Fryssira H - Search Results

1

A clinical study of Sotos syndrome patients with review of the literature.

Leventopoulos G, Kitsiou-Tzeli S, Kritikos K, Psoni S, Mavrou A, Kanavakis E, Fryssira H. Leventopoulos G, et al. Among authors: fryssira h. Pediatr Neurol. 2009 May;40(5):357-64. doi: 10.1016/j.pediatrneurol.2008.11.013. Pediatr Neurol. 2009. PMID: 19380072 Review.

2

Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population.

Amenta S, Sofocleous C, Kolialexi A, Thomaidis L, Giouroukos S, Karavitakis E, Mavrou A, Kitsiou S, Kanavakis E, Fryssira H. Amenta S, et al. Among authors: fryssira h. Pediatr Res. 2005 Jun;57(6):789-95. doi: 10.1203/01.PDR.0000157675.06850.68. Epub 2005 Mar 17. Pediatr Res. 2005. PMID: 15774842

3

Tumor development in three patients with Noonan syndrome.

Fryssira H, Leventopoulos G, Psoni S, Kitsiou-Tzeli S, Stavrianeas N, Kanavakis E. Fryssira H, et al. Eur J Pediatr. 2008 Sep;167(9):1025-31. doi: 10.1007/s00431-007-0636-3. Epub 2007 Dec 5. Eur J Pediatr. 2008. PMID: 18057963

4

Three novel mutations in greek sotos patients with rare clinical manifestations.

Leventopoulos G, Kitsiou-Tzeli S, Psoni S, Mavrou A, Kanavakis E, Willems P, Fryssira H. Leventopoulos G, et al. Among authors: fryssira h. Horm Res. 2009 Jan;71(1):45-51. doi: 10.1159/000173741. Epub 2008 Nov 27. Horm Res. 2009. PMID: 19039236

5

Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.

Syrmou A, Tzetis M, Fryssira H, Kosma K, Oikonomakis V, Giannikou K, Makrythanasis P, Kitsiou-Tzeli S, Kanavakis E. Syrmou A, et al. Among authors: fryssira h. Pediatr Res. 2013 Jun;73(6):772-6. doi: 10.1038/pr.2013.41. Epub 2013 Mar 12. Pediatr Res. 2013. PMID: 23481551

6

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment.

Papadopoulou A, Issakidis M, Gole E, Kosma K, Fryssira H, Fretzayas A, Nicolaidou P, Kitsiou-Tzeli S. Papadopoulou A, et al. Among authors: fryssira h. Eur J Pediatr. 2012 Jan;171(1):51-8. doi: 10.1007/s00431-011-1487-5. Epub 2011 May 18. Eur J Pediatr. 2012. PMID: 21590266

7

Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation.

Tsoutsou E, Tzetis M, Giannikou K, Syrmou A, Oikonomakis V, Kosma K, Kanioura A, Kanavakis E, Fryssira H. Tsoutsou E, et al. Among authors: fryssira h. Eur J Paediatr Neurol. 2013 May;17(3):316-20. doi: 10.1016/j.ejpn.2012.12.004. Epub 2013 Jan 24. Eur J Paediatr Neurol. 2013. PMID: 23352671

8

Non-Hodgkin lymphoma in a child with Williams syndrome.

Amenta S, Moschovi M, Sofocleous C, Kostaridou S, Mavrou A, Fryssira H. Amenta S, et al. Among authors: fryssira h. Cancer Genet Cytogenet. 2004 Oct 1;154(1):86-8. doi: 10.1016/j.cancergencyto.2004.02.004. Cancer Genet Cytogenet. 2004. PMID: 15381380

9

Incontinentia pigmenti revisited. A novel nonsense mutation of the IKBKG gene.

Fryssira H, Kakourou T, Valari M, Stefanaki K, Amenta S, Kanavakis E. Fryssira H, et al. Acta Paediatr. 2011 Jan;100(1):128-33. doi: 10.1111/j.1651-2227.2010.01921.x. Acta Paediatr. 2011. PMID: 20586999

10

A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome.

Settas N, Anapliotou M, Kanavakis E, Fryssira H, Sofocleous C, Dacou-Voutetakis C, Chrousos GP, Voutetakis A. Settas N, et al. Among authors: fryssira h. Menopause. 2015 Nov;22(11):1264-8. doi: 10.1097/GME.0000000000000473. Menopause. 2015. PMID: 25988799

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