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内部出版物
在“
Elsevier电子期刊
”中,
命中:
4
条,耗时:小于0.01 秒
1.
In Vivo Correction of COX Deficiency by Activation of the AMPK/PGC-1α Axis
作者:
Carlo Viscomi
1
;
4
;
Emanuela Bottani
1
;
4
;
Gabriele Civiletto
1
;
Raffaele Cerutti
1
;
Maurizio Moggio
2
;
Gigliola
Fagiolari
2
;
Eric
;
A. Schon
3
;
Costanza Lamperti
1
;
Massimo Zeviani
1
;
zeviani@istituto-besta.it"" rel=""nofollow
刊名:Cell Metabolism
出版年:2011
2.
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP
作者:
Anna Bersano
;
Roberto Del Bo
;
Costanza Lamperti
;
Serena Ghezzi
;
Gigliola
Fagiolari
;
Francesco Fortunato
;
Elena Ballabio
;
Maurizio Moggio
;
Livia C
;
elise
;
Daniela Galimberti
;
Roberta Virgilio
;
Silvia La
关键词:
Inclusion body myopathy
;
Frontotemporal dementia
;
Valosin-containing protein
刊名:Neurobiology of Aging
出版年:2009
3.
Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene
作者:
Costanza Lamperti
;
Rachele Cagliani
;
Patrizia Ciscato
;
Isabella Moroni
;
Maurizio Viri
;
Antonio Romeo
;
Gigliola
Fagiolari
;
Alessandro Prelle
;
Giacomo Pietro Comi
;
Nereo Bresolin and Maurizio Moggio
关键词:
α
;
-Dystroglycan
;
Congenital muscular dystrophy
;
Glycosylation
;
Fukutin-related protein
刊名:Journal of the Neurological Sciences
出版年:2006
4.
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy
作者:
Monica Sciacco
;
Alessandro Prelle
;
Gigliola
Fagiolari
;
Andreina Bordoni
;
Marco Crimi
;
Alessio Di Fonzo
;
Patrizia Ciscato
;
Costanza Lamperti
;
Elisabetta D'Adda
;
Stefano Jann
et al.
关键词:
Myoglobinuria
;
CPT deficiency
;
Mitochondrial disorder
;
RRFs
刊名:Journal of the Neurological Sciences
出版年:2005
1
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