Oxfordshire Childrens Diabetes - The Primary Schools Intervention Programme

Por Pal, Rani, Edge, Julie
Publicado no BMJ Qual Improv Rep (2013)

Protocol for systematic review of evidence on the determinants and influence of early glycaemic control in childhood-onset type 1 diabetes

Por Mazarello Paes, Veena, Charalampopoulos, Dimitrios, Khanolkar, Amal R., Taylor-Robinson, David, Viner, Russell, Edge, Julie, Stephenson, Terence, Amin, Rakesh
Publicado no Syst Rev (2015)

An alternative sensor-based method for glucose monitoring in children and young people with diabetes

Por Edge, Julie, Acerini, Carlo, Campbell, Fiona, Hamilton-Shield, Julian, Moudiotis, Chris, Rahman, Shakeel, Randell, Tabitha, Smith, Anne, Trevelyan, Nicola
Publicado no Arch Dis Child (2017)

Risk of microalbuminuria and progression to macroalbuminuria in a cohort with childhood onset type 1 diabetes: prospective observational study

Por Amin, Rakesh, Widmer, Barry, Prevost, A Toby, Schwarze, Phillip, Cooper, Jason, Edge, Julie, Marcovecchio, Loredana, Neil, Andrew, Dalton, R Neil, Dunger, David B
Publicado em 2008

Maternal but Not Paternal Association of Ambulatory Blood Pressure With Albumin Excretion in Young Offspring With Type 1 Diabetes

Por Marcovecchio, M. Loredana, Tossavainen, Paivi H., Acerini, Carlo L., Barrett, Timothy G., Edge, Julie, Neil, Andrew, Shield, Julian, Widmer, Barry, Dalton, R. Neil, Dunger, David B.
Publicado em 2010

Prevalence of Abnormal Lipid Profiles and the Relationship With the Development of Microalbuminuria in Adolescents With Type 1 Diabetes

Por Marcovecchio, M. Loredana, Dalton, R. Neil, Prevost, A. Toby, Acerini, Carlo L., Barrett, Timothy G., Cooper, Jason D., Edge, Julie, Neil, Andrew, Shield, Julian, Widmer, Barry, Todd, John A., Dunger, David B.
Publicado em 2009

Analysis of Transcription Factors Key for Mouse Pancreatic Development Establishes NKX2-2 and MNX1 Mutations as Causes of Neonatal Diabetes in Man

Por Flanagan, Sarah E., De Franco, Elisa, Lango Allen, Hana, Zerah, Michele, Abdul-Rasoul, Majedah M., Edge, Julie A., Stewart, Helen, Alamiri, Elham, Hussain, Khalid, Wallis, Sam, de Vries, Liat, Rubio-Cabezas, Oscar, Houghton, Jayne A.L., Edghill, Emma L., Patch, Ann-Marie, Ellard, Sian, Hattersley, Andrew T.
Publicado em 2014

Clinical and Molecular Genetic Spectrum of Congenital Deficiency of the Leptin Receptor

Por Farooqi, I. Sadaf, Wangensteen, Teresia, Collins, Stephan, Kimber, Wendy, Matarese, Giuseppe, Keogh, Julia M., Lank, Emma, Bottomley, Bill, Lopez-Fernandez, Judith, Ferraz-Amaro, Ivan, Dattani, Mehul T., Ercan, Oya, Myhre, Anne Grethe, Retterstol, Lars, Stanhope, Richard, Edge, Julie A., McKenzie, Sheila, Lessan, Nader, Ghodsi, Maryam, De Rosa, Veronica, Perna, Francesco, Fontana, Silvia, Barroso, Inês, Undlien, Dag E., O'Rahilly, Stephen
Publicado em 2007