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Items: 1 to 20 of 76

1.

Effects of short-to-long term Enzyme Replacement Therapy (ERT) on skeletal muscle tissue in Late Onset Pompe disease (LOPD).

Ripolone M, Violano R, Ronchi D, Mondello S, Nascimbeni A, Colombo I, Fagiolari G, Bordoni A, Fortunato F, Lucchini V, Saredi S, Filosto M, Musumeci O, Tonin P, Mongini T, Previtali S, Morandi L, Angelini C, Mora M, Sandri M, Sciacco M, Toscano A, Comi GP, Moggio M.

Neuropathol Appl Neurobiol. 2017 Jun 2. doi: 10.1111/nan.12414. [Epub ahead of print]

PMID:
28574618
2.

Genetic predisposition to breath-hold diving-induced hemoptysis: Preliminary study.

Cialoni D, Marabotti C, Sponsiello N, Pieri M, Balestra C, Lucchini V, Marroni A.

Undersea Hyperb Med. 2015 Jan-Feb;42(1):75-83.

PMID:
26094307
3.

Impaired Muscle Mitochondrial Biogenesis and Myogenesis in Spinal Muscular Atrophy.

Ripolone M, Ronchi D, Violano R, Vallejo D, Fagiolari G, Barca E, Lucchini V, Colombo I, Villa L, Berardinelli A, Balottin U, Morandi L, Mora M, Bordoni A, Fortunato F, Corti S, Parisi D, Toscano A, Sciacco M, DiMauro S, Comi GP, Moggio M.

JAMA Neurol. 2015 Jun;72(6):666-75. doi: 10.1001/jamaneurol.2015.0178. Erratum in: JAMA Neurol. 2015 Oct;72(10):1210.

4.

Prevalence of Asymptomatic Vertebral Fractures in Late-Onset Pompe Disease.

Bertoldo F, Zappini F, Brigo M, Moggio M, Lucchini V, Angelini C, Semplicini C, Filosto M, Ravaglia S, Cotelli S, Todeschini A, Scarpelli M, Pancheri S, Tonin P.

J Neuromuscul Dis. 2015;2(s1):S13. No abstract available.

PMID:
27858611
5.

Prevalence of asymptomatic vertebral fractures in late-onset Pompe disease.

Bertoldo F, Zappini F, Brigo M, Moggio M, Lucchini V, Angelini C, Semplicini C, Filosto M, Ravaglia S, Cotelli S, Todeschini A, Scarpelli M, Pancheri S, Tonin P.

J Clin Endocrinol Metab. 2015 Feb;100(2):401-6. doi: 10.1210/jc.2014-2763. Epub 2014 Nov 14.

PMID:
25396301
6.

Novel CLN3 mutation causing autophagic vacuolar myopathy.

Cortese A, Tucci A, Piccolo G, Galimberti CA, Fratta P, Marchioni E, Grampa G, Cereda C, Grieco G, Ricca I, Pittman A, Ciscato P, Napoli L, Lucchini V, Ripolone M, Violano R, Fagiolari G, Mole SE, Hardy J, Moglia A, Moggio M.

Neurology. 2014 Jun 10;82(23):2072-6. doi: 10.1212/WNL.0000000000000490. Epub 2014 May 14.

7.

Mitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock.

Protti A, Fortunato F, Caspani ML, Pluderi M, Lucchini V, Grimoldi N, Solimeno LP, Fagiolari G, Ciscato P, Zella SM, Moggio M, Comi GP, Gattinoni L.

PLoS One. 2014 May 1;9(5):e96205. doi: 10.1371/journal.pone.0096205. eCollection 2014.

8.

Postmortem microcomputed tomography (micro-CT) of small fetuses and hearts.

Lombardi CM, Zambelli V, Botta G, Moltrasio F, Cattoretti G, Lucchini V, Fesslova V, Cuttin MS.

Ultrasound Obstet Gynecol. 2014 Nov;44(5):600-9. doi: 10.1002/uog.13330. Epub 2014 Oct 13.

9.

Null ABCA3 in humans: large homozygous ABCA3 deletion, correlation to clinical-pathological findings.

Carrera P, Ferrari M, Presi S, Ventura L, Vergani B, Lucchini V, Cogo PE, Carnielli VP, Somaschini M, Tagliabue P.

Pediatr Pulmonol. 2014 Mar;49(3):E116-20. doi: 10.1002/ppul.22983. Epub 2014 Jan 14.

PMID:
24420869
10.

POLG1 mutations and stroke like episodes: a distinct clinical entity rather than an atypical MELAS syndrome.

Cheldi A, Ronchi D, Bordoni A, Bordo B, Lanfranconi S, Bellotti MG, Corti S, Lucchini V, Sciacco M, Moggio M, Baron P, Comi GP, Colombo A, Bersano A; Lombardia GENS collaborators.

BMC Neurol. 2013 Jan 15;13:8. doi: 10.1186/1471-2377-13-8.

11.

Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients.

Magri F, Del Bo R, D'Angelo MG, Sciacco M, Gandossini S, Govoni A, Napoli L, Ciscato P, Fortunato F, Brighina E, Bonato S, Bordoni A, Lucchini V, Corti S, Moggio M, Bresolin N, Comi GP.

Neuromuscul Disord. 2012 Nov;22(11):934-43. doi: 10.1016/j.nmd.2012.05.001. Epub 2012 Jun 27.

12.

Cooperative nucleophilic-electrophilic organocatalysis by ionic liquids.

Lucchini V, Noè M, Selva M, Fabris M, Perosa A.

Chem Commun (Camb). 2012 May 25;48(42):5178-80. doi: 10.1039/c2cc31099f. Epub 2012 Apr 19.

PMID:
22517474
13.

Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation.

Ronchi D, Bordoni A, Cosi A, Rizzuti M, Fassone E, Di Fonzo A, Servida M, Sciacco M, Collotta M, Ronzoni M, Lucchini V, Mattioli M, Moggio M, Bresolin N, Corti S, Comi GP.

Biochem Biophys Res Commun. 2011 Aug 26;412(2):245-8. doi: 10.1016/j.bbrc.2011.07.076. Epub 2011 Jul 27.

PMID:
21819970
14.

Metal-promoted synthesis of amidines containing the model nucleobases 1-methylcytosine and 9-methyladenine.

Montagner D, Zangrando E, Borsato G, Lucchini V, Longato B.

Dalton Trans. 2011 Sep 14;40(34):8664-74. doi: 10.1039/c1dt10638d. Epub 2011 Jul 27.

PMID:
21796298
15.

Two novel mutations in PEO1 (twinkle) gene associated with chronic external ophthalmoplegia.

Ronchi D, Fassone E, Bordoni A, Sciacco M, Lucchini V, Di Fonzo A, Rizzuti M, Colombo I, Napoli L, Ciscato P, Moggio M, Cosi A, Collotta M, Corti S, Bresolin N, Comi GP.

J Neurol Sci. 2011 Sep 15;308(1-2):173-6. doi: 10.1016/j.jns.2011.05.042.

16.

Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up.

Magri F, Govoni A, D'Angelo MG, Del Bo R, Ghezzi S, Sandra G, Turconi AC, Sciacco M, Ciscato P, Bordoni A, Tedeschi S, Fortunato F, Lucchini V, Bonato S, Lamperti C, Coviello D, Torrente Y, Corti S, Moggio M, Bresolin N, Comi GP.

J Neurol. 2011 Sep;258(9):1610-23. doi: 10.1007/s00415-011-5979-z. Epub 2011 Mar 12.

PMID:
21399986
17.

Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing.

Magri F, Del Bo R, D'Angelo MG, Govoni A, Ghezzi S, Gandossini S, Sciacco M, Ciscato P, Bordoni A, Tedeschi S, Fortunato F, Lucchini V, Cereda M, Corti S, Moggio M, Bresolin N, Comi GP.

BMC Med Genet. 2011 Mar 11;12:37. doi: 10.1186/1471-2350-12-37.

18.

The reaction of primary aromatic amines with alkylene carbonates for the selective synthesis of bis-N-(2-hydroxy)alkylanilines: the catalytic effect of phosphonium-based ionic liquids.

Selva M, Fabris M, Lucchini V, Perosa A, Noè M.

Org Biomol Chem. 2010 Nov 21;8(22):5187-98. doi: 10.1039/c0ob00105h. Epub 2010 Sep 15.

PMID:
20844790
19.

Interstitial pressure and lung oedema in chronic hypoxia.

Rivolta I, Lucchini V, Rocchetti M, Kolar F, Palazzo F, Zaza A, Miserocchi G.

Eur Respir J. 2011 Apr;37(4):943-9. doi: 10.1183/09031936.00066710. Epub 2010 Aug 6.

20.

Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.

Crugnola V, Lamperti C, Lucchini V, Ronchi D, Peverelli L, Prelle A, Sciacco M, Bordoni A, Fassone E, Fortunato F, Corti S, Silani V, Bresolin N, Di Mauro S, Comi GP, Moggio M.

Arch Neurol. 2010 Jul;67(7):849-54. doi: 10.1001/archneurol.2010.128.

PMID:
20625092

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