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	1.	Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children. [electronic resource] by Teofoli, F Camilot, M Tatò, L Producer: 20070509 In: Journal of endocrinological investigation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation. [electronic resource] by Tagliaro, F Camilot, M Valentini, R Mengarda, F Antoniazzi, F Tatò, L Producer: 19990211 In: Journal of chromatography. B, Biomedical sciences and applications vol. 716 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Thyroxine hair content in congenital hypothyroidism and hyperthyroidism. [electronic resource] by Zamboni, G Camilot, M Francia, G Lauriola, S Arslanoglu, I Isguven, P Tatò, L Producer: 20031106 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis. [electronic resource] by Camilot, M Teofoli, F Longobardi, S Gandini, A Lievore, C Lauriola, S Tatò, L Producer: 20080416 In: Journal of endocrinological investigation vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Osteogenesis imperfecta: clinical, biochemical and molecular findings. [electronic resource] by Venturi, G Tedeschi, E Mottes, M Valli, M Camilot, M Viglio, S Antoniazzi, F Tatò, L Producer: 20061003 In: Clinical genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? [electronic resource] by Cavarzere, P Vincenzi, M Teofoli, F Gaudino, R Lauriola, S Maines, E Camilot, M Antoniazzi, F Producer: 20140923 In: Journal of endocrinological investigation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern Italian neonatal screening. [electronic resource] by Zaffanello, M Zamboni, G Maselli, M Gandini, A Camilot, M Maffeis, C Burlina, A B Tatò, L Producer: 20060517 In: Genetic testing vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Vitamin B [electronic resource] by Maines, E Morandi, G Gugelmo, G Ion-Popa, F Campostrini, N Pasini, A Vincenzi, M Teofoli, F Camilot, M Bordugo, A Publication details: JIMD reports 2017 In: JIMD reports vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up]. [electronic resource] by Franceschi, R Cavarzere, P Gaudino, R Monti, E Perlini, S Vanzati, M Camilot, M Teofoli, F Antoniazzi, F Lauriola, S Albertini, C Tatò, L Producer: 20101004 In: Minerva pediatrica vol. 62 Availability: No items available. Save to lists Add to cart (remove)