Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Nipa, Mitra"'
Autor:
Arthur Abelian, Thomas Mund, Martin D. Curran, Stuart A. Savill, Nipa Mitra, Carol Charan, Amanda L. Ogilvy-Stuart, Hugh R. B. Pelham, Paul H. Dear
Publikováno v:
BMC Infectious Diseases, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract Background PCRctic is an innovative assay based on 16S rDNA PCR technology that has been designed to detect a single intact bacterium in a specimen of cerebro-spinal fluid (CSF). The assay’s potential for accurate, fast and inexpensive dis
Externí odkaz:
https://doaj.org/article/69d6ef3396dd4b6ba0e8579d0f06fd5d
Autor:
Evelina, Carapancea, Marie-Coralie, Cornet, Mathieu, Milh, Lucrezia, De Cosmo, Eric J, Huang, Tiziana, Granata, Pasquale, Striano, Berten, Ceulemans, Anja, Stein, Deborah, Morris-Rosendahl, Greta, Conti, Nipa, Mitra, F Lucy, Raymond, David H, Rowitch, Roberta, Solazzi, Fabiana, Vercellino, Paola, De Liso, Gianluca, D'Onofrio, Clementina, Boniver, Olivier, Danhaive, Katherine, Carkeek, Vincenzo, Salpietro, Sarah, Weckhuysen, Marny, Fedrigo, Annalisa, Angelini, Barbara, Castellotti, Damien, Lederer, Valerie, Benoit, Federico, Raviglione, Renzo, Guerrini, Robertino, Dilena, Maria Roberta, Cilio
Publikováno v:
Neurology
BACKGROUND AND OBJECTIVES: BRAT1 encephalopathy is an ultra-rare autosomal recessive neonatal encephalopathy. We delineate the neonatal electroclinical phenotype at presentation and provide insights for early diagnosis. METHODS: Through a multination
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d587826c6eb7d87fdbd51eb1e1e4b42b
https://pubmed.ncbi.nlm.nih.gov/36599696
https://pubmed.ncbi.nlm.nih.gov/36599696
Autor:
Evelina Carapancea, Marie-Coralie Cornet, Mathieu Milh, Lucrezia De Cosmo, Eric J. Huang, Tiziana Granata, Pasquale Striano, Berten Ceulemans, Anja Stein, Deborah Morris-Rosendahl, Greta Conti, Nipa Mitra, F. Lucy Raymond, David H. Rowitch, Roberta Solazzi, Fabiana Vercellino, Paola De Liso, Gianluca D'Onofrio, Clementina Boniver, Olivier Danhaive, Katherine Carkeek, Vincenzo Salpietro, Sarah Weckhuysen, Marny Fedrigo, Annalisa Angelini, Barbara Castellotti, Damien Lederer, Valerie Benoit, Federico Raviglione, Renzo Guerrini, Robertino Dilena, Maria Roberta Cilio
Publikováno v:
Neurology
Neurology, vol 100, iss 12
Neurology, vol 100, iss 12
Background and ObjectivesBRAT1encephalopathy is an ultra-rare autosomal recessive neonatal encephalopathy. We delineate the neonatal electroclinical phenotype at presentation and provide insights for early diagnosis.MethodsThrough a multinational col
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b4cd442a416c486ed53726277bcfbd7
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85150387701
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85150387701
Autor:
Gusztav Belteki, Nipa Mitra
Publikováno v:
Archives of disease in childhood. Education and practice edition. 106(5)
Modern neonatal intensive care units use a large number of monitoring and therapeutic devices. Most of them have alarms with varying degree of standardisation. Mechanical ventilator alarms alert clinicians about technical problems with equipment, acu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d75bc4957d1236b53746aaaf15aeb36
https://pubmed.ncbi.nlm.nih.gov/33051186
https://pubmed.ncbi.nlm.nih.gov/33051186