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Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.
Dosi C, Rubegni A, Baldacci J, Galatolo D, Doccini S, Astrea G, Berardinelli A, Bruno C, Bruno G, Comi GP, Donati MA, Dotti MT, Filosto M, Fiorillo C, Giannini F, Gigli GL, Grandis M, Lopergolo D, Magri F, Maioli MA, Malandrini A, Massa R, Matà S, Melani F, Messina S, Mignarri A, Moggio M, Pennisi EM, Pegoraro E, Ricci G, Sacchini M, Schenone A, Sampaolo S, Sciacco M, Siciliano G, Tasca G, Tonin P, Tupler R, Valente M, Volpi N, Cassandrini D, Santorelli FM. Dosi C, et al. Among authors: berardinelli a. Genes (Basel). 2023 Jan 23;14(2):298. doi: 10.3390/genes14020298. Genes (Basel). 2023. PMID: 36833224 Free PMC article.
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.
1st Italian SMA Family Association Consensus Meeting: Management and recommendations for respiratory involvement in spinal muscular atrophy (SMA) types I-III, Rome, Italy, 30-31 January 2015.
Sansone VA, Racca F, Ottonello G, Vianello A, Berardinelli A, Crescimanno G, Casiraghi JL; Italian SMA Family Association. Sansone VA, et al. Among authors: berardinelli a. Neuromuscul Disord. 2015 Dec;25(12):979-89. doi: 10.1016/j.nmd.2015.09.009. Epub 2015 Sep 18. Neuromuscul Disord. 2015. PMID: 26453142 No abstract available.
[Ehlers-Danlos syndrome. Description of 2 clinical cases].
Ottolini A, Berardinelli A, Besana D, Cetta G, Dyne KM, Lanzi G. Ottolini A, et al. Among authors: berardinelli a. Minerva Pediatr. 1992 May;44(5):231-6. Minerva Pediatr. 1992. PMID: 1620075 Italian.
168 results