Politano L - Search Results

1

Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.

Pizza A, Picillo E, Onore ME, Scutifero M, Passamano L, Nigro V, Politano L. Pizza A, et al. Among authors: politano l. Acta Myol. 2023 Mar 31;42(1):24-30. doi: 10.36185/2532-1900-246. eCollection 2023. Acta Myol. 2023. PMID: 37091526 Free PMC article. Review.

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

North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy.

Mazzone E, Martinelli D, Berardinelli A, Messina S, D'Amico A, Vasco G, Main M, Doglio L, Politano L, Cavallaro F, Frosini S, Bello L, Carlesi A, Bonetti AM, Zucchini E, De Sanctis R, Scutifero M, Bianco F, Rossi F, Motta MC, Sacco A, Donati MA, Mongini T, Pini A, Battini R, Pegoraro E, Pane M, Pasquini E, Bruno C, Vita G, de Waure C, Bertini E, Mercuri E. Mazzone E, et al. Among authors: politano l. Neuromuscul Disord. 2010 Nov;20(11):712-6. doi: 10.1016/j.nmd.2010.06.014. Epub 2010 Jul 14. Neuromuscul Disord. 2010. PMID: 20634072

10

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.

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