CDC-Authored Genomics and Precision Health Publications Database
Last data update: Sep 03, 2024. (Total: 6282 publications)
Query Trace: Muscular dystrophy[original query] |
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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 34 430-438 |
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 |
Clinical follow-up for Duchenne muscular dystrophy newborn sreening: A proposal
Kwon JM , Abdel-Hamid HZ , Al-Zaidy SA , Mendell JR , Kennedy A , Kinnett K , Cwik VA , Street N , Bolen J , Day JW , Connolly AM . Muscle Nerve 2016 54 (2) 186-91 |
Public Health and Rare Diseases: Oxymoron No More.
Valdez R , Ouyang L , Bolen J . Prev Chronic Dis 2016 13 E05 |
Development of a genomic DNA reference material panel for myotonic dystrophy type 1 (DM1) genetic testing.
Kalman L , Tarleton J , Hitch M , Hegde M , Hjelm N , Berry-Kravis E , Zhou L , Hilbert JE , Luebbe EA , Moxley RT 3rd , Toji L . J Mol Diagn 2013 15 (4) 518-25 |
Reproductive patterns among mothers of males diagnosed with Duchenne or Becker muscular dystrophy.
Nabukera SK , Romitti PA , Caspers KM , Street N , Cunniff C , Mathews KD , Fox DJ , Puzhankara S , Ciafaloni E , James KA , Su Y . Am J Med Genet A 2013 161 (1) 70-75 |
Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Mendell JR , Shilling C , Leslie ND , Flanigan KM , Al-Dahhak R , Gastier-Foster J , Kneile K , Dunn DM , Duval B , Aoyagi A , Hamil C , Mahmoud M , Roush K , Bird L , Rankin C , Lilly H , Street N , Chandrasekar R , Weiss RB . Ann Neurol 2012 71 (3) 304-13 |
Disparities in the diagnostic process of Duchenne and Becker muscular dystrophy
Holtzer C , Meaney FJ , Andrews J , Ciafaloni E , Fox DJ , James KA , Lu Z , Miller L , Pandya S , Ouyang L , Cunniff C . Genet Med 2011 13 (11) 942-7 |
Quality assurance for Duchenne and Becker muscular dystrophy genetic testing: development of a genomic DNA reference material panel.
Kalman L , Leonard J , Gerry N , Tarleton J , Bridges C , Gastier-Foster JM , Pyatt RE , Stonerock E , Johnson MA , Richards CS , Schrijver I , Ma T , Miller VR , Adadevoh Y , Furlong P , Beiswanger C , Toji L . J Mol Diagn 2011 13 (2) 167-74 |
Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005
Kenneson A , Vatave A , Finkel R . Neurology 2010 75 (11) 982-9 |
Evaluation of the validity and utility of genetic testing for rare diseases.
Grosse SD , Kalman L , Khoury MJ . Adv Exp Med Biol 2010 686 115-31 ![]() |
Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management
Bushby K , Finkel R , Birnkrant DJ , Case LE , Clemens PR , Cripe L , Kaul A , Kinnett K , McDonald C , Pandya S , Poysky J , Shapiro F , Tomezsko J , Constantin C , DMD Care Considerations Working Group . Lancet Neurol 2010 9 (1) 77-93 |
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