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The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.
Grugni G, Crinò A, Bosio L, Corrias A, Cuttini M, De Toni T, Di Battista E, Franzese A, Gargantini L, Greggio N, Iughetti L, Livieri C, Naselli A, Pagano C, Pozzan G, Ragusa L, Salvatoni A, Trifirò G, Beccaria L, Bellizzi M, Bellone J, Brunani A, Cappa M, Caselli G, Cerioni V, Delvecchio M, Giardino D, Iannì F, Memo L, Pilotta A, Pomara C, Radetti G, Sacco M, Sanzari A, Sartorio A, Tonini G, Vettor R, Zaglia F, Chiumello G; Genetic Obesity Study Group of Italian Society of Pediatric Endocrinology and Diabetology (ISPED). Grugni G, et al. Among authors: pomara c. Am J Med Genet A. 2008 Apr 1;146A(7):861-72. doi: 10.1002/ajmg.a.32133. Am J Med Genet A. 2008. PMID: 18203198
Cardiac pathology in death from electrocution.
Fineschi V, Karch SB, D'Errico S, Pomara C, Riezzo I, Turillazzi E. Fineschi V, et al. Among authors: pomara c. Int J Legal Med. 2006 Mar;120(2):79-82. doi: 10.1007/s00414-005-0011-8. Epub 2005 Aug 3. Int J Legal Med. 2006. PMID: 16078070
Immunohistochemical marker for Na+ CP type Valpha (C-20) and heterozygous nonsense SCN5A mutation W822X in a sudden cardiac death induced by mild anaphylactic reaction.
Turillazzi E, Pomara C, La Rocca G, Neri M, Riezzo I, Karch SB, Anzalone R, Lo Iacono M, Fineschi V. Turillazzi E, et al. Among authors: pomara c. Appl Immunohistochem Mol Morphol. 2009 Jul;17(4):357-62. doi: 10.1097/PAI.0b013e3181955b37. Appl Immunohistochem Mol Morphol. 2009. PMID: 19318916
146 results