Kanariou M - Search Results

1

Exon-scanning mutation analysis of the ATM gene in patients with ataxia-telangiectasia.

Vorechovský I, Luo L, Prudente S, Chessa L, Russo G, Kanariou M, James M, Negrini M, Webster AD, Hammarström L. Vorechovský I, et al. Among authors: kanariou m. Eur J Hum Genet. 1996;4(6):352-5. doi: 10.1159/000472231. Eur J Hum Genet. 1996. PMID: 9043869

2

Combined microdeletions and CHD7 mutation causing severe CHARGE/DiGeorge syndrome: clinical presentation and molecular investigation by array-CGH.

Kaliakatsos M, Giannakopoulos A, Fryssira H, Kanariou M, Skiathitou AV, Siahanidou T, Giannikou K, Makrythanasis P, Kanavakis E, Tzetis M. Kaliakatsos M, et al. Among authors: kanariou m. J Hum Genet. 2010 Nov;55(11):761-3. doi: 10.1038/jhg.2010.95. Epub 2010 Aug 5. J Hum Genet. 2010. PMID: 20686492

3

Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses.

Siahanidou T, Nikaina E, Kontogiorgou C, Tzanoudaki M, Stefanaki K, Skiathitou AV, Petropoulou T, Kanariou M. Siahanidou T, et al. Among authors: kanariou m. J Clin Immunol. 2019 Apr;39(3):237-240. doi: 10.1007/s10875-019-00611-w. Epub 2019 Mar 12. J Clin Immunol. 2019. PMID: 30864118 No abstract available.

4

The role of basophil activation test in allergic bronchopulmonary aspergillosis and Aspergillus fumigatus sensitization in cystic fibrosis patients.

Katelari A, Tzanoudaki M, Noni M, Kanariou M, Theodoridou M, Kanavakis E, Doudounakis SE, Kanaka-Gantenbein C. Katelari A, et al. Among authors: kanariou m. J Cyst Fibros. 2016 Sep;15(5):587-96. doi: 10.1016/j.jcf.2016.02.004. Epub 2016 Feb 26. J Cyst Fibros. 2016. PMID: 26922860 Free article.

5

Case Report: A Novel Synonymous ARPC1B Gene Mutation Causes a Syndrome of Combined Immunodeficiency, Asthma, and Allergy With Significant Intrafamilial Clinical Heterogeneity.

Papadatou I, Marinakis N, Botsa E, Tzanoudaki M, Kanariou M, Orfanou I, Kanaka-Gantenbein C, Traeger-Synodinos J, Spoulou V. Papadatou I, et al. Among authors: kanariou m. Front Immunol. 2021 Feb 19;12:634313. doi: 10.3389/fimmu.2021.634313. eCollection 2021. Front Immunol. 2021. PMID: 33679784 Free PMC article.

6

Severe combined immunodeficiency in Greek children over a 20-year period: rarity of γc-chain deficiency (X-linked) type.

Michos A, Tzanoudaki M, Villa A, Giliani S, Chrousos G, Kanariou M. Michos A, et al. Among authors: kanariou m. J Clin Immunol. 2011 Oct;31(5):778-83. doi: 10.1007/s10875-011-9564-0. Epub 2011 Jul 6. J Clin Immunol. 2011. PMID: 21732012

7

Novel genetic risk variants for pediatric celiac disease.

Balasopoulou A, Stanković B, Panagiotara A, Nikčevic G, Peters BA, John A, Mendrinou E, Stratopoulos A, Legaki AI, Stathakopoulou V, Tsolia A, Govaris N, Govari S, Zagoriti Z, Poulas K, Kanariou M, Constantinidou N, Krini M, Spanou K, Radlovic N, Ali BR, Borg J, Drmanac R, Chrousos G, Pavlovic S, Roma E, Zukic B, Patrinos GP, Katsila T. Balasopoulou A, et al. Among authors: kanariou m. Hum Genomics. 2016 Oct 24;10(1):34. doi: 10.1186/s40246-016-0091-1. Hum Genomics. 2016. PMID: 27836013 Free PMC article.

8

Absence of Bruton's tyrosine kinase (Btk) mutations in patients with acute myeloid leukaemia.

Ritis K, Speletas M, Tsironidou V, Pardali E, Kanariou M, Moschese V, Orlandi P, Skordala M, Rossi P, Kartalis G, Bourikas G, Sideras P. Ritis K, et al. Among authors: kanariou m. Br J Haematol. 1998 Sep;102(5):1241-8. doi: 10.1046/j.1365-2141.1998.00914.x. Br J Haematol. 1998. PMID: 9753052 Free article.

9

Successful management of cryopyrin-associated periodic syndrome with canakinumab in infancy.

Kanariou M, Tantou S, Varela I, Raptaki M, Petropoulou C, Nikas I, Valari M. Kanariou M, et al. Pediatrics. 2014 Nov;134(5):e1468-73. doi: 10.1542/peds.2013-3185. Pediatrics. 2014. PMID: 25349319

10

Prevalence of antibodies to ganglioside and Hep 2 in Gaucher, Niemann - Pick type C and Sanfilippo diseases.

Dimitriou E, Paschali E, Kanariou M, Michelakakis H. Dimitriou E, et al. Among authors: kanariou m. Mol Genet Metab Rep. 2019 Jun 4;20:100477. doi: 10.1016/j.ymgmr.2019.100477. eCollection 2019 Sep. Mol Genet Metab Rep. 2019. PMID: 31194046 Free PMC article.

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