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Reply: Is SIGMAR1 a confirmed FTD/MND gene?

Bernard-Marissal, Nathalie ; Médard, Jean-Jacques ; Azzedine, Hamid ; Chrast, Roman

In: Brain, 2015, vol. 138, no. 11, p. e394-e394

Consortium of Swiss Academic Libraries

Dysfunction in endoplasmic reticulum-mitochondria crosstalk underlies SIGMAR1 loss of function mediated motor neuron degeneration

Bernard-Marissal, Nathalie ; Médard, Jean-Jacques ; Azzedine, Hamid ; Chrast, Roman

In: Brain, 2015, vol. 138, no. 4, p. 875-890

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PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease

Azzedine, Hamid ; Zavadakova, Petra ; Planté-Bordeneuve, Violaine ; Vaz Pato, Maria ; Pinto, Nuno ; Bartesaghi, Luca ; Zenker, Jennifer ; Poirot, Olivier ; Bernard-Marissal, Nathalie ; Arnaud Gouttenoire, Estelle ; Cartoni, Romain ; Title, Alexandra ; Venturini, Giulia ; Médard, Jean-Jacques ; Makowski, Edward ; Schöls, Ludger ; Claeys, Kristl G. ; Stendel, Claudia ; Roos, Andreas ; Weis, Joachim ; Dubourg, Odile ; Leal Loureiro, José ; Stevanin, Giovanni ; Said, Gérard ; Amato, Anthony ; Baraban, Jay ; LeGuern, Eric ; Senderek, Jan ; Rivolta, Carlo ; Chrast, Roman

In: Human Molecular Genetics, 2013, vol. 22, no. 20, p. 4224-4232

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Expression of mitofusin 2R94Q in a transgenic mouse leads to Charcot-Marie-Tooth neuropathy type 2A

Cartoni, Romain ; Arnaud, Estelle ; Médard, Jean-Jacques ; Poirot, Olivier ; Courvoisier, Delphine S. ; Chrast, Roman ; Martinou, Jean-Claude

In: Brain, 2010, vol. 133, no. 5, p. 1460-1469

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