Read more about the article Learning systems in biosignal analysis.
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Learning systems in biosignal analysis.

Abstract In biosignal analysis, the utility of artificial neural networks (ANN) in classifying electromyographic (EMG) data trained with the momentum back propagation algorithm has recently been demonstrated. In the current…

Continue ReadingLearning systems in biosignal analysis.
Read more about the article Evaluation of the genotoxicity potential (by Mutatox test) of ten pesticides found as water pollutants in Cyprus.
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Evaluation of the genotoxicity potential (by Mutatox test) of ten pesticides found as water pollutants in Cyprus.

Abstract Ten pesticides: aldicarb, aldicard sulfone, aldicarb oxide, carbofuran, propoxur, methomyl, diuron, linuron, alachlor and parathion-methyl, found as water pollutants in Cyprus, were evaluated for their genotoxicity potential with the…

Continue ReadingEvaluation of the genotoxicity potential (by Mutatox test) of ten pesticides found as water pollutants in Cyprus.
Read more about the article Beta thalassaemia.
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Beta thalassaemia.

Abstract

Continue ReadingBeta thalassaemia.
Read more about the article Expression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots.
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Expression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots.

Abstract We previously identified five delta-globin gene alleles associated with reduced hemoglobin (Hb) A2 (Trifillis, P., Ioannou, P., Schwartz, E., and Surrey, S. (1991) Blood 78, 3298-3305). We have now…

Continue ReadingExpression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots.
Read more about the article Description of a symptomless cystic fibrosis L346P/M348K compound heterozygous Cypriot individual.
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Description of a symptomless cystic fibrosis L346P/M348K compound heterozygous Cypriot individual.

Abstract During the past few years we have been testing the hypothesis that Cyprus may have been spared many severe cystic fibrosis (CF) cases but not cystic fibrosis transmembrane conductance…

Continue ReadingDescription of a symptomless cystic fibrosis L346P/M348K compound heterozygous Cypriot individual.
Read more about the article New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians.
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New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians.

Abstract Two novel polymorphisms were identified in the factor V gene by direct sequencing of intronic areas. One of them, located in intron 9, is the marker closest to the…

Continue ReadingNew coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians.
Read more about the article Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
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Evidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.

Abstract The expansion of the trinucleotide repeat (CGG)n in successive generations through maternal meiosis is the cause of fragile X syndrome. Analysis of CA repeat polymorphisms flanking the FMR-1 gene…

Continue ReadingEvidence for high-risk haplotypes and (CGG)n expansion in fragile X syndrome in the Hellenic population of Greece and Cyprus.
Read more about the article A double mutant LDL receptor allele in a cypriot family with heterozygous familial hypercholesterolemia.
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A double mutant LDL receptor allele in a cypriot family with heterozygous familial hypercholesterolemia.

Abstract Two novel mutations Q363X and D365E were identified in the low-density lipoprotein receptor gene in a Cypriot patient with heterozygous familial hypercholesterolemia. Restriction enzyme analysis of the index case…

Continue ReadingA double mutant LDL receptor allele in a cypriot family with heterozygous familial hypercholesterolemia.
Read more about the article A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).
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A translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).

Abstract Mutations in the PKD2 gene on the long arm of chromosome 4 are responsible for approximately 15% of cases of polycystic kidney disease. Perhaps the only difference from the…

Continue ReadingA translation frameshift mutation induced by a cytosine insertion in the polycystic kidney disease 2 gene (PDK2).
Read more about the article The role of electron microscopy in the diagnosis of nonneoplastic muscle diseases.
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The role of electron microscopy in the diagnosis of nonneoplastic muscle diseases.

Abstract Accurate diagnosis of muscle disease is dependent on a careful clinical examination followed by the appropriate laboratory investigations, which in a contemporary diagnostic center should also include ultrastructural investigations.…

Continue ReadingThe role of electron microscopy in the diagnosis of nonneoplastic muscle diseases.