Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Aglaia Giannoulia"'
Autor:
Michael B. Petersen, Manuela Villamar, Maria Grigoriadou, Ignacio del Castillo, Haris Kokotas, Aglaia Giannoulia-Karantana
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:183-187
One specific mutation of the GJB2 gene that encodes the connexin 26 protein, the 35delG mutation, has become a major interest among scientists who focus on the genetics of nonsyndromic hearing loss. The mutation accounts for the majority of GJB2 muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8320e85ed51d7f0e777699922e096c1b
https://doi.org/10.1089/gtmb.2009.0146
https://doi.org/10.1089/gtmb.2009.0146
Autor:
Aglaia Giannoulia-Karantana, Haris Kokotas, Thalia Antoniadi, Maria Grigoriadou, Angeliki Hatzaki, Michael B. Petersen
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:189-192
A variety of techniques have been developed for screening the GJB2 gene for known and unknown mutations, especially the most common mutation in the Caucasian population, the c.35delG. Other mutations that have been so far characterized in the GJB2 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36492030a4304c84a8d957c166beb6af
https://doi.org/10.1089/gtmb.2009.0136
https://doi.org/10.1089/gtmb.2009.0136
Autor:
Stavros Korres, Michael B. Petersen, Maria Grigoriadou, Aglaia Giannoulia-Karantana, Elisabeth Ferekidou, George S. Korres, Dimitrios Kandiloros, Haris Kokotas
Publikováno v:
Journal of Human Genetics. 55:265-269
Hearing impairment is a frequent condition, and genes have an important role in its etiology. The majority of hearing loss occurs in non-syndromic form, with deafness being the only clinically recognizable feature. More than 60 nuclear genes or loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9364e1b75dc6d1567db48eb371c2143f
https://doi.org/10.1038/jhg.2010.23
https://doi.org/10.1038/jhg.2010.23
Autor:
Angeliki Tzagkaraki, Irene Voskaki, Gregory Tripsianis, Vasiliki Arvanitidou, Helen Athanasopoulou, Aglaia Giannoulia-Karantana
Publikováno v:
Biological Trace Element Research. 134:136-145
The aim of this study was to investigate whether there is a correlation between copper (Cu) and zinc (Zn) levels in children and their parents, considering their nutritional habits. Cu and Zn concentrations were measured by flame atomic absorption sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::171f741160d9cbdb0dc8662e514cc04f
https://doi.org/10.1007/s12011-009-8462-2
https://doi.org/10.1007/s12011-009-8462-2
Autor:
Christina Thanopoulou, Ioannis Papassotiriou, Spyros Regoutas, Kleopatra H. Schulpis, Aglaia Giannoulia-Karantana, George A. Karikas, Vassiliki Papaevangelou, Anastasia Bartzeliotou, Athena Fytou-Pallikari
Publikováno v:
Scandinavian Journal of Clinical and Laboratory Investigation. 69:31-35
Valproic acid (VPA) treatment and paraoxonase1/arylesterase (PON1/Aryl) activities are related to the production of free radicals. Our aim was to study the PON1/Aryl activities in children on VPA therapy.Thirty-two children with seizures and 30 healt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38531a4e63fd55a00d2e4ca131becd3d
https://doi.org/10.1080/00365510802248051
https://doi.org/10.1080/00365510802248051
Autor:
Haris Kokotas, Maria Grigoriadou, Margareta Mikkelsen, Aglaia Giannoulia-Karantana, Michael B. Petersen
Publikováno v:
Disease Markers. 27:279-285
Chromosomal aneuploidy consists the leading cause of fetal death in our species. Around 50% of spontaneous abortions until 15 weeks of gestational age are chromosomally aneuploid, with trisomies accounting for 50% of the abnormal abortions. Trisomy 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac76e026069d0bb770ceea44a30473ef
https://doi.org/10.1155/2009/725614
https://doi.org/10.1155/2009/725614
Autor:
Maria Grigoriadou, Aglaia Giannoulia-Karantana, Elisabeth Ferekidou, Stavros Korres, Maria Theodosiou, George N. Korres, Michael B. Petersen, Haris Kokotas
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 72:1735-1740
Mutations of GJB2, the gene encoding connexin 26, have been associated with prelingual, sensorineural hearing loss of mild to profound severity. One specific mutation, the 35delG, has accounted for the majority of mutations detected in the GJB2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c989d493eb7e43d83825e6bce68bf32c
https://doi.org/10.1016/j.ijporl.2008.08.006
https://doi.org/10.1016/j.ijporl.2008.08.006
Autor:
Andreas Fretzayas, Polyxeni Nicolaidou, Georges Tsiftis, Elizabeth Dimitriou, Aglaia Giannoulia-Karantana, Helen Georgouli, Talia Kakourou, Chryssa Bakoula, Helen Tsapra, Anna Papadopoulou, Georges Kavadias
Publikováno v:
Nutrition Research. 26:620-625
Vitamin D status in humans depends on the amount of sun exposure and vitamin D intake. Recent reports suggest that hypovitaminosis D (as defined by serum 25-hydroxyvitamin D [25(OH)D]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8c23cbff91d90705a7fdaf5e1b52037
https://doi.org/10.1016/j.nutres.2006.09.018
https://doi.org/10.1016/j.nutres.2006.09.018
Autor:
Yiannis G. Matsinos, Konstantinos Douros, Andreas Fretzayas, Aglaia Giannoulia-Karantana, Ioannis Papassotiriou, Polyxeni Nicolaidou, Helen Tsapra, Anna Papadopoulou, Helen Georgouli, Georges P Chrousos, Sophia Kitsiou
Publikováno v:
Hormone Research in Paediatrics. 65:83-88
Background/Aims: Hypocalcemic vitamin D-resistant rickets (HVDRR) is a rare monogenic autosomal recessive disorder associated with mutations in the gene of the vitamin D receptor (VDR), the mediator of 1,25(OH)2D3 action. Although many investigations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b33b01626dafeb9916696861ea1fbefc
https://doi.org/10.1159/000091043
https://doi.org/10.1159/000091043
Autor:
Sophia Polychronopoulou, George P. Chrousos, Aglaia Giannoulia-Karantana, Antonia Vlachou, Ioannis Papassotiriou
Publikováno v:
Neuroimmunomodulation. 13:133-144
Melatonin is the main hormone secreted by the pineal gland in the human brain. It has a strong impact on the sleep-wake cycle and is considered a general modulator of the human circadian rhythm. Apart from these well-established properties, melatonin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccea78612660dedde2966066786b7601
https://doi.org/10.1159/000097258
https://doi.org/10.1159/000097258