrello, Michael J., Deuitch, Natalie, Tsai, Wanxia L., Hoffmann, Patrycja, Remmers, Elaine F., Takeuchi, Masaki, Park, Yong Hwan, Chae, JaeJin, Barut, Kenan, Simsek, Dogan, Adrovic, Amra, Sahin, Sezgin, Caliskan, Salim, Chandrasekharappa, Settara C., Hasni, Sarfaraz A., Ombrello, Amanda K., Gadina, Massimo, Kastner, Daniel L., Kaplan, Mariana J., Kasapcopur, Ozgur, Aksentijevich, Ivona

Volltext

Evaluation of KIR3DL1/KIR3DS1 polymorphism in Behçet’s disease von Erer, B, Takeuchi, M, Ustek, D, Tugal-Tutkun, I, Seyahi, E, Özyazgan, Y, Duymaz-Tozkir, J, Gül, A, Kastner, D L, Remmers, E F, Ombrello, M J

Volltext

A Schizophrenia-Linked KALRN Coding Variant Alters Neuron Morphology, Protein Function, and Transcript Stability von Russell, Theron A., Grubisha, Melanie J., Remmers, Christine L., Kang, Seok Kyu, Forrest, Marc P., Smith, Katharine R., Kopeikina, Katherine J., Gao, Ruoqi, Sweet, Robert A., Penzes, Peter

Volltext