Politano L - Search Results

1

Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function.

Onore ME, Savarese M, Picillo E, Passamano L, Nigro V, Politano L. Onore ME, et al. Among authors: politano l. Int J Mol Sci. 2022 Dec 14;23(24):15906. doi: 10.3390/ijms232415906. Int J Mol Sci. 2022. PMID: 36555543 Free PMC article.

2

Pulsed Doppler tissue imaging in dystrophinopathic cardiomyopathy.

Agretto A, Politano L, Bossone E, Petretta VR, D'Isa S, Passamano L, Comi LI, Erbel R. Agretto A, et al. Among authors: politano l. J Am Soc Echocardiogr. 2002 Sep;15(9):891-9. doi: 10.1067/mje.2002.121197. J Am Soc Echocardiogr. 2002. PMID: 12221405 Clinical Trial.

3

A preliminary randomized study of growth hormone administration in Becker and Duchenne muscular dystrophies.

Cittadini A, Ines Comi L, Longobardi S, Rocco Petretta V, Casaburi C, Passamano L, Merola B, Durante-Mangoni E, Saccà L, Politano L. Cittadini A, et al. Among authors: politano l. Eur Heart J. 2003 Apr;24(7):664-72. doi: 10.1016/s0195-668x(02)00740-6. Eur Heart J. 2003. PMID: 12657225 Clinical Trial.

4

Molecular and muscle pathology in a series of caveolinopathy patients.

Fulizio L, Nascimbeni AC, Fanin M, Piluso G, Politano L, Nigro V, Angelini C. Fulizio L, et al. Among authors: politano l. Hum Mutat. 2005 Jan;25(1):82-9. doi: 10.1002/humu.20119. Hum Mutat. 2005. PMID: 15580566

5

Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H.

Saccone V, Palmieri M, Passamano L, Piluso G, Meroni G, Politano L, Nigro V. Saccone V, et al. Among authors: politano l. Hum Mutat. 2008 Feb;29(2):240-7. doi: 10.1002/humu.20633. Hum Mutat. 2008. PMID: 17994549

6

Log-PCR: a new tool for immediate and cost-effective diagnosis of up to 85% of dystrophin gene mutations.

Trimarco A, Torella A, Piluso G, Maria Ventriglia V, Politano L, Nigro V. Trimarco A, et al. Among authors: politano l. Clin Chem. 2008 Jun;54(6):973-81. doi: 10.1373/clinchem.2007.097881. Epub 2008 Apr 10. Clin Chem. 2008. PMID: 18403565

7

One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatography.

Torella A, Trimarco A, Blanco Fdel V, Cuomo A, Aurino S, Piluso G, Minetti C, Politano L, Nigro V. Torella A, et al. Among authors: politano l. J Mol Diagn. 2010 Jan;12(1):65-73. doi: 10.2353/jmoldx.2010.090074. Epub 2009 Dec 3. J Mol Diagn. 2010. PMID: 19959795 Free PMC article.

8

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: politano l. 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

9

Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations.

Cacciottolo M, Numitone G, Aurino S, Caserta IR, Fanin M, Politano L, Minetti C, Ricci E, Piluso G, Angelini C, Nigro V. Cacciottolo M, et al. Among authors: politano l. Eur J Hum Genet. 2011 Sep;19(9):974-80. doi: 10.1038/ejhg.2011.70. Epub 2011 Apr 27. Eur J Hum Genet. 2011. PMID: 21522182 Free PMC article.

10

Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders.

Piluso G, Dionisi M, Del Vecchio Blanco F, Torella A, Aurino S, Savarese M, Giugliano T, Bertini E, Terracciano A, Vainzof M, Criscuolo C, Politano L, Casali C, Santorelli FM, Nigro V. Piluso G, et al. Among authors: politano l. Clin Chem. 2011 Nov;57(11):1584-96. doi: 10.1373/clinchem.2011.168898. Epub 2011 Sep 6. Clin Chem. 2011. PMID: 21896784 Free article.

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