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Kidney International, ISSN 0085-2538, 04/2013, Volume 83, Issue 4, pp. 749 - 756
The Nephrotic Syndrome Study Network (NEPTUNE) is a North American multicenter collaborative consortium established to develop a translational research... 
clinical trial | focal segmental glomerulosclerosis | membranous nephropathy | nephrotic syndrome | CLINICAL SPECTRUM | BIOLOGY | UROLOGY & NEPHROLOGY | GENETIC-HETEROGENEITY | CLASSIFICATION | RENAL-DISEASE | IDIOPATHIC MEMBRANOUS NEPHROPATHY | Predictive Value of Tests | Glomerulonephritis - therapy | Prognosis | Prospective Studies | Age Factors | Glomerulosclerosis, Focal Segmental - genetics | Humans | Nephrosis, Lipoid - epidemiology | Glomerulonephritis, Membranous - genetics | Glomerulonephritis, Membranous - epidemiology | Nephrotic Syndrome - genetics | Systems Biology | Time Factors | Adult | Registries | Surveys and Questionnaires | Nephrotic Syndrome - therapy | Translational Medical Research - methods | Child | Glomerulonephritis, Membranous - therapy | Glomerulonephritis - epidemiology | Glomerulosclerosis, Focal Segmental - epidemiology | Glomerulonephritis, Membranous - pathology | Risk Factors | Glomerulonephritis - genetics | Cooperative Behavior | Nephrotic Syndrome - pathology | Genotype | Nephrosis, Lipoid - therapy | Nephrosis, Lipoid - genetics | Phenotype | Pilot Projects | Nephrosis, Lipoid - pathology | Biopsy | Glomerulonephritis - pathology | Nephrotic Syndrome - epidemiology | Glomerulosclerosis, Focal Segmental - therapy | North America - epidemiology | Longitudinal Studies | Research Design | Glomerulosclerosis, Focal Segmental - pathology
Journal Article
Book
by Godoy, Patricio and Hewitt, Nicola J and Albrecht, Ute and Andersen, Melvin E and Ansari, Nariman and Bhattacharya, Sudin and Bode, Johannes Georg and Bolleyn, Jennifer and Borner, Christoph and Böttger, Jan and Braeuning, Albert and Budinsky, Robert A and Burkhardt, Britta and Cameron, Neil R and Camussi, Giovanni and Cho, Chong-Su and Choi, Yun-Jaie and Craig Rowlands, J and Dahmen, Uta and Damm, Georg and Dirsch, Olaf and Donato, María Teresa and Dong, Jian and Dooley, Steven and Drasdo, Dirk and Eakins, Rowena and Ferreira, Karine Sá and Fonsato, Valentina and Fraczek, Joanna and Gebhardt, Rolf and Gibson, Andrew and Glanemann, Matthias and Goldring, Chris E. P and Gómez-Lechón, María José and Groothuis, Geny M. M and Gustavsson, Lena and Guyot, Christelle and Hallifax, David and Hammad, Seddik and Hayward, Adam and Häussinger, Dieter and Hellerbrand, Claus and Hewitt, Philip and Hoehme, Stefan and Holzhütter, Hermann-Georg and Houston, J Brian and Hrach, Jens and Ito, Kiyomi and Jaeschke, Hartmut and Keitel, Verena and Kelm, Jens M and Kevin Park, B and Kordes, Claus and Kullak-Ublick, Gerd A and LeCluyse, Edward L and Lu, Peng and Luebke-Wheeler, Jennifer and Lutz, Anna and Maltman, Daniel J and Matz-Soja, Madlen and McMullen, Patrick and Merfort, Irmgard and Messner, Simon and Meyer, Christoph and Mwinyi, Jessica and Naisbitt, Dean J and Nussler, Andreas K and Olinga, Peter and Pampaloni, Francesco and Pi, Jingbo and Pluta, Linda and Przyborski, Stefan A and Ramachandran, Anup and Rogiers, Vera and Rowe, Cliff and Schelcher, Celine and Schmich, Kathrin and Schwarz, Michael and Singh, Bijay and Stelzer, Ernst H. K and Stieger, Bruno and Stöber, Regina and Sugiyama, Yuichi and Tetta, Ciro and Thasler, Wolfgang E and Vanhaecke, Tamara and Vinken, Mathieu and Weiss, Thomas S and Widera, Agata and Woods, Courtney G and Xu, Jinghai James and Yarborough, Kathy M and Hengstler, Jan G
Archives of Toxicology, ISSN 0340-5761, 8/2013, Volume 87, Issue 8, pp. 1315 - 1530
Journal Article
by Majounie, Elisa, PhD and Renton, Alan E, PhD and Mok, Kin, MSc and Dopper, Elise GP and Waite, Adrian, PhD and Rollinson, Sara, PhD and Chiò, Adriano, MD and Restagno, Gabriella, MD and Nicolaou, Nayia, MSc and Simon-Sanchez, Javier, PhD and van Swieten, John C, Prof and Abramzon, Yevgeniya and Johnson, Janel O, PhD and Sendtner, Michael, Prof and Pamphlett, Roger, MD and Orrell, Richard W, MD and Mead, Simon, MD and Sidle, Katie C, MD and Houlden, Henry, Prof and Rohrer, Jonathan D, MD and Morrison, Karen E, Prof and Pall, Hardev, MD and Talbot, Kevin, Prof and Ansorge, Olaf, MD and Hernandez, Dena G, MSc and Arepalli, Sampath, MS and Sabatelli, Mario, MD and Mora, Gabriele, MD and Corbo, Massimo, MD and Giannini, Fabio, MD and Calvo, Andrea, MD and Englund, Elisabet, MD and Borghero, Giuseppe, MD and Floris, Gian Luca, MD and Remes, Anne M, Prof and Laaksovirta, Hannu, MD and McCluskey, Leo, MD and Trojanowski, John Q, Prof and Van Deerlin, Vivianna M, MD and Schellenberg, Gerard D, Prof and Nalls, Michael A, PhD and Drory, Vivian E, MD and Lu, Chin-Song, Prof and Yeh, Tu-Hsueh, MD and Ishiura, Hiroyuki, MD and Takahashi, Yuji, MD and Tsuji, Shoji, Prof and Le Ber, Isabelle, MD and Brice, Alexis, Prof and Drepper, Carsten, PhD and Williams, Nigel, PhD and Kirby, Janine, PhD and Shaw, Pamela, Prof and Hardy, John, Prof and Tienari, Pentti J, MD and Heutink, Peter, Prof and Morris, Huw R, MD and Pickering-Brown, Stuart, Prof and Traynor, Bryan J, Dr and The Chromosome 9-ALS/FTD Consortium and The ITALSGEN Consortium and The French research network on FTLD/FTLD/ALS and Chromosome 9-ALS FTD Consortium and French Res Network FTLD FTLD ALS and ITALSGEN Consortium and French research network on FTLD/FTLD/ALS and Chromosome 9-ALS/FTD Consortium
Lancet Neurology, The, ISSN 1474-4422, 2012, Volume 11, Issue 4, pp. 323 - 330
Summary Background We aimed to accurately estimate the frequency of a hexanucleotide repeat expansion in C9orf72 that has been associated with a large... 
Neurology | PREVALENCE | MUTATIONS | LOBAR DEGENERATION | GENETICS | TDP-43 | CLINICAL NEUROLOGY | Frontotemporal Dementia - genetics | Cross-Sectional Studies | DNA Repeat Expansion - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Middle Aged | Child, Preschool | Genotype | Male | Genetic Loci | Open Reading Frames - genetics | Young Adult | Chromosomes, Human, Pair 9 - genetics | Adolescent | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Child | Cohort Studies | Medical research | Medical colleges | Care and treatment | Nervous system diseases | Neurosciences | Molecular genetics | Oncology, Experimental | Questions and answers | Amyotrophic lateral sclerosis | Research | Medicine, Experimental | Agriculture | Physicians (General practice) | Alzheimer's disease | Dementia | Cancer | Biomedical engineering | Haplotypes | Polymerase chain reaction | Neurodegenerative diseases | Ethnic groups | Data processing | Mutation | Frontotemporal dementia | Genetic counselling | Islands | Age | Toll-Like Receptor 4 | Open Reading Frames | Adaptor Proteins, Vesicular Transport | Lipopolysaccharides | Life Sciences | DNA Repeat Expansion | Interferon Regulatory Factor-3 | Transfection | Amyotrophic Lateral Sclerosis | RNA Interference | HEK293 Cells | Membrane Glycoproteins | Vesicular Transport Proteins | Protein Structure, Tertiary | Cell Line | Chemokine CCL5 | Frontotemporal Dementia | Signal Transduction | Myeloid Differentiation Factor 88 | Chromosomes, Human, Pair 9 | Protein Transport | Adaptor Proteins, Signal Transducing | Santé publique et épidémiologie | RNA, Small Interfering | Endosomes | Neurologi | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
Journal Article