Your search returned 9 results.

Results
	1.	[Autism and epigenetics. A model of explanation for the understanding of the genesis in autism spectrum disorders]. [electronic resource] by Arberas, Claudia Ruggieri, Víctor Producer: 20140715 In: Medicina vol. 73 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Pervasive developmental disorders. Clinical and genetics aspects]. [electronic resource] by Ruggieri, Victor Arberas, Claudia Producer: 20081208 In: Medicina vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Autism. Genetic and biological aspects]. [electronic resource] by Arberas, Claudia Ruggieri, Víctor Producer: 20200311 In: Medicina vol. 79 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Genetic syndromes recognizable in the neonatal period]. [electronic resource] by Ruggieri, Víctor L Arberas, Claudia L Producer: 20100205 In: Medicina vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Non-epileptic motor paroxysmal phenomena in wakefulness in childhood]. [electronic resource] by Ruggieri, Víctor L Arberas, Claudia L Producer: 20140630 In: Revista de neurologia vol. 57 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	6.	[Therapeutic approaches in autism spectrum disorders]. [electronic resource] by Ruggieri, Víctor L Arberas, Claudia L Producer: 20160222 In: Revista de neurologia vol. 60 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	7.	Aging and Autism: Understanding, Intervention and Proposals to Improve Quality of Life. [electronic resource] by Ruggieri, Victor Gómez, José Luis Cuesta Martínez, María Merino Arberas, Claudia Producer: 20200617 In: Current pharmaceutical design vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Terminal osseous dysplasia with pigmentary defects (TODPD) due to a recurrent filamin A (FLNA) mutation. [electronic resource] by Brunetti-Pierri, Nicola Torrado, Maria Fernandez, Maria Del Carmen Tello, Ana Maria Arberas, Claudia L Cardinale, Antonella Piccolo, Pasquale Bacino, Carlos A Producer: 20150123 In: Molecular genetics & genomic medicine vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A homozygous mutation in the highly conserved Tyr60 of the mature IGF1 peptide broadens the spectrum of IGF1 deficiency. [electronic resource] by Keselman, Ana Claudia Martin, Ayelen Scaglia, Paula Alejandra Sanguineti, Nora María Armando, Romina Gutiérrez, Mariana Braslavsky, Débora Ballerini, María Gabriela Ropelato, María Gabriela Ramirez, Laura Landi, Estefanía Domené, Sabina Castro, Julia F Cassinelli, Hamilton Casali, Bárbara Del Rey, Graciela Barros, Ángel Campos Nevado Blanco, Julián Domené, Horacio Jasper, Héctor Arberas, Claudia Rey, Rodolfo A Lapunzina-Badía, Pablo Bergadá, Ignacio Pennisi, Patricia A Producer: 20191129 In: European journal of endocrinology vol. 181 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)