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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2011 | 1 |
2012 | 1 |
2014 | 1 |
2015 | 1 |
2016 | 1 |
2017 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
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7 results
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Page 1
Spectrum of muscular dystrophies associated with sarcolemmal-protein genetic defects.
Biochim Biophys Acta. 2015 Apr;1852(4):585-93. doi: 10.1016/j.bbadis.2014.07.023. Epub 2014 Jul 30.
Biochim Biophys Acta. 2015.
PMID: 25086336
Free article.
Review.
Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial.
Perrone F, Piccirillo MC, Ascierto PA, Salvarani C, Parrella R, Marata AM, Popoli P, Ferraris L, Marrocco-Trischitta MM, Ripamonti D, Binda F, Bonfanti P, Squillace N, Castelli F, Muiesan ML, Lichtner M, Calzetti C, Salerno ND, Atripaldi L, Cascella M, Costantini M, Dolci G, Facciolongo NC, Fraganza F, Massari M, Montesarchio V, Mussini C, Negri EA, Botti G, Cardone C, Gargiulo P, Gravina A, Schettino C, Arenare L, Chiodini P, Gallo C; TOCIVID-19 investigators, Italy.
Perrone F, et al.
J Transl Med. 2020 Oct 21;18(1):405. doi: 10.1186/s12967-020-02573-9.
J Transl Med. 2020.
PMID: 33087150
Free PMC article.
Clinical Trial.
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Correction to: Tocilizumab for patients with COVID-19 pneumonia. The single-arm TOCIVID-19 prospective trial.
Perrone F, Piccirillo MC, Ascierto PA, Salvarani C, Parrella R, Marata AM, Popoli P, Ferraris L, Marrocco-Trischitta MM, Ripamonti D, Binda F, Bonfanti P, Squillace N, Castelli F, Muiesan ML, Lichtner M, Calzetti C, Salerno ND, Atripaldi L, Cascella M, Costantini M, Dolci G, Facciolongo NC, Fraganza F, Massari M, Montesarchio V, Mussini C, Negri EA, Botti G, Cardone C, Gargiulo P, Gravina A, Schettino C, Arenare L, Chiodini P, Gallo C; TOCIVID-19 investigators, Italy.
Perrone F, et al.
J Transl Med. 2021 Oct 21;19(1):442. doi: 10.1186/s12967-021-03094-9.
J Transl Med. 2021.
PMID: 34674735
Free PMC article.
No abstract available.
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Limb girdle muscular dystrophies: update on genetic diagnosis and therapeutic approaches.
Nigro V, Aurino S, Piluso G.
Nigro V, et al.
Curr Opin Neurol. 2011 Oct;24(5):429-36. doi: 10.1097/WCO.0b013e32834aa38d.
Curr Opin Neurol. 2011.
PMID: 21825984
Review.
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Next generation sequencing (NGS) strategies for the genetic testing of myopathies.
Nigro V, Piluso G.
Nigro V, et al.
Acta Myol. 2012 Dec;31(3):196-200.
Acta Myol. 2012.
PMID: 23620651
Free PMC article.
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Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis.
Grandone A, Torella A, Santoro C, Giugliano T, Del Vecchio Blanco F, Mutarelli M, Cirillo M, Cirillo G, Piluso G, Capristo C, Festa A, Marzuillo P, Miraglia Del Giudice E, Perrone L, Nigro V.
Grandone A, et al.
Clin Genet. 2016 Nov;90(5):445-450. doi: 10.1111/cge.12771. Epub 2016 Apr 29.
Clin Genet. 2016.
PMID: 26940245
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Long term variation of serum levels of uremic toxins in patients treated by post-dilution high volume on-line hemodiafiltration in comparison to standard low-flux bicarbonate dialysis: results from the REDERT study.
Panichi V, Rocchetti MT, Scatena A, Rosati A, Migliori M, Pizzarelli F, Gesualdo L; REDERT Study group.
Panichi V, et al.
J Nephrol. 2017 Aug;30(4):583-591. doi: 10.1007/s40620-017-0381-2. Epub 2017 Mar 24.
J Nephrol. 2017.
PMID: 28337716
Clinical Trial.
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