Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2 von Stemerdink, M., García-Bohórquez, B., Schellens, R., Garcia-Garcia, G., Van Wijk, E., Millan, J. M.

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Agomelatine: mechanism of action and pharmacological profile in relation to antidepressant properties von Guardiola‐Lemaitre, B, De Bodinat, C, Delagrange, P, Millan, M J, Munoz, C, Mocaër, E

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The Added Value of Apparent Diffusion Coefficient to Cerebral Blood Volume in the Preoperative Grading of Diffuse Gliomas von HILARIO, A, RAMOS, A, PEREZ-NUNEZ, A, SALVADOR, E, MILLAN, J. M, LAGARES, A, SEPULVEDA, J. M, GONZALEZ-LEON, P, HERNANDEZ-LAIN, A, RICOY, J. R

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The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells von Jacoupy, M., Hamon-Keromen, E., Ordureau, A., Erpapazoglou, Z., Coge, F., Corvol, J.-C., Nosjean, O., Mannoury la Cour, C., Millan, M. J., Boutin, J. A., Harper, J. W., Brice, A., Guedin, D., Gautier, C. A., Corti, O.

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Physical interaction between the serotonin transporter and neuronal nitric oxide synthase underlies reciprocal modulation of their activity von Chanrion, B, Mannoury la Cour, C, Bertaso, F, Lerner-Natoli, M, Freissmuth, M, Millan, M.J, Bockaert, J, Marin, P

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Severe Traumatic Head Injury: Prognostic Value of Brain Stem Injuries Detected at MRI von HILARIO, A, RAMOS, A, MILLAN, J. M, SALVADOR, E, GOMEZ, P. A, CICUENDEZ, M, DIEZ-LOBATO, R, LAGARES, A

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The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor von Bernal, S, Alías, L, Barceló, M J, Also-Rallo, E, Martínez-Hernández, R, Gámez, J, Guillén-Navarro, E, Rosell, J, Hernando, I, Rodríguez-Alvarez, F J, Borrego, S, Millán, J M, Hernández-Chico, C, Baiget, M, Fuentes-Prior, P, Tizzano, E F

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Genetics of Charcot-Marie-Tooth disease type 4A: mutations, inheritance, phenotypic variability, and founder effect von Claramunt, R, Pedrola, L, Sevilla, T, López de Munain, A, Berciano, J, Cuesta, A, Sánchez-Navarro, B, Millán, J M, Saifi, G M, Lupski, J R, Vílchez, J J, Espinós, C, Palau, F

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Synergistic activation of AMPK prevents from polyglutamine-induced toxicity in Caenorhabditis elegans von Gómez-Escribano, AP, Bono-Yagüe, J, García-Gimeno, MA, Sequedo, MD, Hervás, D, Fornés-Ferrer, V, Torres-Sánchez, SC, Millán, JM, Sanz, P, Vázquez-Manrique, RP

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Improving detection and genetic counseling in carriers of spinal muscular atrophy with two copies of the SMN1 gene von Alías, L., Barceló, M.J., Bernal, S., Martínez-Hernández, R., Also-Rallo, E., Vázquez, C., Santana, A., Millán, J.M., Baiget, M., Tizzano, E.F.

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The induction of pain: an integrative review von Millan, M J

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Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth von Sevilla, T, Martínez-Rubio, D, Márquez, C, Paradas, C, Colomer, J, Jaijo, T, Millán, JM, Palau, F, Espinós, C

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Ketamine enhances structural plasticity in mouse mesencephalic and human iPSC-derived dopaminergic neurons via AMPAR-driven BDNF and mTOR signaling von Cavalleri, L, Merlo Pich, E, Millan, M J, Chiamulera, C, Kunath, T, Spano, P F, Collo, G

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Acute perfusion changes after spontaneous SAH: a perfusion CT study von Lagares, Alfonso, Cicuendez, Marta, Ramos, Ana, Salvador, Elena, Alén, Jose F., Kaen, Ariel, Jiménez-Roldán, Luis, Millán, J. M.

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Spanish MYH7 founder mutation of Italian ancestry causing a large cluster of Laing myopathy patients von Muelas, N, Hackman, P, Luque, H, Suominen, T, Espinós, C, Garcés-Sánchez, M, Sevilla, T, Azorín, I, Millán, JM, Udd, B, Vílchez, JJ

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Simultaneous quantification of serotonin, dopamine and noradrenaline levels in single frontal cortex dialysates of freely-moving rats reveals a complex pattern of reciprocal auto-... von Gobert, A, Rivet, J.-M, Audinot, V, Newman-Tancredi, A, Cistarelli, L, Millan, M.J

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The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4 von Claramunt, R, Sevilla, T, Lupo, V, Cuesta, A, Millán, JM, Vílchez, JJ, Palau, F, Espinós, C

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Functional analysis of splicing mutations in MYO7A and USH2A genes von Jaijo, T, Aller, E, Aparisi, MJ, García-García, G, Hernan, I, Gamundi, MJ, Nájera, C, Carballo, M, Millán, JM

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Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II von Aller, E, Jaijo, T, Beneyto, M, Nájera, C, Oltra, S, Ayuso, C, Baiget, M, Carballo, M, Antiñolo, G, Valverde, D, Moreno, F, Vilela, C, Collado, D, Pérez-Garrigues, H, Navea, A, Millán, J M

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CRF1 receptor antagonists do not reverse pharmacological disruption of prepulse inhibition in rodents von Douma, T. N., Millan, M. J., Boulay, D., Griebel, G., Verdouw, P. M., Westphal, K. G., Olivier, B., Groenink, L.

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