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Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study.
Brogna C, Pane M, Coratti G, D'Amico A, Pegoraro E, Bello L, Sansone VAM, Albamonte E, Messina S, Pini A, D'Angelo MG, Bruno C, Mongini T, Ricci FS, Berardinelli A, Battini R, Masson R, Bertini ES, Politano L, Mercuri E, Italian Dmd Group. Brogna C, et al. Among authors: berardinelli a. Children (Basel). 2023 Apr 19;10(4):746. doi: 10.3390/children10040746. Children (Basel). 2023. PMID: 37189996 Free PMC article.
Long-term growth hormone therapy in mitochondrial cytopathy.
Barberi S, Bozzola E, Berardinelli A, Meazza C, Bozzola M. Barberi S, et al. Among authors: berardinelli a. Horm Res. 2004;62(2):103-6. doi: 10.1159/000080451. Epub 2004 Aug 25. Horm Res. 2004. PMID: 15331853
Response to carbamazepine of recessive-type myotonia congenita.
Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Muscle Nerve. 2000 Jan;23(1):138-9. doi: 10.1002/(sici)1097-4598(200001)23:1<138::aid-mus23>3.0.co;2-4. Muscle Nerve. 2000. PMID: 10590422 No abstract available.
Large-scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy.
Scionti I, Greco F, Ricci G, Govi M, Arashiro P, Vercelli L, Berardinelli A, Angelini C, Antonini G, Cao M, Di Muzio A, Moggio M, Morandi L, Ricci E, Rodolico C, Ruggiero L, Santoro L, Siciliano G, Tomelleri G, Trevisan CP, Galluzzi G, Wright W, Zatz M, Tupler R. Scionti I, et al. Among authors: berardinelli a. Am J Hum Genet. 2012 Apr 6;90(4):628-35. doi: 10.1016/j.ajhg.2012.02.019. Am J Hum Genet. 2012. PMID: 22482803 Free PMC article.
168 results