Camilot M - Search Results

1

A young boy with ventricular arrhythmias and thyroid dysgenesis: two genes are not enough?

Franceschi R, Maines E, Bellizzi M, Rivieri F, Bacca A, Filippi A, Valente EM, Plumari M, Soffiati M, Vincenzi M, Teofoli F, Camilot M. Franceschi R, et al. Among authors: camilot m. Arch Endocrinol Metab. 2023 Jan 18;67(1):143-149. doi: 10.20945/2359-3997000000546. Epub 2022 Dec 1. Arch Endocrinol Metab. 2023. PMID: 36468928 Free PMC article.

2

Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern Italian neonatal screening.

Zaffanello M, Zamboni G, Maselli M, Gandini A, Camilot M, Maffeis C, Burlina AB, Tatò L. Zaffanello M, et al. Among authors: camilot m. Genet Test. 2005 Summer;9(2):133-7. doi: 10.1089/gte.2005.9.133. Genet Test. 2005. PMID: 15943553

3

Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation.

Tagliaro F, Camilot M, Valentini R, Mengarda F, Antoniazzi F, Tatò L. Tagliaro F, et al. Among authors: camilot m. J Chromatogr B Biomed Sci Appl. 1998 Sep 25;716(1-2):77-82. doi: 10.1016/s0378-4347(98)00196-0. J Chromatogr B Biomed Sci Appl. 1998. PMID: 9824220

4

Neonatal screening for congenital adrenal hyperplasia in North-Eastern Italy: a report three years into the program.

Cavarzere P, Camilot M, Teofoli F, Tatò L. Cavarzere P, et al. Among authors: camilot m. Horm Res. 2005;63(4):180-6. doi: 10.1159/000085021. Epub 2005 Apr 7. Horm Res. 2005. PMID: 15818055

5

Thyrotropin receptor gene mutations and TSH resistance: variable expressivity in the heterozygotes.

Camilot M, Teofoli F, Gandini A, Franceschi R, Rapa A, Corrias A, Bona G, Radetti G, Tatò L. Camilot M, et al. Clin Endocrinol (Oxf). 2005 Aug;63(2):146-51. doi: 10.1111/j.1365-2265.2005.02314.x. Clin Endocrinol (Oxf). 2005. PMID: 16060907

6

Circulating ghrelin levels in girls with central precocious puberty are reduced during treatment with LHRH analog.

Maffeis C, Franceschi R, Moghetti P, Camilot M, Lauriola S, Tatò L. Maffeis C, et al. Among authors: camilot m. Eur J Endocrinol. 2007 Jan;156(1):99-103. doi: 10.1530/eje.1.02320. Eur J Endocrinol. 2007. PMID: 17218731

7

Lack of association between thyrotropin receptor gene polymorphisms and subclinical hypothyroidism in children.

Teofoli F, Camilot M, Tatò L. Teofoli F, et al. Among authors: camilot m. J Endocrinol Invest. 2007 Feb;30(2):163-6. doi: 10.1007/BF03347416. J Endocrinol Invest. 2007. PMID: 17392608

8

Prepubertal serum inhibin B in cryptorchid infants and in monorchid boys with compensatory testicular hypertrophy.

Gaudino R, Cavarzere P, Camilot M, Teofoli F, Zampieri N, Tatò L. Gaudino R, et al. Among authors: camilot m. Fertil Steril. 2008 Dec;90(6):2217-21. doi: 10.1016/j.fertnstert.2007.10.017. Epub 2008 Jan 14. Fertil Steril. 2008. PMID: 18191850 Free article.

9

Implementation of a congenital hypothyroidism newborn screening procedure with mutation detection on genomic DNA extracted from blood spots: the experience of the Italian northeastern reference center.

Camilot M, Teofoli F, Vincenzi M, Federici F, Perlini S, Tatò L. Camilot M, et al. Genet Test. 2007 Winter;11(4):387-90. doi: 10.1089/gte.2007.0033. Genet Test. 2007. PMID: 18294054

10

A technique of mRNA extraction and labeling from circulating lymphocytes of children treated with growth hormone replacement therapy for microarray analysis.

Camilot M, Teofoli F, Longobardi S, Gandini A, Lievore C, Lauriola S, Tatò L. Camilot M, et al. J Endocrinol Invest. 2008 Jan;31(1):1-7. doi: 10.1007/BF03345559. J Endocrinol Invest. 2008. PMID: 18296898

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