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期刊名:Epma journal

缩写:EPMA J

ISSN:1878-5077

e-ISSN:1878-5085

IF/分区:5.9/Q1

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共收录本刊相关文章索引67
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Andreas Dietz,Gunnar Wichmann Andreas Dietz
This article focuses on squamous cell carcinomas of the larynx, pharynx and oral cavity which count nearly 90% of the head and neck squamous cell carcinomas (HNSCC). Individual susceptibility depends on an individually given genetic backgro...
Maurizio Scarpa,Adriana Ceci,Rosella Tomanin et al. Maurizio Scarpa et al.
The development of personalised medicine is of considerable importance for paediatric patient populations, and represents a move away from the use of treatment dosages based on experience with the same compounds in adults. Currently, howeve...
Paola Morales,Diego Bustamante,Pablo Espina-Marchant et al. Paola Morales et al.
Perinatal asphyxia occurs still with great incidence whenever delivery is prolonged, despite improvements in perinatal care. After asphyxia, infants can suffer from short- to long-term neurological sequelae, their severity depend upon the e...
Olga Golubnitschaja,Kristina Yeghiazaryan,Melanie Cebioglu et al. Olga Golubnitschaja et al.
Perinatal Asphyxia-oxygen deficit at delivery-can lead to severe hypoxic ischaemic organ damage in newborns followed by a fatal outcome or severe life-long pathologies. The severe insults often cause neurodegenerative diseases, mental retar...
Munis Dundar,Asli Subasioglu Uzak,Murat Erdogan et al. Munis Dundar et al.
Genetic testing usually helps physicians to determine possible genetic diseases in unborn babies, genetic disorders of patients and the carriers who might pass the mutant gene on to their children. They are performed on blood, tissues or ot...
Meral Ozgüç Meral Ozgüç
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 the human genome. One important...
Georgia Tounta,Aggeliki Kolialexi,Nikolas Papantoniou et al. Georgia Tounta et al.
The discovery of circulating cell-free fetal DNA (cffDNA) in maternal plasma allowed for the development of alternative methodologies that may facilitate safe non-invasive prenatal diagnosis (NIPD). The low concentration of cffDNA in matern...
Aggeliki Kolialexi,Athanasios K Anagnostopoulos,Georgia Tounta et al. Aggeliki Kolialexi et al.
Current non-invasive prenatal diagnosis for fetal aneuploidies is based on biochemical and ultrasound markers and needs to be improved in order to reduce the number of pregnant women subjected to invasive diagnostic procedures. Proteomic te...
George Th Tsangaris,Athanasios K Anagnostopoulos,Georgia Tounta et al. George Th Tsangaris et al.
Proteomics-based identification of biomarkers for fetal abnormalities and pregnancy complications in amniotic fluid (AF) has made significant progress in the past 5 years. This is attributed mainly to advances in mass spectrometry-based pro...