Keywords
> MYOBASE > HEALTH > medicine > disease > disease by system > metabolic diseases > hereditary metabolic diseases > mitochondrial diseases
mitochondrial diseasesSynonymscytopathie mitochondriale ;mitochondrial cytopathy ;mitochondrial disorder ;troubles mitochondriaux ;mitochondrial diseases mitochondriopathieSee also: |
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Ronchi D, Author ; Liu C ; Caporali L ; Piga D ; Li H ; Tagliavini F ; Valentino ML ; Ferro MT ; Bini P ; Zheng L ; Carelli V ; Shen B ; Comi GP | United States | 09/2019Article
Vazquez-Fonseca L, Author ; Schaefer J ; Navas-Enamorado I ; Santos-Ocana C ; Hernandez-Camacho JD ; Guerra I ; Cascajo MV ; Sanchez-Cuesta A ; Horvath Z ; Siendones E ; Jou C ; Casado M ; Gutierrez P ; Brea-Calvo G ; Lopez-Lluch G ; Fernandez-Ayala DJM ; Cortes-Rodriguez AB ; Rodriguez-Aguilera JC ; Matte C ; Ribes A ; Prieto-Soler SY ; Dominguez-Del-Toro E ; Francesco AD ; Aon MA ; Bernier M ; Salviati L ; Artuch R ; Cabo R ; Jackson S ; Navas P | Switzerland | 09/2019Article
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Poulsen NS, Author ; Madsen KL ; Hornsyld TM ; Eisum AV ; Fornander F ; Buch AE ; Stemmerik MG ; Ruiz-Ruiz C ; Krag TO ; Vissing J | Netherlands | 2019Article
Wang J ; El-Hattab AW | 26/07/2018Initial Posting: December 6, 2012; Last Update: July 26, 2018. Clinical characteristics. TK2-related mitochondrial DNA (mtDNA) maintenance defect is a phenotypic continuum that ranges from severe to mild. To date, approximately 107 individua[...]Article
Poulsen NS, Author ; Poulsen NS ; Dahlqvist JR ; Hedermann G ; Lokken N ; Vissing J | 11/07/2018Article
Ohsawa Y, Author ; Hagiwara H ; Nishimatsu SI ; Hirakawa A ; Kamimura N ; Ohtsubo H ; Fukai Y ; Murakami T ; Koga Y ; Goto YI ; Ohta S ; Sunada Y | 17/04/2018Article
Garone C, Author ; Taylor RW ; Nascimento A ; Poulton J ; Fratter C ; Dominguez Gonzalez C ; Evans JC ; Loos M ; Isohanni P ; Suomalainen A ; Ram D ; Hughes MI ; McFarland R ; Barca E ; Lopez Gomez C ; Jayawant S ; Thomas ND ; Manzur AY ; Kleinsteuber K ; Martin MA ; Kerr T ; Gorman GS ; Sommerville EW ; Chinnery PF ; Hofer M ; Karch C ; Ralph J ; Camara Y ; Madruga-Garrido M ; Dominguez-Carral J ; Ortez C ; Emperador S ; Montoya J ; Chakrapani A ; Kriger JF ; Schoenaker R ; Levin B ; Thompson JLP ; Long Y ; Rahman S ; Donati MA ; DiMauro S ; Hirano M | 30/03/2018Article
Comment in: Remodel mitochondria and get energized. [Neurology. 2018]Article
Torres-Torronteras J, Author ; Cabrera-Pérez R ; Vila-Julia F ; Viscomi C ; Camara Y ; Hirano M ; Zeviani M ; Marti R | 26/02/2018Article
Hedermann G, Author ; Dahlqvist JR ; Lokken N ; Vissing CR ; Knak KL ; Andersen LK ; Thomsen C ; Vissing J | 21/02/2018Article
Fontaine M, Author ; Kim I ; Dessein AF ; Mention-Mulliez K ; Dobbelaere D ; Douillard C ; Sole G ; Schiff M ; Jaussaud R ; Espil Taris C ; Boutron A ; Wuyts W ; Acquaviva C ; Vianey-Saban C ; Roland D ; Joncquel-Chevalier Curt M ; Vamecq J | 12/02/2018Article
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Bakhoum MF, Author ; Wu WP ; White EC ; Sengillo JD ; Sanfilippo C ; Morcos MM ; Freund KB ; Perry HD ; Sarraf D ; Tsang SH | 2018Comment in: Polymegathism as a biomarker of mitochondrial disorders. [Graefes Arch Clin Exp Ophthalmol. 2018] Mitochondrial A3243G mutation results in corneal endothelial polymegathism. [Graefes Arch Clin Exp Ophthalmol. 2018]Article
Bartsakoulia M, Author ; Pyle A ; Troncosco D ; Vial J ; Paz-Fiblas MV ; Duff J ; Griffin H ; Boczonadi V ; Lochmuller H ; Kleinle S ; Chinnery PF ; Grunert S ; Kirschner J ; Eisner V ; Horvath R | 2018