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Helen Fryssira

Showing results (11-20 of 43) with videos related to

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Brain & Development|October 11, 2011
MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disordersStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Hormone Research|November 29, 2008
Three novel mutations in greek sotos patients with rare clinical manifestationsGeorge Leventopoulos, Sophia Kitsiou-Tzeli, Stavroula Psoni, et al.
Pediatric Neurology|April 22, 2009
A clinical study of Sotos syndrome patients with review of the literatureGeorge Leventopoulos, Sophia Kitsiou-Tzeli, Konstantinos Kritikos, et al.
Hormone Research in Paediatrics|July 27, 2012
A rare case of a male with 45, XO, SRY+, ZFY+ with short stature and mild Turner stigmataGeorgia Ntali, Christalena Sofocleous, Elisabeth Kouvidi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 30, 2006
Two years of growth hormone treatment in the first growth hormone deficient patient with cerebrofaciothoracic dysplasiaChristina Kanaka-Gantenbein, Helen Fryssira, Konstantinos Kakavakis, et al.
Pediatric Research|January 26, 2010
Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletionStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Endocrine|May 28, 2025
A rare combination of hypogonadotropic hypogonadism, GH deficiency and rectal atresia in a female with an FGFR1 variant: a case report and systematic review of the literatureKrystallenia I Alexandraki, Odysseas Violetis, Eleni Memi, et al.
European Journal of Pediatrics|May 19, 2011
Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessmentAnna Papadopoulou, Michalis Issakidis, Evangelia Gole, et al.
Gene|July 7, 2012
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotypeKrinio Giannikou, Helen Fryssira, Vasilis Oikonomakis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Growth hormone deficiency in a child with Williams-Beuren syndrome. The response to growth hormone therapyParaskevi Xekouki, Helen Fryssira, Maria Maniati-Christidi, et al.
Pageof 5

Showing results (11-20 of 43) with videos related to

Sort By:
Pageof 5
Brain & Development|October 11, 2011
MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disordersStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Hormone Research|November 29, 2008
Three novel mutations in greek sotos patients with rare clinical manifestationsGeorge Leventopoulos, Sophia Kitsiou-Tzeli, Stavroula Psoni, et al.
Pediatric Neurology|April 22, 2009
A clinical study of Sotos syndrome patients with review of the literatureGeorge Leventopoulos, Sophia Kitsiou-Tzeli, Konstantinos Kritikos, et al.
Hormone Research in Paediatrics|July 27, 2012
A rare case of a male with 45, XO, SRY+, ZFY+ with short stature and mild Turner stigmataGeorgia Ntali, Christalena Sofocleous, Elisabeth Kouvidi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 30, 2006
Two years of growth hormone treatment in the first growth hormone deficient patient with cerebrofaciothoracic dysplasiaChristina Kanaka-Gantenbein, Helen Fryssira, Konstantinos Kakavakis, et al.
Pediatric Research|January 26, 2010
Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletionStavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, et al.
Endocrine|May 28, 2025
A rare combination of hypogonadotropic hypogonadism, GH deficiency and rectal atresia in a female with an FGFR1 variant: a case report and systematic review of the literatureKrystallenia I Alexandraki, Odysseas Violetis, Eleni Memi, et al.
European Journal of Pediatrics|May 19, 2011
Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessmentAnna Papadopoulou, Michalis Issakidis, Evangelia Gole, et al.
Gene|July 7, 2012
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotypeKrinio Giannikou, Helen Fryssira, Vasilis Oikonomakis, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Growth hormone deficiency in a child with Williams-Beuren syndrome. The response to growth hormone therapyParaskevi Xekouki, Helen Fryssira, Maria Maniati-Christidi, et al.
Pageof 5