Osteoporosis Syndrome in Thalassaemia Major: An Overview

por Toumba, Meropi, Skordis, Nicos
Publicado 2010

Thalassaemia and Aberrations of Growth and Puberty

por Kyriakou, Andreas, Skordis, Nicos
Publicado 2009

Current approach to the clinical care of adolescents with gender dysphoria

por Kyriakou, Andreas, Nicolaides, Nicolas C., Skordis, Nicos
Publicado en Acta Biomed (2020)

Genotype Is Associated to the Degree of Virilization in Patients With Classic Congenital Adrenal Hyperplasia

por Neocleous, Vassos, Fanis, Pavlos, Phylactou, Leonidas A., Skordis, Nicos
Publicado en Front Endocrinol (Lausanne) (2018)

Polycystic ovarian syndrome in adolescents: from diagnostic criteria to therapeutic management

por Nicolaides, Nicolas C., Matheou, Andreas, Vlachou, Florentia, Neocleous, Vassos, Skordis, Nicos
Publicado en Acta Biomed (2020)

Phenotypic variability of hyperandrogenemia in females heterozygous for CYP21A2 mutations

por Neocleous, Vassos, Shammas, Christos, Phedonos, Alexia AP, Phylactou, Leonidas A, Skordis, Nicos
Publicado en Indian J Endocrinol Metab (2014)

Combined effect of glutamine at position 70 of HLA-DRB1 and alanine at position 57 of HLA-DQB1 in type 1 diabetes: An epitope analysis

por Gerasimou, Petroula, Nicolaidou, Vicky, Skordis, Nicos, Picolos, Michalis, Monos, Demetrios, Costeas, Paul A.
Publicado en PLoS One (2018)

Type 2 Diabetes Susceptibility in the Greek-Cypriot Population: Replication of Associations with TCF7L2, FTO, HHEX, SLC30A8 and IGF2BP2 Polymorphisms

por Votsi, Christina, Toufexis, Costas, Michailidou, Kyriaki, Antoniades, Athos, Skordis, Nicos, Karaolis, Minas, Pattichis, Constantinos S., Christodoulou, Kyproula
Publicado en Genes (Basel) (2017)

Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5′-UTR Region of the Imprinted MKRN3 Gene

por Fanis, Pavlos, Skordis, Nicos, Toumba, Meropi, Papaioannou, Nikoletta, Makris, Anestis, Kyriakou, Andreas, Neocleous, Vassos, Phylactou, Leonidas A.
Publicado en Front Endocrinol (Lausanne) (2019)

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin

por Tsinopoulou, Assimina Galli, Serbis, Anastasios, Kotanidou, Eleni P., Litou, Eleni, Dokousli, Vaia, Mouzaki, Konstantina, Fanis, Pavlos, Neocleous, Vassos, Skordis, Nicos
Publicado en J Clin Res Pediatr Endocrinol (2018)

Endocrine check-up in adolescents and indications for referral: A guide for health care providers

por De Sanctis, Vincenzo, Soliman, Ashraf T, Fiscina, Bernadette, Elsedfy, Heba, Elalaily, Rania, Yassin, Mohamed, Skordis, Nicos, Di Maio, Salvatore, Piacentini, Giorgio, Kholy, Mohamed El
Publicado en Indian J Endocrinol Metab (2014)

The ICET-A Recommendations for the Diagnosis and Management of Disturbances of Glucose Homeostasis in Thalassemia Major Patients

por De Sanctis, Vincenzo, Soliman, Ashraf T., Elsedfy, Heba, Yaarubi, Saif AL, Skordis, Nicos, Khater, Doaa, El Kholy, Mohamed, Stoeva, Iva, Fiscina, Bernadette, Angastiniotis, Michael, Daar, Shahina, Kattamis, Christos
Publicado en Mediterr J Hematol Infect Dis (2016)

Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia

por Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Phedonos, Alexia A. P., Picolos, Michalis, Andreou, Elena, Kyriakides, Tassos C., Tanteles, George A., Shammas, Christos, Phylactou, Leonidas A., Skordis, Nicos
Publicado en Int J Endocrinol (2017)

Position effect, cryptic complexity, and direct gene disruption as disease mechanisms in de novo apparently balanced translocation cases

por Aristidou, Constantia, Theodosiou, Athina, Bak, Mads, Mehrjouy, Mana M., Constantinou, Efthymia, Alexandrou, Angelos, Papaevripidou, Ioannis, Christophidou-Anastasiadou, Violetta, Skordis, Nicos, Kitsiou-Tzeli, Sophia, Tommerup, Niels, Sismani, Carolina
Publicado en PLoS One (2018)

GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in ANOS1, RNF216, WDR11, FGFR1, CHD7, and POLR3A Genes in a Case Series and Review of...

por Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Tanteles, George A., Schiza, Melpo, Cinarli, Feride, Nicolaides, Nicolas C., Oulas, Anastasis, Spyrou, George M., Mantzoros, Christos S., Vlachakis, Dimitrios, Skordis, Nicos, Phylactou, Leonidas A.
Publicado en Front Endocrinol (Lausanne) (2020)

FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation

por Koumbaris, George, Hatzisevastou-Loukidou, Hariklia, Alexandrou, Angelos, Ioannides, Marios, Christodoulou, Christodoulos, Fitzgerald, Tomas, Rajan, Diana, Clayton, Stephen, Kitsiou-Tzeli, Sophia, Vermeesch, Joris R., Skordis, Nicos, Antoniou, Pavlos, Kurg, Ants, Georgiou, Ioannis, Carter, Nigel P., Patsalis, Philippos C.
Publicado 2011

Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines

por De Sanctis, Vincenzo, Soliman, Ashraf T., Elsedfy, Heba, Skordis, Nicos, Kattamis, Christos, Angastiniotis, Michael, Karimi, Mehran, Yassin, Mohd Abdel Daem Mohd, El Awwa, Ahmed, Stoeva, Iva, Raiola, Giuseppe, Galati, Maria Concetta, Bedair, Elsaid M., Fiscina, Bernadette, El Kholy, Mohamed
Publicado 2013

Insulin-like Growth Factor-1 (IGF-1): Demographic, Clinical and Laboratory Data in 120 Consecutive Adult Patients with Thalassaemia Major

por De Sanctis, Vincenzo, Soliman, Ashraf T, Candini, Giancarlo, Yassin, Mohamed, Raiola, Giuseppe, Galati, Maria Concetta, Elalaily, Rania, Elsedfy, Heba, Skordis, Nicos, Garofalo, Piernicola, Anastasi, Salvatore, Campisi, Saveria, Karimi, Mehran, Kattamis, Christos, Canatan, Duran, Kilinc, Yurdanur, Sobti, Praveen, Fiscina, Bernadette, El Kholy, Mohamed
Publicado en Mediterr J Hematol Infect Dis (2014)

The ICET-A Survey on Current Criteria Used by Clinicians for the Assessment of Central Adrenal Insufficiency in Thalassemia: Analysis of Results and Recommendations

por De Sanctis, Vincenzo, Soliman, Ashraf T., Elsedfy, Heba, Albu, Alice, Al Jaouni, Soad, Yaarubi, Saif AL, Anastasi, Salvatore, Canatan, Duran, Di Maio, Massimo, Di Maio, Salvatore, El Kholy, Mohamed, Karimi, Mehran, Khater, Doaa, Kilinc, Yurdanur, Lum, Su Han, Skordis, Nicos, Sobti, Praveen, Stoeva, Iva, Tzoulis, Ploutarchos, Wali, Yasser, Kattamis, Christos
Publicado en Mediterr J Hematol Infect Dis (2016)

Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism

por Badiu, Corin, Bonomi, Marco, Borshchevsky, Ivan, Cools, Martine, Craen, Margarita, Ghervan, Cristina, Hauschild, Michael, Hershkovitz, Eli, Hrabovszky, Erik, Juul, Anders, Kim, Soo-Hyun, Kumanov, Phillip, Lecumberri, Beatriz, Lemos, Manuel C., Neocleous, Vassos, Niedziela, Marek, Djurdjevic, Sandra Pekic, Persani, Luca, Phan-Hug, Franziska, Pignatelli, Duarte, Pitteloud, Nelly, Popovic, Vera, Quinton, Richard, Skordis, Nicos, Smith, Neil, Stefanija, Magdalena Avbelj, Xu, Cheng, Young, Jacques, Dwyer, Andrew A.
Publicado en Orphanet J Rare Dis (2017)