Assessing the population impact of low rates of vitamin D supplementation on type 1 diabetes using a new statistical method

por Zipitis, Christos S, Mughal, Zulf M, Clayton, Peter E
Publicado 2016

Role of ZBTB38 Genotype and Expression in Growth and Response to Recombinant Human Growth Hormone Treatment

por Parsons, Samuel, Stevens, Adam, Whatmore, Andrew, Clayton, Peter E, Murray, Philip G
Publicado 2022

Identifying biological pathways that underlie primordial short stature using network analysis

por Hanson, Dan, Stevens, Adam, Murray, Philip G, Black, Graeme C M, Clayton, Peter E
Publicado 2014

Glucose uptake as an alternative to oxygen uptake for assessing metabolic rate in Danio rerio larvae

por Evans, Bridget L., Hurlstone, Adam F.L., Clayton, Peter E., Stevens, Adam, Shiels, Holly A.
Publicado 2022

Maternal malaria status and metabolic profiles in pregnancy and in cord blood: relationships with birth size in Nigerian infants

por Ayoola, Omolola O, Whatmore, Andrew, Balogun, Williams O, Jarrett, Olatokunbo O, Cruickshank, John K, Clayton, Peter E
Publicado 2012

Can network biology unravel the aetiology of congenital hyperinsulinism?

por Stevens, Adam, Cosgrove, Karen E, Padidela, Raja, Skae, Mars S, Clayton, Peter E, Banerjee, Indraneel, Dunne, Mark J
Publicado 2013

Metabolites involved in Glycolysis and Amino Acid Metabolism are Altered in Short Children Born Small for Gestational Age

por Murray, Philip G, Butcher, Imogen, Dunn, Warwick B, Stevens, Adam, Perchard, Reena, Hanson, Daniel, Whatmore, Andrew, Westwood, Melissa, Clayton, Peter E
Publicado 2016

Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism

por Banerjee, Indraneel, Forsythe, Lynette, Skae, Mars, Avatapalle, Hima Bindu, Rigby, Lindsey, Bowden, Louise E., Craigie, Ross, Padidela, Raja, Ehtisham, Sarah, Patel, Leena, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado 2016

Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R)

por Skae, Mars, Avatapalle, Hima Bindu, Banerjee, Indraneel, Rigby, Lindsey, Vail, Andy, Foster, Peter, Charalambous, Christiana, Bowden, Louise, Padidela, Raja, Patel, Leena, Ehtisham, Sarah, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado 2014

Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism

por Avatapalle, Hima Bindu, Banerjee, Indraneel, Shah, Sajni, Pryce, Megan, Nicholson, Jacqueline, Rigby, Lindsey, Caine, Louise, Didi, Mohammed, Skae, Mars, Ehtisham, Sarah, Patel, Leena, Padidela, Raja, Cosgrove, Karen E., Dunne, Mark J., Clayton, Peter E.
Publicado 2013

Response to Letter to the Editor From Virú-Loza and Chávez-Nomberto: “Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort”

por Maghnie, Mohamad, Ranke, Michael B, Geffner, Mitchell E, Vlachopapadopoulou, Elpis, Ibáñez, Lourdes, Carlsson, Martin, Cutfield, Wayne, Rooman, Raoul, Gomez, Roy, Wajnrajch, Michael P, Linglart, Agnès, Stawerska, Renata, Clayton, Peter E, Darendeliler, Feyza, Hokken-Koelega, Anita C S, Horikawa, Reiko, Tanaka, Toshiaki, Dörr, Helmuth-Günther, Albertsson-Wikland, Kerstin, Polak, Michel, Grimberg, Adda
Publicado 2023

Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort

por Maghnie, Mohamad, Ranke, Michael B, Geffner, Mitchell E, Vlachopapadopoulou, Elpis, Ibáñez, Lourdes, Carlsson, Martin, Cutfield, Wayne, Rooman, Raoul, Gomez, Roy, Wajnrajch, Michael P, Linglart, Agnès, Stawerska, Renata, Clayton, Peter E, Darendeliler, Feyza, Hokken-Koelega, Anita C S, Horikawa, Reiko, Tanaka, Toshiaki, Dörr, Helmuth-Günther, Albertsson-Wikland, Kerstin, Polak, Michel, Grimberg, Adda
Publicado 2022

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

por Alston, Charlotte L, Howard, Caoimhe, Oláhová, Monika, Hardy, Steven A, He, Langping, Murray, Philip G, O'Sullivan, Siobhan, Doherty, Gary, Shield, Julian P H, Hargreaves, Iain P, Monavari, Ardeshir A, Knerr, Ina, McCarthy, Peter, Morris, Andrew A M, Thorburn, David R, Prokisch, Holger, Clayton, Peter E, McFarland, Robert, Hughes, Joanne, Crushell, Ellen, Taylor, Robert W
Publicado 2016

Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption

por Meyer, Stefan, Stevens, Adam, Paredes, Roberto, Schneider, Marion, Walker, Michael J, Williamson, Andrew J K, Gonzalez-Sanchez, Maria-Belen, Smetsers, Stephanie, Dalal, Vineet, Teng, Hsiang Ying, White, Daniel J, Taylor, Sam, Muter, Joanne, Pierce, Andrew, de Leonibus, Chiara, Rockx, Davy A P, Rooimans, Martin A, Spooncer, Elaine, Stauffer, Stacey, Biswas, Kajal, Godthelp, Barbara, Dorsman, Josephine, Clayton, Peter E, Sharan, Shyam K, Whetton, Anthony D
Publicado 2017

Growth Hormone Research Society perspective on biomarkers of GH action in children and adults

por Johannsson, Gudmundur, Bidlingmaier, Martin, Biller, Beverly M K, Boguszewski, Margaret, Casanueva, Felipe F, Chanson, Philippe, Clayton, Peter E, Choong, Catherine S, Clemmons, David, Dattani, Mehul, Frystyk, Jan, Ho, Ken, Hoffman, Andrew R, Horikawa, Reiko, Juul, Anders, Kopchick, John J, Luo, Xiaoping, Neggers, Sebastian, Netchine, Irene, Olsson, Daniel S, Radovick, Sally, Rosenfeld, Ron, Ross, Richard J, Schilbach, Katharina, Solberg, Paulo, Strasburger, Christian, Trainer, Peter, Yuen, Kevin C J, Wickstrom, Kerstin, Jorgensen, Jens O L
Publicado 2018

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia

por Vaz, Frédéric M, McDermott, John H, Alders, Mariëlle, Wortmann, Saskia B, Kölker, Stefan, Pras-Raves, Mia L, Vervaart, Martin A T, van Lenthe, Henk, Luyf, Angela C M, Elfrink, Hyung L, Metcalfe, Kay, Cuvertino, Sara, Clayton, Peter E, Yarwood, Rebecca, Lowe, Martin P, Lovell, Simon, Rogers, Richard C, van Kampen, Antoine H C, Ruiter, Jos P N, Wanders, Ronald J A, Ferdinandusse, Sacha, van Weeghel, Michel, Engelen, Marc, Banka, Siddharth
Publicado 2019

Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years’ Experience in the UK

por Buonocore, Federica, Maharaj, Avinaash, Qamar, Younus, Koehler, Katrin, Suntharalingham, Jenifer P, Chan, Li F, Ferraz-de-Souza, Bruno, Hughes, Claire R, Lin, Lin, Prasad, Rathi, Allgrove, Jeremy, Andrews, Edward T, Buchanan, Charles R, Cheetham, Tim D, Crowne, Elizabeth C, Davies, Justin H, Gregory, John W, Hindmarsh, Peter C, Hulse, Tony, Krone, Nils P, Shah, Pratik, Shaikh, M Guftar, Roberts, Catherine, Clayton, Peter E, Dattani, Mehul T, Thomas, N Simon, Huebner, Angela, Clark, Adrian J, Metherell, Louise A, Achermann, John C
Publicado 2021

Safety of growth hormone replacement in survivors of cancer and intracranial and pituitary tumours: a consensus statement

por Boguszewski, Margaret C S, Boguszewski, Cesar L, Chemaililly, Wassim, Cohen, Laurie E, Gebauer, Judith, Higham, Claire, Hoffman, Andrew R, Polak, Michel, Yuen, Kevin C J, Alos, Nathalie, Antal, Zoltan, Bidlingmaier, Martin, Biller, Beverley M K, Brabant, George, Choong, Catherine S Y, Cianfarani, Stefano, Clayton, Peter E, Coutant, Regis, Cardoso-Demartini, Adriane A, Fernandez, Alberto, Grimberg, Adda, Guðmundsson, Kolbeinn, Guevara-Aguirre, Jaime, Ho, Ken K Y, Horikawa, Reiko, Isidori, Andrea M, Jørgensen, Jens Otto Lunde, Kamenicky, Peter, Karavitaki, Niki, Kopchick, John J, Lodish, Maya, Luo, Xiaoping, McCormack, Ann I, Meacham, Lillian, Melmed, Shlomo, Mostoufi Moab, Sogol, Müller, Hermann L, Neggers, Sebastian J C M M, Aguiar Oliveira, Manoel H, Ozono, Keiichi, Pennisi, Patricia A, Popovic, Vera, Radovick, Sally, Savendahl, Lars, Touraine, Philippe, van Santen, Hanneke M, Johannsson, Gudmundur
Publicado 2022