Saredi S - Search Results

1

Altered extracellular matrix transcript expression and protein modulation in primary Duchenne muscular dystrophy myotubes.

Zanotti S, Saredi S, Ruggieri A, Fabbri M, Blasevich F, Romaggi S, Morandi L, Mora M. Zanotti S, et al. Among authors: saredi s. Matrix Biol. 2007 Oct;26(8):615-24. doi: 10.1016/j.matbio.2007.06.004. Epub 2007 Jun 27. Matrix Biol. 2007. PMID: 17662584

2

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: saredi s. Matrix Biol. 2018 Dec;74:77-100. doi: 10.1016/j.matbio.2018.07.003. Epub 2018 Jul 5. Matrix Biol. 2018. PMID: 29981373

3

Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement.

Saredi S, Ruggieri A, Mottarelli E, Ardissone A, Zanotti S, Farina L, Morandi L, Mora M, Moroni I. Saredi S, et al. Muscle Nerve. 2009 Jun;39(6):845-8. doi: 10.1002/mus.21271. Muscle Nerve. 2009. PMID: 19396839

4

A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation.

Saredi S, Gibertini S, Ardissone A, Fusco I, Zanotti S, Blasevich F, Morandi L, Moroni I, Mora M. Saredi S, et al. Eur J Paediatr Neurol. 2014 May;18(3):404-8. doi: 10.1016/j.ejpn.2013.10.005. Epub 2013 Oct 27. Eur J Paediatr Neurol. 2014. PMID: 24183756

5

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: saredi s. 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

6

Fibrosis and inflammation are greater in muscles of beta-sarcoglycan-null mouse than mdx mouse.

Gibertini S, Zanotti S, Savadori P, Curcio M, Saredi S, Salerno F, Andreetta F, Bernasconi P, Mantegazza R, Mora M. Gibertini S, et al. Among authors: saredi s. Cell Tissue Res. 2014 May;356(2):427-43. doi: 10.1007/s00441-014-1854-4. Epub 2014 Apr 11. Cell Tissue Res. 2014. PMID: 24723230

7

DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies.

Ruggieri A, Saredi S, Zanotti S, Pasanisi MB, Maggi L, Mora M. Ruggieri A, et al. Among authors: saredi s. Front Mol Biosci. 2016 Sep 30;3:63. doi: 10.3389/fmolb.2016.00063. eCollection 2016. Front Mol Biosci. 2016. PMID: 27747217 Free PMC article. Review.

8

Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease.

Saredi S, Ardissone A, Ruggieri A, Mottarelli E, Farina L, Rinaldi R, Silvestri E, Gandioli C, D'Arrigo S, Salerno F, Morandi L, Grammatico P, Pantaleoni C, Moroni I, Mora M. Saredi S, et al. J Neurol Sci. 2012 Jul 15;318(1-2):45-50. doi: 10.1016/j.jns.2012.04.008. Epub 2012 May 2. J Neurol Sci. 2012. PMID: 22554691 Free PMC article.

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: saredi s. 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

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: saredi s. Acta Myol. 2013 Oct;32(2):85-90. Acta Myol. 2013. PMID: 24399864 Free PMC article.

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