Pusiol E - Search Results

1

Very early detection of RET proto-oncogene mutation is crucial for preventive thyroidectomy in multiple endocrine neoplasia type 2 children: presence of C-cell malignant disease in asymptomatic carriers.

Sanso GE, Domene HM, Garcia R, Pusiol E, de M, Roque M, Ring A, Perinetti H, Elsner B, Iorcansky S, Barontini M. Sanso GE, et al. Among authors: pusiol e. Cancer. 2002 Jan 15;94(2):323-30. doi: 10.1002/cncr.10228. Cancer. 2002. PMID: 11900218 Free article.

2

[Detection of a non-standard mutation in the ret protoncogene by site directed mutagenesis].

Real S, Gómez L, Perinetti H, Mayorga LS, Pusiol E, Roqué M. Real S, et al. Among authors: pusiol e. Medicina (B Aires). 2005;65(1):41-6. Medicina (B Aires). 2005. PMID: 15830792 Spanish.

3

A PCR-mutagenesis strategy for rapid detection of mutations in codon 634 of the ret proto-oncogene related to MEN 2A.

Roqué M, Pusiol E, Perinetti H, Godoy CP, Mayorga LS. Roqué M, et al. Among authors: pusiol e. BMC Med Genet. 2002 May 21;3:4. doi: 10.1186/1471-2350-3-4. Epub 2002 May 21. BMC Med Genet. 2002. PMID: 12033991 Free PMC article.

4

Milos IN, Frank-Raue K, Wohllk N, Maia AL, Pusiol E, Patocs A, Robledo M, Biarnes J, Barontini M, Links TP, de Groot JW, Dvorakova S, Peczkowska M, Rybicki LA, Sullivan M, Raue F, Zosin I, Eng C, Neumann HP. Milos IN, et al. Among authors: pusiol e. Endocr Relat Cancer. 2008 Dec;15(4):1035-41. doi: 10.1677/ERC-08-0105. Epub 2008 Sep 15. Endocr Relat Cancer. 2008. PMID: 18794325

5

[Diagnosis by directed mutagenesis of a mutation at the hMSH2 gene associated with hereditary nonpolyposis colorectal cancer].

Roqué M, Pusiol E, Giribet G, Perinetti H, Mayorga LS. Roqué M, et al. Among authors: pusiol e. Medicina (B Aires). 2000;60(2):188-94. Medicina (B Aires). 2000. PMID: 10962807 Spanish.

6

[Molecular biology diagnosis of hereditary non-polyposis colorectal cancer (HNPCC)].

Roqué M, Pusiol E, Perinetti H, Mayorga L. Roqué M, et al. Among authors: pusiol e. Acta Gastroenterol Latinoam. 1999;29(5):341-4. Acta Gastroenterol Latinoam. 1999. PMID: 10668072 Spanish. No abstract available.

7

Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.

Roqué M, Godoy CP, Castellanos M, Pusiol E, Mayorga LS. Roqué M, et al. Among authors: pusiol e. Hum Mutat. 2001 Aug;18(2):167. doi: 10.1002/humu.1173. Hum Mutat. 2001. PMID: 11462248

8

Increased prevalence of insulin resistance in patients with differentiated thyroid carcinoma.

Rezzónico JN, Rezzónico M, Pusiol E, Pitoia F, Niepomniszcze H. Rezzónico JN, et al. Among authors: pusiol e. Metab Syndr Relat Disord. 2009 Aug;7(4):375-80. doi: 10.1089/met.2008.0062. Metab Syndr Relat Disord. 2009. PMID: 19320560

9

Management of overt and subclinical hypothyroidism. Factors influencing L-thyroxine dosage.

Rezzónico JN, Pusiol E, Saravi FD, Rezzónico M, Bossa N. Rezzónico JN, et al. Among authors: pusiol e. Medicina (B Aires). 1999;59(6):698-704. Medicina (B Aires). 1999. PMID: 10752211

10

High prevalence of thyroid nodules in patients with achrocordons (skin tags). Possible role of insulin-resistance.

Rezzónico J, Rezzónico M, Pusiol E, Pitoia F, Niepomniszcze H. Rezzónico J, et al. Among authors: pusiol e. Medicina (B Aires). 2009;69(3):302-4. Medicina (B Aires). 2009. PMID: 19622476

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