Search Results - "Katzos, G."
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A 2-year prospective densitometric study on the influence of Fok-I gene polymorphism in young patients with thalassaemia major
Published in Osteoporosis international (01-02-2016)“…Summary This study is to estimate the degree of genetic contribution of Fok-I gene polymorphism of Vitamin D receptor to bone mass in patients with…”
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2
Evaluation of pelvic ultrasonography in the diagnosis and differentiation of various forms of sexual precocity in girls
Published in Ultrasound in obstetrics & gynecology (01-11-2008)“…Objectives This study was conducted to assess the role of pelvic ultrasound variables in discriminating between normal girls and girls with different forms of…”
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3
Clonidine and glucagon stimulation for testing growth hormone secretion in children and adolescents: Can we make it with fewer samples?
Published in Journal of endocrinological investigation (01-12-2013)“…Background: Our aim was to retrospectively evaluate the possibility to reduce the number of GH analyses during clonidine and glucagon tests without…”
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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
Published in Journal of endocrinological investigation (01-09-2011)“…Background: fl/d3 polymorphism in human GH receptor was correlated with the response to GH therapy in different groups of children with short stature. Aim:…”
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5
Defining overweight and obesity among Greek children living in Thessaloniki: International versus local reference standards
Published in Hippokratia (01-01-2011)“…Body Mass Index (BMI) offers a simple and reasonable measure of obesity that, with the use of the appropriate reference, can help in the early detection of…”
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Bone mineral density and quantitative ultrasound in children and adolescents with cystic fibrosis
Published in Journal of cystic fibrosis (2010)Get full text
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7
Alterations of bone mineral metabolism of children with different cell lineage types of acute lymphoblastic leukaemia under chemotherapy
Published in Hippokratia (01-01-2011)“…Children with haematological malignancies such as acute lymphoblastic leukaemia (ALL) may have alteration of bone mineral metabolism therefore increased risk…”
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A patient with Klinefelter's syndrome and thalassemia intermedia
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-04-2005)“…Klinefelter's syndrome (KS) is associated with a wide spectrum of clinical features, such as tall stature, eunuchoid proportions, testes disproportionately…”
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Growth hormone treatment in short children with beta-thalassemia major
Published in Journal of pediatric endocrinology & metabolism : JPEM (01-02-2000)“…The effect of one year recombinant human growth hormone (rhGH) treatment on growth rate and bone age was studied in ten short prepubertal children with…”
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10
Serial magnetic resonance imaging findings in mucopolysaccharidosis IIIB (Sanfilippo's syndrome B)
Published in Brain & development (Tokyo. 1979) (01-10-2001)“…Sanfillippo B syndrome (mucopolysaccharidosis (MPS) III, type B) is characterized by mild expression of the characteristic ‘Hurler’ phenotype and a severe…”
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Atypical and variable clinical presentation of glutaric aciduria type I
Published in Neuropediatrics (01-12-2000)“…We report atypical and variable clinical presentation of glutaric aciduria type I (GA I) in four children from two Greek families. In one family, a boy with…”
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Clinical features, laboratory findings and differential diagnosis of benign acute childhood myositis
Published in Acta Paediatrica (01-12-2000)“…We report clinical and laboratory data from 32 children with benign acute childhood myositis (BACM), children who presented with calf tenderness and gait…”
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13
Early infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies
Published in Brain & development (Tokyo. 1979) (01-11-1997)“…Early infantile Krabbe disease is a progressive neurodegenerative disease caused by deficiency of lysosomal enzyme galactocerebroside β-galactosidase, with…”
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Circadian growth hormone secretion in short multitransfused prepubertal children with thalassaemia major
Published in European journal of pediatrics (01-06-1995)“…Growth hormone (GH) secretion was determined by evaluating circadian GH profiles for 24 h and GH responses to clonidine stimulation test and insulin-stimulated…”
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Single High-Dose Immunoglobulin Therapy for Childhood Guillain-Barré Syndrome
Published in Journal of child neurology (01-07-1999)Get full text
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Single dose immunoglobulin therapy for childhood Guillain-Barré syndrome
Published in Brain & development (Tokyo. 1979) (01-07-1997)“…To establish the efficacy of intravenous immunoglobulins (IVIG) in the treatment of acute Guillain-Barré syndrome (GBS), we treated nine consecutive pediatric…”
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Magnetic resonance imaging findings in mild mucopolysaccharidosis II (Hunter's syndrome)
Published in European journal of paediatric neurology (1998)Get full text
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18
Bone mineral density in children and young adults with beta-thalassemia major conventionally treated
Published in Pediatric Blood & Cancer (01-07-2006)Get full text
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Hypoparathyroidism and intracranial calcifications in β-thalassemia major
Published in The Journal of pediatrics (01-03-2001)Get full text
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20
Castleman's disease presenting as a goiter in a child
Published in Hormone research (2003)Get more information
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