Výsledky vyhledávání - "Manara Elena"

Akademický článek

The Biennial report: The collaboration between MAGI Research, Diagnosis and Treatment Center of Genetic and Rare Diseases and Near East University DESAM Institute

Autor: Ergoren Mahmut Cerkez, Manara Elena, Paolacci Stefano, Cobanogullari Havva, Tuncel Gulten, Betmezoglu Meryem, Bertelli Matteo, Sanlidag Tamer

Publikováno v: The EuroBiotech Journal, Vol 4, Iss 4, Pp 167-170 (2020)

Scientific collaboration is more common now than it was before. In many areas of biomedical science, collaborations between researchers with different scientific backgrounds and perspectives have enabled researchers to address complicated questions a

Externí odkaz: https://doaj.org/article/3755d2d044fc4d96896ef5c5fb715530

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Akademický článek

Quality assurance of genetic laboratories and the EBTNA practice certification, a simple standardization assurance system for a laboratory network

Autor: Precone Vincenza, Dundar Munis, Beccari Tommaso, Turanli Eda Tahir, Cecchin Stefano, Marceddu Giuseppe, Manara Elena, Bertelli Matteo

Publikováno v: The EuroBiotech Journal, Vol 2, Iss 4, Pp 215-222 (2018)

Analytical laboratory results greatly influence medical diagnosis, about 70% of medical decisions are based on laboratory results. Quality assurance and quality control are designed to detect and correct errors in a laboratory’s analytical process

Externí odkaz: https://doaj.org/article/912a888d314e4480aa0aa6cc8ac3430a

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Akademický článek

What is Magi?

Autor: Manara Elena, Abeshi Andi, Bertelli Matteo

Publikováno v: The EuroBiotech Journal, Vol 1, Iss s2, Pp 115-118 (2017)

MAGI is concerned with research and diagnosis of rare genetic diseases. It has been operating since 2006 in Italy and abroad. Today it has three centers in Italy, including a medical genetics laboratory specialized in next generation sequencing in Bo

Externí odkaz: https://doaj.org/article/6c9f42ac5a4a41fab9645e0f0be57772

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Akademický článek

MAGI Balkans, a laboratory for the diagnosis of rare genetic diseases

Autor: Manara Elena, Maltese Paolo E., Guerri Giulia, Marceddu Giuseppe, Capodicasa Natale, Abeshi Andi, Bertelli Matteo

Publikováno v: The EuroBiotech Journal, Vol 1, Iss s2, Pp 128-130 (2017)

Molecular diagnosis relieves patients of uncertainty, aids informed decisions about health and reproductive choices, and helps them join clinical trials or access available therapy. Genetic testing by next generation sequencing (NGS) is the suggested

Externí odkaz: https://doaj.org/article/fd19a9385ea946edbd8f2d3cc3f15945

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