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	1.	Proposal for a standardized protocol for the systematic orofacial examination of patients with Hereditary Sensory Radicular Neuropathy. [electronic resource] by Siqueira, S R D T Okada, M Lino, A M M Teixeira, M J Siqueira, J T T Producer: 20070109 In: International endodontic journal vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Recurrent neuromyelitis optica in Brazilian patients: clinical, immunological, and neuroimaging characteristics. [electronic resource] by Adoni, T Lino, A M M da Gama, P D Apóstolos-Pereira, S L Marchiori, P E Kok, F Callegaro, D Producer: 20100308 In: Multiple sclerosis (Houndmills, Basingstoke, England) vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel stop codon mutation in the PMP22 gene associated with a variable phenotype. [electronic resource] by Abe, K T Lino, A M M Hirata, M T A Pavanello, R C M Brotto, M W I Marchiori, P E Zatz, M Producer: 20040621 In: Neuromuscular disorders : NMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Beyond neuropathy in hereditary sensory and autonomic neuropathy type V: cognitive evaluation. [electronic resource] by de Andrade, D C Baudic, S Attal, N Rodrigues, C L Caramelli, P Lino, A M M Marchiori, P E Okada, M Scaff, M Bouhassira, D Teixeira, M J Producer: 20080812 In: European journal of neurology vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)