Kattamis A - Search Results

1

Heterozygosity of the Complex Corfu δ0β+ Thalassemic Allele (HBD Deletion and HBB:c.92+5G>A) Revisited.

Kattamis C, Skafida M, Delaporta P, Vrettou C, Traeger-Synodinos J, Sofocleous C, Kattamis A. Kattamis C, et al. Among authors: kattamis a. Biology (Basel). 2022 Mar 11;11(3):432. doi: 10.3390/biology11030432. Biology (Basel). 2022. PMID: 35336809 Free PMC article.

2

Clinical response and adverse events in young patients with sickle cell disease treated with hydroxyurea.

Kattamis A, Lagona E, Orfanou I, Psichou F, Ladis V, Kanavakis E, Metaxotou-Mavrommati A, Kattamis C. Kattamis A, et al. Among authors: kattamis c. Pediatr Hematol Oncol. 2004 Jun;21(4):335-42. doi: 10.1080/08880010490440473. Pediatr Hematol Oncol. 2004. PMID: 15205096 Clinical Trial.

3

Iron chelation treatment with combined therapy with deferiprone and deferioxamine: a 12-month trial.

Kattamis A, Ladis V, Berdousi H, Kelekis NL, Alexopoulou E, Papasotiriou I, Drakaki K, Kaloumenou I, Galani A, Kattamis C. Kattamis A, et al. Among authors: kattamis c. Blood Cells Mol Dis. 2006 Jan-Feb;36(1):21-5. doi: 10.1016/j.bcmd.2005.11.002. Epub 2006 Jan 4. Blood Cells Mol Dis. 2006. PMID: 16386928 Clinical Trial.

4

Cystatin C levels in patients with beta-thalassemia during deferasirox treatment.

Papassotiriou I, Margeli A, Hantzi E, Delaporta P, Sergounioti A, Goussetis E, Ladis V, Kattamis A. Papassotiriou I, et al. Among authors: kattamis a. Blood Cells Mol Dis. 2010 Mar 15;44(3):152-5. doi: 10.1016/j.bcmd.2010.01.001. Epub 2010 Jan 29. Blood Cells Mol Dis. 2010. PMID: 20110177

5

Investigation of FANCA mutations in Greek patients.

Selenti N, Sofocleous C, Kattamis A, Kolialexi A, Kitsiou S, Fryssira E, Polychronopoulou S, Kanavakis E, Mavrou A. Selenti N, et al. Among authors: kattamis a. Anticancer Res. 2013 Aug;33(8):3369-74. Anticancer Res. 2013. PMID: 23898106

6

Clinical phenotype and genetic analysis of RPS19, RPL5, and RPL11 genes in Greek patients with Diamond Blackfan Anemia.

Delaporta P, Sofocleous C, Stiakaki E, Polychronopoulou S, Economou M, Kossiva L, Kostaridou S, Kattamis A. Delaporta P, et al. Among authors: kattamis a. Pediatr Blood Cancer. 2014 Dec;61(12):2249-55. doi: 10.1002/pbc.25183. Epub 2014 Aug 17. Pediatr Blood Cancer. 2014. PMID: 25132370

7

Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to α-thalassemia intermedia, when in trans to a single α-globin gene deletion.

Kattamis A, Delaporta P, Fylaktou I, Vrettou C, Kyriakopoulou D, Stamoulakatou A, Papassotiriou I, Kanavakis E, Traeger-Synodinos J. Kattamis A, et al. Hemoglobin. 2015;39(1):55-7. doi: 10.3109/03630269.2014.981827. Epub 2014 Dec 5. Hemoglobin. 2015. PMID: 25476779

8

Evaluation of Intracranial Cerebral Blood Flow Velocities in Splenectomised and Non-Splenectomised Patients with β-Thalassemia Intermedia Using Transcranial Doppler Sonography.

Kanavaki A, Kattamis A, Delaporta P, Papassotiriou I, Spengos K. Kanavaki A, et al. Among authors: kattamis a. In Vivo. 2015 Jul-Aug;29(4):501-4. In Vivo. 2015. PMID: 26130796

9

Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing.

Kakourou G, Vrettou C, Kattamis A, Destouni A, Poulou M, Moutafi M, Kokkali G, Pantos K, Davies S, Kitsiou-Tzeli S, Kanavakis E, Traeger-Synodinos J. Kakourou G, et al. Among authors: kattamis a. Syst Biol Reprod Med. 2016;62(1):69-76. doi: 10.3109/19396368.2015.1100692. Epub 2015 Dec 4. Syst Biol Reprod Med. 2016. PMID: 26636621

10

The Greek Registry of Shwachman Diamond-Syndrome: Molecular and clinical data.

Delaporta P, Sofocleous C, Economou M, Makis A, Kostaridou S, Kattamis A. Delaporta P, et al. Among authors: kattamis a. Pediatr Blood Cancer. 2017 Nov;64(11). doi: 10.1002/pbc.26630. Epub 2017 May 16. Pediatr Blood Cancer. 2017. PMID: 28509441

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