Read more about the article Ultrasound plaque characterisation, genetic markers and risks.
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Ultrasound plaque characterisation, genetic markers and risks.

Abstract The arterial wall changes detected by ultrasound are the end result of all risk factors (exogenous, endogenous and genetic) known and unknown and are better predictors of risk than…

Continue ReadingUltrasound plaque characterisation, genetic markers and risks.
Read more about the article A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.
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A gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.

Abstract Nonsyndromic X-linked mental retardation (MRX) is a highly heterogeneous condition in which mental retardation appears to be the only consistent manifestation. According to the most recent data, 77 MRX…

Continue ReadingA gene for nonsyndromic X-linked mental retardation (MRX77) maps to Xq12-Xq21.33.
Read more about the article From symptoms to leg edema: efficacy of Daflon 500 mg.
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From symptoms to leg edema: efficacy of Daflon 500 mg.

Abstract This article reviews the mechanisms by which micronized purified flavonoid fraction (MPFF; Daflon 500 mg) acts on symptoms as well as on edema in patients with chronic venous disease,…

Continue ReadingFrom symptoms to leg edema: efficacy of Daflon 500 mg.
Read more about the article Texture-based classification of atherosclerotic carotid plaques.
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Texture-based classification of atherosclerotic carotid plaques.

Abstract There are indications that the morphology of atherosclerotic carotid plaques, obtained by high-resolution ultrasound imaging, has prognostic implications. The objective of this study was to develop a computer-aided system…

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Read more about the article Photosensitivity during the hypersomnic phase in a patient with Kleine-Levin syndrome.
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Photosensitivity during the hypersomnic phase in a patient with Kleine-Levin syndrome.

Abstract The case of an adolescent with Kleine-Levin syndrome is presented who exhibited a consistent and predictable photoparoxysmal self-limited response to intermittent photic stimulation during all relapses of his hypersomnic…

Continue ReadingPhotosensitivity during the hypersomnic phase in a patient with Kleine-Levin syndrome.
Read more about the article Woodchuck post-transcriptional element induces nuclear export of myotonic dystrophy 3′ untranslated region transcripts.
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Woodchuck post-transcriptional element induces nuclear export of myotonic dystrophy 3′ untranslated region transcripts.

Abstract The woodchuck post-transcriptional regulatory element (WPRE) can naturally accumulate hepatitis transcripts in the cytoplasm, and has been recently exploited as an enhancer of transgene expression. The retention of mutant…

Continue ReadingWoodchuck post-transcriptional element induces nuclear export of myotonic dystrophy 3′ untranslated region transcripts.
Read more about the article Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.
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Complete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.

Abstract Complete androgen insensitivity syndrome (CAIS) is characterized by a completely female phenotype in a 46,XY individual and is caused by mutations in the androgen receptor (AR) gene. A 5…

Continue ReadingComplete androgen insensitivity syndrome caused by the R855H mutation in the androgen receptor gene.
Read more about the article 5alpha-reductase 2 gene mutations in three unrelated patients of Greek Cypriot origin: identification of an ancestral founder effect.
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5alpha-reductase 2 gene mutations in three unrelated patients of Greek Cypriot origin: identification of an ancestral founder effect.

Abstract 5alpha-Steroid reductase deficiency (5alphaSRD) is an autosomal recessive enzymatic deficiency. Mutations in the 5alpha-steroid reductase type 2 gene (SRD5A2) result in male pseudohermaphroditism caused by decreased dihydrotestosterone (DHT) synthesis--a…

Continue Reading5alpha-reductase 2 gene mutations in three unrelated patients of Greek Cypriot origin: identification of an ancestral founder effect.
Read more about the article Neurogenic vestibular evoked potentials in three cases of vestibular system dysfunction.
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Neurogenic vestibular evoked potentials in three cases of vestibular system dysfunction.

Abstract To demonstrate that neurogenic vestibular evoked potentials (NVsEP) may be specific to the vestibular system using three cases of vestibular system dysfunction and normal auditory function, Neurogenic vestibular evoked…

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Read more about the article Evidence for association of endothelial cell nitric oxide synthase gene polymorphism with earlier progression to end-stage renal disease in a cohort of Hellens from Greece and Cyprus.
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Evidence for association of endothelial cell nitric oxide synthase gene polymorphism with earlier progression to end-stage renal disease in a cohort of Hellens from Greece and Cyprus.

Abstract Nitric oxide (NO) is thought to be an important factor in the deterioration of renal function. A variable-number tandem 27-bp repeat in intron 4 of the endothelial cell nitric…

Continue ReadingEvidence for association of endothelial cell nitric oxide synthase gene polymorphism with earlier progression to end-stage renal disease in a cohort of Hellens from Greece and Cyprus.