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	21.	[Pyelonephritis in childhood]. [electronic resource] by Ortiz, F E Caria, M A Traverso, M A De Fernandez, N R De Veber, I de C Canepa, C Caceres, H Hurtig, C Producer: 19711130 In: Revista chilena de pediatria vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	22.	[Pharmaceutical care for older adults. Application of STOPP-START criteria]. [electronic resource] by Palchik, V Bianchi, M Colautti, M Salamano, M Pires, N Catena, J M Dolza, M L Tassone, V Lillini, G Paciaroni, J Traverso, M L Producer: 20210701 In: Journal of healthcare quality research vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Novel FAM126A mutations in hypomyelination and congenital cataract disease. [electronic resource] by Traverso, M Assereto, S Gazzerro, E Savasta, S Abdalla, E M Rossi, A Baldassari, S Fruscione, F Ruffinazzi, G Fassad, M R El Beheiry, A Minetti, C Zara, F Biancheri, R Producer: 20131118 In: Biochemical and biophysical research communications vol. 439 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Truncation of Caveolin-3 causes autosomal-recessive Rippling Muscle Disease. [electronic resource] by Traverso, M Bruno, C Broccolini, A Sotgia, F Donati, M A Assereto, S Gazzerro, E Lo Monaco, M Modoni, A D'Amico, A Gasperini, S Ricci, E Zara, F Lisanti, M Minetti, C Producer: 20080530 In: Journal of neurology, neurosurgery, and psychiatry vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	West syndrome associated with 14q12 duplications harboring FOXG1. [electronic resource] by Striano, P Paravidino, R Sicca, F Chiurazzi, P Gimelli, S Coppola, A Robbiano, A Traverso, M Pintaudi, M Giovannini, S Operto, F Vigliano, P Granata, T Coppola, G Romeo, A Specchio, N Giordano, L Osborne, L R Gimelli, G Minetti, C Zara, F Producer: 20110725 In: Neurology vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV). [electronic resource] by Bruno, C van Diggelen, O P Cassandrini, D Gimpelev, M Giuffrè, B Donati, M A Introvini, P Alegria, A Assereto, S Morandi, L Mora, M Tonoli, E Mascelli, S Traverso, M Pasquini, E Bado, M Vilarinho, L van Noort, G Mosca, F DiMauro, S Zara, F Minetti, C Producer: 20050518 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. [electronic resource] by Agostinelli, S Traverso, M Accorsi, P Beccaria, F Belcastro, V Capovilla, G Cappanera, S Coppola, A Dalla Bernardina, B Darra, F Ferretti, M Elia, M Galeone, D Giordano, L Gobbi, G Nicita, F Parisi, P Pezzella, M Spalice, A Striano, S Tozzi, E Vignoli, A Minetti, C Zara, F Striano, P Verrotti, A Producer: 20131028 In: European journal of neurology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)