Sertedaki, A: search on Z-Library

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1

Correction:Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene

Chiara Redaelli, Rosalind A Coleman, Laura Moro, Amalia Sertedaki, Talia Kakourou, Solaf Mohamed Elsayed, Daniele Prati, Agostino Colli, Donatella Mela, Roberto Colombo, Daniela Tavian

Journal:

Orphanet Journal of Rare Diseases

Year:

2011

Language:

english

File:

PDF, 185 KB

english, 2011

2

CAC – the neglected repeat

Amalia Sertedaki, Susan Lindsay

Journal:

Year:

1996

Language:

english

File:

PDF, 837 KB

english, 1996

3

Oligonucleotide (CAC)5 fingerprinting: Validity and reliability in paternity testing

Dr. Surinder S. Papiha, Amalia Sertedaki

Journal:

ELECTROPHORESIS

Year:

1995

Language:

english

File:

PDF, 337 KB

english, 1995

4

Conception and pregnancy outcome in a patient with 11-bp deletion of the steroidogenic acute regulatory protein gene

Amalia Sertedaki, Kostas Pantos, Christina Vrettou, Georgia Kokkali, Christina Christofidou, Emmanouel Kanavakis, Catherine Dacou-Voutetakis

Journal:

Fertility and Sterility

Year:

2009

Language:

english

File:

PDF, 101 KB

english, 2009

5

A Novel Point Mutation in the KCNJ5 Gene Causing Primary Hyperaldosteronism and Early-Onset Autosomal Dominant Hypertension

Charmandari, Evangelia, Sertedaki, Amalia, Kino, Tomoshige, Merakou, Christina, Hoffman, Dax A., Hatch, Michael M., Hurt, Darrell E., Lin, Lin, Xekouki, Paraskevi, Stratakis, Constantine A., Chrousos,

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2012

Language:

english

File:

PDF, 1.32 MB

english, 2012

6

Ovulation induction and successful pregnancy outcome in two patients with Prop1 gene mutations

Antonis Voutetakis, Amalia Sertedaki, Sarantis Livadas, Maria Maniati-Christidi, Ioannis Mademtzis, Ioannis Bossis, Catherine Dacou-Voutetakis, Ioannis E Messinis

Journal:

Fertility and Sterility

Year:

2004

Language:

english

File:

PDF, 163 KB

english, 2004

7

Pituitary Stalk Interruption Syndrome and Isolated Pituitary Hypoplasia May Be Caused by Mutations in Holoprosencephaly-Related Genes

Tatsi, Christina, Sertedaki, Amalia, Voutetakis, Antonis, Valavani, Eleni, Magiakou, Maria-Alexandra, Kanaka-Gantenbein, Christina, Chrousos, George P., Dacou-Voutetakis, Catherine

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2013

Language:

english

File:

PDF, 965 KB

english, 2013

8

The spectrum of HNF1A gene mutations in Greek patients with MODY3: relative frequency and identification of seven novel germline mutations

Tatsi, Christina, Kanaka-Gantenbein, Christina, Vazeou-Gerassimidi, Adriani, Chrysis, Dionysios, Delis, Dimitrios, Tentolouris, Nikolaos, Dacou-Voutetakis, Catherine, Chrousos, George P, Sertedaki, Am

Journal:

Pediatric Diabetes

Year:

2013

Language:

english

File:

PDF, 533 KB

english, 2013

9

A Novel Point Mutation in the DNA-Binding Domain (DBD) of the Human Glucocorticoid Receptor Causes Primary Generalized Glucocorticoid Resistance by Disrupting the Hydrophobic Structure of its DBD

Roberts, Michael L., Kino, Tomoshige, Nicolaides, Nicolas C., Hurt, Darrell E., Katsantoni, Eleni, Sertedaki, Amalia, Komianou, Filadelfia, Kassiou, Korina, Chrousos, George P., Charmandari, Evangelia

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2013

Language:

english

File:

PDF, 607 KB

english, 2013

10

A Novel Point Mutation of the Human Glucocorticoid Receptor Gene Causes Primary Generalized Glucocorticoid Resistance Through Impaired Interaction With the LXXLL Motif of the p160 Coactivators: Dissociation of the Transactivating and Transreppressive Activities

Nicolaides, Nicolas C., Roberts, Michael L., Kino, Tomoshige, Braatvedt, Geoffrey, Hurt, Darrell E., Katsantoni, Eleni, Sertedaki, Amalia, Chrousos, George P., Charmandari, Evangelia

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2014

Language:

english

File:

PDF, 485 KB

english, 2014

11

Comparative functional analysis of two fibroblast growth factor receptor 1 (FGFR1) mutations affecting the same residue (R254W and R254Q) in isolated hypogonadotropic hypogonadism (IHH)

Koika, Vasiliki, Varnavas, Petros, Valavani, Helen, Sidis, Yisrael, Plummer, Lacey, Dwyer, Andrew, Quinton, Richard, Kanaka-Gantenbein, Christine, Pitteloud, Nelly, Sertedaki, Amalia, Dacou-Voutetakis

Journal:

Year:

2013

Language:

english

File:

PDF, 377 KB

english, 2013

12

Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism?

Voutetakis, A., Sertedaki, A., Livadas, S., Xekouki, P., Bossis, I., Dacou-Voutetakis, C., Argyropoulou, M. I.

Journal:

Journal of Endocrinological Investigation

Year:

2006

Language:

english

File:

PDF, 225 KB

english, 2006

13

The IVS1- 2A>G mutation in theSRD5A2gene predominates in Cypriot patients with 5α reductase deficiency

Skordis, N., Neocleous, V., Kyriakou, A., Efstathiou, E., Sertedaki, A., Philibert, P., Phylactou, L. A., Lumbroso, S., Sultan, C.

Journal:

Journal of Endocrinological Investigation

Year:

2010

Language:

english

File:

PDF, 162 KB

english, 2010

14

The spectrum of clinical, hormonal and molecular findings in 280 individuals with nonclassical congenital adrenal hyperplasia caused by mutations of the CYP21A2 gene

Livadas, S., Dracopoulou, M., Dastamani, A., Sertedaki, A., Maniati-Christidi, M., Magiakou, A.-M., Kanaka-Gantenbein, C., Chrousos, G.P., Dacou-Voutetakis, C.

Journal:

Clinical Endocrinology

Year:

2015

Language:

english

File:

PDF, 101 KB

english, 2015

15

Study of three hypervariable DNA loci (D1S7; D7S22 and D12S11) in three European populations

Papiha, S.S., Calderon, R., Sertedaki, A., Pena, J., Zhong, Y., Chakraborty, R.

Journal:

Annals of Human Biology

Year:

1998

Language:

english

File:

PDF, 899 KB

english, 1998

16

Long-term clinical data and molecular defects in the STAR gene in five Greek patients

Sertedaki, A., Dracopoulou, M., Voutetakis, A., Stefanaki, K., Rontogianni, D., Magiakou, A.-M., Kanaka-Gantenbein, C., Chrousos, G., Dacou-Voutetakis, C.

Journal:

European Journal of Endocrinology

Year:

2013

Language:

english

File:

PDF, 243 KB

english, 2013

17

PROP1 Gene Mutations and Pituitary Size: A Unique Case of Two Consecutive Cycles of Enlargement and Regression

Xekouki, Paraskevi, Sertedaki, Amalia, Livadas, Sarantis, Argyropoulou, Maria, Voutetakis, Antonis

Journal:

Hormone Research

Year:

2007

Language:

english

File:

PDF, 183 KB

english, 2007

18

Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X)

Voutetakis, A, Maniati-Christidi, M, Kanaka-Gantenbein, C, Dracopoulou, M, Argyropoulou, M, Livadas, S, Dacou-Voutetakis, C, Sertedaki, A

Journal:

European Journal of Endocrinology

Year:

2004

Language:

english

File:

PDF, 166 KB

english, 2004

19

A Favorable Metabolic and Antiatherogenic Profile in Carriers of CYP21A2 Gene Mutations Supports the Theory of a Survival Advantage in This Population

Livadas, Sarantis, Dracopoulou, Maria, Lazaropoulou, Christina, Papassotiriou, Ioannis, Sertedaki, Amalia, Angelopoulos, G. Nick, Chrousos, George P., Dacou-Voutetakis, Catherine

Journal:

Hormone Research

Year:

2009

Language:

english

File:

PDF, 142 KB

english, 2009

20

Molecular Defects in the Hypothalamic-Pituitary-Thyroid Axis Leading to Congenital Hypothyroidism

Sertedaki, Amalia, Voutetakis, Antony, Dacou-Voutetakis, Catherine

Journal:

Current Pediatric Reviews

Year:

2005

Language:

english

File:

PDF, 143 KB

english, 2005

21

Stress-induced Aldosterone Hyper-Secretion in a Substantial Subset of Patients With Essential Hypertension

Markou, Athina, Sertedaki, Amalia, Kaltsas, Gregory, Androulakis, Ioannis I., Marakaki, Chrisanthi, Pappa, Theodora, Gouli, Aggeliki, Papanastasiou, Labrini, Fountoulakis, Stelios, Zacharoulis, Achill

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2015

Language:

english

File:

PDF, 985 KB

english, 2015

22

Low TSH Congenital Hypothyroidism: Identification of a Novel Mutation of the TSH ß-Subunit Gene in One Sporadic Case (C85R) and of Mutation Q49stop in Two Siblings with Congenital Hypothyroidism

Sertedaki, Amalia, Papadimitriou, Anastasios, Voutetakis, Antony, Dracopoulou, Maria, Maniati-Christidi, Maria, Dacou-Voutetakis, Catherine

Journal:

Pediatric Research

Year:

2002

Language:

english

File:

PDF, 241 KB

english, 2002

23

Pituitary Magnetic Resonance Imaging in 15 Patients with Prop1 Gene Mutations: Pituitary Enlargement May Originate from the Intermediate Lobe

Voutetakis, Antonis, Argyropoulou, Maria, Sertedaki, Amalia, Livadas, Sarantis, Xekouki, Paraskevi, Maniati-Christidi, Maria, Bossis, Ioannis, Thalassinos, Nicolas, Patronas, Nicholas, Dacou-Voutetaki

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 188 KB

english, 2004

24

Misfolding Ectodomain Mutations of the Lutropin Receptor Increase Efficacy of Hormone Stimulation

Charmandari, E., Guan, R., Zhang, M., Silveira, L. G., Fan, Q. R., Chrousos, G. P., Sertedaki, A. C., Latronico, A. C., Segaloff, D. L.

Journal:

Molecular Endocrinology

Year:

2016

Language:

english

File:

PDF, 2.24 MB

english, 2016

25

Sequencing analysis of the human glucocorticoid receptor (NR3C1) gene in multiple sclerosis patients

Kassi, Eva, Semaniakou, Anna, Sertedaki, Amalia, Evangelopoulos, Maria-Eleftheria, Kazazoglou, Theodosia, Kominakis, Antonios, Sfagos, Constantinos, Charmandari, Evangelia, Chrousos, George P., Moutsa

Journal:

Journal of the Neurological Sciences

Year:

2016

Language:

english

File:

PDF, 225 KB

english, 2016

26

A novel mutation of the hGR gene causing Chrousos syndrome

Nicolaides, Nicolas C., Geer, Eliza B., Vlachakis, Dimitrios, Roberts, Michael L., Psarra, Anna-Maria G., Moutsatsou, Paraskevi, Sertedaki, Amalia, Kossida, Sophia, Charmandari, Evangelia

Journal:

European Journal of Clinical Investigation

Year:

2015

Language:

english

File:

PDF, 800 KB

english, 2015

27

Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion

Sertedaki, Amalia, Markou, Athina, Vlachakis, Dimitrios, Kossida, Sophia, Campanac, Emilie, Hoffman, Dax A., Sierra, Maria De La Luz, Xekouki, Paraskevi, Stratakis, Constantine A., Kaltsas, Gregory, P

Journal:

Clinical Endocrinology

Year:

2016

Language:

english

File:

PDF, 733 KB

english, 2016

28

Functional characterization of the hGRαT556I causing Chrousos syndrome

Nicolaides, Nicolas C., Skyrla, Eirini, Vlachakis, Dimitrios, Psarra, Anna-Maria G., Moutsatsou, Paraskevi, Sertedaki, Amalia, Kossida, Sophia, Charmandari, Evangelia

Journal:

European Journal of Clinical Investigation

Year:

2016

Language:

english

File:

PDF, 655 KB

english, 2016

29

Insufficient Adrenarche in Patients with Combined Pituitary Hormone Deficiency Caused by a PROP A Gene Defect

Voutetakis, A., Livadas, S., Sertedaki, A., Maniati-Christidi, M., Dacou-Voutetakis, C.

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2001

Language:

english

File:

PDF, 361 KB

english, 2001

30

Increased glucocorticoid receptor expression in sepsis is related to heat shock proteins, cytokines, and cortisol and is associated with increased mortality

Vardas, Konstantinos, Ilia, Stavroula, Sertedaki, Amalia, Charmandari, Evangelia, Briassouli, Efrossini, Goukos, Dimitris, Apostolou, Kleovoulos, Psarra, Katerina, Botoula, Efthimia, Tsagarakis, Styli

Journal:

Intensive Care Medicine Experimental

Year:

2017

Language:

english

File:

PDF, 1.83 MB

english, 2017

31

Pituitary stalk interruption syndrome

Voutetakis, Antonis, Sertedaki, Amalia, Dacou-Voutetakis, Catherine

Journal:

Current Opinion in Pediatrics

Year:

2016

Language:

english

File:

PDF, 868 KB

english, 2016

32

The effect of HPV infection on IVF outcomes: a systematic review and meta-analysis

Siristatidis, Charalampos, Vaidakis, Dennis, Sertedaki, Eleni, Martins, Wellington

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2017

Language:

english

File:

PDF, 1.15 MB

english, 2017

33

Metabolomics for improving pregnancy outcomes in women undergoing assisted reproductive technologies

Siristatidis, Charalampos S, Sertedaki, Eleni, Vaidakis, Dennis, Varounis, Christos, Trivella, Marialena

Journal:

Cochrane database of systematic reviews

Year:

2018

Language:

english

File:

PDF, 659 KB

english, 2018

34

P26.05: The possible effect of HPV infection on IVF outcomes: a systematic review and meta-analysis

Siristatidis, C., Vaidakis, D., Sertedaki, E., Belba, M., Dafopoulos, K., Martins, W.P.

Journal:

Ultrasound in Obstetrics & Gynecology

Year:

2017

Language:

english

File:

PDF, 41 KB

english, 2017

35

Endometrial injection of embryo culture supernatant for subfertile women in assisted reproduction

Siristatidis, Charalampos S, Sertedaki, Eleni, Vaidakis, Dennis

Journal:

Cochrane database of systematic reviews

Year:

2018

Language:

english

File:

PDF, 200 KB

english, 2018

36

PROP-1 gene mutations in a 63-year-old woman presenting with osteoporosis and hyperlipidaemia

Andrikoula, Maria, Sertedaki, Amalia, Andrikoula, Sofia, Dacou-Voutetakis, Catherine, Tsatsoulis, Agathocles

Journal:

Year:

2013

Language:

english

File:

PDF, 245 KB

english, 2013

37

Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance

Nicolaides, Nicolas C., Lamprokostopoulou, Agaristi, Sertedaki, Amalia, Charmandari, Evangelia

Journal:

Year:

2016

Language:

english

File:

PDF, 800 KB

english, 2016

38

Transcriptomics in Tissue Glucocorticoid Sensitivity

Nicolaides, Nicolas C., Polyzos, Alexandros, Koniari, Eleni, Lamprokostopoulou, Agaristi, Papageorgiou, Ifigeneia, Golfinopoulou, Eleni, Papathanasiou, Chrysanthi, Sertedaki, Amalia, Thanos, Dimitris,

Journal:

European Journal of Clinical Investigation

Year:

2019

Language:

english

File:

PDF, 405 KB

english, 2019

39

First Report of Diabetes Phenotype due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism

Koufakis, Theocharis, Sertedaki, Amalia, Tatsi, Elizabeth-Barbara, Trakatelli, Christina-Maria, Karras, Spyridon N., Manthou, Eleni, Kanaka-Gantenbein, Christina, Kotsa, Kalliopi

Journal:

Case Reports in Genetics

Year:

2019

Language:

english

File:

PDF, 1.50 MB

english, 2019

40

Next Generation Sequencing Targeted Gene Panel in Greek MODY patients increases diagnostic accuracy

Tatsi, Elizabeth Barbara, Kanaka‐Gantenbein, Christina, Scorilas, Andreas, Chrousos, George P., Sertedaki, Amalia

Journal:

Pediatric Diabetes

Year:

2019

Language:

english

File:

PDF, 1.85 MB

english, 2019

41

Next Generation Sequencing Targeted Gene Panel in Greek MODY patients increases diagnostic accuracy

Tatsi, Elizabeth Barbara, Kanaka‐Gantenbein, Christina, Scorilas, Andreas, Chrousos, George P., Sertedaki, Amalia

Journal:

Pediatric Diabetes

Year:

2019

File:

PDF, 1.85 MB

2019

42

Adrenal Steroids in Female Hypothyroid Neonates: Unraveling an Association Between Thyroid Hormones and Adrenal Remodeling

Galanou, Sofia, Chouliaras, Giorgos, Girginoudis, Panagiotis, Mengreli, Chryssanthi, Sertedaki, Amalia, Dracopoulou, Maria, Farakla, Ioanna, Platis, Dimitris, Iliadi, Alexandra, Chrousos, George P, Da

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2019

Language:

english

File:

PDF, 700 KB

english, 2019

43

Emerging technologies in pediatrics: the paradigm of neonatal diabetes mellitus

Nicolaides, Nicolas C., Kanaka-Gantenbein, Christina, Papadopoulou-Marketou, Nektaria, Sertedaki, Amalia, Chrousos, George P., Papassotiriou, Ioannis

Journal:

Critical Reviews in Clinical Laboratory Sciences

Year:

2020

File:

PDF, 1.23 MB

2020

44

Drug Repurposing and DNA Damage in Cancer Treatment: Facts and Misconceptions

Sertedaki, Eleni, Kotsinas, Athanassios

Journal:

Year:

2020

File:

PDF, 183 KB

2020

45

Carotid Disease and Ageing: A Literature Review on the Pathogenesis of Vascular Senescence in Older Subjects

Sertedaki, Eleni, Veroutis, Dimitris, Zagouri, Flora, Galyfos, George, Filis, Konstadinos, Papalambros, Alexandros, Aggeli, Konstantina, Tsioli, Panagiota, Charalambous, George, Zografos, George, Siga

Journal:

Current Gerontology and Geriatrics Research

Year:

2020

File:

PDF, 1.36 MB

2020

46

Endometrial injection of embryo culture supernatant for subfertile women in assisted reproduction

Siristatidis, Charalampos S, Sertedaki, Eleni, Karageorgiou, Vasilios, Vaidakis, Dennis

Journal:

Cochrane database of systematic reviews

Year:

2020

File:

PDF, 649 KB

2020

47

Molecular analysis of the CYP11B2 gene in 62 patients with Hypoaldosteronism due to Aldosterone Synthase Deficiency

Merakou, Christina, Fylaktou, Irene, Sertedaki, Amalia, Dracopoulou, Maria, Voutetakis, Antonis, Efthymiadou, Alexandra, Christoforidis, Athanasios, Dacou-Voutetakis, Catherine, Chrysis, Dionisios, Ka

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2020

File:

PDF, 934 KB

2020

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