Blasevich F - Search Results

1

Therapeutic efficacy of 3,4-Diaminopyridine phosphate on neuromuscular junction in Pompe disease.

Bragato C, Blasevich F, Ingenito G, Mantegazza R, Maggi L. Bragato C, et al. Among authors: blasevich f. Biomed Pharmacother. 2021 May;137:111357. doi: 10.1016/j.biopha.2021.111357. Epub 2021 Feb 19. Biomed Pharmacother. 2021. PMID: 33724918 Free article.

2

Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy.

Di Blasi C, Blasevich F, Bellafiore E, Mottarelli E, Gibertini S, Zanotti S, Saredi S, Mantegazza R, Morandi L, Mora M. Di Blasi C, et al. Among authors: blasevich f. Neuromuscul Disord. 2010 May;20(5):326-9. doi: 10.1016/j.nmd.2010.02.003. Epub 2010 Mar 7. Neuromuscul Disord. 2010. PMID: 20211563

3

Novel PTRF mutation in a child with mild myopathy and very mild congenital lipodystrophy.

Ardissone A, Bragato C, Caffi L, Blasevich F, Maestrini S, Bianchi ML, Morandi L, Moroni I, Mora M. Ardissone A, et al. Among authors: blasevich f. BMC Med Genet. 2013 Sep 11;14:89. doi: 10.1186/1471-2350-14-89. BMC Med Genet. 2013. PMID: 24024685 Free PMC article.

4

Familial adult-onset Pompe disease associated with unusual clinical and histological features.

Maggi L, Salerno F, Bragato C, Saredi S, Blasevich F, Maccagnano E, Pasanisi B, Danesino C, Mora M, Morandi L. Maggi L, et al. Among authors: blasevich f. Acta Myol. 2013 Oct;32(2):85-90. Acta Myol. 2013. PMID: 24399864 Free PMC article.

5

SEPN1-related myopathy in three patients: novel mutations and diagnostic clues.

Ardissone A, Bragato C, Blasevich F, Maccagnano E, Salerno F, Gandioli C, Morandi L, Mora M, Moroni I. Ardissone A, et al. Among authors: blasevich f. Eur J Pediatr. 2016 Aug;175(8):1113-8. doi: 10.1007/s00431-015-2685-3. Epub 2016 Jan 16. Eur J Pediatr. 2016. PMID: 26780752

6

Zebrafish as a Model to Investigate Dynamin 2-Related Diseases.

Bragato C, Gaudenzi G, Blasevich F, Pavesi G, Maggi L, Giunta M, Cotelli F, Mora M. Bragato C, et al. Among authors: blasevich f. Sci Rep. 2016 Feb 4;6:20466. doi: 10.1038/srep20466. Sci Rep. 2016. PMID: 26842864 Free PMC article.

7

Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvement.

Missaglia S, Maggi L, Mora M, Gibertini S, Blasevich F, Agostoni P, Moro L, Cassandrini D, Santorelli FM, Gerevini S, Tavian D. Missaglia S, et al. Among authors: blasevich f. Neuromuscul Disord. 2017 May;27(5):481-486. doi: 10.1016/j.nmd.2017.01.011. Epub 2017 Jan 17. Neuromuscul Disord. 2017. PMID: 28258942 Free PMC article.

8

Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosis.

Zanotti S, Gibertini S, Blasevich F, Bragato C, Ruggieri A, Saredi S, Fabbri M, Bernasconi P, Maggi L, Mantegazza R, Mora M. Zanotti S, et al. Among authors: blasevich f. Matrix Biol. 2018 Dec;74:77-100. doi: 10.1016/j.matbio.2018.07.003. Epub 2018 Jul 5. Matrix Biol. 2018. PMID: 29981373

9

Long term follow-up and further molecular and histopathological studies in the LGMD1F sporadic TNPO3-mutated patient.

Gibertini S, Ruggieri A, Saredi S, Salerno F, Blasevich F, Napoli L, Moggio M, Nigro V, Morandi L, Maggi L, Mora M. Gibertini S, et al. Among authors: blasevich f. Acta Neuropathol Commun. 2018 Dec 19;6(1):141. doi: 10.1186/s40478-018-0648-4. Acta Neuropathol Commun. 2018. PMID: 30567601 Free PMC article. No abstract available.

10

Glycogen storage in a zebrafish Pompe disease model is reduced by 3-BrPA treatment.

Bragato C, Carra S, Blasevich F, Salerno F, Brix A, Bassi A, Beltrame M, Cotelli F, Maggi L, Mantegazza R, Mora M. Bragato C, et al. Among authors: blasevich f. Biochim Biophys Acta Mol Basis Dis. 2020 May 1;1866(5):165662. doi: 10.1016/j.bbadis.2020.165662. Epub 2020 Jan 7. Biochim Biophys Acta Mol Basis Dis. 2020. PMID: 31917327 Free article.

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