Adamtziki E - Search Results

1

Two de novo factor VIII gene mutations in the family of an isolated severe haemophilia A patient.

Kapsimali Z, Pavlova A, Pergantou H, Adamtziki E, Oldenburg J, Platokouki H. Kapsimali Z, et al. Among authors: adamtziki e. Haemophilia. 2012 Jan;18(1):e3-4. doi: 10.1111/j.1365-2516.2011.02609.x. Epub 2011 Jul 11. Haemophilia. 2012. PMID: 21740484 No abstract available.

2

The challenging management of a child with type 3 von Willebrand disease and antibodies to von Willebrand factor.

Pergantou H, Xafaki P, Adamtziki E, Koletsi P, Komitopoulou A, Platokouki H. Pergantou H, et al. Among authors: adamtziki e. Haemophilia. 2012 May;18(3):e66-7. doi: 10.1111/j.1365-2516.2012.02799.x. Haemophilia. 2012. PMID: 22531022 No abstract available.

3

Prevalence of inhibitor formation in a cohort of haemophilic children exposed to several products of various purities.

Aronis S, Platokouki H, Kapsimali Z, Adamtziki E, Kolokithas A, Mitsika A. Aronis S, et al. Among authors: adamtziki e. Haemophilia. 1995 Oct;1(4):236-42. doi: 10.1111/j.1365-2516.1995.tb00082.x. Haemophilia. 1995. PMID: 27214630

4

Mutations and polymorphisms in genes affecting hemostasis proteins and homocysteine metabolism in children with arterial ischemic stroke.

Komitopoulou A, Platokouki H, Kapsimali Z, Pergantou H, Adamtziki E, Aronis S. Komitopoulou A, et al. Among authors: adamtziki e. Cerebrovasc Dis. 2006;22(1):13-20. doi: 10.1159/000092332. Epub 2006 Mar 27. Cerebrovasc Dis. 2006. PMID: 16567932

5

Venous thromboembolism at uncommon sites in neonates and children.

Pergantou H, Avgeri M, Komitopoulou A, Xafaki P, Kapsimali Z, Mazarakis M, Adamtziki E, Platokouki H. Pergantou H, et al. Among authors: adamtziki e. J Pediatr Hematol Oncol. 2014 Nov;36(8):624-9. doi: 10.1097/MPH.0000000000000116. J Pediatr Hematol Oncol. 2014. PMID: 24517966

6

Indications of coagulation and/or fibrinolytic system activation in healthy and sick very-low-birth-weight neonates.

Aronis S, Platokouki H, Photopoulos S, Adamtziki E, Xanthou M. Aronis S, et al. Among authors: adamtziki e. Biol Neonate. 1998 Nov;74(5):337-44. doi: 10.1159/000014051. Biol Neonate. 1998. PMID: 9742262

7

Haemostatic variables in phenylketonuric children under dietary treatment.

Schulpis KH, Platokouki H, Papakonstantinou ED, Adamtziki E, Bargeliotis A, Aronis S. Schulpis KH, et al. Among authors: adamtziki e. J Inherit Metab Dis. 1996;19(5):603-9. doi: 10.1007/BF01799833. J Inherit Metab Dis. 1996. PMID: 8892015

8

Association of lupus anticoagulant with transient antibodies to prothrombin in a patient with hypoprothrombinemia.

Amiral J, Aronis S, Adamtziki E, Garoufi A, Karpathios T. Amiral J, et al. Among authors: adamtziki e. Thromb Res. 1997 Apr 1;86(1):73-8. doi: 10.1016/s0049-3848(97)00047-9. Thromb Res. 1997. PMID: 9172289 No abstract available.

9

Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.

Gupta PK, Saxena R, Adamtziki E, Budde U, Oyen F, Obser T, Schneppenheim R. Gupta PK, et al. Among authors: adamtziki e. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):219-22. doi: 10.1016/j.bcmd.2008.03.004. Epub 2008 May 16. Blood Cells Mol Dis. 2008. PMID: 18485763

10

Gene conversions are a common cause of von Willebrand disease.

Gupta PK, Adamtziki E, Budde U, Jaiprakash M, Kumar H, Harbeck-Seu A, Kannan M, Oyen F, Obser T, Wedekind I, Saxena R, Schneppenheim R. Gupta PK, et al. Among authors: adamtziki e. Br J Haematol. 2005 Sep;130(5):752-8. doi: 10.1111/j.1365-2141.2005.05660.x. Br J Haematol. 2005. PMID: 16115133 Free article.

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