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4. Newborn screening for Duchenne muscular dystrophy: A two-year pilot study. Tavakoli NP; Gruber D; Armstrong N; Chung WK; Maloney B; Park S; Wynn J; Koval-Burt C; Verdade L; Tegay DH; Cohen LL; Shapiro N; Kennedy A; Noritz G; Ciafaloni E; Weinberger B; Ellington M; Schleien C; Spinazzola R; Sood S; Brower A; Lloyd-Puryear M; Caggana M; Ann Clin Transl Neurol; 2023 Aug; 10(8):1383-1396. PubMed ID: 37350320 [TBL] [Abstract][Full Text] [Related]
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6. Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy. Ke Q; Zhao ZY; Mendell JR; Baker M; Wiley V; Kwon JM; Alfano LN; Connolly AM; Jay C; Polari H; Ciafaloni E; Qi M; Griggs RC; Gatheridge MA World J Pediatr; 2019 Jun; 15(3):219-225. PubMed ID: 30904991 [TBL] [Abstract][Full Text] [Related]
7. Three years' experience with neonatal screening for Duchenne/Becker muscular dystrophy: gene analysis, gene expression, and phenotype prediction. Greenberg CR; Jacobs HK; Halliday W; Wrogemann K Am J Med Genet; 1991 Apr; 39(1):68-75. PubMed ID: 1867267 [TBL] [Abstract][Full Text] [Related]
8. Neonatal screening for Duchenne muscular dystrophy: a novel semiquantitative application of the bioluminescence test for creatine kinase in a pilot national program in Cyprus. Drousiotou A; Ioannou P; Georgiou T; Mavrikiou E; Christopoulos G; Kyriakides T; Voyasianos M; Argyriou A; Middleton L Genet Test; 1998; 2(1):55-60. PubMed ID: 10464597 [TBL] [Abstract][Full Text] [Related]
9. Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment. Ke Q; Zhao ZY; Griggs R; Wiley V; Connolly A; Kwon J; Qi M; Sheehan D; Ciafaloni E; Howell RR; Furu P; Sazani P; Narayana A; Gatheridge M World J Pediatr; 2017 Jun; 13(3):197-201. PubMed ID: 28466241 [TBL] [Abstract][Full Text] [Related]
10. Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy. Farrar MA; Kariyawasam D; Grattan S; Bayley K; Davis M; Holland S; Waddel LB; Jones K; Lorentzos M; Ravine A; Wotton T; Wiley V; J Neuromuscul Dis; 2023; 10(1):15-28. PubMed ID: 36373292 [TBL] [Abstract][Full Text] [Related]
11. [Anesthetic complications. The incidence of severe anesthetic complications in patients and families with progressive muscular dystrophy of the Duchenne and Becker types]. Breucking E; Reimnitz P; Schara U; Mortier W Anaesthesist; 2000 Mar; 49(3):187-95. PubMed ID: 10788987 [TBL] [Abstract][Full Text] [Related]
12. Framing optional genetic testing in the context of mandatory newborn screening tests. Lillie SE; Tarini BA; Janz NK; Zikmund-Fisher BJ BMC Med Inform Decis Mak; 2015 Jun; 15():50. PubMed ID: 26123051 [TBL] [Abstract][Full Text] [Related]
13. Report of MDA muscle disease symposium on newborn screening for Duchenne muscular dystrophy. Mendell JR; Lloyd-Puryear M Muscle Nerve; 2013 Jul; 48(1):21-6. PubMed ID: 23716304 [TBL] [Abstract][Full Text] [Related]
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15. Duchenne muscular dystrophy: systematic neonatal screening and earlier detection of carriers. Plauchu H; Dellamonica C; Cotte J; Robert JM J Genet Hum; 1980 Dec; 28(4):65-82. PubMed ID: 7205199 [TBL] [Abstract][Full Text] [Related]
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19. [Differential diagnosis of Becker and Duchenne muscular dystrophy]. Alvarez Leal M; Hernández Sifuentes PM; Pérez-Zuno JA Gac Med Mex; 1994; 130(6):454-8. PubMed ID: 7557060 [TBL] [Abstract][Full Text] [Related]