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

CDC-Authored Genomics and Precision Health Publications Database


Last data update: May 30, 2023. (Total: 4302 publications since 2011)
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Records 1-10 (of 10 Records)
Query Trace: Muscular dystrophy[original query]
Seroprevalence of AAV neutralizing antibodies in males with Duchenne muscular dystrophy.
Verma S , Nwosu SN , Razdan R , Upadhyayula SR , Phan HC , Koroma AA , Leguizamo I , Correa NS , Kuipa M , Lee D , Vanderford TH , Gardner MR .
Hum Gene Ther 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.
Paramsothy P , Wang Y , Cai B , Conway KM , Johnson NE , Pandya S , Ciafaloni E , Mathews KD , Romitti PA , Howard JFJr , Riley C .
Neuromuscul Disord 2022 32 (6) 468-476
Role Attainment in Emerging Adulthood: Subjective Evaluation by Male Adolescents and Adults with Duchenne and Becker Muscular Dystrophy1.
Peay HL , Do BT , Khosla N , Paramsothy P , Erickson SW , Lamb MM , Whitehead N , Fox DJ , Pandya S , Kinnett K , Wolff J , Howard JF .
J Neuromuscul Dis 2022 9 (3) 447-456
Time to Diagnosis of Duchenne Muscular Dystrophy Remains Unchanged: Findings from the Muscular Dystrophy Surveillance, Tracking, and Research Network (MD STARnet), 2000-2015.
Thomas S , Conway KM , Fapo O , Street N , Mathews KD , Mann J , Romitti PA , Soim A , Westfield C , Fox DJ , Ciafaloni E .
Muscle Nerve 2022 66 (2) 193-197
Duchenne and Becker Muscular Dystrophies' Prevalence in MD STARnet Surveillance Sites: An Examination of Racial and Ethnic Differences.
Zhang Y , Mann JR , James KA , McDermott S , Conway KM , Paramsothy P , Smith T , Cai B .
Neuroepidemiology 2021 55 (1) 1-9
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.
Birnkrant DJ , Bushby K , Bann CM , Apkon SD , Blackwell A , Brumbaugh D , Case LE , Clemens PR , Hadjiyannakis S , Pandya S , Street N , Tomezsko J , Wagner KR , Ward LM , Weber DR .
Lancet Neurol 2018 17 (3) 251-267
Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management.
Birnkrant DJ , Bushby K , Bann CM , Alman BA , Apkon SD , Blackwell A , Case LE , Cripe L , Hadjiyannakis S , Olson AK , Sheehan DW , Bolen J , Weber DR , Ward LM .
Lancet Neurol 2018 17 (4) 347-361
Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy.
Nabukera Sarah K, Romitti Paul A, Caspers Kristin M, Street Natalie, Cunniff Christopher, Mathews Katherine D, Fox Deborah J, Puzhankara Soman, Ciafaloni Emma, James Katherine A, Su Yin, . Am. J. Med. Genet. A 2013 Jan 161A(1) 70-5 .
Am. J. Med. Genet. A 2013 Jan 161A(1) 70-5
Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Mendell Jerry R, Shilling Chris, Leslie Nancy D, Flanigan Kevin M, al-Dahhak Roula, Gastier-Foster Julie, Kneile Kelley, Dunn Diane M, Duval Brett, Aoyagi Alexander, Hamil Cindy, Mahmoud Maha, Roush Kandice, Bird Lauren, Rankin Chelsea, Lilly Heather, Street Natalie, Chandrasekar Ram, Weiss Robert B. Ann. Neurol. 2012 Mar 71(3) 304-13 .
Ann. Neurol. 2012 Mar 71(3) 304-13
Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.
Kalman Lisa, Leonard Jay, Gerry Norman, Tarleton Jack, Bridges Christina, Gastier-Foster Julie M, Pyatt Robert E, Stonerock Eileen, Johnson Monique A, Richards C Sue, Schrijver Iris, Ma Tianhui, Miller Vanessa Rangel, Adadevoh Yetsa, Furlong Pat, Beiswanger Christine, Toji Lorraine. The Journal of molecular diagnostics : JMD 2011 Mar 13(2) 167-74 .
The Journal of molecular diagnostics : JMD 2011 Mar 13(2) 167-74
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