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Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
J Med Genet. 2005 Sep;42(9):686-93. doi: 10.1136/jmg.2004.028738.
J Med Genet. 2005.
PMID: 16141003
Free PMC article.
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
Fanin M, Fulizio L, Nascimbeni AC, Spinazzi M, Piluso G, Ventriglia VM, Ruzza G, Siciliano G, Trevisan CP, Politano L, Nigro V, Angelini C.
Fanin M, et al. Among authors: ventriglia vm.
Hum Mutat. 2004 Jul;24(1):52-62. doi: 10.1002/humu.20058.
Hum Mutat. 2004.
PMID: 15221789
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Corneal thickness and endothelial cell characteristics in patients with myotonic dystrophy.
Rosa N, Lanza M, Borrelli M, Filosa ML, De Bernardo M, Ventriglia VM, Cecio MR, Politano L.
Rosa N, et al. Among authors: ventriglia vm.
Ophthalmology. 2010 Feb;117(2):223-5. doi: 10.1016/j.ophtha.2009.07.003. Epub 2009 Dec 6.
Ophthalmology. 2010.
PMID: 19969362
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Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients.
Rinaldi F, Botta A, Vallo L, Contino G, Morgante A, Iraci R, Catalli C, Silvestri G, Ventriglia VM, Politano L, Novelli G.
Rinaldi F, et al. Among authors: ventriglia vm.
Acta Myol. 2008 Dec;27(3):82-9.
Acta Myol. 2008.
PMID: 19472917
Free PMC article.
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Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy.
Nigro G, Russo V, Ventriglia VM, Della Cioppa N, Palladino A, Nigro V, Calabrò R, Nigro G, Politano L.
Nigro G, et al. Among authors: ventriglia vm.
Neuromuscul Disord. 2010 Mar;20(3):174-7. doi: 10.1016/j.nmd.2009.12.004. Epub 2010 Feb 10.
Neuromuscul Disord. 2010.
PMID: 20149661
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