Philip Robinson - Concepedia

Author

Philip Robinson

Also Known As

Jérémy Jové, Maximilian F. Reiser, P J A ROBINSON, P J A Robinson, P J RObinson, P J Robinson, P J. Robinson, P ROBINSON, P Robinson, P. J Robinson

525

Publications

13K

Citations

H-Index

334

Concepts

All Affiliations

Royal Children's Hospital St James's University Hospital Murdoch Children's Research Institute Inserm The University of Melbourne

About

Philip Robinson is an author at Royal Children's Hospital specializing in medicine, pathology, and health sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Health Sciences	20	29	1.2K
2	Engineering	8	8	195
3	Arts	6	6	262
4	Education	4	4	96
5	Language Studies	1	1	43

Philip Robinson

195

Publications

10.7K

Citations

H-Index

Page 1

	Year	Citations
Lung Disease at Diagnosis in Infants with Cystic Fibrosis Detected by Newborn Screening Peter D. Sly, Siobhain Brennan, Catherine Gangell, American Journal of Respiratory and Critical Care Medicine	2009	544
Improved Detection of Focal Liver Lesions at MR Imaging: Multicenter Comparison of Gadoxetic Acid–enhanced MR Images with Intraoperative Findings Alexander Huppertz, Thomas Balzer, A. Blakeborough, Radiology	2004	395
A two-year randomized, placebo-controlled trial of dornase alfa in young patients with cystic fibrosis with mild lung function abnormalities Joanne Quan, Harm A.W.M. Tiddens, Judy P. Sy, The Journal of Pediatrics Two-year RandomizedPulmonary CareAdvanced Lung DiseasePulmonary FibrosisPulmonary Medicine	2001	299
Efficacy and safety of lumacaftor and ivacaftor in patients aged 6–11 years with cystic fibrosis homozygous for F508del-CFTR : a randomised, placebo-controlled phase 3 trial Félix Ratjen, Christopher Hug, Gautham Marigowda, The Lancet Respiratory Medicine Pulmonary FibrosisMedicinePlacebo-controlled Phase 3	2017	291
Infection, Inflammation, and Lung Function Decline in Infants with Cystic Fibrosis Naveen Pillarisetti, Elizabeth Williamson, Barry Linnane, American Journal of Respiratory and Critical Care Medicine	2011	282
Progression of early structural lung disease in young children with cystic fibrosis assessed using CT Lauren S. Mott, Judy Park, Conor Murray, Thorax	2011	272
Ivacaftor treatment of cystic fibrosis in children aged 12 to <24 months and with a CFTR gating mutation (ARRIVAL): a phase 3 single-arm study Margaret Rosenfeld, Claire Wainwright, Mark Higgins, The Lancet Respiratory Medicine MedicineCftr Gating MutationPediatricsIvacaftor Treatment	2018	262
Hepatocellular Carcinoma in the Cirrhotic Liver: Double-Contrast MR Imaging for Diagnosis Janice Ward, J. Ashley Guthrie, D Scott, Radiology	2000	190
Lung Function in Infants with Cystic Fibrosis Diagnosed by Newborn Screening Barry Linnane, Graham L. Hall, Siobhan Brennan, American Journal of Respiratory and Critical Care Medicine	2008	186
The mental health and wellbeing of children and adolescents in home‐based foster care Michael G. Sawyer, Josephine A. Carbone, Amelia Searle, The Medical Journal of Australia	2007	161

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