Search Results - "Georgouli, H"

Endothelin 1 levels in relation to clinical presentation and outcome of Henoch Schonlein purpura by Fessatou, S, Nicolaidou, P, Gourgiotis, D, Georgouli, H, Douros, K, Moustaki, M, Fretzayas, A

“…Henoch Schonlein purpura (HSP) is a common vasculitis of small vessels whereas endothelin-1 (ET-1) is usually reported elevated in vasculities and systematic…”
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Persistent coagulopathy during Escherichia coli sepsis in a previously healthy infant revealed undiagnosed tyrosinaemia type 1 by Georgouli, H, Schulpis, K H, Michelakaki, H, Kaltsa, M, Sdogou, T, Kossiva, L

“…Hereditary tyrosinaemia type 1 (HT1) is caused by an enzymatic defect in tyrosine metabolism. It is an autosomal recessive disorder and affects both sexes…”
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Hereditary vitamin D-resistant rickets in Greek children: genotype, phenotype, and long-term response to treatment by Nicolaidou, P, Tsitsika, A, Papadimitriou, A, Karantana, A, Papadopoulou, A, Psychou, F, Liakopoulou, D, Georgouli, H, Kakourou, T, Chrousos, G

“…We describe four patients (two pairs of children from two unrelated kindreds) from a Greek island, suffering from hereditary vitamin D-resistant rickets…”
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Invasive meningococcal disease presenting as Henoch-Schönlein purpura by TSOLIA, M. N, FRETZAYAS, A, GEORGOULI, H, TZANAKAKI, G, FESSATOU, S, LIAPI-ADAMIDOU, G, CONSTANTOPOULOS, A

“…Henoch-Schonlein purpura (HSP) is an acute systemic form of vasculitis that has been associated with a number of viral and bacterial infections. Described here…”
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Family pattern of idiopathic hypercalciuria and its subtypes by Nicolaidou, P, Themeli, S, Karpathios, T, Georgouli, H, Athanassaki, K, Xaidara, A, Messaritakis, J

“…We determined the mode of inheritance of idiopathic hypercalciuria and its subtypes. We evaluated 40 children with symptomatic idiopathic hypercalciuria and…”
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Hypercalciuria in children with febrile convulsions by Papadimitriou, Anastasios, Nicolaidou, Polyxeni, Garoufi, Anastasia, Georgouli, Helen

“…Background : The purpose of the present study was to investigate whether idiopathic hypercalciuria may be implicated in the pathogenesis of febrile…”
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Increased Serum Hepcidin in Children with Infection and Correlation with Ferritin Level by Kossiva, L, Vassilenko, H, Gouriotis, D, Tsentidis, C, Anastassiou, T, Sdogou, T, Georgouli, H

“…Background and aims: Hepcidin is a recently discovered peptide produced by hepatocytes and macrophages in response to inflammatory stimuli. It is markedly…”
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THE 'FRYING PANS' OF THE EARLY BRONZE AGE AEGEAN: AN EXPERIMENTAL APPROACH TO THEIR POSSIBLE USE AS LIQUID MIRRORS by PAPATHANASSOGLOU, D. A., GEORGOULI, CH. A.

“…The so‐called ‘frying pans’ are peculiar vessels, most of them made of terracotta, flat and shallow, usually decorated on the outside part and dated to the…”
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142 The Effect of Vitamin K Supplementation on BMD in Children and Adolescent with Cystic Fibrosis by Nicolaidou, P, Georgouli, H, Stavrinadis, I, Loukou, J, Papadopoulou, A, Douros, K, Gourgiotis, D, Antoniou, A, Doudounakis, S

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Invasive meningococcal disease presenting as Henoch-Schoenlein purpura by Tsolia, M N, Fretzayas, A, Georgouli, H, Tzanakaki, G, Fessatou, S, Liapi-Adamidou, G, Constantopoulos, A

“…Henoch-Schoenlein purpura (HSP) is an acute systemic form of vasculitis that has been associated with a number of viral and bacterial infections. Described…”
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Invasive meningococcal disease presenting as Henoch-Sch nlein purpura by Tsolia, M. N., Fretzayas, A., Georgouli, H., Tzanakaki, G., Fessatou, S., Liapi-Adamidou, G., Constantopoulos, A.

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Low vitamin D status in preschool children in Greece by Nicolaidou, Polyxeni, Kakourou, Talia, Papadopoulou, Anna, Kavadias, Georges, Dimitriou, Elizabeth, Georgouli, Helen, Tsapra, Helen, Giannoulia-Karantana, Aglaia, Fretzayas, Andreas, Tsiftis, Georges, Bakoula, Chryssa

“…Vitamin D status in humans depends on the amount of sun exposure and vitamin D intake. Recent reports suggest that hypovitaminosis D (as defined by serum…”
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Vitamin D receptor polymorphisms in hypocalcemic vitamin D-resistant rickets carriers by Nicolaidou, Polyxeni, Papadopoulou, Anna, Matsinos, Y G, Georgouli, Helen, Fretzayas, Andreas, Papadimitriou, Anastasios, Priftis, Kostantinos, Douros, Konstantinos, Chrousos, George P

“…Hypocalcemic vitamin D-resistant rickets (HVDRR) is a rare autosomal recessive disorder characterized by severe rickets, hypocalcemia, secondary…”
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Calcium and vitamin D metabolism in hypocalcemic vitamin D-resistant rickets carriers by Nicolaidou, Polyxeni, Papadopoulou, Anna, Georgouli, Helen, Matsinos, Y G, Tsapra, Helen, Fretzayas, Andreas, Giannoulia-Karantana, Aglaia, Kitsiou, Sophia, Douros, Konstantinos, Papassotiriou, Ioannis, Chrousos, Georges P

“…Hypocalcemic vitamin D-resistant rickets (HVDRR) is a rare monogenic autosomal recessive disorder associated with mutations in the gene of the vitamin D…”
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Urinary excretion of endothelin-1 in children with absorptive idiopathic hypercalciuria by NICOLAIDOU, Polyxeni, GEORGOULI, Helen, GETSI, Vasiliki, TSAPRA, Helen, PSYCHOU, Fotini, MATSINOS, Yiannis G, ZEIS, Petros M, GOURGIOTIS, Dimitris

“…Urinary excretion of endothelin-1 (ET-1) and plasma ET-1 were measured in 21 children with absorptive idiopathic hypercalciuria (AIH) and 22 controls. The…”
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Endothelin‐1 in children with acute poststreptococcal glomerulonephritis and hypertension by NICOLAIDOU, POLYXENI, GEORGOULI, HELEN, MATSINOS, YIANNIS, PSYCHOU, FOTINI, MESSARITAKI, ANNA, GOURGIOTIS, DIMITRIS, ZEIS, PETROS

“…Background : Endothelin‐1 (ET‐1), the most potent vasoconstrictor peptide, is known to play a role in arterial hypertension. In patients with acute…”
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Atrial natriuretic peptide in children with idiopathic hypercalciuria by NICOLAIDOU, P, NYKTARI, G, GEORGOULI, H, ATHANASSAKI, K, GAROUFI, A, PAPADIMITRIOU, A, KAVAZARAKIS, E, KARPATHIOS, T

“…We measured plasma atrial natriuretic peptide (ANP) levels in 30 children with idiopathic hypercalciuria (IH) and 19 normal controls (NC). A calcium (Ca)…”
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Persistent coagulopathy during Escherichia coli sepsis in a previously healthy infant revealed undiagnosed tyrosinaemia type 1 by Georgouli, H, Schulpis, K H, Michelakaki, H, Kaltsa, M, Sdogou, T, Kossiva, L

“…Hereditary tyrosinaemia type 1 (HT1) is caused by an enzymatic defect in tyrosine metabolism. It is an autosomal recessive disorder and affects both sexes…”
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Severe disseminated tuberculosis in a 4-month-old infant initially presenting with multiform cutaneous lesions by Spyridis, Nikos, Georgouli, Heleni, Tsoukatou, Theano, Sakou, Irini, Tsolia, Maria, Miriokefalitakis, Nikos, Spyridis, Panayiotis

“…A 4-month-old female infant presented with 1 month history of horizontal nystagmus and discrete multiform skin lesions. The patient was initially diagnosed…”
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