CNS Myelination Requires Cytoplasmic Dynein Function

Yazar: Yang, Michele L., Shin, Jimann, Kearns, Christina A., Langworthy, Melissa M., Snell, Heather, Walker, Macie B., Appel, Bruce
Yayımlandı Dev Dyn (2015)

Health Care Transition Experiences of Males with Childhood-onset Duchenne and Becker Muscular Dystrophy: Findings from the Muscular Dystrophy Surveillance Tracking and Research Net...

Yazar: Paramsothy, Pangaja, Herron, Adrienne R., Lamb, Molly M., Kinnett, Kathi, Wolff, Jodi, Yang, Michele L., Oleszek, Joyce, Pandya, Shree, Kennedy, Annie, Cooney, Darryl, Fox, Deborah, Sheehan, Daniel
Yayımlandı PLoS Curr (2018)

The motor neuron response to SMN1 deficiency in spinal muscular atrophy

Yazar: Kang, Peter B., Gooch, Clifton L., McDermott, Michael P., Darras, Basil T., Finkel, Richard S., Yang, Michele L., Sproule, Douglas M., Chung, Wendy K., Kaufmann, Petra, De Vivo, Darryl C.
Baskı/Yayın Bilgisi 2014

Quality and Safety Analysis of 2,999 Telemedicine Encounters During the COVID-19 Pandemic

Yazar: Joshi, Charuta N., Yang, Michele L., Eschbach, Krista, Tong, Suhong, Jacobson, Mona P., Stillman, Chelsey, Kropp, Annmarie E., Shea, Stephanie A., Frunzi, Gerard M., Thomas, J. Fred, Olson, Christina A.
Yayımlandı Neurol Clin Pract (2021)

Outcomes of Colorado children with acute flaccid myelitis at 1 year

Yazar: Martin, Jan A., Messacar, Kevin, Yang, Michele L., Maloney, John A., Lindwall, Jennifer, Carry, Terri, Kenyon, Patricia, Sillau, Stefan H., Oleszek, Joyce, Tyler, Kenneth L., Dominguez, Samuel R., Schreiner, Teri L.
Yayımlandı Neurology (2017)

A multicenter, retrospective medical record review of X‐linked myotubular myopathy: The recensus study

Yazar: Beggs, Alan H., Byrne, Barry J., De Chastonay, Sabine, Haselkorn, Tmirah, Hughes, Imelda, James, Emma S., Kuntz, Nancy L., Simon, Jennifer, Swanson, Lindsay C., Yang, Michele L., Yu, Zi‐Fan, Yum, Sabrina W., Prasad, Suyash
Yayımlandı Muscle Nerve (2017)

Mortality and respiratory support in X-linked myotubular myopathy: a RECENSUS retrospective analysis

Yazar: Graham, Robert J, Muntoni, Francesco, Hughes, Imelda, Yum, Sabrina W, Kuntz, Nancy L, Yang, Michele L, Byrne, Barry J, Prasad, Suyash, Alvarez, Rachel, Genetti, Casie A, Haselkorn, Tmirah, James, Emma S, LaRusso, Laurie B, Noursalehi, Mojtaba, Rico, Salvador, Beggs, Alan H
Yayımlandı Arch Dis Child (2020)

A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity

Yazar: Beck, David B., Subramanian, T., Vijayalingam, S., Ezekiel, Uthayashankar R., Donkervoort, Sandra, Yang, Michele L., Dubbs, Holly A., Ortiz-Gonzalez, Xilma R., Lakhani, Shenela, Segal, Devorah, Au, Margaret, Graham, John M., Verma, Sumit, Waggoner, Darrel, Shinawi, Marwan, Bönnemann, Carsten G., Chung, Wendy K., Chinnadurai, G.
Yayımlandı Neurogenetics (2019)

Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family

Yazar: Zukosky, Kristen, Meilleur, Katherine, Traynor, Bryan J., Dastgir, Jahannaz, Medne, Livija, Devoto, Marcella, Collins, James, Rooney, Jachinta, Zou, Yaqun, Yang, Michele L., Gibbs, J. Raphael, Meier, Markus, Stetefeld, Joerg, Finkel, Richard S., Schessl, Joachim, Elman, Lauren, Felice, Kevin, Ferguson, Toby A., Ceyhan-Birsoy, Ozge, Beggs, Alan H., Tennekoon, Gihan, Johnson, Janel O., Bönnemann, Carsten G.
Yayımlandı JAMA Neurol (2015)

Prospective cohort study of spinal muscular atrophy types 2 and 3

Yazar: Kaufmann, Petra, McDermott, Michael P., Darras, Basil T., Finkel, Richard S., Sproule, Douglas M., Kang, Peter B., Oskoui, Maryam, Constantinescu, Andrei, Gooch, Clifton L., Foley, A. Reghan, Yang, Michele L., Tawil, Rabi, Chung, Wendy K., Martens, William B., Montes, Jacqueline, Battista, Vanessa, O'Hagen, Jessica, Dunaway, Sally, Flickinger, Jean, Quigley, Janet, Riley, Susan, Glanzman, Allan M., Benton, Maryjane, Ryan, Patricia A., Punyanitya, Mark, Montgomery, Megan J., Marra, Jonathan, Koo, Benjamin, De Vivo, Darryl C.
Baskı/Yayın Bilgisi 2012