Dias-da-Silva MR - Search Results

1

Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study.

Maciel RMB, Camacho CP, Assumpção LVM, Bufalo NE, Carvalho AL, de Carvalho GA, Castroneves LA, de Castro FM, Ceolin L, Cerutti JM, Corbo R, Ferraz TMBL, Ferreira CV, França MIC, Galvão HCR, Germano-Neto F, Graf H, Jorge AAL, Kunii IS, Lauria MW, Leal VLG, Lindsey SC, Lourenço DM, Maciel LMZ, Magalhães PKR, Martins JRM, Martins-Costa MC, Mazeto GMFS, Impellizzeri AI, Nogueira CR, Palmero EI, Pessoa CHCN, Prada B, Siqueira DR, Sousa MSA, Toledo RA, Valente FOF, Vaisman F, Ward LS, Weber SS, Weiss RV, Yang JH, Dias-da-Silva MR, Hoff AO, Toledo SPA, Maia AL. Maciel RMB, et al. Endocr Connect. 2019 Mar 1;8(3):289-298. doi: 10.1530/EC-18-0506. Endocr Connect. 2019. PMID: 30763276 Free PMC article.

2

Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel alpha1 subunit gene (Cav1.1) are not associated with thyrotoxic hypokalaemic periodic paralysis.

Dias da Silva MR, Cerutti JM, Tengan CH, Furuzawa GK, Vieira TC, Gabbai AA, Maciel RM. Dias da Silva MR, et al. Clin Endocrinol (Oxf). 2002 Mar;56(3):367-75. doi: 10.1046/j.1365-2265.2002.01481.x. Clin Endocrinol (Oxf). 2002. PMID: 11940049

3

A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.

Dias Da Silva MR, Cerutti JM, Arnaldi LA, Maciel RM. Dias Da Silva MR, et al. J Clin Endocrinol Metab. 2002 Nov;87(11):4881-4. doi: 10.1210/jc.2002-020698. J Clin Endocrinol Metab. 2002. PMID: 12414843

4

Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay.

Vieira TC, Dias da Silva MR, Cerutti JM, Brunner E, Borges M, Arnaldi LT, Kopp P, Abucham J. Vieira TC, et al. J Clin Endocrinol Metab. 2003 Jan;88(1):38-44. doi: 10.1210/jc.2001-011872. J Clin Endocrinol Metab. 2003. PMID: 12519826

5

Three years follow-up of pamidronate therapy in two brothers with osteoporosis-pseudoglioma syndrome (OPPG) carrying an LRP5 mutation.

Barros ER, Dias da Silva MR, Kunii IS, Lazaretti-Castro M. Barros ER, et al. J Pediatr Endocrinol Metab. 2008 Aug;21(8):811-8. doi: 10.1515/jpem.2008.21.8.811. J Pediatr Endocrinol Metab. 2008. PMID: 18825883

6

Novel etiopathophysiological aspects of thyrotoxic periodic paralysis.

Maciel RM, Lindsey SC, Dias da Silva MR. Maciel RM, et al. Nat Rev Endocrinol. 2011 May 10;7(11):657-67. doi: 10.1038/nrendo.2011.58. Nat Rev Endocrinol. 2011. PMID: 21556020 Review.

7

Extended RET gene analysis in patients with apparently sporadic medullary thyroid cancer: clinical benefits and cost.

Lindsey SC, Kunii IS, Germano-Neto F, Sittoni MY, Camacho CP, Valente FO, Yang JH, Signorini PS, Delcelo R, Cerutti JM, Maciel RM, Dias-da-Silva MR. Lindsey SC, et al. Horm Cancer. 2012 Aug;3(4):181-6. doi: 10.1007/s12672-012-0109-7. Epub 2012 May 31. Horm Cancer. 2012. PMID: 22648435 Free PMC article.

8

Measurement of calcitonin and calcitonin gene-related peptide mRNA refines the management of patients with medullary thyroid cancer and may replace calcitonin-stimulation tests.

Camacho CP, Lindsey SC, Melo MC, Yang JH, Germano-Neto F, Valente Fde O, Lima TR, Biscolla RP, Vieira JG, Cerutti JM, Dias-da-Silva MR, Maciel RM. Camacho CP, et al. Thyroid. 2013 Mar;23(3):308-16. doi: 10.1089/thy.2012.0361. Thyroid. 2013. PMID: 23259706 Free PMC article.

9

Optimizing nucleic acid extraction from thyroid fine-needle aspiration cells in stained slides, formalin-fixed/paraffin-embedded tissues, and long-term stored blood samples.

Kizys MM, Cardoso MG, Lindsey SC, Harada MY, Soares FA, Melo MC, Montoya MZ, Kasamatsu TS, Kunii IS, Giannocco G, Martins JR, Cerutti JM, Maciel RM, Dias-da-Silva MR. Kizys MM, et al. Arq Bras Endocrinol Metabol. 2012 Dec;56(9):618-26. doi: 10.1590/s0004-27302012000900004. Arq Bras Endocrinol Metabol. 2012. PMID: 23329184

10

A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian families.

Giuffrida FM, Calliari LE, Manna TD, Ferreira JG, Saddi-Rosa P, Kunii IS, Furuzawa GK, Dias-da-Silva MR, Reis AF. Giuffrida FM, et al. Diabetes Res Clin Pract. 2013 May;100(2):e42-5. doi: 10.1016/j.diabres.2013.01.029. Epub 2013 Feb 19. Diabetes Res Clin Pract. 2013. PMID: 23433541

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