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CDC-Authored Genomics and Precision Health Publications Database|Home|PHGKB

CDC-Authored Genomics and Precision Health Publications Database


Rare Diseases

Last data update: Mar 31, 2023. (Total: 4252 publications since 2011)
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Records 1-6 (of 6 Records)
Query Trace: Duchenne Muscular Dystrophy[original query]
Seroprevalence of AAV neutralizing antibodies in males with Duchenne muscular dystrophy.
Sumit Verma, Stella N Nwosu, Raj Razdan, Saila R Upadhyayula, Han C Phan, Abubakarr A Koroma, Isai Leguizamo, Natalie S Correa, Michael Kuipa, David Lee, Thomas H Vanderford, and Matthew R Gardner
Human gene therapy 2022
Selected clinical and demographic factors and all-cause mortality among individuals with Duchenne muscular dystrophy in the Muscular Dystrophy Surveillance, Tracking, and Research Network.
Pangaja Paramsothy, Yinding Wang, Bo Cai, Kristin M Conway, Nicholas E Johnson, Shree Pandya, Emma Ciafaloni, Katherine D Mathews, Paul A Romitti, James F Howard, and Catharine Riley
Neuromuscular disorders : NMD 2022
Time to Diagnosis of Duchenne Muscular Dystrophy Remains Unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet), 2000-2015.
Shiny Thomas, Kristin M Conway, Olushola Fapo, Natalie Street, Katherine D Mathews, Joshua Mann, Paul A Romitti, Aida Soim, Christina Westfield, Deborah J Fox, Emma Ciafaloni, and
Muscle & nerve 2022
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.
David J Birnkrant, Katharine Bushby, Carla M Bann, Susan D Apkon, Angela Blackwell, David Brumbaugh, Laura E Case, Paula R Clemens, Stasia Hadjiyannakis, Shree Pandya, Natalie Street, Jean Tomezsko, Kathryn R Wagner, Leanne M Ward, David R Weber, and
The Lancet. Neurology 2018 Jan
Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management.
David J Birnkrant, Katharine Bushby, Carla M Bann, Benjamin A Alman, Susan D Apkon, Angela Blackwell, Laura E Case, Linda Cripe, Stasia Hadjiyannakis, Aaron K Olson, Daniel W Sheehan, Julie Bolen, David R Weber, Leanne M Ward, and
The Lancet. Neurology 2018 Jan
Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Jerry R Mendell, Chris Shilling, Nancy D Leslie, Kevin M Flanigan, Roula al-Dahhak, Julie Gastier-Foster, Kelley Kneile, Diane M Dunn, Brett Duval, Alexander Aoyagi, Cindy Hamil, Maha Mahmoud, Kandice Roush, Lauren Bird, Chelsea Rankin, Heather Lilly, Natalie Street, Ram Chandrasekar, and Robert B Weiss
Ann. Neurol. 2012 Mar 71(3) 304-13
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