The Relationship Between Bone Mineral Density and Cardiovascular Function in Duchenne Muscular Dystrophy: A Retrospective Cohort Study

por Kervin, Tara, Thangarajh, Mathula
Publicado no PLoS Curr (2018)

Longitudinal Evaluation of Working Memory in Duchenne Muscular Dystrophy

por Thangarajh, Mathula, Elfring, Gary L., Trifillis, Panayiota
Publicado no J Clin Med (2020)

The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy

por Thangarajh, Mathula, Elfring, Gary L., Trifillis, Panayiota, McIntosh, Joseph, Peltz, Stuart W.
Publicado no Neurology (2018)

Relationships between DMD mutations and neurodevelopment in dystrophinopathy

por Thangarajh, Mathula, Hendriksen, Jos, McDermott, Michael P., Martens, William, Hart, Kimberly A., Griggs, Robert C.
Publicado no Neurology (2019)

The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy

por Thangarajh, Mathula, Kaat, Aaron J., Bibat, Genila, Mansour, Jennifer, Summerton, Katherine, Gioia, Anthony, Berger, Carly, Hardy, Kristina K., Wagner, Kathryn R.
Publicado no Ann Clin Transl Neurol (2019)

Neurodevelopmental Needs in Young Boys with Duchenne Muscular Dystrophy (DMD): Observations from the Cooperative International Neuromuscular Research Group (CINRG) DMD Natural Hist...

por Thangarajh, Mathula, Spurney, Christopher F., Gordish-Dressman, Heather, Clemens, Paula R., Hoffman, Eric P., McDonald, Craig M., Henricson, Erik K., Investigators, CINRG
Publicado no PLoS Curr (2018)

Discovery of potential urine-accessible metabolite biomarkers associated with muscle disease and corticosteroid response in the mdx mouse model for Duchenne

por Thangarajh, Mathula, Zhang, Aiping, Gill, Kirandeep, Ressom, Habtom W., Li, Zhenzhi, Varghese, Rency S., Hoffman, Eric P., Nagaraju, Kanneboyina, Hathout, Yetrib, Boca, Simina M.
Publicado no PLoS One (2019)

Dystrophic muscle distribution in late-stage muscular dystrophy

por Pilato, Celeste Michelle, Walker, Melissa Sue, Nguyen, Andrea M., Hanna, McKay Elizabeth, Huang, Scott Lanxing, Lutins, Erika Morgan, Meredith, M. Alex, Haar, Peter Jacob, Thangarajh, Mathula, Richard, Hope Theresa, Chow, Woon Nam
Publicado no Autops Case Rep (2020)

Cytoplasmic body pathology in severe ACTA1-related myopathy in the absence of typical nemaline rods

por Donkervoort, Sandra, Chan, Sophelia H.S., Hayes, Leslie H., Bradley, Nathaniel, Nguyen, David, Leach, Meganne E., Mohassel, Payam, Hu, Ying, Thangarajh, Mathula, Bharucha-Goebel, Diana, Kan, Amanda, Ho, Ronnie S.L., Reyes, Christine A., Nance, Jessica, Moore, Steven A., Foley, A. Reghan, Bönnemann, Carsten G.
Publicado no Neuromuscul Disord (2017)

Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle...

por Thangarajh, Mathula, Yang, Genyan, Fuchs, Dana, Ponisio, Maria R., McKinstry, Robert C., Jaju, Alok, Noetzel, Michael J., Casella, James F., Barron-Casella, Emily, Hooper, W. Craig, Boulet, Sheree L., Bean, Christopher J., Pyle, Meredith E., Payne, Amanda B., Driggers, Jennifer, Trau, Heidi A., Vendt, Bruce A., Rodeghier, Mark, DeBaun, Michael R.
Publicado em 2012

A multinational study on motor function in early-onset FSHD

por Mah, Jean K., Feng, Jia, Jacobs, Marni B., Duong, Tina, Carroll, Kate, de Valle, Katy, Carty, Cara L., Morgenroth, Lauren P., Guglieri, Michela, Ryan, Monique M., Clemens, Paula R., Thangarajh, Mathula, Webster, Richard, Smith, Edward, Connolly, Anne M., McDonald, Craig M., Karachunski, Peter, Tulinius, Mar, Harper, Amy, Cnaan, Avital, Chen, Yi-Wen
Publicado no Neurology (2018)

Multi-Omics Identifies Circulating miRNA and Protein Biomarkers for Facioscapulohumeral Dystrophy

por Heier, Christopher R., Zhang, Aiping, Nguyen, Nhu Y, Tully, Christopher B., Panigrahi, Aswini, Gordish-Dressman, Heather, Pandey, Sachchida Nand, Guglieri, Michela, Ryan, Monique M., Clemens, Paula R., Thangarajh, Mathula, Webster, Richard, Smith, Edward C., Connolly, Anne M., McDonald, Craig M., Karachunski, Peter, Tulinius, Mar, Harper, Amy, Mah, Jean K., Fiorillo, Alyson A., Chen, Yi-Wen
Publicado no J Pers Med (2020)

The CINRG Becker Natural History Study: Baseline Characteristics

por Clemens, Paula R., Niizawa, Gabriela, Feng, Jia, Florence, Julaine, D’Alessandro, Andrea Smith, Morgenroth, Lauren P., Gorni, Ksenija, Guglieri, Michela, Connolly, Anne, Wicklund, Matthew, Bertorini, Tulio, Mah, Jean K., Thangarajh, Mathula, Smith, Edward, Kuntz, Nancy, McDonald, Craig M., Henricson, Erik K., Upadhyayula, Saila, Byrne, Barry, Manousakis, Georgios, Harper, Amy, Bravver, Elena, Iannaccone, Susan, Spurney, Christopher, Cnaan, Avital, Gordish-Dressman, Heather
Publicado no Muscle Nerve (2020)

Recruitment & retention program for the NeuroNEXT SMA Biomarker Study: Super Babies for SMA!

por Bartlett, Amy, Kolb, Stephen J., Kingsley, Allison, Swoboda, Kathryn J., Reyna, Sandra P., Sakonju, Ai, Darras, Basil T., Shell, Richard, Kuntz, Nancy, Castro, Diana, Iannaccone, Susan T., Parsons, Julie, Connolly, Anne M., Chiriboga, Claudia A., McDonald, Craig, Burnette, W. Bryan, Werner, Klaus, Thangarajh, Mathula, Shieh, Perry B., Finanger, Erika, Coffey, Christopher S., Yankey, Jon W., Cudkowicz, Merit E., McGovern, Michelle M., McNeil, D. Elizabeth, Arnold, W. David, Kissel, John T.
Publicado no Contemp Clin Trials Commun (2018)

Baseline results of the NeuroNEXT spinal muscular atrophy infant biomarker study

por Kolb, Stephen J., Coffey, Christopher S., Yankey, Jon W., Krosschell, Kristin, Arnold, W. David, Rutkove, Seward B., Swoboda, Kathryn J., Reyna, Sandra P., Sakonju, Ai, Darras, Basil T., Shell, Richard, Kuntz, Nancy, Castro, Diana, Iannaccone, Susan T., Parsons, Julie, Connolly, Anne M., Chiriboga, Claudia A., McDonald, Craig, Burnette, W. Bryan, Werner, Klaus, Thangarajh, Mathula, Shieh, Perry B., Finanger, Erika, Cudkowicz, Merit E., McGovern, Michelle M., McNeil, D. Elizabeth, Finkel, Richard, Kaye, Edward, Kingsley, Allison, Renusch, Samantha R., McGovern, Vicki L., Wang, Xueqian, Zaworski, Phillip G., Prior, Thomas W., Burghes, Arthur H.M., Bartlett, Amy, Kissel, John T.
Publicado no Ann Clin Transl Neurol (2016)

Natural History of Infantile-Onset Spinal Muscular Atrophy

por Kolb, Stephen J., Coffey, Christopher S., Yankey, Jon W., Krosschell, Kristin, Arnold, W. David, Rutkove, Seward B., Swoboda, Kathryn J., Reyna, Sandra P., Sakonju, Ai, Darras, Basil T., Shell, Richard, Kuntz, Nancy, Castro, Diana, Parsons, Julie, Connolly, Anne M., Chiriboga, Claudia A., McDonald, Craig, Burnette, W. Bryan, Werner, Klaus, Thangarajh, Mathula, Shieh, Perry B., Finanger, Erika, Cudkowicz, Merit E., McGovern, Michelle M., McNeil, D. Elizabeth, Finkel, Richard, Iannaccone, Susan T., Kaye, Edward, Kingsley, Allison, Renusch, Samantha R., McGovern, Vicki L., Wang, Xueqian, Zaworski, Phillip G., Prior, Thomas W., Burghes, Arthur H.M., Bartlett, Amy, Kissel, John T.
Publicado no Ann Neurol (2017)

Developing Standardized Corticosteroid Treatment for Duchenne Muscular Dystrophy

por Guglieri, Michela, Bushby, Kate, McDermott, Michael P., Hart, Kimberly A., Tawil, Rabi, Martens, William B., Herr, Barbara E., McColl, Elaine, Wilkinson, Jennifer, Kirschner, Janbernd, King, Wendy M., Eagle, Michele, Brown, Mary W., Willis, Tracey, Hirtz, Deborah, Shieh, Perry B., Straub, Volker, Childs, Anne-Marie, Ciafaloni, Emma, Butterfield, Russell J., Horrocks, Iain, Spinty, Stefan, Flanigan, Kevin M., Kuntz, Nancy L., Baranello, Giovanni, Roper, Helen, Morrison, Leslie, Mah, Jean K., Manzur, Adnan Y., McDonald, Craig M., Schara, Ulrike, von der Hagen, Maja, Barohn, Richard J., Campbell, Craig, Darras, Basil T., Finkel, Richard S., Vita, Giuseppe, Hughes, Imelda, Mongini, Tiziana, Pegoraro, Elena, Wicklund, Matthew, Wilichowski, Ekkehard, Burnette, W. Bryan, Howard, James F., McMillan, Hugh J., Thangarajh, Mathula, Griggs, Robert C.
Publicado no Contemp Clin Trials (2017)

A checklist for clinical trials in rare disease: obstacles and anticipatory actions—lessons learned from the FOR-DMD trial

por Crow, Rebecca A., Hart, Kimberly A., McDermott, Michael P., Tawil, Rabi, Martens, William B., Herr, Barbara E., McColl, Elaine, Wilkinson, Jennifer, Kirschner, Janbernd, King, Wendy M., Eagle, Michele, Brown, Mary W., Hirtz, Deborah, Lochmuller, Hanns, Straub, Volker, Ciafaloni, Emma, Shieh, Perry B., Spinty, Stefan, Childs, Anne-Marie, Manzur, Adnan Y., Morandi, Lucia, Butterfield, Russell J., Horrocks, Iain, Roper, Helen, Flanigan, Kevin M., Kuntz, Nancy L., Mah, Jean K., Morrison, Leslie, Darras, Basil T., von der Hagen, Maja, Schara, Ulrike, Wilichowski, Ekkehard, Mongini, Tiziana, McDonald, Craig M., Vita, Giuseppe, Barohn, Richard J., Finkel, Richard S., Wicklund, Matthew, McMillan, Hugh J., Hughes, Imelda, Pegoraro, Elena, Bryan Burnette, W., Howard, James F., Thangarajh, Mathula, Campbell, Craig, Griggs, Robert C., Bushby, Kate, Guglieri, Michela
Publicado no Trials (2018)