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	81.	Hepatic neddylation targets and stabilizes electron transfer flavoproteins to facilitate fatty acid β-oxidation. [electronic resource] by Zhang, Xueying Zhang, Yao-Lin Qiu, Guihua Pian, Lili Guo, Lu Cao, Huanling Liu, Jian Zhao, Yawei Li, Xin Xu, Zhe Huang, Xiaofeng Huang, Jingru Dong, Jie Shen, Beifen Wang, Hong-Xia Ying, Xiaomin Zhang, Weiping J Cao, Xuetao Zhang, Jiyan Producer: 20200615 In: Proceedings of the National Academy of Sciences of the United States of America vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	Equine acquired multiple acyl-CoA dehydrogenase deficiency (MADD) in 14 horses associated with ingestion of Maple leaves (Acer pseudoplatanus) covered with European tar spot (Rhytisma acerinum). [electronic resource] by van der Kolk, J H Wijnberg, I D Westermann, C M Dorland, L de Sain-van der Velden, M G M Kranenburg, L C Duran, M Dijkstra, J A van der Lugt, J J Wanders, R J A Gruys, E Producer: 20110127 In: Molecular genetics and metabolism vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	A boy with neck weakness. [electronic resource] by Yiş, Uluç Becker, Kerstin Çırak, Sebahattin Producer: 20191021 In: Neuromuscular disorders : NMD vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patients. [electronic resource] by Gitiaux, Cyril Roze, Emmanuel Kinugawa, Kiyoka Flamand-Rouvière, Constance Boddaert, Nathalie Apartis, Emmanuelle Valayannopoulos, Vassili Touati, Guy Motte, Jacques Devos, David Mention, Karine Dobbelaere, Dries Rodriguez, Diana Roubertie, Agathe Chabrol, Brigitte Feillet, François Vidailhet, Marie Bahi-Buisson, Nadia Producer: 20090408 In: Movement disorders : official journal of the Movement Disorder Society vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Pregnancy of a patient with multiple Acyl-CoA dehydrogenation deficiency (MADD). [electronic resource] by Trakadis, Y Kadlubowska, D Barnes, R Mitchell, J Spector, E Frerman, F Melancon, S Producer: 20121203 In: Molecular genetics and metabolism vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Brown-Vialetto-Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment. [electronic resource] by Bosch, Annet M Abeling, Nico G G M Ijlst, Lodewijk Knoester, Hennie van der Pol, W Ludo Stroomer, Alida E M Wanders, Ronald J Visser, Gepke Wijburg, Frits A Duran, Marinus Waterham, Hans R Producer: 20110512 In: Journal of inherited metabolic disease vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	87.	Mitochondrial fatty acid oxidation defects--remaining challenges. [electronic resource] by Gregersen, Niels Andresen, Brage S Pedersen, Christina B Olsen, Rikke K J Corydon, Thomas J Bross, Peter Producer: 20090128 In: Journal of inherited metabolic disease vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Evidence for genetic heterogeneity in D-2-hydroxyglutaric aciduria. [electronic resource] by Kranendijk, Martijn Struys, Eduard A Gibson, K Michael Wickenhagen, Wjera V Abdenur, Jose E Buechner, Jochen Christensen, Ernst de Kremer, Raquel Dodelson Errami, Abdellatif Gissen, Paul Gradowska, Wanda Hobson, Emma Islam, Lily Korman, Stanley H Kurczynski, Thaddeus Maranda, Bruno Meli, Concetta Rizzo, Cristiano Sansaricq, Claude Trefz, Friedrich K Webster, Rachel Jakobs, Cornelis Salomons, Gajja S Producer: 20101029 In: Human mutation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	Glutaric aciduria type 2, late onset type in Thai siblings with myopathy. [electronic resource] by Wasant, Pornswan Kuptanon, Chulaluck Vattanavicharn, Nithiwat Liammongkolkul, Somporn Ratanarak, Pisanu Sangruchi, Tumtip Yamaguchi, Seiji Producer: 20110121 In: Pediatric neurology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	A 3-Month-Old Boy With Progressive Weakness. [electronic resource] by Kim, Soo Yeon Ko, Jung Min Choi, Sun Ah Cho, Anna Lee, Jin Sook Lim, Byung Chan Kim, Ki Joong Chae, Jong-Hee Producer: 20190305 In: Brain pathology (Zurich, Switzerland) vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	A Historical Cohort Study on the Efficacy of Glucocorticoids and Riboflavin Among Patients with Late-onset Multiple Acyl-CoA Dehydrogenase Deficiency. [electronic resource] by Liu, Xin-Yi Wang, Zhi-Qiang Wang, Dan-Ni Lin, Min-Ting Wang, Ning Producer: 20170123 In: Chinese medical journal vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency with unknown genetic defect. [electronic resource] by Cotelli, Maria Sofia Vielmi, Valentina Rimoldi, Marco Rizzetto, Manuela Castellotti, Barbara Bertasi, Valeria Todeschini, Alice Gregorelli, Valeria Baronchelli, Carla Gellera, Cinzia Padovani, Alessandro Filosto, Massimiliano Producer: 20130905 In: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	93.	Mutations at the flavin binding site of ETF:QO yield a MADD-like severe phenotype in Drosophila. [electronic resource] by Alves, Ema Henriques, Bárbara J Rodrigues, João V Prudêncio, Pedro Rocha, Hugo Vilarinho, Laura Martinho, Rui G Gomes, Cláudio M Producer: 20130118 In: Biochimica et biophysica acta vol. 1822 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	94.	Use of guidelines improves the neurological outcome in glutaric aciduria type I. [electronic resource] by Heringer, Jana Boy, S P Nikolas Ensenauer, Regina Assmann, Birgit Zschocke, Johannes Harting, Inga Lücke, Thomas Maier, Esther M Mühlhausen, Chris Haege, Gisela Hoffmann, Georg F Burgard, Peter Kölker, Stefan Producer: 20101129 In: Annals of neurology vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	95.	Some notes on fatal acquired multiple acyl-CoA dehydrogenase deficiency (MADD) in a two-year-old warmblood stallion and European tar spot (Rhytisma acerinum). [electronic resource] by van der Kolk, J H Boelens, R Halkes, S B A Wijnberg, I D de Sain-van der Velden, M G M Ippel, J H Producer: 20131119 In: The veterinary quarterly vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	96.	Quantification of hypoglycin A as butyl ester. [electronic resource] by Sander, Johannes Terhardt, Michael Sander, Stefanie Janzen, Nils Producer: 20170213 In: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences vol. 1029-1030 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	97.	Conformational analysis of the riboflavin-responsive ETF:QO-p.Pro456Leu variant associated with mild multiple acyl-CoA dehydrogenase deficiency. [electronic resource] by Lucas, Tânia G Henriques, Bárbara J Gomes, Cláudio M Producer: 20200720 In: Biochimica et biophysica acta. Proteins and proteomics vol. 1868 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	98.	Long-term outcomes of a patient with late-onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutations in ETFDH: A case report. [electronic resource] by Wang, Juan Wu, Jun-Cang Yu, Xu-En Han, Yong-Zhu Yang, Ren-Min Producer: 20190107 In: Medicine vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	99.	Nucleotide exchange factor Rab3GEP requires DENN and non-DENN elements for activation and targeting of Rab27a. [electronic resource] by Sanzà, Paolo Evans, Richard D Briggs, Deborah A Cantero, Marta Montoliu, Lluis Patel, Shyamal Sviderskaya, Elena V Itzen, Aymelt Figueiredo, Ana C Seabra, Miguel C Hume, Alistair N Producer: 20200611 In: Journal of cell science vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	100.	MR imaging findings of glutaric aciduria type II. [electronic resource] by Mumtaz, H A Gupta, V Singh, P Marwaha, R K Khandelwal, N Producer: 20100928 In: Singapore medical journal vol. 51 Availability: No items available. Save to lists Add to cart (remove)

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