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Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report.
Ronchi D, Cosi A, Tonduti D, Orcesi S, Bordoni A, Fortunato F, Rizzuti M, Sciacco M, Collotta M, Cagdas S, Capovilla G, Moggio M, Berardinelli A, Veggiotti P, Comi GP. Ronchi D, et al. Among authors: orcesi s. BMC Neurol. 2011 Jul 12;11:85. doi: 10.1186/1471-2377-11-85. BMC Neurol. 2011. PMID: 21749722 Free PMC article.
Fate of melatonin orally administered in preterm newborns: Antioxidant performance and basis for neuroprotection.
Garofoli F, Franco V, Accorsi P, Albertini R, Angelini M, Asteggiano C, Aversa S, Ballante E, Borgatti R, Cabini RF, Caporali C, Chiapparini L, Cociglio S, Fazzi E, Longo S, Malerba L, Materia V, Mazzocchi L, Naboni C, Palmisani M, Pichiecchio A, Pinelli L, Pisoni C, Preda L, Riboli A, Risso FM, Rizzo V, Rognone E, Simoncelli AM, Villani P, Tzialla C, Ghirardello S, Orcesi S. Garofoli F, et al. Among authors: orcesi s. J Pineal Res. 2024 Jan;76(1):e12932. doi: 10.1111/jpi.12932. Epub 2023 Dec 18. J Pineal Res. 2024. PMID: 38111174 Clinical Trial.
Expanding the Natural History of SNORD118-Related Ribosomopathy: Hints from an Early-Diagnosed Patient with Leukoencephalopathy with Calcifications and Cysts and Overview of the Literature.
Politano D, Catalano G, Pezzotti E, Varesio C, Sirchia F, Casella A, Rognone E, Pichiecchio A, Borgatti R, Orcesi S. Politano D, et al. Among authors: orcesi s. Genes (Basel). 2023 Sep 19;14(9):1817. doi: 10.3390/genes14091817. Genes (Basel). 2023. PMID: 37761957 Free PMC article.
AAEM news and comments.
Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Among authors: orcesi s. Muscle Nerve. 2000 Jan;23(1):142-6. Muscle Nerve. 2000. PMID: 10590423 No abstract available.
Dystrophinopathies: peculiar clinical and laboratory aspects.
Berardinelli A, Gorni K, Orcesi S, Tagliabue A, Uggetti C, Lanzi G. Berardinelli A, et al. Among authors: orcesi s. Funct Neurol. 2001;16(4 Suppl):255-62. Funct Neurol. 2001. PMID: 11996522 No abstract available.
New case of 4H syndrome and a review of the literature.
Orcesi S, Tonduti D, Uggetti C, Larizza D, Fazzi E, Balottin U. Orcesi S, et al. Pediatr Neurol. 2010 May;42(5):359-64. doi: 10.1016/j.pediatrneurol.2010.01.015. Pediatr Neurol. 2010. PMID: 20399393 Review.
159 results