Read more about the article Molecular epidemiology of rhinoviruses in Cyprus over three consecutive seasons.
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Molecular epidemiology of rhinoviruses in Cyprus over three consecutive seasons.

Abstract Human rhinoviruses (HRVs) are widespread respiratory pathogens and a major cause of acute respiratory tract infections. The aim of this study was to investigate the molecular epidemiology of rhinovirus…

Continue ReadingMolecular epidemiology of rhinoviruses in Cyprus over three consecutive seasons.
Read more about the article Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol.
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Characterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol.

Abstract Prognostic stratification is critical for making therapeutic decisions and maximizing survival of patients with acute myeloid leukemia. Advances in the genomics of acute myeloid leukemia have identified several recurrent…

Continue ReadingCharacterization of gene mutations and copy number changes in acute myeloid leukemia using a rapid target enrichment protocol.
Read more about the article Prevalence of overweight and obesity in European children below the age of 10.
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Prevalence of overweight and obesity in European children below the age of 10.

Abstract There is a lack of common surveillance systems providing comparable figures and temporal trends of the prevalence of overweight (OW), obesity and related risk factors among European preschool and…

Continue ReadingPrevalence of overweight and obesity in European children below the age of 10.
Read more about the article Recent trends in the gene therapy of β-thalassemia.
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Recent trends in the gene therapy of β-thalassemia.

Abstract The β-thalassemias are a group of hereditary hematological diseases caused by over 300 mutations of the adult β-globin gene. Together with sickle cell anemia, thalassemia syndromes are among the…

Continue ReadingRecent trends in the gene therapy of β-thalassemia.
Read more about the article Impacts of biological globalization in the Mediterranean: unveiling the deep history of human-mediated gamebird dispersal.
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Impacts of biological globalization in the Mediterranean: unveiling the deep history of human-mediated gamebird dispersal.

Abstract Humans have a long history of moving wildlife that over time has resulted in unprecedented biotic homogenization. It is, as a result, often unclear whether certain taxa are native…

Continue ReadingImpacts of biological globalization in the Mediterranean: unveiling the deep history of human-mediated gamebird dispersal.
Read more about the article Transcriptional silencing and activation of paternal DNA during Plasmodium berghei zygotic development and transformation to oocyst.
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Transcriptional silencing and activation of paternal DNA during Plasmodium berghei zygotic development and transformation to oocyst.

Abstract The malaria parasite develops sexually in the mosquito midgut upon entry with the ingested blood meal before it can invade the midgut epithelium and embark on sporogony. Recent data…

Continue ReadingTranscriptional silencing and activation of paternal DNA during Plasmodium berghei zygotic development and transformation to oocyst.
Read more about the article A prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus.
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A prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus.

Abstract Terminal deletions in the long arm of chromosome 1 result in a postnatally recognizable disorder described as 1q43q44 deletion syndrome. The size of the deletions and the resulting phenotype…

Continue ReadingA prenatally ascertained de novo terminal deletion of chromosomal bands 1q43q44 associated with multiple congenital abnormalities in a female fetus.
Read more about the article Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.
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Novel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.

Abstract Greig cephalopolysyndactyly syndrome (GCPS) is typically characterized by preaxial or mixed preaxial and postaxial polydactyly with or without syndactyly and craniofacial features including hypertelorism and macrocephaly. Although GLI3 shows…

Continue ReadingNovel GLI3 mutation in a Greek-Cypriot patient with Greig cephalopolysyndactyly syndrome.
Read more about the article The evidence is finally here: Ocular vestibular evoked myogenic potentials are mainly dependent on utricular pathway function.
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The evidence is finally here: Ocular vestibular evoked myogenic potentials are mainly dependent on utricular pathway function.

Abstract

Continue ReadingThe evidence is finally here: Ocular vestibular evoked myogenic potentials are mainly dependent on utricular pathway function.
Read more about the article Clinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients.
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Clinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients.

Abstract Despite the manifestations of primary ciliary dyskinesia (PCD) in early life, the diagnosis is often much delayed. Since 1998 in Cyprus, we have established the only national diagnostic and…

Continue ReadingClinical features of primary ciliary dyskinesia in Cyprus with emphasis on lobectomized patients.