Rezultati pretrage - Giurgea, I

Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome od Benit, P, Slama, A, Cartault, F, Giurgea, I, Chretien, D, Lebon, S, Marsac, C, Munnich, A, Rotig, A, Rustin, P

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Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency od Lebon, S, Chol, M, Benit, P, Mugnier, C, Chretien, D, Giurgea, I, Kern, I, Girardin, E, Hertz-Pannier, L, de Lonlay, P, Rotig, A, Rustin, P, Munnich, A

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Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke‐like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal deve... od Bouchet, C, Steffann, J, Corcos, J, Monnot, S, Paquis, V, Rötig, A, Lebon, S, Levy, P, Royer, G, Giurgea, I, Gigarel, N, Benachi, A, Dumez, Y, Munnich, A, Bonnefont, J P

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Congenital hyperinsulinism and mosaic abnormalities of the ploidy od Giurgea, I, Sanlaville, D, Fournet, J‐C, Sempoux, C, Bellanné‐Chantelot, C, Touati, G, Hubert, L, Groos, M‐S, Brunelle, F, Rahier, J, Henquin, J‐C, Dunne, M J, Jaubert, F, Robert, J‐J, Nihoul‐Fékété, C, Vekemans, M, Junien, C, de Lonlay, P

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