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	81.	Cancer causes metabolic perturbations associated with reduced insulin-stimulated glucose uptake in peripheral tissues and impaired muscle microvascular perfusion. [electronic resource] by Han, Xiuqing Raun, Steffen H Carlsson, Michala Sjøberg, Kim A Henriquez-Olguín, Carlos Ali, Mona Lundsgaard, Anne-Marie Fritzen, Andreas M Møller, Lisbeth L V Li, Zhen Li, Jinwen Jensen, Thomas E Kiens, Bente Sylow, Lykke Producer: 20200427 In: Metabolism: clinical and experimental vol. 105 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Aberrant expression of miR-218 and miR-204 in human mesial temporal lobe epilepsy and hippocampal sclerosis-convergence on axonal guidance. [electronic resource] by Kaalund, Sanne S Venø, Morten T Bak, Mads Møller, Rikke S Laursen, Henning Madsen, Flemming Broholm, Helle Quistorff, Bjørn Uldall, Peter Tommerup, Niels Kauppinen, Sakari Sabers, Anne Fluiter, Kees Møller, Lisbeth B Nossent, Anne Y Silahtaroglu, Asli Kjems, Jørgen Aronica, Eleonora Tümer, Zeynep Producer: 20150304 In: Epilepsia vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin. [electronic resource] by Huppke, Peter Brendel, Cornelia Kalscheuer, Vera Korenke, Georg Christoph Marquardt, Iris Freisinger, Peter Christodoulou, John Hillebrand, Merle Pitelet, Gaele Wilson, Callum Gruber-Sedlmayr, Ursula Ullmann, Reinhard Haas, Stefan Elpeleg, Orly Nürnberg, Gudrun Nürnberg, Peter Dad, Shzeena Møller, Lisbeth Birk Kaler, Stephen G Gärtner, Jutta Producer: 20120312 In: American journal of human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Missense dopamine transporter mutations associate with adult parkinsonism and ADHD. [electronic resource] by Hansen, Freja H Skjørringe, Tina Yasmeen, Saiqa Arends, Natascha V Sahai, Michelle A Erreger, Kevin Andreassen, Thorvald F Holy, Marion Hamilton, Peter J Neergheen, Viruna Karlsborg, Merete Newman, Amy H Pope, Simon Heales, Simon J R Friberg, Lars Law, Ian Pinborg, Lars H Sitte, Harald H Loland, Claus Shi, Lei Weinstein, Harel Galli, Aurelio Hjermind, Lena E Møller, Lisbeth B Gether, Ulrik Producer: 20141006 In: The Journal of clinical investigation vol. 124 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. [electronic resource] by Bonnet, Crystel Riahi, Zied Chantot-Bastaraud, Sandra Smagghe, Luce Letexier, Mélanie Marcaillou, Charles Lefèvre, Gaëlle M Hardelin, Jean-Pierre El-Amraoui, Aziz Singh-Estivalet, Amrit Mohand-Saïd, Saddek Kohl, Susanne Kurtenbach, Anne Sliesoraityte, Ieva Zobor, Ditta Gherbi, Souad Testa, Francesco Simonelli, Francesca Banfi, Sandro Fakin, Ana Glavač, Damjan Jarc-Vidmar, Martina Zupan, Andrej Battelino, Saba Martorell Sampol, Loreto Claveria, Maria Antonia Catala Mora, Jaume Dad, Shzeena Møller, Lisbeth B Rodriguez Jorge, Jesus Hawlina, Marko Auricchio, Alberto Sahel, José-Alain Marlin, Sandrine Zrenner, Eberhart Audo, Isabelle Petit, Christine Producer: 20170711 In: European journal of human genetics : EJHG vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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