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Search Results - Burren, CP
Search Results - Burren, CP
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Risedronate in children with osteogenesis imperfecta: a randomised, double-blind, placebo-controlled trial
by
Bishop, Nick, Prof
,
Adami, Silvano, MD
,
Ahmed, S Faisal, MD
,
Antón, Jordi, MD
,
Arundel, Paul, MD
,
Burren, Christine P, MD
,
Devogelaer, Jean-Pierre, MD
,
Hangartner, Thomas, PhD
,
Hosszú, Eva, MD
,
Lane, Joseph M, MD
,
Lorenc, Roman, MD
,
Mäkitie, Outi, MD
,
Munns, Craig F, MD
,
Paredes, Ana, MD
,
Pavlov, Helene, MD
,
Plotkin, Horacio, MD
,
Raggio, Cathleen L, MD
,
Reyes, Maria Loreto, MD
,
Schoenau, Eckhard, MD
,
Semler, Oliver, MD
,
Sillence, David O, MD
,
Steiner, Robert D, MD
Published in
The Lancet (British edition)
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TRPV6 compound heterozygous variants result in impaired placental calcium transport and severe undermineralization and dysplasia of the fetal skeleton
by
Burren, Christine P.
,
Caswell, Richard
,
Castle, Bruce
,
Welch, C. Ross
,
Hilliard, Tom N.
,
Smithson, Sarah F.
,
Ellard, Sian
Published in
American journal of medical genetics. Part A
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Growth reference charts for children with hypochondroplasia
by
Cheung, Moira S.
,
Cole, Tim J.
,
Arundel, Paul
,
Bridges, Nicola
,
Burren, Christine P.
,
Cole, Trevor
,
Davies, Justin Huw
,
Hagenäs, Lars
,
Högler, Wolfgang
,
Hulse, Anthony
,
Mason, Avril
,
McDonnell, Ciara
,
Merker, Andrea
,
Mohnike, Klaus
,
Sabir, Ataf
,
Skae, Mars
,
Rothenbuhler, Anya
,
Warner, Justin
,
Irving, Melita
Published in
American journal of medical genetics. Part A
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G206(P) Recognising the risk factors: missed opportunities to prevent rickets
by
Hutchings, FA
,
Oliver, N
,
Thursby-Pelham, A
,
Burren, CP
Published in
Archives of disease in childhood
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G224(P) Developing a Patient Reported Outcome and Experience Measure for a Specialised Paediatric Service
by
Ryninks, KE
,
Burren, CP
,
Garratt, VL
Published in
Archives of disease in childhood
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G485(P) Acquired hypothyroidism in infantile peritoneal dialysis: the role of iatrogenic iodine exposure
by
Prasad, R
,
Mallett, T
,
Burren, CP
,
Crowne, EC
,
Dudley, JA
Published in
Archives of disease in childhood
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Developing a patient reported outcome and experience measure for a specialised paediatric service
by
Ryninks, KE
,
Burren, CP
,
Garratt, VL
Published in
Archives of disease in childhood
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The IGF-I generation test revisited : A marker of GH sensitivity
by
BUCKWAY, C. K
,
GUEVARA-AGUIRRE, J
,
PRATT, K. L
,
BURREN, C. P
,
ROSENFELD, R. G
Published in
The journal of clinical endocrinology and metabolism
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Improving the communication pathway for eye screening in paediatric diabetes
by
McIntyre, B
,
Chatterjee, Sumana
,
Cole, Abosede
,
Burren, CP
Published in
Practical diabetes (2011)
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Binding properties and distribution of insulin-like growth factor binding protein-related protein 3 (IGFBP-rP3/NovH), an additional member of the IGFBP superfamily
by
BURREN, C. P
,
WILSON, E. M
,
HWA, V
,
OH, Y
,
ROSENFELD, R. G
Published in
The journal of clinical endocrinology and metabolism
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Serum levels of insulin-like growth factor binding proteins in Ecuadorean children with growth hormone insensitivity
by
Burren, CP
,
Wanek, D
,
Mohan, S
,
Cohen, P
,
Guevara-Aguirre, J
,
Rosenfeld, RG
Published in
Acta Paediatrica
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Type 2 diabetes in adolescence – unearthed at the time of registration with the general practitioner (GP)
by
Ng, GYT
,
Burren, CP
Published in
Practical diabetes international
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Localization studies of IGFBP-2 and IGFBP-5 in the anterior compartment of the eye
by
Burren, Christine P.
,
Berka, Jennifer L.A.
,
Batch, Jennifer A.
Published in
Current eye research
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Type 2 diabetes in adolescence - unearthed at the time of registration with the general practitioner (GP)
by
Ng, GYT
,
Burren, CP
Published in
Practical Diabetes International
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Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from...
by
De Castro, Sandra C. P.
,
Leung, Kit-yi
,
Savery, Dawn
,
Burren, Katie
,
Rozen, Rima
,
Copp, Andrew J.
,
Greene, Nicholas D. E.
Published in
Birth defects research. A Clinical and molecular teratology
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