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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2012 | 1 |
2013 | 1 |
2014 | 1 |
2015 | 1 |
2017 | 1 |
2018 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
Congenital myopathies: clinical phenotypes and new diagnostic tools.
Ital J Pediatr. 2017 Nov 15;43(1):101. doi: 10.1186/s13052-017-0419-z.
Ital J Pediatr. 2017.
PMID: 29141652
Free PMC article.
Review.
The empowerment of translational research: lessons from laminopathies.
Benedetti S, Bernasconi P, Bertini E, Biagini E, Boriani G, Capanni C, Carboni N, Cenacchi G, Columbaro M, D'Adamo M, D'Amico A, D'Apice MR, Fontana M, Gambineri A, Lattanzi G, Liguori R, Maraldi NM, Mazzanti L, Mercuri E, Mongini T, Morandi LO, Neri I, Nigro G, Novelli G, Ortolani M, Pasquali R, Pini A, Petrini S, Politano L, Previtali S, Pucci L, Rapezzi C, Ricci G, Rodolico C, Sbraccia P, Scarano E, Siciliano G, Squarzoni S, Toscano A, Vercelli L, Ziacchi M.
Benedetti S, et al. Among authors: morandi lo.
Orphanet J Rare Dis. 2012 Jun 12;7:37. doi: 10.1186/1750-1172-7-37.
Orphanet J Rare Dis. 2012.
PMID: 22691392
Free PMC article.
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SMA-miRs (miR-181a-5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples.
Abiusi E, Infante P, Cagnoli C, Lospinoso Severini L, Pane M, Coratti G, Pera MC, D'Amico A, Diano F, Novelli A, Spartano S, Fiori S, Baranello G, Moroni I, Mora M, Pasanisi MB, Pocino K, Le Pera L, D'Amico D, Travaglini L, Ria F, Bruno C, Locatelli D, Bertini ES, Morandi LO, Mercuri E, Di Marcotullio L, Tiziano FD.
Abiusi E, et al. Among authors: morandi lo.
Elife. 2021 Sep 20;10:e68054. doi: 10.7554/eLife.68054.
Elife. 2021.
PMID: 34542403
Free PMC article.
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Undiagnosed myopathy before surgery and safe anaesthesia table.
Trevisan CP, Accorsi A, Morandi LO, Mongini T, Savoia G, Gravino E, Angelini C, Tegazzin V.
Trevisan CP, et al. Among authors: morandi lo.
Acta Myol. 2013 Oct;32(2):100-5.
Acta Myol. 2013.
PMID: 24399867
Free PMC article.
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Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study.
Astrea G, Romano A, Angelini C, Antozzi CG, Barresi R, Battini R, Battisti C, Bertini E, Bruno C, Cassandrini D, Fanin M, Fattori F, Fiorillo C, Guerrini R, Maggi L, Mercuri E, Morani F, Mora M, Moro F, Pezzini I, Picillo E, Pinelli M, Politano L, Rubegni A, Sanseverino W, Savarese M, Striano P, Torella A, Trevisan CP, Trovato R, Zaraieva I, Muntoni F, Nigro V, D'Amico A, Santorelli FM; Italian CMD Network.
Astrea G, et al.
Orphanet J Rare Dis. 2018 Sep 26;13(1):170. doi: 10.1186/s13023-018-0863-x.
Orphanet J Rare Dis. 2018.
PMID: 30257713
Free PMC article.
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A chaperone enhances blood α-glucosidase activity in Pompe disease patients treated with enzyme replacement therapy.
Parenti G, Fecarotta S, la Marca G, Rossi B, Ascione S, Donati MA, Morandi LO, Ravaglia S, Pichiecchio A, Ombrone D, Sacchini M, Pasanisi MB, De Filippi P, Danesino C, Della Casa R, Romano A, Mollica C, Rosa M, Agovino T, Nusco E, Porto C, Andria G.
Parenti G, et al. Among authors: morandi lo.
Mol Ther. 2014 Nov;22(11):2004-12. doi: 10.1038/mt.2014.138. Epub 2014 Jul 23.
Mol Ther. 2014.
PMID: 25052852
Free PMC article.
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Changing Characteristics of Late-Onset Pompe Disease Patients in Italy: Data from the Pompe Registry.
Angelini C, Bembi B, Burlina A, Filosto M, Maioli MA, Morandi LO, Parini R, Pegoraro E, Ravaglia S, Servidei S, Toscano A, Tugnoli V.
Angelini C, et al. Among authors: morandi lo.
J Neuromuscul Dis. 2015;2(s1):S36-S37.
J Neuromuscul Dis. 2015.
PMID: 27858631
No abstract available.
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