| Diagnosis and management of Silver–Russell syndrome: first international consensus statement EL Wakeling, F Brioude, O Lokulo-Sodipe, SM O'Connell, J Salem, J Bliek, ... Nature Reviews Endocrinology 13 (2), 105-124, 2017 | 462 | 2017 |
| Endocrine complications in patients with Thalassaemia Major M Toumba, A Sergis, C Kanaris, N Skordis Pediatric endocrinology reviews 5 (2), 642, 2007 | 251 | 2007 |
| High prevalence of congenital hypothyroidism in the Greek Cypriot population: results of the neonatal screening program 1990-2000 N Skordis, M Toumba, SC Savva, E Erakleous, M Topouzi, M Vogazianos, ... Journal of Pediatric Endocrinology and Metabolism 18 (5), 453-462, 2005 | 121 | 2005 |
| Osteoporosis syndrome in thalassaemia major: an overview M Toumba, N Skordis Journal of osteoporosis 2010, 2010 | 96 | 2010 |
| Update on fertility in thalassaemia major. N Skordis, L Petrikkos, M Toumba, M Hadjigavriel, M Sitarou, A Kolnakou, ... Pediatric endocrinology reviews: PER 2, 296-302, 2004 | 68 | 2004 |
| Effect of long-term growth hormone treatment on final height of children with Russell-Silver syndrome M Toumba, A Albanese, C Azcona, R Stanhope Hormone research in paediatrics 74 (3), 212-217, 2010 | 59 | 2010 |
| Bone disease in thalassaemia major: recent advances in pathogenesis and clinical aspects. N Skordis, M Toumba Pediatric endocrinology reviews: PER 8, 300-306, 2011 | 49 | 2011 |
| Outcome and management of pregnancy in women with thalassaemia in Cyprus M Toumba, C Kanaris, K Simamonian, N Skordis EMHJ-Eastern Mediterranean Health Journal, 14 (3), 628-635, 2008, 2008 | 38 | 2008 |
| Hormonal dysregulation and bones in thalassaemia--an overview. N Skordis, E Efstathiou, A Kyriakou, M Toumba Pediatric endocrinology reviews: PER 6, 107-115, 2008 | 29 | 2008 |
| 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 … V Neocleous, P Fanis, M Toumba, GA Tanteles, M Schiza, F Cinarli, ... Frontiers in endocrinology 11, 550772, 2020 | 27 | 2020 |
| The impact of iron overload and genotype on gonadal function in women with thalassaemia major. N Skordis, M Gourni, C Kanaris, M Toumba, M Kleanthous, N Karatzia, ... Pediatric Endocrinology Reviews: PER 2, 292-295, 2004 | 27 | 2004 |
| Central precocious puberty caused by novel mutations in the promoter and 5′-UTR region of the imprinted MKRN3 gene P Fanis, N Skordis, M Toumba, N Papaioannou, A Makris, A Kyriakou, ... Frontiers in Endocrinology 10, 460982, 2019 | 26 | 2019 |
| Evaluation of the auxological and metabolic status in prepubertal children born small for gestational age M Toumba, A Hadjidemetriou, M Topouzi, SC Savva, R Demetriadou, ... Journal of Pediatric Endocrinology and Metabolism 18 (7), 677-688, 2005 | 26 | 2005 |
| Morbidity and mortality associated with vasopressin analogue treatment M Toumba, R Stanhope Journal of Pediatric Endocrinology and Metabolism 19 (3), 197-202, 2006 | 22 | 2006 |
| Evidence of digenic inheritance in autoinflammation-associated genes V Neocleous, S Byrou, M Toumba, C Costi, C Shammas, C Kyriakou, ... Journal of genetics 95, 761-766, 2016 | 20 | 2016 |
| Overview of genetic defects in endocrinopathies in the island of Cyprus; evidence of a founder effect C Shammas, V Neocleous, M Toumba, C Costi, AAP Phedonos, ... Genetic testing and molecular biomarkers 16 (9), 1073-1079, 2012 | 20 | 2012 |
| Expensive therapies in children: benefit versus cost of combined treatment of recombinant human growth hormone and gonadotropin-releasing hormone analogue in girls with poor … M Toumba, V Kokotsis, SC Savva, N Skordis Journal of Pediatric Endocrinology and Metabolism 27 (3-4), 311-316, 2014 | 19 | 2014 |
| Stress, thyroid dysregulation, and thyroid cancer in children and adolescents: proposed impending mechanisms A Kyriacou, V Tziaferi, M Toumba Hormone Research in Paediatrics 96 (1), 44-53, 2023 | 18 | 2023 |
| Genetic defects of the CYP21A2 gene in girls with premature adrenarche N Skordis, C Shammas, AAP Phedonos, A Kyriakou, M Toumba, ... Journal of endocrinological investigation 38, 535-539, 2015 | 18 | 2015 |
| Genetic defects in the cyp21a2 gene in heterozygous girls with premature adrenarche and adolescent females with hyperandrogenemia. V Neocleous, C Shammas, AP Phedonos, E Karaoli, A Kyriakou, ... Georgian medical news, 40-47, 2012 | 18 | 2012 |
Nicos SkordisProfessor of Pediatrics, St George's University London Medical School at the University of NicosiaVerified email at paedi.org.cy
