Contactin-1 links autoimmune neuropathy and membranous glomerulonephritis von Fehmi, Janev, Davies, Alexander J, Antonelou, Marilina, Keddie, Stephen, Pikkupeura, Sonja, Querol, Luis, Delmont, Emilien, Cortese, Andrea, Franciotta, Diego, Persson, Staffan, Barratt, Jonathan, Pepper, Ruth, Farinha, Filipa, Rahman, Anisur, Canetti, Diana, Gilbertson, Janet A, Rendell, Nigel B, Radunovic, Aleksandar, Minton, Thomas, Fuller, Geraint, Murphy, Sinead M, Carr, Aisling S, Reilly, Mary R, Eftimov, Filip, Wieske, Luuk, Teunissen, Charlotte E, Roberts, Ian S D, Ashman, Neil, Salama, Alan D, Rinaldi, Simon

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Contactin-1 links autoimmune neuropathy and membranous glomerulonephritis von Janev Fehmi, Alexander J. Davies, Marilina Antonelou, Stephen Keddie, Sonja Pikkupeura, Luis Querol, Emilien Delmont, Andrea Cortese, Diego Franciotta, Staffan Persson, Jonathan Barratt, Ruth Pepper, Filipa Farinha, Anisur Rahman, Diana Canetti, Janet A. Gilbertson, Nigel B. Rendell, Aleksandar Radunovic, Thomas Minton, Geraint Fuller, Sinead M. Murphy, Aisling S. Carr, Mary R. Reilly, Filip Eftimov, Luuk Wieske, Charlotte E. Teunissen, Ian S. D. Roberts, Neil Ashman, Alan D. Salama, Simon Rinaldi

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Contactin-1 links autoimmune neuropathy and membranous glomerulonephritis von Fehmi, Janev, Davies, Alexander J, Antonelou, Marilina, Keddie, Stephen, Pikkupeura, Sonja, Querol, Luis, Delmont, Emilien, Cortese, Andrea, Franciotta, Diego, Persson, Staffan, Barratt, Jonathan, Pepper, Ruth, Farinha, Filipa, Rahman, Anisur, Canetti, Diana, Gilbertson, Janet A, Rendell, Nigel B, Radunovic, Aleksandar, Minton, Thomas, Fuller, Geraint, Murphy, Sinead M, Carr, Aisling S, Reilly, Mary R, Eftimov, Filip, Wieske, Luuk, Teunissen, Charlotte E, Roberts, Ian S. D, Ashman, Neil, Salama, Alan D, Rinaldi, Simon, Universitat Autònoma de Barcelona

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USER FRIENDLY SYSTEMS AND DEVICES FACILITATING WATER CONSERVATION IN THE SMART HOME von Reilly, JR., Mary, Chang, Lawrence, Silverstein, Brian, Sloo, David

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Combined Angiotensin Inhibition for the Treatment of Diabetic Nephropathy von Fried, Linda F, Emanuele, Nicholas, Zhang, Jane H, Brophy, Mary, Conner, Todd A, Duckworth, William, Leehey, David J, McCullough, Peter A, O'Connor, Theresa, Palevsky, Paul M, Reilly, Robert F, Seliger, Stephen L, Warren, Stuart R, Watnick, Suzanne, Peduzzi, Peter, Guarino, Peter

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Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies von Burnor, Elisabeth, Yang, Li, Zhou, Hao, Patterson, Kristina R, Quinn, Colin, Reilly, Mary M, Rossor, Alexander M, Scherer, Steven S, Lancaster, Eric

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Mutations in BICD2 Cause Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraplegia von Oates, Emily C., Rossor, Alexander M., Hafezparast, Majid, Gonzalez, Michael, Speziani, Fiorella, MacArthur, Daniel G., Lek, Monkol, Cottenie, Ellen, Scoto, Mariacristina, Foley, A. Reghan, Hurles, Matthew, Houlden, Henry, Greensmith, Linda, Auer-Grumbach, Michaela, Pieber, Thomas R., Strom, Tim M., Schule, Rebecca, Herrmann, David N., Sowden, Janet E., Acsadi, Gyula, Menezes, Manoj P., Clarke, Nigel F., Züchner, Stephan, Muntoni, Francesco, North, Kathryn N., Reilly, Mary M.

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A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families von Scriba, Carolin K, Beecroft, Sarah J, Clayton, Joshua S, Cortese, Andrea, Sullivan, Roisin, Yau, Wai Yan, Dominik, Natalia, Rodrigues, Miriam, Walker, Elizabeth, Dyer, Zoe, Wu, Teddy Y, Davis, Mark R, Chandler, David C, Weisburd, Ben, Houlden, Henry, Reilly, Mary M, Laing, Nigel G, Lamont, Phillipa J, Roxburgh, Richard H, Ravenscroft, Gianina

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Upper Limb Evaluation in Duchenne Muscular Dystrophy: Fat-Water Quantification by MRI, Muscle Force and Function Define Endpoints for Clinical Trials von Ricotti, Valeria, Evans, Matthew R B, Sinclair, Christopher D J, Butler, Jordan W, Ridout, Deborah A, Hogrel, Jean-Yves, Emira, Ahmed, Morrow, Jasper M, Reilly, Mary M, Hanna, Michael G, Janiczek, Robert L, Matthews, Paul M, Yousry, Tarek A, Muntoni, Francesco, Thornton, John S

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Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications von Mathew, Divij, Giles, Josephine R, Baxter, Amy E, Oldridge, Derek A, Greenplate, Allison R, Wu, Jennifer E, Alanio, Cécile, Kuri-Cervantes, Leticia, Pampena, M Betina, D'Andrea, Kurt, Manne, Sasikanth, Chen, Zeyu, Huang, Yinghui Jane, Reilly, John P, Weisman, Ariel R, Ittner, Caroline A G, Kuthuru, Oliva, Dougherty, Jeanette, Nzingha, Kito, Han, Nicholas, Kim, Justin, Pattekar, Ajinkya, Goodwin, Eileen C, Anderson, Elizabeth M, Weirick, Madison E, Gouma, Sigrid, Arevalo, Claudia P, Bolton, Marcus J, Chen, Fang, Lacey, Simon F, Ramage, Holly, Cherry, Sara, Hensley, Scott E, Apostolidis, Sokratis A, Huang, Alexander C, Vella, Laura A, Betts, Michael R, Meyer, Nuala J, Wherry, E John

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Gene replacement therapy in a model of Charcot-Marie-Tooth 4C neuropathy von Schiza, Natasa, Georgiou, Elena, Kagiava, Alexia, Médard, Jean-Jacques, Richter, Jan, Tryfonos, Christina, Sargiannidou, Irene, Heslegrave, Amanda J, Rossor, Alexander M, Zetterberg, Henrik, Reilly, Mary M, Christodoulou, Christina, Chrast, Roman, Kleopa, Kleopas A

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Sexual and social stimuli elicit rapid and contrasting genomic responses von Cummings, Molly E, Larkins-Ford, Jonah, Reilly, Christian R.L, Wong, Ryan Y, Ramsey, Mary, Hofmann, Hans A

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Hereditary sensory neuropathy type 1-associated deoxysphingolipids cause neurotoxicity, acute calcium handling abnormalities and mitochondrial dysfunction in vitro von Wilson, Emma R., Kugathasan, Umaiyal, Abramov, Andrey Y., Clark, Alex J., Bennett, David L.H., Reilly, Mary M., Greensmith, Linda, Kalmar, Bernadett

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Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders von Gilley, Jonathan, Jackson, Oscar, Pipis, Menelaos, Estiar, Mehrdad A, Al-Chalabi, Ammar, Danzi, Matt C, van Eijk, Kristel R, Goutman, Stephen A, Harms, Matthew B, Houlden, Henry, Iacoangeli, Alfredo, Kaye, Julia, Lima, Leandro, Ravits, John, Rouleau, Guy A, Schüle, Rebecca, Xu, Jishu, Züchner, Stephan, Cooper-Knock, Johnathan, Gan-Or, Ziv, Reilly, Mary M, Coleman, Michael P

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Comparative safety of antiepileptic drugs during pregnancy von HERNANDEZ-DIAZ, S, SMITH, C. R, SHEN, A, MITTENDORF, R, HAUSER, W. A, YERBY, M, HOLMES, L. B

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Ascorbic acid in Charcot–Marie–Tooth disease type 1A (CMT-TRI AA L and CMT-TRAUK): a double-blind randomised trial von Pareyson, Davide, Dr, Reilly, Mary M, Prof, Schenone, Angelo, MD, Fabrizi, Gian Maria, MD, Cavallaro, Tiziana, MD, Santoro, Lucio, Prof, Vita, Giuseppe, Prof, Quattrone, Aldo, Prof, Padua, Luca, MD, Gemignani, Franco, MD, Visioli, Francesco, PhD, Laurà, Matilde, MD, Radice, Davide, MSc, Calabrese, Daniela, MSc, Hughes, Richard AC, Prof, Solari, Alessandra, MD

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Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V von Beetz, Christian, Pieber, Thomas R., Hertel, Nicole, Schabhüttl, Maria, Fischer, Carina, Trajanoski, Slave, Graf, Elisabeth, Keiner, Silke, Kurth, Ingo, Wieland, Thomas, Varga, Rita-Eva, Timmerman, Vincent, Reilly, Mary M., Strom, Tim M., Auer-Grumbach, Michaela

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Targeted High-Throughput Sequencing Identifies Mutations in atlastin-1 as a Cause of Hereditary Sensory Neuropathy Type I von Guelly, Christian, Zhu, Peng-Peng, Leonardis, Lea, Papić, Lea, Zidar, Janez, Schabhüttl, Maria, Strohmaier, Heimo, Weis, Joachim, Strom, Tim M., Baets, Jonathan, Willems, Jan, De Jonghe, Peter, Reilly, Mary M., Fröhlich, Eleonore, Hatz, Martina, Trajanoski, Slave, Pieber, Thomas R., Janecke, Andreas R., Blackstone, Craig, Auer-Grumbach, Michaela

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A Dominant Mutation in FBXO38 Causes Distal Spinal Muscular Atrophy with Calf Predominance von Sumner, Charlotte J., d’Ydewalle, Constantin, Wooley, Joe, Fawcett, Katherine A., Hernandez, Dena, Gardiner, Alice R., Kalmar, Bernadett, Baloh, Robert H., Gonzalez, Michael, Züchner, Stephan, Stanescu, Horia C., Kleta, Robert, Mankodi, Ami, Cornblath, David R., Boylan, Kevin B., Reilly, Mary M., Greensmith, Linda, Singleton, Andrew B., Harms, Matthew B., Rossor, Alexander M., Houlden, Henry

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Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease von Cornett, Kayla MD, Menezes, Manoj P, Bray, Paula, Halaki, Mark, Shy, Rosemary R, Yum, Sabrina W, Estilow, Timothy, Moroni, Isabella, Foscan, Maria, Pagliano, Emanuela, Pareyson, Davide, Laurá, Matilde, Bhandari, Trupti, Muntoni, Francesco, Reilly, Mary M, Finkel, Richard S, Sowden, Janet, Eichinger, Katy J, Herrmann, David N, Shy, Michael E, Burns, Joshua

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