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Minerva Anestesiologica|October 24, 2007
Epidural analgesia in children: planning, organization and development of a new programP M Ingelmo, C Gelsumino, A P Acosta, et al.
Brain : a Journal of Neurology|January 20, 2018
SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiencyAdriana P Rebelo, Dimah Saade, Claudia V Pereira, et al.
Neurology|June 20, 1998
Clinical manifestations of mitochondrial DNA depletionT H Vu, M Sciacco, K Tanji, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2024
The contribution of mitochondria-associated ER membranes to cholesterol homeostasisJ Montesinos, K Kabra, M Uceda, et al.
The EMBO Journal|August 16, 2012
Upregulated function of mitochondria-associated ER membranes in Alzheimer diseaseEstela Area-Gomez, Maria Del Carmen Lara Castillo, Marc D Tambini, et al.
The American Journal of Pathology|October 17, 2009
Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondriaEstela Area-Gomez, Ad J C de Groof, Istvan Boldogh, et al.
Human Molecular Genetics|March 14, 2008
A functionally dominant mitochondrial DNA mutationSabrina Sacconi, Leonardo Salviati, Yutaka Nishigaki, et al.
Orphanet Journal of Rare Diseases|April 21, 2012
Copper and bezafibrate cooperate to rescue cytochrome c oxidase deficiency in cells of patients with SCO2 mutationsAlberto Casarin, Gianpietro Giorgi, Vanessa Pertegato, et al.
Human Molecular Genetics|January 17, 2019
MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergeticsDelfina Larrea, Marta Pera, Adriano Gonnelli, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 30, 2015
ATP-binding cassette transporters and sterol O-acyltransferases interact at membrane microdomains to modulate sterol uptake and esterificationSonia Gulati, Dina Balderes, Christine Kim, et al.
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