Inflammation in ALS/FTD pathogenesis

por McCauley, Madelyn E., Baloh, Robert H.
Publicado 2018

Patients with ALS show highly correlated progression rates in left and right limb muscles

por Rushton, David J., Andres, Patricia L., Allred, Peggy, Baloh, Robert H., Svendsen, Clive N.
Publicado 2017

MFN1 augmentation prevents retinal degeneration in a Charcot-Marie-Tooth type 2A mouse model

por Shahin, Saba, Lu, Bin, Zhou, Yueqin, Xu, Hui, Chetsawang, Jason, Baloh, Robert H., Wang, Shaomei
Publicado 2023

Mitochondrial Phenotypes in Genetically Diverse Neurodegenerative Diseases and Their Response to Mitofusin Activation

por Dang, Xiawei, Walton, Emily K., Zablocka, Barbara, Baloh, Robert H., Shy, Michael E., Dorn, Gerald W.
Publicado 2022

Valosin-containing protein (VCP) is required for autophagy and is disrupted in VCP disease

por Ju, Jeong-Sun, Fuentealba, Rodrigo A., Miller, Sara E., Jackson, Erin, Piwnica-Worms, David, Baloh, Robert H., Weihl, Conrad C.
Publicado 2009

ALS disrupts spinal motor neuron maturation and aging pathways within gene co-expression networks

por Ho, Ritchie, Sances, Samuel, Gowing, Genevieve, Amoroso, Mackenzie Weygandt, O'Rourke, Jacqueline G., Sahabian, Anais, Wichterle, Hynek, Baloh, Robert H., Sareen, Dhruv, Svendsen, Clive N.
Publicado 2016

Cell transplantation strategies for acquired and inherited disorders of peripheral myelin

por Muhammad, A. K. M. G., Kim, Kevin, Epifantseva, Irina, Aghamaleky‐Sarvestany, Arwin, Simpkinson, Megan E., Carmona, Sharon, Landeros, Jesse, Bell, Shaughn, Svaren, John, Baloh, Robert H.
Publicado 2018

Burst mitofusin activation reverses neuromuscular dysfunction in murine CMT2A

por Franco, Antonietta, Dang, Xiawei, Walton, Emily K, Ho, Joshua N, Zablocka, Barbara, Ly, Cindy, Miller, Timothy M, Baloh, Robert H, Shy, Michael E, Yoo, Andrew S, Dorn, Gerald W
Publicado 2020

Sizing, stabilising, and cloning repeat-expansions for gene targeting constructs

por Nair, Remya R., Tibbit, Charlotte, Thompson, David, McLeod, Ross, Nakhuda, Asif, Simon, Michelle M., Baloh, Robert H., Fisher, Elizabeth M.C., Isaacs, Adrian M., Cunningham, Thomas J.
Publicado 2021

Addressing heterogeneity in amyotrophic lateral sclerosis CLINICAL TRIALS

por Goyal, Namita A., Berry, James D., Windebank, Anthony, Staff, Nathan P., Maragakis, Nicholas J., van den Berg, Leonard H., Genge, Angela, Miller, Robert, Baloh, Robert H., Kern, Ralph, Gothelf, Yael, Lebovits, Chaim, Cudkowicz, Merit
Publicado 2020

C9orf72 in myeloid cells suppresses STING-induced inflammation

por McCauley, Madelyn E., O’Rourke, Jacqueline Gire, Yáñez, Alberto, Markman, Janet L., Ho, Ritchie, Wang, Xinchen, Chen, Shuang, Lall, Deepti, Jin, Mengyao, Muhammad, A.K.M.G, Bell, Shaughn, Landeros, Jesse, Valencia, Viviana, Harms, Matthew, Arditi, Moshe, Jefferies, Caroline, Baloh, Robert H.
Publicado 2020

Neural crest‐derived mesenchymal progenitor cells enhance cranial allograft integration

por Glaeser, Juliane D., Behrens, Phillip, Stefanovic, Tina, Salehi, Khosrowdad, Papalamprou, Angela, Tawackoli, Wafa, Metzger, Melodie F., Eberlein, Samuel, Nelson, Trevor, Arabi, Yasaman, Kim, Kevin, Baloh, Robert H., Ben‐David, Shiran, Cohn‐Schwartz, Doron, Ryu, Robert, Bae, Hyun W., Gazit, Zulma, Sheyn, Dmitriy
Publicado 2021

Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder

por Mukherjee-Clavin, Bipasha, Mi, Ruifa, Kern, Barbara, Choi, In Young, Lim, Hotae, Oh, Yohan, Lannon, Benjamin, Kim, Kevin J., Bell, Shaughn, Hur, Junho K., Hwang, Woochang, Hyun Che, Young, Habib, Omer, Baloh, Robert H., Eggan, Kevin, Brandacher, Gerald, Hoke, Ahmet, Studer, Lorenz, Jun Kim, Yong, Lee, Gabsang
Publicado 2019

Revised Airlie House consensus guidelines for design and implementation of ALS clinical trials

por van den Berg, Leonard H., Sorenson, Eric, Gronseth, Gary, Macklin, Eric A., Andrews, Jinsy, Baloh, Robert H., Benatar, Michael, Berry, James D., Chio, Adriano, Corcia, Philippe, Genge, Angela, Gubitz, Amelie K., Lomen-Hoerth, Catherine, McDermott, Christopher J., Pioro, Erik P., Rosenfeld, Jeffrey, Silani, Vincenzo, Turner, Martin R., Weber, Markus, Brooks, Benjamin Rix, Miller, Robert G., Mitsumoto, Hiroshi
Publicado 2019

A randomized placebo‐controlled phase 3 study of mesenchymal stem cells induced to secrete high levels of neurotrophic factors in amyotrophic lateral sclerosis

por Cudkowicz, Merit E., Lindborg, Stacy R., Goyal, Namita A., Miller, Robert G., Burford, Matthew J., Berry, James D., Nicholson, Katharine A., Mozaffar, Tahseen, Katz, Jonathan S., Jenkins, Liberty J., Baloh, Robert H., Lewis, Richard A., Staff, Nathan P., Owegi, Margaret A., Berry, Donald A., Gothelf, Yael, Levy, Yossef S., Aricha, Revital, Kern, Ralph Z., Windebank, Anthony J., Brown, Robert H.
Publicado 2022

Moderate intrinsic phenotypic alterations in C9orf72 ALS/FTD iPSC-microglia despite the presence of C9orf72 pathological features

por Lorenzini, Ileana, Alsop, Eric, Levy, Jennifer, Gittings, Lauren M., Lall, Deepti, Rabichow, Benjamin E., Moore, Stephen, Pevey, Ryan, Bustos, Lynette M., Burciu, Camelia, Bhatia, Divya, Singer, Mo, Saul, Justin, McQuade, Amanda, Tzioras, Makis, Mota, Thomas A., Logemann, Amber, Rose, Jamie, Almeida, Sandra, Gao, Fen-Biao, Marks, Michael, Donnelly, Christopher J., Hutchins, Elizabeth, Hung, Shu-Ting, Ichida, Justin, Bowser, Robert, Spires-Jones, Tara, Blurton-Jones, Mathew, Gendron, Tania F., Baloh, Robert H., Van Keuren-Jensen, Kendall, Sattler, Rita
Publicado 2023

Transplantation of human neural progenitor cells secreting GDNF into the spinal cord of patients with ALS: a phase 1/2a trial

por Baloh, Robert H., Johnson, J. Patrick, Avalos, Pablo, Allred, Peggy, Svendsen, Soshana, Gowing, Genevieve, Roxas, Kristina, Wu, Amanda, Donahue, Becky, Osborne, Sheryl, Lawless, George, Shelley, Brandon, Wheeler, Koral, Prina, Carolyn, Fine, Dana, Kendra-Romito, Tami, Stokes, Haniah, Manoukian, Vicki, Muthukumaran, Abirami, Garcia, Leslie, Bañuelos, Maria G., Godoy, Marlesa, Bresee, Catherine, Yu, Hong, Drazin, Doniel, Ross, Lindsey, Naruse, Robert, Babu, Harish, Macklin, Eric A., Vo, Ashley, Elsayegh, Ashraf, Tourtellotte, Warren, Maya, Marcel, Burford, Matthew, Diaz, Frank, Patil, Chirag G., Lewis, Richard A., Svendsen, Clive N.
Publicado 2022

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis

por Johnson, Janel O., Pioro, Erik P., Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E., Pliner, Hannah A., Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J., Gibbs, J Raphael, Nalls, Michael A., Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W., Malaspina, Andrea, Sidle, Katie C., Fratta, Pietro, Harms, Matthew B., Baloh, Robert H., Pestronk, Alan, Weihl, Conrad C., Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E., Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D., Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B., Taylor, J. Paul, Cookson, Mark R., Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J.
Publicado 2014

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

por van Rheenen, Wouter, van der Spek, Rick A. A., Bakker, Mark K., van Vugt, Joke J. F. A., Hop, Paul J., Zwamborn, Ramona A. J., de Klein, Niek, Westra, Harm-Jan, Bakker, Olivier B., Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot M., Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H. P., van Eijk, Kristel R., Kooyman, Maarten, Byrne, Ross P., Doherty, Mark, Heverin, Mark, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley N., Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Orrell, Richard W., Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J., Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D’Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert H., Bell, Shaughn, Vourc’h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Mora Pardina, Jesus S., Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick A., Ross, Jay P., Ludolph, Albert C., Weishaupt, Jochen H., Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine A. M., Saker-Delye, Safa, Wood, Nicholas W., Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia, Whiteman, David C., Olsen, Catherine M., Uitterlinden, Andre G., Hofman, Albert, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Amouyel, Philippe, Traynor, Bryan J., Singleton, Andrew B., Mitne Neto, Miguel, Cauchi, Ruben J., Ophoff, Roel A., Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, van Deerlin, Vivianna M., Grosskreutz, Julian, Roediger, Annekathrin, Gaur, Nayana, Jörk, Alexander, Barthel, Tabea, Theele, Erik, Ilse, Benjamin, Stubendorff, Beatrice, Witte, Otto W., Steinbach, Robert, Hübner, Christian A., Graff, Caroline, Brylev, Lev, Fominykh, Vera, Demeshonok, Vera, Ataulina, Anastasia, Rogelj, Boris, Koritnik, Blaž, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Stević, Zorica, Drory, Vivian, Povedano, Monica, Blair, Ian P., Kiernan, Matthew C., Benyamin, Beben, Henderson, Robert D., Furlong, Sarah, Mathers, Susan, McCombe, Pamela A., Needham, Merrilee, Ngo, Shyuan T., Nicholson, Garth A., Pamphlett, Roger, Rowe, Dominic B., Steyn, Frederik J., Williams, Kelly L., Mather, Karen A., Sachdev, Perminder S., Henders, Anjali K., Wallace, Leanne, de Carvalho, Mamede, Pinto, Susana, Petri, Susanne, Weber, Markus, Rouleau, Guy A., Silani, Vincenzo, Curtis, Charles J., Breen, Gerome, Glass, Jonathan D., Brown, Robert H., Landers, John E., Shaw, Christopher E., Andersen, Peter M., Groen, Ewout J. N., van Es, Michael A., Pasterkamp, R. Jeroen, Fan, Dongsheng, Garton, Fleur C., McRae, Allan F., Davey Smith, George, Gaunt, Tom R., Eberle, Michael A., Mill, Jonathan, McLaughlin, Russell L., Hardiman, Orla, Kenna, Kevin P., Wray, Naomi R., Tsai, Ellen, Runz, Heiko, Franke, Lude, Al-Chalabi, Ammar, Van Damme, Philip, van den Berg, Leonard H., Veldink, Jan H.
Publicado 2021

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biolo...

por van Rheenen, Wouter, van der Spek, Rick A. A., Bakker, Mark K., van Vugt, Joke J. F. A., Hop, Paul J., Zwamborn, Ramona A. J., de Klein, Niek, Westra, Harm-Jan, Bakker, Olivier B., Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot M., Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H. P., van Eijk, Kristel R., Kooyman, Maarten, Byrne, Ross P., Doherty, Mark, Heverin, Mark, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley N., Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Orrell, Richard W., Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J., Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D’Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert H., Bell, Shaughn, Vourc’h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Mora Pardina, Jesus S., Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick A., Ross, Jay P., Ludolph, Albert C., Weishaupt, Jochen H., Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine A. M., Saker-Delye, Safa, Wood, Nicholas W., Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia, Whiteman, David C., Olsen, Catherine M., Uitterlinden, Andre G., Hofman, Albert, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Amouyel, Philippe, Traynor, Bryan J., Singleton, Andrew B., Mitne Neto, Miguel, Cauchi, Ruben J., Ophoff, Roel A., Wiedau-Pazos, Martina, Lomen-Hoerth, Catherine, van Deerlin, Vivianna M., Grosskreutz, Julian, Roediger, Annekathrin, Gaur, Nayana, Jörk, Alexander, Barthel, Tabea, Theele, Erik, Ilse, Benjamin, Stubendorff, Beatrice, Witte, Otto W., Steinbach, Robert, Hübner, Christian A., Graff, Caroline, Brylev, Lev, Fominykh, Vera, Demeshonok, Vera, Ataulina, Anastasia, Rogelj, Boris, Koritnik, Blaž, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Stević, Zorica, Drory, Vivian, Povedano, Monica, Blair, Ian P., Kiernan, Matthew C., Benyamin, Beben, Henderson, Robert D., Furlong, Sarah, Mathers, Susan, McCombe, Pamela A., Needham, Merrilee, Ngo, Shyuan T., Nicholson, Garth A., Pamphlett, Roger, Rowe, Dominic B., Steyn, Frederik J., Williams, Kelly L., Mather, Karen A., Sachdev, Perminder S., Henders, Anjali K., Wallace, Leanne, de Carvalho, Mamede, Pinto, Susana, Petri, Susanne, Weber, Markus, Rouleau, Guy A., Silani, Vincenzo, Curtis, Charles J., Breen, Gerome, Glass, Jonathan D., Brown, Robert H., Landers, John E., Shaw, Christopher E., Andersen, Peter M., Groen, Ewout J. N., van Es, Michael A., Pasterkamp, R. Jeroen, Fan, Dongsheng, Garton, Fleur C., McRae, Allan F., Davey Smith, George, Gaunt, Tom R., Eberle, Michael A., Mill, Jonathan, McLaughlin, Russell L., Hardiman, Orla, Kenna, Kevin P., Wray, Naomi R., Tsai, Ellen, Runz, Heiko, Franke, Lude, Al-Chalabi, Ammar, Van Damme, Philip, van den Berg, Leonard H., Veldink, Jan H.
Publicado 2022