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What Have We Learned from Patients Who Have Arboleda-Tham Syndrome Due to a De Novo KAT6A Pathogenic Variant with Impaired Histone Acetyltransferase Function? A Precise Clinical Description May Be Critical for Genetic Testing Approach and Final Diagnosis.
Bukvic N, Chetta M, Bagnulo R, Leotta V, Pantaleo A, Palumbo O, Palumbo P, Oro M, Rivieccio M, Laforgia N, De Rinaldis M, Rosati A, Kerkhof J, Sadikovic B, Resta N. Bukvic N, et al. Among authors: de rinaldis m. Genes (Basel). 2023 Jan 7;14(1):165. doi: 10.3390/genes14010165. Genes (Basel). 2023. PMID: 36672906 Free PMC article.
Charcot-Marie-Tooth type 1a in a child with Long QT syndrome.
Losito L, De Rinaldis M, Gennaro L, Priori SG, Bloise R, Bassi MT, Bresolin N, Trabacca A. Losito L, et al. Among authors: de rinaldis m. Eur J Paediatr Neurol. 2009 Sep;13(5):459-62. doi: 10.1016/j.ejpn.2008.07.011. Epub 2008 Sep 16. Eur J Paediatr Neurol. 2009. PMID: 18799333
It's time to measure disability in spinal muscular atrophy.
Trabacca A, Ferrante C, De Rinaldis M. Trabacca A, et al. Among authors: de rinaldis m. Acta Myol. 2022 Jun 30;41(2):57-58. doi: 10.36185/2532-1900-070. eCollection 2022 Jun. Acta Myol. 2022. PMID: 35832503 Free PMC article. No abstract available.
35 results