Máximo V - Search Results

1

Mitochondrial DNA alteration in gastric cancer.

Máximo V, Soares P, Machado JC, Seruca R, Sobrinho-Simões M. Máximo V, et al. Gastroenterology. 2000 Dec;119(6):1808-9. doi: 10.1016/s0016-5085(00)70044-8. Gastroenterology. 2000. PMID: 11187439 No abstract available.

2

Investigation of the clinical utility of adhesion molecules in the management of thyroid nodules.

Rabi LT, Peres KC, Nascimento M, de Souza Teixeira E, de Freitas LLL, Barreto IS, Geraldo MV, Assumpção LVM, Máximo V, Tincani AJ, Bufalo NE, Ward LS. Rabi LT, et al. Among authors: maximo v. Sci Rep. 2023 Mar 11;13(1):4069. doi: 10.1038/s41598-023-31302-7. Sci Rep. 2023. PMID: 36906717 Free PMC article.

3

The common deletion of mitochondrial DNA is found in goiters and thyroid tumors with and without oxyphil cell change.

Máximo V, Sores P, Rocha AS, Sobrinho-Simões M. Máximo V, et al. Ultrastruct Pathol. 1998 May-Jun;22(3):271-3. doi: 10.3109/01913129809033479. Ultrastruct Pathol. 1998. PMID: 9793208 No abstract available.

4

Comments on: mutations in mitochondrial control region DNA in gastric tumours of Japanese patients, Tamura, et al. Eur J Cancer 1999, 35, 316-319.

Máximo V, Soares P, Seruca R, Sobrinho-Simões M. Máximo V, et al. Eur J Cancer. 1999 Sep;35(9):1407-8. doi: 10.1016/s0959-8049(99)00126-4. Eur J Cancer. 1999. PMID: 10658535 No abstract available.

5

Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance.

Máximo V, Sobrinho-Simões M. Máximo V, et al. Virchows Arch. 2000 Aug;437(2):107-15. doi: 10.1007/s004280000219. Virchows Arch. 2000. PMID: 10993269 Review.

6

Mitochondrial DNA 'common' deletion in Hürthle cell lesions of the thyroid.

Máximo V, Sobrinho-Simões M. Máximo V, et al. J Pathol. 2000 Dec;192(4):561-2. doi: 10.1002/1096-9896(200012)192:4<561::AID-PATH790>3.0.CO;2-3. J Pathol. 2000. PMID: 11113879 No abstract available.

7

Abnormalities of the E-cadherin/catenin adhesion complex in classical papillary thyroid carcinoma and in its diffuse sclerosing variant.

Rocha AS, Soares P, Seruca R, Máximo V, Matias-Guiu X, Cameselle-Teijeiro J, Sobrinho-Simões M. Rocha AS, et al. Among authors: maximo v. J Pathol. 2001 Jul;194(3):358-66. doi: 10.1002/path.905. J Pathol. 2001. PMID: 11439369

8

Microsatellite instability, mitochondrial DNA large deletions, and mitochondrial DNA mutations in gastric carcinoma.

Máximo V, Soares P, Seruca R, Rocha AS, Castro P, Sobrinho-Simões M. Máximo V, et al. Genes Chromosomes Cancer. 2001 Oct;32(2):136-43. doi: 10.1002/gcc.1175. Genes Chromosomes Cancer. 2001. PMID: 11550281

9

Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors.

Máximo V, Soares P, Lima J, Cameselle-Teijeiro J, Sobrinho-Simões M. Máximo V, et al. Am J Pathol. 2002 May;160(5):1857-65. doi: 10.1016/S0002-9440(10)61132-7. Am J Pathol. 2002. PMID: 12000737 Free PMC article.

10

Mucoepidermoid carcinoma of the thyroid: a tumour histotype characterised by P-cadherin neoexpression and marked abnormalities of E-cadherin/catenins complex.

Rocha AS, Soares P, Machado JC, Máximo V, Fonseca E, Franssila K, Sobrinho-Simões M. Rocha AS, et al. Among authors: maximo v. Virchows Arch. 2002 May;440(5):498-504. doi: 10.1007/s00428-002-0622-0. Epub 2002 Mar 21. Virchows Arch. 2002. PMID: 12021924

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