Hasil Pencarian - Rodney D Gilbert
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1
Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm oleh Eleanor G. Seaby, Rodney D. Gilbert, Rodney D. Gilbert, Gaia Andreoletti, Reuben J. Pengelly, Catherine Mercer, David Hunt, Sarah Ennis
Diterbitkan 2017-05-01Dapatkan teks lengkap
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2
A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project) oleh Gary Leggatt, Guo Cheng, Sumit Narain, Luis BriseƱo-Roa, Jean-Philippe Annereau, The Genomics England Research Consortium, Christine Gast, Rodney D. Gilbert, Sarah Ennis
Diterbitkan 2023-06-01Dapatkan teks lengkap
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3
Efficacy and safety of eculizumab in children with Shiga-toxin-producing Escherichia coli haemolytic uraemic syndrome: the ECUSTEC RCT oleh Natalie Ives, Rebecca Woolley, Moin A Saleem, Catherine A Moakes, Aoife Waters, Rodney D Gilbert, Hugh Jarrett, Elizabeth Brettell, Steve Nash, Louise K Farmer, Khadija Ourradi, Sally A Johnson
Diterbitkan 2024-07-01Dapatkan teks lengkap
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4
Daily low-dose prednisolone to prevent relapse of steroid-sensitive nephrotic syndrome in children with an upper respiratory tract infection: PREDNOS2 RCT oleh Martin T Christian, Nicholas JA Webb, Rebecca L Woolley, Nafsika Afentou, Samir Mehta, Emma Frew, Elizabeth A Brettell, Adam R Khan, David V Milford, Detlef Bockenhauer, Moin A Saleem, Angela S Hall, Ania Koziell, Heather Maxwell, Shivaram Hegde, Eric R Finlay, Rodney D Gilbert, Caroline Jones, Karl McKeever, Wendy Cook, Natalie Ives
Diterbitkan 2022-01-01Dapatkan teks lengkap
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