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Page 1
[Metabolic syndrome in children and in adults: is it an autonomous nosological entity?].
Recenti Prog Med. 2012 Apr;103(4):158-63. doi: 10.1701/1068.11706.
Recenti Prog Med. 2012.
PMID: 22561995
Italian.
12q14.3 microdeletion involving HMGA2 gene cause a Silver-Russell syndrome-like phenotype: a case report and review of the literature.
Mercadante F, Busè M, Salzano E, Fragapane T, Palazzo D, Malacarne M, Piccione M.
Mercadante F, et al. Among authors: fragapane t.
Ital J Pediatr. 2020 Jul 28;46(1):108. doi: 10.1186/s13052-020-00866-9.
Ital J Pediatr. 2020.
PMID: 32723361
Free PMC article.
Review.
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Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes.
Balistreri CR, Ammoscato CL, Scola L, Fragapane T, Giarratana RM, Lio D, Piccione M.
Balistreri CR, et al. Among authors: fragapane t.
Genes (Basel). 2020 Nov 28;11(12):1428. doi: 10.3390/genes11121428.
Genes (Basel). 2020.
PMID: 33260695
Free PMC article.
Clinical Trial.
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Response to Stanich et al.: Correspondence regarding-PTEN hamartoma tumor syndromes in childhood-Description of two cases and a proposal for follow-up protocol.
Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G.
Piccione M, et al. Among authors: fragapane t.
Am J Med Genet A. 2014 Jul;164A(7):1871. doi: 10.1002/ajmg.a.36527. Epub 2014 Apr 3.
Am J Med Genet A. 2014.
PMID: 24700784
No abstract available.
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PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.
Piccione M, Fragapane T, Antona V, Giachino D, Cupido F, Corsello G.
Piccione M, et al. Among authors: fragapane t.
Am J Med Genet A. 2013 Nov;161A(11):2902-8. doi: 10.1002/ajmg.a.36266. Epub 2013 Oct 7.
Am J Med Genet A. 2013.
PMID: 24123798
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