Rare Diseases
Integrative PPPM Approach as the Medicine of the Future
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Open AccessDiscovery of biomarkers in rare diseases: innovative approaches by predictive and personalized medicine
There are more than 8000 rare diseases (RDs) that affect >5 % of the world’s population. Many of the RDs have no effective treatment and lack of knowledge creates delayed diagnosis making management difficult....
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Open AccessEPMA-World Congress 2015
A1 Predictive and prognostic biomarker panel for targeted application of radioembolisation improving individual outcomes in hepatocellular carcinoma
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Bioethical Challenges of the Ebola Outbreak
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Book
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Open AccessEducation for all in the era of personalized medicine
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Open AccessA new book “Rare Diseases: Integrative PPPM Approach as the Medicine of the Future”
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Open AccessGenetic testing: predictive value of genoty** for diagnosis and management of disease
This article describes predictive, preventive value of genetic tests and the implication of the use of testing for personalized treatment. This year marks the 10th anniversity of publishing of the sequence of ...
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Changes in the Expression of Selenoproteins in Mesial Temporal Lobe Epilepsy Patients
Selenoproteins are enzymes containing selenium in their structure and are involved in cellular processes such as defense against oxidative stress and cell survival. The aim of this study is to investigate the ...
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Expression of matrix metalloproteinases in vasculitic neuropathy
The aim of this study was to investigate the expression pattern and cellular source of matrix metalloproteinases (MMP) in vasculitic neuropathy. Matrix metalloproteinases are endopeptidases degrading component...
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Sodium chloride deficiency in cystic fibrosis patients
Sodium chloride deficiency (SCD) was observed within the 1st year of life in 12 of 46 cystic fibrosis (CF) patients between July 1989 and September 1992. All patients showed sweating, loss of appetite, fever, ...
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DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population
Thirty-nine Turkish phenylketonuria (PKU) families were investigated for their DNA haplotypes at the phenylalanine hydroxylase (PAH) locus. There was a threefold higher incidence of consanguinity in the popula...
