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A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major

Osteoporosis international, 2016-02, Vol.27 (2), p.781-788

2016

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Evaluation of pelvic ultrasonography in the diagnosis and differentiation of various forms of sexual precocity in girls

Ultrasound in obstetrics & gynecology, 2008-11, Vol.32 (6), p.819-827

2008

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Clonidine and glucagon stimulation for testing growth hormone secretion in children and adolescents: Can we make it with fewer samples?

Journal of endocrinological investigation, 2013-12, Vol.36 (11), p.1046-1050

2013

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Correlation of fl/d3 polymorphism of growth hormone receptor with the first- and second-year response to recombinant human growth hormone therapy in pre-pubertal Greek children with idiopathic isolated growth hormone deficiency

Journal of endocrinological investigation, 2011-09, Vol.34 (8), p.609-614

2011

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Defining overweight and obesity among Greek children living in Thessaloniki: International versus local reference standards

Hippokratia, 2011-01, Vol.15 (2), p.141-146

2011

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Bone mineral density and quantitative ultrasound in children and adolescents with cystic fibrosis

Journal of cystic fibrosis, 2010, Vol.9, p.S84-S84

2010

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Alterations of bone mineral metabolism of children with different cell lineage types of acute lymphoblastic leukaemia under chemotherapy

Hippokratia, 2011-01, Vol.15 (1), p.43-47

2011

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Serial magnetic resonance imaging findings in mucopolysaccharidosis IIIB (Sanfilippo's syndrome B)

Brain & development (Tokyo. 1979), 2001-10, Vol.23 (6), p.385-389

2001

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A patient with Klinefelter's syndrome and thalassemia intermedia

Journal of Pediatric Endocrinology and Metabolism, 2005-04, Vol.18 (4), p.413

2005

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Growth hormone treatment in short children with beta-thalassemia major

Journal of pediatric endocrinology & metabolism : JPEM, 2000-02, Vol.13 (2), p.163

2000

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Early infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies

Brain & development (Tokyo. 1979), 1997-11, Vol.19 (7), p.488-491

1997

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Single High-Dose Immunoglobulin Therapy for Childhood Guillain-Barré Syndrome

Journal of child neurology, 1999-07, Vol.14 (7), p.480-481

1999

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Single dose immunoglobulin therapy for childhood Guillain-Barré syndrome

Brain & development (Tokyo. 1979), 1997-07, Vol.19 (5), p.323-325

1997

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Atypical and variable clinical presentation of glutaric aciduria type I

Neuropediatrics, 2000-12, Vol.31 (6), p.303-306

2000

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Clinical features, laboratory findings and differential diagnosis of benign acute childhood myositis

Acta Paediatrica, 2000-12, Vol.89 (12), p.1493-1494

2000

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Circadian growth hormone secretion in short multitransfused prepubertal children with thalassaemia major

European journal of pediatrics, 1995-06, Vol.154 (6), p.445-449

1995

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Magnetic resonance imaging findings in mild mucopolysaccharidosis II (Hunter's syndrome)

European journal of paediatric neurology, 1998, Vol.2 (3), p.153-156

1998

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Bone mineral density in children and young adults with beta-thalassemia major conventionally treated

Pediatric Blood & Cancer, 2006-07, Vol.47 (1), p.113-114

2006

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Thelarche variant in a girl with Angelman syndrome

Brain & development (Tokyo. 1979), 2004-08, Vol.26 (5), p.339-341

2004

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Familial moyamoya disease in a Greek family

Brain & development (Tokyo. 1979), 2003-06, Vol.25 (4), p.288-290

2003

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Hypoparathyroidism and intracranial calcifications in β-thalassemia major

The Journal of pediatrics, 2001-03, Vol.138 (3), p.411-411

2001

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Castleman's disease presenting as a goiter in a child

Hormone research, 2003, Vol.59 (1), p.42-42

2003

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L-2-Hydroxyglutaric aciduria presenting as status epilepticus

Brain & development (Tokyo. 1979), 2001-07, Vol.23 (4), p.255-257

2001

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Hypoparathyroidism in beta-thalassemic patients

Journal of pediatric hematology/oncology, 2003-03, Vol.25 (3), p.275-276

2003

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Growth Hormone Treatment in Short Children with ß-Thalassaemia Major

Journal of Pediatric Endocrinology and Metabolism, 2000-01, Vol.13 (2)

2000

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A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major

Evaluation of pelvic ultrasonography in the diagnosis and differentiation of various forms of sexual precocity in girls

Clonidine and glucagon stimulation for testing growth hormone secretion in children and adolescents: Can we make it with fewer samples?

Correlation of fl/d3 polymorphism of growth hormone receptor with the first- and second-year response to recombinant human growth hormone therapy in pre-pubertal Greek children with idiopathic isolated growth hormone deficiency

Defining overweight and obesity among Greek children living in Thessaloniki: International versus local reference standards

Bone mineral density and quantitative ultrasound in children and adolescents with cystic fibrosis

Alterations of bone mineral metabolism of children with different cell lineage types of acute lymphoblastic leukaemia under chemotherapy

Serial magnetic resonance imaging findings in mucopolysaccharidosis IIIB (Sanfilippo's syndrome B)

A patient with Klinefelter's syndrome and thalassemia intermedia

Growth hormone treatment in short children with beta-thalassemia major

Early infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies

Single High-Dose Immunoglobulin Therapy for Childhood Guillain-Barré Syndrome

Single dose immunoglobulin therapy for childhood Guillain-Barré syndrome

Atypical and variable clinical presentation of glutaric aciduria type I

Clinical features, laboratory findings and differential diagnosis of benign acute childhood myositis

Circadian growth hormone secretion in short multitransfused prepubertal children with thalassaemia major

Magnetic resonance imaging findings in mild mucopolysaccharidosis II (Hunter's syndrome)

Bone mineral density in children and young adults with beta-thalassemia major conventionally treated

Thelarche variant in a girl with Angelman syndrome

Familial moyamoya disease in a Greek family

Hypoparathyroidism and intracranial calcifications in β-thalassemia major

Castleman's disease presenting as a goiter in a child

L-2-Hydroxyglutaric aciduria presenting as status epilepticus

Hypoparathyroidism in beta-thalassemic patients

Growth Hormone Treatment in Short Children with ß-Thalassaemia Major

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