Your search returned 4 results.

Results
	1.	Diseases of the Synaptic Vesicle: A Potential New Group of Neurometabolic Disorders Affecting Neurotransmission. [electronic resource] by Cortès-Saladelafont, E Tristán-Noguero, A Artuch, R Altafaj, X Bayès, A García-Cazorla, A Producer: 20180126 In: Seminars in pediatric neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Sotos syndrome: a novel nonsense mutation in NSD1 gene, presenting with neonatal cutis laxa]. [electronic resource] by Cortès-Saladelafont, E Arias-Sáez, K Esteban-Oliva, D Coroleu-Lletget, W Martín-Jiménez, P Pintos-Morell, G Producer: 20111129 In: Anales de pediatria (Barcelona, Spain : 2003) vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Infantile parkinsonism and GABAergic hypotransmission in a patient with pyruvate carboxylase deficiency. [electronic resource] by Ortez, C Jou, C Cortès-Saladelafont, E Moreno, J Pérez, A Ormazábal, A Pérez-Cerdá, C Pérez, B Artuch, R Cusi, V García-Cazorla, A Producer: 20131224 In: Gene vol. 532 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial-peroxisomal protein. [electronic resource] by Díez, H Cortès-Saladelafont, E Ormazábal, A Marmiese, A Fernández Armstrong, J Matalonga, Leslie Bravo, Miren Briones, Paz Emperador, Sonia Montoya, Julio Artuch, Rafael Giros, Marisa Garcia-Cazorla, Àngels Producer: 20190104 In: Movement disorders : official journal of the Movement Disorder Society vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)