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S. Kitsiou‐Tzeli
Observed names:
S Kitsiou-Tzeli,
S. Kitsiou-Tzeli,
Sofia Kitsiou-Tzeli,
Sophia Kitsiou–Tzeli
Institutions:
National and Kapodistrian University of Athens,
Children's Hospital Agia Sophia
Observed institutions:
National and Kapodistrian University of Athens,
Children's Hospital Agia Sophia,
Panagiotis & Aglaia Kyriakou Children's Hospital
OpenAlex ID:
A5110149700
Spontaneous Ovulation in a True Hermaphrodite with Normal Male Phenotype and a Rare 46,XX/47,XXY Klinefelter’s Mosaic Karyotype
2007
·
Ch. Kanaka-Gantenbein
, E. Papandreou
, et al.
·
Hormone Research in Paediatrics
·
54
Cell-free DNA levels in acute myocardial infarction patients during hospitalization
2009
·
A. Destouni
, C. Vrettou
, et al.
·
Acta Cardiologica
·
50
Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
2004
·
S Kitsiou-Tzeli
, A Kolialexi
, et al.
·
PubMed
·
41
High Nitrate Content in Drinking Water: Cytogenetic Effects in Exposed Children
1996
·
Aspasia Tsezou
, S. Kitsiou-Tzeli
, et al.
·
Archives of Environmental Health An International Journal
·
36
Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications
2016
·
V. Oikonomakis
, K. Kosma
, et al.
·
Clinical Genetics
·
35
miR-15a and miR-24-1 as putative prognostic microRNA signatures for pediatric pilocytic astrocytomas and ependymomas
2016
·
M. Braoudaki
, G. I. Lambrou
, et al.
·
Tumor Biology
·
30
GILBERT SYNDROME ASSOCIATED WITH β-THALASSEMIA
2001
·
M. Tzetis
, E. Kanavakis
, et al.
·
Pediatric Hematology and Oncology
·
20
Early onset posterior subscapular cataract in a series of myotonic dystrophy type 2 patients
2017
·
C Papadopoulos
, K Kekou
, et al.
·
Eye
·
19
PDF
Aberrant microRNA expression in tumor mycosis fungoides
2016
·
E. Papadavid
, M. Braoudaki
, et al.
·
Tumor Biology
·
19
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
2011
·
G. Christopoulou
, M. Tzetis
, et al.
·
European Journal of Medical Genetics
·
10
Steroid hormones polymorphisms and cholelithiasis in Greek population
2006
·
S. Kitsiou‐Tzeli
, E. Giannatou
, et al.
·
Liver International
·
8
Constitutive Heterochromatin Polymorphisms in Children with Acute Lymphoblastic Leukemia
1993
·
Aspasia Tsezoil
, Sofia Kitsiou-Tzeli
, et al.
·
Pediatric Hematology and Oncology
·
7
An unusual case of cat‐eye syndrome phenotype and extragonadal mature teratoma: Review of the literature
2012
·
Maria Tzetis
, Kalliopi Stefanaki
, et al.
·
Birth Defects Research Part A Clinical and Molecular Teratology
·
3
Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pter.
2007
·
V Touliatou
, A Mavrou
, et al.
·
PubMed
·
2
Diagnosis of Fanconi Anemia
1999
·
N. G. Papadopoulos
, E. Papadaki
, et al.
·
Pediatric Hematology and Oncology
·
1
A Case of non-Fanconi Anemia Bone Marrow Dysfunction with Familial Involvement
1998
·
N. G. Papadopoulos
, E. Papadaki
, et al.
·
Pediatric Hematology and Oncology
·
1
Early onset cataract: prominent feature in myotonic dystrophy type 2
2017
·
C. Papadopoulos
, S. Xirou
, et al.
·
Neuromuscular Disorders
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Works count:
17
Citation count:
336
H-index:
10
I10-index:
10
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