Tzetis M - Search Results

1

Frequencies of pathogenic CFTR variants in Greek cystic fibrosis patients with allergic bronchopulmonary aspergillosis and Aspergillus fumigatus chronic colonization: A retrospective cohort study.

Noni M, Katelari A, Poulou M, Ioannidis D, Kapasouri EM, Tzetis M, Doudounakis SE, Kanaka-Gantenbein C, Spoulou V. Noni M, et al. Among authors: tzetis m. J Mycol Med. 2023 Mar;33(1):101326. doi: 10.1016/j.mycmed.2022.101326. Epub 2022 Aug 7. J Mycol Med. 2023. PMID: 36272381

2

New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12.

Pagani F, Stuani C, Tzetis M, Kanavakis E, Efthymiadou A, Doudounakis S, Casals T, Baralle FE. Pagani F, et al. Among authors: tzetis m. Hum Mol Genet. 2003 May 15;12(10):1111-20. doi: 10.1093/hmg/ddg131. Hum Mol Genet. 2003. PMID: 12719375

3

Evidence for a common ethnic origin of cystic fibrosis mutation 3120+1G-->A in diverse populations.

Dörk T, El-Harith EH, Stuhrmann M, Macek M Jr, Egan M, Cutting GR, Tzetis M, Kanavakis E, Carles S, Claustres M, Padoa C, Ramsay M, Schmidtke J. Dörk T, et al. Among authors: tzetis m. Am J Hum Genet. 1998 Aug;63(2):656-62. doi: 10.1086/301950. Am J Hum Genet. 1998. PMID: 9683582 Free PMC article. No abstract available.

4

Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7B.

Loudianos G, Lovicu M, Dessi V, Tzetis M, Kanavakis E, Zancan L, Zelante L, Galvèz-Galvèz C, Cao A. Loudianos G, et al. Among authors: tzetis m. Hum Mutat. 2002 Oct;20(4):260-6. doi: 10.1002/humu.10121. Hum Mutat. 2002. PMID: 12325021

5

A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.

Tsezou A, Tzetis M, Kitsiou S, Kavazarakis E, Galla A, Kanavakis E. Tsezou A, et al. Among authors: tzetis m. Haematologica. 2000 Mar;85(3):319. Haematologica. 2000. PMID: 10702824 No abstract available.

6

Haplotype and mutation analysis in Greek patients with Wilson disease.

Loudianos G, Dessì V, Lovicu M, Angius A, Kanavakis E, Tzetis M, Kattamis C, Manolaki N, Vassiliki G, Karpathios T, Cao A, Pirastu M. Loudianos G, et al. Among authors: tzetis m. Eur J Hum Genet. 1998 Sep-Oct;6(5):487-91. doi: 10.1038/sj.ejhg.5200219. Eur J Hum Genet. 1998. PMID: 9801873

7

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Castellani C, Cuppens H, Macek M Jr, Cassiman JJ, Kerem E, Durie P, Tullis E, Assael BM, Bombieri C, Brown A, Casals T, Claustres M, Cutting GR, Dequeker E, Dodge J, Doull I, Farrell P, Ferec C, Girodon E, Johannesson M, Kerem B, Knowles M, Munck A, Pignatti PF, Radojkovic D, Rizzotti P, Schwarz M, Stuhrmann M, Tzetis M, Zielenski J, Elborn JS. Castellani C, et al. Among authors: tzetis m. J Cyst Fibros. 2008 May;7(3):179-96. doi: 10.1016/j.jcf.2008.03.009. J Cyst Fibros. 2008. PMID: 18456578 Free PMC article. Review.

8

Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.

Christopoulou G, Tzetis M, Konstantinidou AE, Tsezou A, Kanavakis E, Kitsiou-Tzeli S, Velissariou V. Christopoulou G, et al. Among authors: tzetis m. Eur J Med Genet. 2012 Jan;55(1):75-9. doi: 10.1016/j.ejmg.2011.08.002. Epub 2011 Sep 9. Eur J Med Genet. 2012. PMID: 21914491

9

CFTR localization in native airway cells and cell lines expressing wild-type or F508del-CFTR by a panel of different antibodies.

Carvalho-Oliveira I, Efthymiadou A, Malhó R, Nogueira P, Tzetis M, Kanavakis E, Amaral MD, Penque D. Carvalho-Oliveira I, et al. Among authors: tzetis m. J Histochem Cytochem. 2004 Feb;52(2):193-203. doi: 10.1177/002215540405200207. J Histochem Cytochem. 2004. PMID: 14729871

10

Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population.

Kavazarakis E, Tsezou A, Tzetis M, Hadjidimoula A, Kitsiou S, Kanavakis E, Karpathios T. Kavazarakis E, et al. Among authors: tzetis m. Eur J Pediatr. 2000 Nov;159(11):873-4. doi: 10.1007/s004310000603. Eur J Pediatr. 2000. PMID: 11079211 No abstract available.

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