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Editorial: Rickets and osteomalacia, from genes to nutrition

Frontiers in endocrinology (Lausanne), 2023-01, Vol.14, p.1141888-1141888

2023

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Bone health assessment of food allergic children on restrictive diets: a practical guide

Journal of pediatric endocrinology & metabolism : JPEM, 2017-02, Vol.30 (2), p.133

2017

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Higher Adiponectin Levels in Children and Adolescents with T1D Probably Contribute to the Osteopenic Phenotype through the RANKL/OPG System Activation

Endocrines, 2023-11, Vol.4 (4), p.709-719

2023

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A novel frameshift deletion in PLS3 causing severe primary osteoporosis

Journal of human genetics, 2018-08, Vol.63 (8), p.923-926

2018

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Hypophosphatasia

Journal of clinical medicine, 2021-12, Vol.10 (23), p.5676

2021

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Body composition of patients with Duchenne muscular dystrophy: the Greek experience

Acta neurologica Belgica, 2016-12, Vol.116 (4), p.565-572

2016

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Parietal aplasia and hypophosphatasia in a child harboring a novel mutation in RUNX2 and a likely pathogenic variant in TNSALP

Bone (New York, N.Y.), 2021-05, Vol.146, p.115904-115904, Article 115904

2021

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Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report

Journal of pediatric endocrinology & metabolism : JPEM, 2023-07, Vol.36 (7), p.712

2023

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Uncoupling of Bone Turnover may Compromise Skeletal Health of Young Patients With Haemophilia A

Journal of clinical densitometry, 2022-01, Vol.25 (1), p.89-96

2022

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Circulating Irisin Levels in Preadolescents and Adolescents Born Preterm

Hormone research in paediatrics, 2022-03, Vol.94 (11-12), p.416-425

2022

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Sclerostin distribution in children and adolescents with type 1 diabetes mellitus and correlation with bone metabolism and bone mineral density

Pediatric diabetes, 2016-06, Vol.17 (4), p.289-299

2016

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Parental attitudes towards head lice infestation in Greece

International journal of dermatology, 2011-06, Vol.50 (6), p.689-692

2011

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A toddler with severe vitamin D-dependent rickets type 1 A (VDDR1A), hungry bone syndrome, and severe RSV infection: presentation and therapeutic challenges

Hormones (Athens, Greece), 2024-07

2024

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Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation

Calcified tissue international, 2018-09, Vol.103 (3), p.353-358

2018

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Body composition and lung function in children with cystic fibrosis and meconium ileus

European journal of pediatrics, 2017-06, Vol.176 (6), p.737-743

2017

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Serum Spexin is Correlated with Lipoprotein(a) and Androgens in Female Adolescents

Journal of clinical medicine, 2019-12, Vol.8 (12), p.2103

2019

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Body composition profile of young patients with phenylketonuria and mild hyperphenylalaninemia

International journal of endocrinology and metabolism, 2014-07, Vol.12 (3), p.e16061-e16061

2014

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Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy

Molecular syndromology, 2021-06, Vol.12 (3), p.194-200

2021

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Sclerostin distribution in children and adolescents with type 1 diabetes mellitus and correlation with bone metabolism and bone mineral density: Sclerostin in T1DM children and adolescents

Pediatric diabetes, 2016-06, Vol.17 (4), p.289-299

2016

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Long-term follow-up of a child with Klinefelter syndrome and achondroplasia from infancy to 16 years

Journal of pediatric endocrinology & metabolism : JPEM, 2017-07, Vol.30 (7), p.797

2017

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Identification of a Novel Nonsense Mutation in the Ligand-Binding Domain of the Vitamin D Receptor Gene and Clinical Description of Two Greek Patients with Hereditary Vitamin D-Resistant Rickets and Alopecia

Hormone research in paediatrics, 2014-01, Vol.82 (3), p.206-212

2014

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Changes of the Brain Synapses During Aging. New Aspects

Zeitschrift für Naturforschung C. A journal of biosciences, 2001-12, Vol.56 (11), p.921-929

2001

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Body composition in young patients with galactose metabolic disorders: a preliminary report

Journal of pediatric endocrinology & metabolism : JPEM, 2014-01, Vol.27 (1-2), p.81

2014

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Bone health evaluation of children and adolescents with homozygous β-thalassemia: implications for practice

Journal of pediatric hematology/oncology, 2012-07, Vol.34 (5), p.344-348

2012

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Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis

JIMD Reports, Volume 35, 2017, Vol.35, p.87-96

2017

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Editorial: Rickets and osteomalacia, from genes to nutrition

Bone health assessment of food allergic children on restrictive diets: a practical guide

Higher Adiponectin Levels in Children and Adolescents with T1D Probably Contribute to the Osteopenic Phenotype through the RANKL/OPG System Activation

A novel frameshift deletion in PLS3 causing severe primary osteoporosis

Hypophosphatasia

Body composition of patients with Duchenne muscular dystrophy: the Greek experience

Parietal aplasia and hypophosphatasia in a child harboring a novel mutation in RUNX2 and a likely pathogenic variant in TNSALP

Severe hypophosphataemia can be an early sign of osteopetrorickets: a case report

Uncoupling of Bone Turnover may Compromise Skeletal Health of Young Patients With Haemophilia A

Circulating Irisin Levels in Preadolescents and Adolescents Born Preterm

Sclerostin distribution in children and adolescents with type 1 diabetes mellitus and correlation with bone metabolism and bone mineral density

Parental attitudes towards head lice infestation in Greece

A toddler with severe vitamin D-dependent rickets type 1 A (VDDR1A), hungry bone syndrome, and severe RSV infection: presentation and therapeutic challenges

Autosomal Recessive Osteogenesis Imperfecta Caused by a Novel Homozygous COL1A2 Mutation

Body composition and lung function in children with cystic fibrosis and meconium ileus

Serum Spexin is Correlated with Lipoprotein(a) and Androgens in Female Adolescents

Body composition profile of young patients with phenylketonuria and mild hyperphenylalaninemia

Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy

Sclerostin distribution in children and adolescents with type 1 diabetes mellitus and correlation with bone metabolism and bone mineral density: Sclerostin in T1DM children and adolescents

Long-term follow-up of a child with Klinefelter syndrome and achondroplasia from infancy to 16 years

Identification of a Novel Nonsense Mutation in the Ligand-Binding Domain of the Vitamin D Receptor Gene and Clinical Description of Two Greek Patients with Hereditary Vitamin D-Resistant Rickets and Alopecia

Changes of the Brain Synapses During Aging. New Aspects

Body composition in young patients with galactose metabolic disorders: a preliminary report

Bone health evaluation of children and adolescents with homozygous β-thalassemia: implications for practice

Bone Health in Classic Galactosemia: Systematic Review and Meta-Analysis

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