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Author Scaglia F |
Available item(s) by this author (7)
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Article
Karaa A ; Bertini E ; Carelli V ; Cohen BH ; Enns GM ; Falk MJ ; Goldstein A ; Gorman GS ; Haas R ; Hirano M ; Klopstock T ; Koenig MK ; Kornblum C ; Lamperti C ; Lehman A ; Longo N ; Molnar MJ ; Parikh S ; Phan H ; Pitceathly RDS ; Saneto R ; Scaglia F ; Servidei S ; Tarnopolsky M ; Toscano A ; van Hove JLK ; Vissing J ; Vockley J ; Finman JS ; Brown DA ; Shiffer JA ; Mancuso M | 02/06/2023Article
Pillai NR ; Amin H ; Gijavanekar C ; Liu N ; Issaq N ; Broniowska KA ; Bertuch AA ; Sutton VR ; Elsea SH ; Scaglia F | United States | 2020Article
Xiao C ; Astiazaran-Symonds E ; Basu S ; Kisling M ; Scaglia F ; Chapman KA ; Wang Y ; Vockley J ; Ferreira CR | United States | 2020Article
Neurology Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy (MOTOR trial)
Madsen KL ; Buch AE ; Cohen BH ; Falk MJ ; Goldsberry A ; Goldstein A ; Karaa A ; Koenig MK ; Muraresku CC ; Meyer C ; O'Grady M ; Scaglia F ; Shieh PB ; Vockley J ; Zolkipli-Cunningham Z ; Haller RG ; Vissing J | United States | 01/2020Article
El-Hattab AW ; Almannai M ; Scaglia F | 29/11/2018Initial Posting: February 27, 2001; Last Update: November 29, 2018. Clinical characteristics. MELAS (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes) is a multisystem disorder with protean manifestations. The vast [...]Article
El-Hattab AW ; Scaglia F | 18/05/2017Initial Posting: May 26, 2009; Last Revision: May 18, 2017. Clinical characteristics. SUCLA2-related mitochondrial DNA (mtDNA) depletion syndrome, encephalomyopathic form with methylmalonic aciduria is characterized by onset of the following[...]