HATZAKI A[au] - Search Results

Year	Number of Results
1995	1
2000	1
2001	1
2002	1
2003	1
2004	2
2005	1
2006	3
2007	1
2008	1
2009	2
2010	1
2011	2
2012	1
2018	1
2022	0

1

A novel de novo mutation within EFNB1 gene in a young girl with craniofrontonasal syndrome.

Apostolopoulou D, Stratoudakis A, Hatzaki A, Kaxira OS, Panagopoulos KP, Kollia P, Aleporou V. Apostolopoulou D, et al. Among authors: hatzaki a. Cleft Palate Craniofac J. 2012 Jan;49(1):109-13. doi: 10.1597/10-247. Epub 2011 Feb 27. Cleft Palate Craniofac J. 2012. PMID: 21385071

2

The effect of alcohol and gemfibrozil co-administration in Wistar rats.

Kolovou GD, Mikhailidis DP, Kafaltis N, Adamopoulou EN, Yazitsoglou E, Hatzaki A, Pilatis N, Margeli AP, Salpea KD, Mykoniatis M, Cokkinos DV. Kolovou GD, et al. Among authors: hatzaki a. In Vivo. 2004 Jan-Feb;18(1):49-53. In Vivo. 2004. PMID: 15011751 Free article.

3

Genetic Analysis of Syndromic and Nonsyndromic Patients With Craniosynostosis Identifies Novel Mutations in the TWIST1 and EFNB1 Genes.

Apostolopoulou D, Kaxira OS, Hatzaki A, Panagopoulos KP, Alexandrou K, Stratoudakis A, Kollia P, Aleporou V. Apostolopoulou D, et al. Among authors: hatzaki a. Cleft Palate Craniofac J. 2018 Sep;55(8):1092-1102. doi: 10.1177/1055665618760412. Epub 2018 Mar 21. Cleft Palate Craniofac J. 2018. PMID: 29561715

4

Genetic skeletal disorders of the fetus and infant: pathologic and molecular findings in a series of 41 cases.

Konstantinidou AE, Agrogiannis G, Sifakis S, Karantanas A, Harakoglou V, Kaminopetros P, Hatzaki A, Petersen MB, Karadimas C, Velissariou V, Velonis S, Papantoniou N, Antsaklis A, Patsouris E. Konstantinidou AE, et al. Among authors: hatzaki a. Birth Defects Res A Clin Mol Teratol. 2009 Oct;85(10):811-21. doi: 10.1002/bdra.20617. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19637253

5

Prenatal diagnosis of hypochondroplasia: report of two cases.

Karadimas C, Sifakis S, Valsamopoulos P, Makatsoris C, Velissariou V, Nasioulas G, Petersen MB, Koumantakis E, Hatzaki A. Karadimas C, et al. Among authors: hatzaki a. Am J Med Genet A. 2006 May 1;140(9):998-1003. doi: 10.1002/ajmg.a.31177. Am J Med Genet A. 2006. PMID: 16575888

6

Rare XXY/XX mosaicism in a phenotypic male with Klinefelter syndrome: case report.

Velissariou V, Christopoulou S, Karadimas C, Pihos I, Kanaka-Gantenbein C, Kapranos N, Kallipolitis G, Hatzaki A. Velissariou V, et al. Among authors: hatzaki a. Eur J Med Genet. 2006 Jul-Aug;49(4):331-7. doi: 10.1016/j.ejmg.2005.09.001. Epub 2005 Oct 21. Eur J Med Genet. 2006. PMID: 16829354

7

Prenatal diagnosis of achondroplasia presenting with multiple-suture synostosis: a novel association.

Karadimas C, Trouvas D, Haritatos G, Makatsoris C, Dedoulis E, Velissariou V, Antoniadi T, Hatzaki A, Petersen MB. Karadimas C, et al. Among authors: hatzaki a. Prenat Diagn. 2006 Mar;26(3):258-61. doi: 10.1002/pd.1392. Prenat Diagn. 2006. PMID: 16475234

8

The implications of using mutagenic primers in combination with Taq polymerase having proofreading activity.

Papadopoulou E, Metaxa-Mariatou V, Hatzaki A, Hatzis T, Nasioulas G. Papadopoulou E, et al. Among authors: hatzaki a. Biologicals. 2004 Jun;32(2):84-7. doi: 10.1016/j.biologicals.2004.01.001. Biologicals. 2004. PMID: 15454186

9

Easy, rapid, and cost-effective methods for identifying carriers of recurrent GJB2 mutations causing nonsyndromic hearing impairment in the Greek population.

Kokotas H, Grigoriadou M, Hatzaki A, Antoniadi T, Giannoulia-Karantana A, Petersen MB. Kokotas H, et al. Among authors: hatzaki a. Genet Test Mol Biomarkers. 2010 Apr;14(2):189-92. doi: 10.1089/gtmb.2009.0136. Genet Test Mol Biomarkers. 2010. PMID: 20059378

10

Prevalence of GJB2 mutations in prelingual deafness in the Greek population.

Pampanos A, Economides J, Iliadou V, Neou P, Leotsakos P, Voyiatzis N, Eleftheriades N, Tsakanikos M, Antoniadi T, Hatzaki A, Konstantopoulou I, Yannoukakos D, Gronskov K, Brondum-Nielsen K, Grigoriadou M, Gyftodimou J, Iliades T, Skevas A, Petersen MB. Pampanos A, et al. Among authors: hatzaki a. Int J Pediatr Otorhinolaryngol. 2002 Sep 2;65(2):101-8. doi: 10.1016/s0165-5876(02)00177-5. Int J Pediatr Otorhinolaryngol. 2002. PMID: 12176179

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