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

di Kervin, Tara, Thangarajh, Mathula
Pubblicato in PLoS Curr (2018)

Longitudinal Evaluation of Working Memory in Duchenne Muscular Dystrophy

di Thangarajh, Mathula, Elfring, Gary L., Trifillis, Panayiota
Pubblicato in J Clin Med (2020)

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

di Thangarajh, Mathula, Elfring, Gary L., Trifillis, Panayiota, McIntosh, Joseph, Peltz, Stuart W.
Pubblicato in Neurology (2018)

Relationships between DMD mutations and neurodevelopment in dystrophinopathy

di Thangarajh, Mathula, Hendriksen, Jos, McDermott, Michael P., Martens, William, Hart, Kimberly A., Griggs, Robert C.
Pubblicato in Neurology (2019)

The NIH Toolbox for cognitive surveillance in Duchenne muscular dystrophy

di Thangarajh, Mathula, Kaat, Aaron J., Bibat, Genila, Mansour, Jennifer, Summerton, Katherine, Gioia, Anthony, Berger, Carly, Hardy, Kristina K., Wagner, Kathryn R.
Pubblicato in 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...

di Thangarajh, Mathula, Spurney, Christopher F., Gordish-Dressman, Heather, Clemens, Paula R., Hoffman, Eric P., McDonald, Craig M., Henricson, Erik K., Investigators, CINRG
Pubblicato in PLoS Curr (2018)

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

di Thangarajh, Mathula, Zhang, Aiping, Gill, Kirandeep, Ressom, Habtom W., Li, Zhenzhi, Varghese, Rency S., Hoffman, Eric P., Nagaraju, Kanneboyina, Hathout, Yetrib, Boca, Simina M.
Pubblicato in PLoS One (2019)

Dystrophic muscle distribution in late-stage muscular dystrophy

di 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
Pubblicato in Autops Case Rep (2020)

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

di 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.
Pubblicato in 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...

di 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.
Pubblicazione 2012

A multinational study on motor function in early-onset FSHD

di 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
Pubblicato in Neurology (2018)

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

di 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
Pubblicato in J Pers Med (2020)

The CINRG Becker Natural History Study: Baseline Characteristics

di 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
Pubblicato in Muscle Nerve (2020)

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

di 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.
Pubblicato in Contemp Clin Trials Commun (2018)

Baseline results of the NeuroNEXT spinal muscular atrophy infant biomarker study

di 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.
Pubblicato in Ann Clin Transl Neurol (2016)

Natural History of Infantile-Onset Spinal Muscular Atrophy

di 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.
Pubblicato in Ann Neurol (2017)

Developing Standardized Corticosteroid Treatment for Duchenne Muscular Dystrophy

di 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.
Pubblicato in Contemp Clin Trials (2017)

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

di 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
Pubblicato in Trials (2018)