Netherlands (NL)

Sp2 is the only glutamine-rich Specificity protein with minor impact on development and differentiation in myelinating glia. (2017) Wegener A, Küspert M, Sock E, Philipsen S, Suske G, Wegner M Journal article, Original article The TH1 phenotype of follicular helper T cells indicates an IFN-?-associated immune dysregulation in patients with CD21low common variable immunodeficiency (2017) Unger S, Seidl M, van Schouwenburg P, Rakhmanov M, Bulashevska A, Frede N, Grimbacher B, et al. Journal article Prevention of Mental Health Disorders using Internet and mobile-based Interventions: a narrative review and recommendations for future research (2017) Ebert D, Cuijpers P, Munoz R, Baumeister H Journal article, Review article Analysis of ATP8B4 F436L missense variant in a large Systemic sclerosis cohort (2017) Lopez-Isac E, Bossini-Castillo L, Palma AB, Assassi S, Mayes MD, Simeon CP, Ortego-Centeno N, et al. Journal article ESRD After Heart Failure, Myocardial Infarction, or Stroke in Type 2 Diabetic Patients With CKD (2017) Charytan DM, Solomon SD, Ivanovich P, Remuzzi G, Cooper ME, McGill JB, Parving HH, et al. Journal article A dual role for UCMA in osteoarthritis-Inhibition of aggrecanases and promotion of bone turnover (2017) Stock M, Menges S, Eitzinger N, Gesslein M, Botschner R, Wormser L, Distler A, et al. Journal article Renal function in patients with non-dialysis chronic kidney disease receiving intravenous ferric carboxymaltose: an analysis of the randomized FIND-CKD trial (2017) Macdougall IC, Bock AH, Carrera F, Eckardt KU, Gaillard C, Van Wyck D, Meier Y, et al. Journal article Immunohistochemical and molecular characterizations in urothelial carcinoma of bladder in patients less than 45 years (2017) Weyerer V, Schneckenpointner R, Filbeck T, Burger M, Hofstaedter F, Wild PJ, Fine SW, et al. Journal article Safety of intravenous ferric carboxymaltose versus oral iron in patients with nondialysis-dependent CKD: an analysis of the 1-year FIND-CKD trial (2017) Roger SD, Gaillard CA, Bock AH, Carrera F, Eckardt KU, Van Wyck DB, Cronin M, et al. Journal article STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability (2017) Lehalle D, Mosca-Boidron AL, Begtrup A, Boute-Benejean O, Charles P, Cho MT, Clarkson A, et al. Journal article