Gonadal function and fertility issues in Thalassaemia by Nicos Skordis

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Osteoporosis Syndrome in Thalassaemia Major: An Overview by Meropi Toumba, Nicos Skordis

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THALASSAEMIA AND ABERRATIONS OF GROWTH AND PUBERTY by Andreas Kyriakou, Nicos Skordis

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Genotype Is Associated to the Degree of Virilization in Patients With Classic Congenital Adrenal Hyperplasia by Vassos Neocleous, Vassos Neocleous, Pavlos Fanis, Pavlos Fanis, Leonidas A. Phylactou, Leonidas A. Phylactou, Nicos Skordis, Nicos Skordis, Nicos Skordis

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The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes by Pavlos Fanis, Nicos Skordis, Nicos Skordis, Nicos Skordis, Meropi Toumba, Meropi Toumba, Michalis Picolos, George A. Tanteles, Vassos Neocleous, Leonidas A. Phylactou

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Methylation status of hypothalamic Mkrn3 promoter across puberty by Pavlos Fanis, Maria Morrou, Marios Tomazou, Kyriaki Michailidou, George M. Spyrou, Meropi Toumba, Meropi Toumba, Nicos Skordis, Nicos Skordis, Nicos Skordis, Vassos Neocleous, Leonidas A. Phylactou

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Obesogens in Adolescence: Challenging Aspects and Prevention Strategies by Marina Nicolaou, Meropi Toumba, Alexandros Kythreotis, Habib Daher, Nicos Skordis

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Genetic diagnosis of endocrine disorders in Cyprus through the Cyprus Institute of Neurology and Genetics: an ENDO-ERN Reference Center by Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Nicos Skordis, Leonidas A. Phylactou

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RET Proto-Oncogene Variants in Patients with Medullary Thyroid Carcinoma from the Mediterranean Basin: A Brief Report by Vassos Neocleous, Pavlos Fanis, Savvas Frangos, Nicos Skordis, Leonidas A. Phylactou

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Central Precocious Puberty Caused by Novel Mutations in the Promoter and 5′-UTR Region of the Imprinted MKRN3 Gene by Pavlos Fanis, Pavlos Fanis, Nicos Skordis, Nicos Skordis, Meropi Toumba, Meropi Toumba, Nikoletta Papaioannou, Nikoletta Papaioannou, Anestis Makris, Andreas Kyriakou, Vassos Neocleous, Vassos Neocleous, Leonidas A. Phylactou, Leonidas A. Phylactou

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Seminoma in 46, XY Gonadal Dysgenesis: Rare Presentation and Review of the Literature by Maamoun Adra, Hayato Nakanishi, Eleni Papachristodoulou, Evangelia Karaoli, Petroula Gerasimou, Antri Miltiadous, Katerina Nicolaou, Loizos Loizou, Nicos Skordis

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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... by Vassos Neocleous, Vassos Neocleous, Pavlos Fanis, Pavlos Fanis, Meropi Toumba, Meropi Toumba, George A. Tanteles, George A. Tanteles, Melpo Schiza, Melpo Schiza, Feride Cinarli, Feride Cinarli, Nicolas C. Nicolaides, Nicolas C. Nicolaides, Anastasis Oulas, Anastasis Oulas, George M. Spyrou, George M. Spyrou, Christos S. Mantzoros, Christos S. Mantzoros, Dimitrios Vlachakis, Dimitrios Vlachakis, Dimitrios Vlachakis, Nicos Skordis, Nicos Skordis, Nicos Skordis, Leonidas A. Phylactou, Leonidas A. Phylactou

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Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty by Vassos Neocleous, Vassos Neocleous, Pavlos Fanis, Pavlos Fanis, Meropi Toumba, Meropi Toumba, Barbara Gorka, Ioanna Kousiappa, Ioanna Kousiappa, George A. Tanteles, George A. Tanteles, Michalis Iasonides, Michalis Iasonides, Nicolas C. Nicolaides, Nicolas C. Nicolaides, Yiolanda P. Christou, Yiolanda P. Christou, Kyriaki Michailidou, Kyriaki Michailidou, Stella Nicolaou, Savvas S. Papacostas, Savvas S. Papacostas, Savvas S. Papacostas, Savvas S. Papacostas, Athanasios Christoforidis, Andreas Kyriakou, Andreas Kyriakou, Dimitrios Vlachakis, Dimitrios Vlachakis, Dimitrios Vlachakis, Nicos Skordis, Nicos Skordis, Nicos Skordis, Leonidas A. Phylactou, Leonidas A. Phylactou

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Position effect, cryptic complexity, and direct gene disruption as disease mechanisms in de novo apparently balanced translocation cases. by Constantia Aristidou, Athina Theodosiou, Mads Bak, Mana M Mehrjouy, Efthymia Constantinou, Angelos Alexandrou, Ioannis Papaevripidou, Violetta Christophidou-Anastasiadou, Nicos Skordis, Sophia Kitsiou-Tzeli, Niels Tommerup, Carolina Sismani

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Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia by Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Alexia A. P. Phedonos, Michalis Picolos, Elena Andreou, Tassos C. Kyriakides, George A. Tanteles, Christos Shammas, Leonidas A. Phylactou, Nicos Skordis

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Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines by Vincenzo De Sanctis, Ashraf T Soliman, Heba Elsedfy, Nicos Skordis, Christos Kattamis, Michael Angastiniotis, Mehran Karimi, Mohd Abdel Daem Mohd Yassin, Ahmed El Awwa, Iva Stoeva, Giuseppe Raiola, Maria Concetta Galati, Elsaid M Bedair, Bernadette Fiscina, Mohamed El Kholy

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Inherited metabolic disorders in Cyprus by Theodoros Georgiou, Petros P. Petrou, Anna Malekkou, Ioannis Ioannou, Marina Gavatha, Nicos Skordis, Paola Nicolaidou, Irini Savvidou, Emilia Athanasiou, Sofia Ourani, Elena Papamichael, Marios Vogazianos, Maria Dionysiou, Gabriella Mavrikiou, Olga Grafakou, George A. Tanteles, Violetta Anastasiadou, Anthi Drousiotou

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