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Early-Onset Shapiro Syndrome Variant Treated with Pizotifen: A Case Report.
Neurodiagn J. 2017;57(2):139-146. doi: 10.1080/21646821.2017.1309941.
Neurodiagn J. 2017.
PMID: 28622125
Expanded spectrum of Pelizaeus-Merzbacher-like disease: literature revision and description of a novel GJC2 mutation in an unusually severe form.
Biancheri R, Rosano C, Denegri L, Lamantea E, Pinto F, Lanza F, Severino M, Filocamo M.
Biancheri R, et al. Among authors: denegri l.
Eur J Hum Genet. 2013 Jan;21(1):34-9. doi: 10.1038/ejhg.2012.93. Epub 2012 Jun 6.
Eur J Hum Genet. 2013.
PMID: 22669416
Free PMC article.
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Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literature.
Tassano E, Biancheri R, Denegri L, Porta S, Novara F, Zuffardi O, Gimelli G, Cuoco C.
Tassano E, et al. Among authors: denegri l.
Eur J Med Genet. 2014 Nov-Dec;57(11-12):626-9. doi: 10.1016/j.ejmg.2014.09.007.
Eur J Med Genet. 2014.
PMID: 25451713
Review.
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