Read more about the article Mutations of the human polycystic kidney disease 2 (PKD2) gene.
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Mutations of the human polycystic kidney disease 2 (PKD2) gene.

Abstract Autosomal dominant polycystic kidney disease (ADPKD) is an inherited nephropathy, usually of late onset (onset between third to seventh decade), primarily characterized by the formation of fluid-filled cysts in…

Continue ReadingMutations of the human polycystic kidney disease 2 (PKD2) gene.
Read more about the article Evidence of two distinct subsubtypes within the HIV-1 subtype A radiation.
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Evidence of two distinct subsubtypes within the HIV-1 subtype A radiation.

Abstract Members of HIV-1 group M are responsible for the vast majority of AIDS cases worldwide and have been classified on the basis of their phylogenetic relationships into nine roughly…

Continue ReadingEvidence of two distinct subsubtypes within the HIV-1 subtype A radiation.
Read more about the article Alpha-thalassaemia prenatal diagnosis by two PCR-based methods.
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Alpha-thalassaemia prenatal diagnosis by two PCR-based methods.

Abstract In Cyprus all couples carrying alpha0-thalassaemia mutations are detected in the course of the thalassaemia carrier screening program and prenatal diagnosis is offered to all of them. Prenatal diagnosis…

Continue ReadingAlpha-thalassaemia prenatal diagnosis by two PCR-based methods.
Read more about the article The MNSs blood group system in the population of South Backa.
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The MNSs blood group system in the population of South Backa.

Abstract Blood groups represent qualitative characteristics of humans which are controlled by one or a few genetic loci and due to this it is easy to determine various kinds of…

Continue ReadingThe MNSs blood group system in the population of South Backa.
Read more about the article Population genetics of factor V Leiden in Europe.
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Population genetics of factor V Leiden in Europe.

Abstract We have analyzed 5971 control individuals originating from 26 geographically defined populations in Europe and neighboring countries for the presence of factor V Leiden, an important genetic risk factor…

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Read more about the article The molecular characterization of 16 new sequence variants of Hop stunt viroid reveals the existence of invariable regions and a conserved hammerhead-like structure on the viroid molecule.
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The molecular characterization of 16 new sequence variants of Hop stunt viroid reveals the existence of invariable regions and a conserved hammerhead-like structure on the viroid molecule.

Abstract At present isolates of Hop stunt viroid (HSVd) are divided into five groups: three major groups (plum-type, hop-type and citrus-type) each containing isolates from only a limited number of…

Continue ReadingThe molecular characterization of 16 new sequence variants of Hop stunt viroid reveals the existence of invariable regions and a conserved hammerhead-like structure on the viroid molecule.
Read more about the article Familial homozygous hypercholesterolemia: effective long-term treatment with cascade double filtration plasmapheresis.
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Familial homozygous hypercholesterolemia: effective long-term treatment with cascade double filtration plasmapheresis.

Abstract Homozygous familial hypercholesterolemia (FH) is a rare disease with an incidence of 1 in 1 million births. It is characterized by blood cholesterol levels over 600 mg/dl and the…

Continue ReadingFamilial homozygous hypercholesterolemia: effective long-term treatment with cascade double filtration plasmapheresis.
Read more about the article Genetic diversity among accessions of an ancient olive variety of Cyprus.
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Genetic diversity among accessions of an ancient olive variety of Cyprus.

Abstract To evaluate germplasm variability and to discriminate between accessions of 'Ladolia', an ancient olive variety of Cyprus, different accessions from a germplasm collection were screened with 11 selected oligonucleotide…

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Read more about the article Compressive lumbar myelopathy presenting as segmental motor neuron disease.
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Compressive lumbar myelopathy presenting as segmental motor neuron disease.

Abstract Four patients presented with slowly progressive, bilateral, asymmetric weakness and muscle atrophy in the lower extremities, accompanied by cramps and fasciculations. Sensory symptoms were insignificant. There was no bladder…

Continue ReadingCompressive lumbar myelopathy presenting as segmental motor neuron disease.
Read more about the article Clinical results with direct thrombin inhibitors.
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Clinical results with direct thrombin inhibitors.

Abstract Direct thrombin inhibitors inactivate thrombin without the need for antithrombin and some inactivate not only thrombin but also fibrin-bound thrombin. Hirudin has been shown to be more effective than…

Continue ReadingClinical results with direct thrombin inhibitors.