Search Results - "Petropoulou, Theoni"
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1
Chronic granulomatous disease: the European experience
Published in PloS one (21-04-2009)“…CGD is an immunodeficiency caused by deletions or mutations in genes that encode subunits of the leukocyte NADPH oxidase complex. Normally, assembly of the…”
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2
Hematopoietic stem cell gene therapy for adenosine deaminase-deficient severe combined immunodeficiency leads to long-term immunological recovery and metabolic correction
Published in Science translational medicine (24-08-2011)“…Genetic defects in the purine salvage enzyme adenosine deaminase (ADA) lead to severe combined immunodeficiency (SCID) with profound depletion of T, B, and…”
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3
425 A case of a 13-year-old boy with parapneumonic effusion caused by Streptococcus constellatus
Published in Archives of disease in childhood (11-10-2021)“…A 13-year-old previously healthy male presented with a two-week history of intermittent fever and left subcostal pain, which had previously been attributed to…”
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4
Mild nocturnal hypoxaemia and elevated pulse rate in infants with viral bronchiolitis: An oximetry‐based study
Published in Acta Paediatrica (01-03-2022)Get full text
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5
A Syndrome with Congenital Neutropenia and Mutations in G6PC3
Published in The New England journal of medicine (01-01-2009)“…Five children from two consanguineous families were born with severe congenital neutropenia, prominent venous angiectasia, and congenital heart defects,…”
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6
Teeth and Tongue Discoloration After Linezolid Treatment in Children
Published in The Pediatric infectious disease journal (01-11-2013)“…We describe 3 children who developed teeth and tongue discoloration while receiving intravenous linezolid for 2 to 3 weeks. Linezolid was coadministered with…”
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7
Autoinflammation with Infantile Enterocolitis Associated with Recurrent Perianal Abscesses
Published in Journal of clinical immunology (01-04-2019)Get full text
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8
Thyroid Function in Greek Patients with Thalassemia Major
Published in Blood (16-11-2012)“…Abstract 5176 Disturbances of thyroid function is known to frequently occur in Thalassemia Major (TM); its types prevalence and severity vary in different…”
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9
Longitudinal Changes in Iron Overload Parameters and Iron Chelation Therapy in Young Patients with Thalassemia Major
Published in Blood (18-11-2011)“…Abstract 3202 New modalities for the assessment of iron overload and the availability of new oral chelators have led to important changes in the iron load…”
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10
Iron Chelation Therapy in Transfusion Dependent Patients with Thalassemia and Minimal Liver Iron Load
Published in Blood (19-11-2010)“…Abstract 4270 Recent advances in the treatment of iron overload in patients with transfusion- dependent thalassemia have dramatically changed iron related…”
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11
Traffic Load Prediction in SDN/OpenFlow Networks
Published 01-01-2016“…This thesis is an experimental attempt at applying machine learning techniques to predict the load of a network within an SDN (Software Defined Networking)…”
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Dissertation -
12
Long-term follow-up and outcome of 39 patients with chronic granulomatous disease
Published in The Journal of pediatrics (01-11-2000)“…Objectives: To evaluate the clinical long-term course in patients with chronic granulomatous disease (CGD) with respect to different CGD subtypes and currently…”
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13
Cases of Tinea capitis due to pale isolates of Trichophyton violaceum (Trichophyton glabrum) in South-East Europe. A challenge to the clinical laboratory
Published in Medical mycology case reports (01-01-2012)“…Two recent indigenous cases of tinea capitis in children due to pale isolates of Trichophyton violaceum are reported herein for the first time from South-East…”
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14
A novel syndrome with congenital neutropenia caused by mutations in G6PC3
Published in The New England journal of medicine (01-01-2009)Get full text
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15
A Novel Clinical Syndrome Associating Severe Congenital Neutropenia and Complex Developmental Aberrations Caused by Deficiency of G6PC3
Published in Blood (16-11-2008)“…We here describe a previously unrecognized nosological entity in 12 patients from 8 unrelated pedigrees. All patients presented with severe congenital…”
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16
Changes in hypervariable region 1 of the envelope 2 glycoprotein of hepatitis C virus in children and adults with humoral immune defects
Published in Journal of medical virology (01-03-2003)“…The N‐terminal end of the hepatitis C virus (HCV) envelope glycoprotein E2 contains a stretch of 27 amino acids that exhibit increased variability. This…”
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17
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections
Published in Blood (01-08-2002)“…In this study the blood cells of 4 male patients from 2 unrelated families with chronic nonspherocytic anemia and recurrent bacterial infections were…”
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18
Comparison of two antiretroviral triple combinations including the protease inhibitor indinavir in children infected with human immunodeficiency virus
Published in The Pediatric infectious disease journal (01-06-1998)“…OBJECTIVE.The effects of two antiretroviral triple combinations including the protease inhibitor indinavir on the surrogate markers, viral load and CD4 cells…”
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19
Lupus erythematosus tumidus and chronic discoid lupus erythematosus in carriers of X-linked chronic granulomatous disease
Published in EJD. European journal of dermatology (01-04-2000)“…Two Caucasian carriers for chronic granulomatous disease (CGD) developed cutaneous lupus erythematosus (LE) with clinically and morphologically characteristic…”
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20
Successful Hematopoietic Stem Cell Transplantation in 2 Children with X-Linked Chronic Granulomatous Disease from Their Unaffected HLA-Identical Siblings Selected Using Preimplantation Genetic Diagnosis Combined with HLA Typing
Published in Biology of blood and marrow transplantation (01-03-2010)“…We report 2 children with X-linked chronic granulomatous disease (X-CGD) who underwent hematopoietic stem cell transplantation (HSCT) using grafts from their…”
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