Fryssira H - Search Results

1

Two years of growth hormone treatment in the first growth hormone deficient patient with cerebrofaciothoracic dysplasia.

Kanaka-Gantenbein C, Fryssira H, Kakavakis K, Bouzas E, Thomaidis L, Chrousos G, Mastorakos G. Kanaka-Gantenbein C, et al. Among authors: fryssira h. J Pediatr Endocrinol Metab. 2006 Sep;19(9):1179-83. doi: 10.1515/jpem.2006.19.9.1179. J Pediatr Endocrinol Metab. 2006. PMID: 17128568

2

Growth hormone deficiency in a child with Williams-Beuren syndrome. The response to growth hormone therapy.

Xekouki P, Fryssira H, Maniati-Christidi M, Amenta S, Karavitakis EM, Kanaka-Gantenbein C, Dacou-Voutetakis C. Xekouki P, et al. Among authors: fryssira h. J Pediatr Endocrinol Metab. 2005 Feb;18(2):205-7. doi: 10.1515/jpem.2005.18.2.205. J Pediatr Endocrinol Metab. 2005. PMID: 15751610

3

Growth hormone deficiency in a case of cerebrofaciothoracic syndrome in one of two affected siblings.

Kanaka-Gantenbein C, Fryssira H, Chrousos G, Mastorakos G. Kanaka-Gantenbein C, et al. Among authors: fryssira h. Am J Med Genet A. 2004 Sep 1;129A(3):330. doi: 10.1002/ajmg.a.30151. Am J Med Genet A. 2004. PMID: 15326640 No abstract available.

4

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

5

Central precocious puberty in a boy with 22q13 deletion syndrome and NOTCH-1 gene duplication.

Giannakopoulos A, Fryssira H, Tzetis M, Xaidara A, Kanaka-Gantenbein C. Giannakopoulos A, et al. Among authors: fryssira h. J Pediatr Endocrinol Metab. 2016 Nov 1;29(11):1307-1311. doi: 10.1515/jpem-2015-0484. J Pediatr Endocrinol Metab. 2016. PMID: 27235670

6

A novel large deletion of the ICR1 region including H19 and putative enhancer elements.

Fryssira H, Amenta S, Kanber D, Sofocleous C, Lykopoulou E, Kanaka-Gantenbein C, Cerrato F, Lüdecke HJ, Bens S, Riccio A, Buiting K. Fryssira H, et al. BMC Med Genet. 2015 May 6;16:30. doi: 10.1186/s12881-015-0173-2. BMC Med Genet. 2015. PMID: 25943194 Free PMC article.

7

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

8

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.

9

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

10

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

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