Works matching AU Clayton, Peter E

Results: 52

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

Published in:

Journal of the Endocrine Society, 2022, v. 6, n. 3, p. 1, doi. 10.1210/jendso/bvac006

By:

Parsons, Samuel;
Stevens, Adam;
Whatmore, Andrew;
Clayton, Peter E;
Murray, Philip G

Publication type:

Article

Expanding the Spectrum of Mutations in GH1 and GHRHR: Genetic Screening in a Large Cohort of Patients with Congenital Isolated Growth Hormone Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2009, v. 94, n. 9, p. 3191, doi. 10.1210/jc.2008-2783

By:

Alatzoglou, Kyriaki S.;
Turton, James P.;
Kelberman, Daniel;
Clayton, Peter E.;
Mehta, Ameeta;
Buchanan, Charles;
Aylwin, Simon;
Crowne, Elisabeth C.;
Christesen, Henrik T.;
Hertel, Niels T.;
Trainer, Peter J.;
Savage, Martin O.;
Raza, Jamal;
Banerjee, Kausik;
Sinha, Sunil K.;
Ten, Svetlana;
Mushtaq, Talat;
Brauner, Raja;
Cheetham, Timothy D.;
Hindmarsh, Peter C.

Publication type:

Article

Association studies of common variants in 10 hypogonadotropic hypogonadism genes with age at menarche.

Published in:

2008

By:

Gajdos, Zofia K Z;
Butler, Johannah L;
Henderson, Katherine DeLellis;
He, Chunyan;
Supelak, Pamela J;
Egyud, Matthew;
Price, Alkes;
Reich, David;
Clayton, Peter E;
Le Marchand, Loic;
Hunter, David J;
Henderson, Brian E;
Palmert, Mark R;
Hirschhorn, Joel N

Publication type:

journal article

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

Published in:

2007

By:

Petkovic, Vibor;
Lochmatter, Didier;
Turton, James;
Clayton, Peter E;
Trainer, Peter J;
Dattani, Mehul T;
Eblé, Andrée;
Robinson, Iain C;
Flück, Christa E;
Mullis, Primus E

Publication type:

journal article

Adiponectin in Umbilical Cord Blood Is Inversely Related to Low-Density Lipoprotein Cholesterol But Not Ethnicity.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 6, p. 2244, doi. 10.1210/jc.2005-2714

By:

Bansal, Narinder;
Charlton-Menys, Valentine;
Pemberton, Philip;
McElduff, Patrick;
Oldroyd, John;
Vyas, Avni;
Koudsi, Abir;
Clayton, Peter E.;
Cruickshank, J. Kennedy;
Durrington, Paul N.

Publication type:

Article

Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 8, p. 4762, doi. 10.1210/jc.2005-0570

By:

Turton, James P. G.;
Reynaud, Rachel;
Mehta, Ameeta;
Torpian, John;
Saveanu, Alexandru;
Woods, Kathryn S.;
Tiulpakov, Anatoly;
Zdravkovic, Vera;
Hamilton, Jill;
Attard-Montalto, Simon;
Parascandalo, Ray;
Vella, Cecil;
Clayton, Peter E.;
Shalet, Stephen;
Barton, John;
Brue, Thierry;
Dattani, Mehul T.

Publication type:

Article

Novel Mutations within the POU1F1 Gene Associated with Variable Combined Pituitary Hormone Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 6, p. 4762, doi. 10.1210/jc.2005-0570

By:

Turton, James P. G.;
Reynaud, Rachel;
Mehta, Ameeta;
Torpiano, John;
Saveanu, Alexandru;
Woods, Kathryn S.;
Tiulpakov, Anatoly;
Zdravkovic, Vera;
Hamilton, Jill;
Attard-Montalto, Simon;
Parascandalo, Ray;
Vella, Cecil;
Clayton, Peter E.;
Shalet, Stephen;
Barton, John;
Brue, Thierry;
Dattani, Mehul T.

Publication type:

Article

Determination of Sequence Variation and Haplotype Structure for the Gonadotropin-Releasing Hormone (GnRH) and GnRH Receptor Genes: Investigation of Role in Pubertal Timing.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 1091, doi. 10.1210/jc.2004-0649

By:

Sedlmeyer, Ines L.;
Pearce, Celeste Leigh;
Trueman, Julie A.;
Butler, Johannah L.;
Bersaglieri, Todd;
Read, Andrew P.;
Clayton, Peter E.;
Kolonel, Laurence N.;
Henderson, Brian E.;
Hirschhorn, Joel N.;
Palmert, Mark R.

Publication type:

Article

Behavioral and physical masculinization are related to genotype in girls with congenital adrenal hyperplasia.

Published in:

2004

By:

Hall, Catherine M;
Jones, Julie A;
Meyer-Bahlburg, Heino F L;
Dolezal, Curtis;
Coleman, Michelle;
Foster, Peter;
Price, David A;
Clayton, Peter E

Publication type:

journal article

Familial Isolated Growth Hormone Deficiency Is Associated with Increased Systolic Blood Pressure, Central Obesity, and Dyslipidemia.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 5, p. 2018, doi. 10.1210/jcem.87.5.8474

By:

Soares Barreto-Filho, José Augusto;
Alcântara, Marta Regina S.;
Salvatori, Roberto;
Barreto, Martha Azevedo;
Sobral Sousa, Antônio Carlos;
Bastos, Valquíria;
Souza, Anita Hermínia;
C. Pereira, Rossana Maria;
Clayton, Peter E.;
Gill, Matthew S.;
Aguiar-Oliveira, Manuel Hermínio

Publication type:

Article

Patterns of GH Output and Their Synchrony with Short-Term Height Increments Influence Stature and Growth Performance in Normal Children.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 12, p. 5860, doi. 10.1210/jcem.86.12.8116

By:

GILL, MATTHEW S.;
TILLMANN, VALLO;
VELDHUIS, JOHANNES D.;
CLAYTON, PETER E.

Publication type:

Article

The Acute Leptin Response to GH.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 9, p. 4412, doi. 10.1210/jcem.86.9.7796

By:

LISSETT, CATHERINE A.;
CLAYTON, PETER E.;
SHALET, STEPHEN M.

Publication type:

Article

Effect of Severe Growth Hormone (GH) Deficiency due to a Mutation in the GH-Releasing Hormone Receptor on Insulin-Like Growth Factors (IGFs), IGF-Binding Proteins, and Ternary Complex Formation Throughout Life.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 11, p. 4118, doi. 10.1210/jcem.84.11.6133

By:

AGUIAR-OLIVEIRA, MANUEL H.;
GILL, MATTHEW S.;
BARRETTO, ELENILDE S. DE A.;
ALCANTARA, MARTA R. S.;
MIRAKI-MOUD, FARIDEH;
MENEZES, CARLOS A.;
SOUZA, ANITA H. O.;
MARTINELLI, CARLOS E.;
PEREIRA, F. A.;
SALVATORI, ROBERTO;
LEVINE, MICHAEL A.;
SHALET, STEPHEN M.;
CAMACHO-HUBNER, CECILIA;
CLAYTON, PETER E.

Publication type:

Article

Biochemical Tests in the Diagnosis of Childhood Growth Hormone Deficiency.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 2, p. 531, doi. 10.1210/jcem.82.2.3750

By:

TILLMANN, VALLO;
BUCKLER, JOHN M. H.;
KIBIRIGE, MOHAMMED S.;
PRICE, DAVID A.;
SHALET, STEPHEN M.;
WALES, JEREMY K. H.;
ADDISON, MICHAEL G.;
GILL, MATHEW S.;
WHATMORE, ANDY J.;
CLAYTON, PETER E.

Publication type:

Article

Infradian Rhythms in Urinary Growth Hormone Excretion.

Published in:

Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 1, p. 100, doi. 10.1210/jc.81.1.100

By:

THALANGE, NANDU K. S.;
GILL, MATTHEW S.;
GILL, LEN;
WHATMORE, ANDREW J.;
ADDISON, G. MICHAEL;
PRICE, D. ANTHONY;
CLAYTON, PETER E.

Publication type:

Article

The challenge of delivering endocrine care and successful transition to adult services in adolescents with congenital adrenal hyperplasia: experience in a single centre over 18 years.

Published in:

Clinical Endocrinology, 2013, v. 78, n. 1, p. 23, doi. 10.1111/cen.12053

By:

Gleeson, Helena;
Davis, Joanne;
Jones, Julie;
O'Shea, Elaine;
Clayton, Peter E.

Publication type:

Article

Transition in endocrinology: the challenge of maintaining continuity.

Published in:

Clinical Endocrinology, 2013, v. 78, n. 1, p. 29, doi. 10.1111/j.1365-2265.2012.04473.x

By:

Downing, Jennifer;
Gleeson, Helena K.;
Clayton, Peter E.;
Davis, Julian R. E.;
Wales, Jerry K.;
Callery, Peter

Publication type:

Article

Exploring the spectrum of 3-M syndrome, a primordial short stature disorder of disrupted ubiquitination.

Published in:

Clinical Endocrinology, 2012, v. 77, n. 3, p. 335, doi. 10.1111/j.1365-2265.2012.04428.x

By:

Clayton, Peter E.;
Hanson, Dan;
Magee, Lucia;
Murray, Philip G.;
Saunders, Emma;
Abu-Amero, Sayeda N.;
Moore, Gudrun E.;
Black, Graeme C. M.

Publication type:

Article

A pilot study to evaluate gene expression profiles in peripheral blood mononuclear cells (PBMCs) from children with GH deficiency and Turner syndrome in response to GH treatment.

Published in:

Clinical Endocrinology, 2009, v. 70, n. 3, p. 429, doi. 10.1111/j.1365-2265.2008.03477.x

By:

Whatmore, Andrew J.;
Patel, Leena;
Clayton, Peter E.

Publication type:

Article

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

Published in:

2019

By:

Vaz, Frédéric M;
McDermott, John H;
Alders, Mariëlle;
Wortmann, Saskia B;
Kölker, Stefan;
Pras-Raves, Mia L;
Vervaart, Martin A T;
Lenthe, Henk van;
Luyf, Angela C M;
Elfrink, Hyung L;
Metcalfe, Kay;
Cuvertino, Sara;
Clayton, Peter E;
Yarwood, Rebecca;
Lowe, Martin P;
Lovell, Simon;
Rogers, Richard C;
Study, Deciphering Developmental Disorders;
Kampen, Antoine H C van;
Ruiter, Jos P N

Publication type:

journal article

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

Published in:

European Journal of Endocrinology, 2022, v. 186, n. 6, p. P35, doi. 10.1530/eje-21-1186

By:

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;
K Biller, Beverley M;
Brabant, George;
Choong, Catherine S. Y.;
Cianfarani, Stefano;
Clayton, Peter E.;
Coutant, Regis;
Cardoso-Demartini, Adriane A.;
Fernandez, Alberto

Publication type:

Article

Phenotypic spectrum and responses to recombinant human IGF1 (rhIGF1) therapy in patients with homozygous intronic pseudoexon growth hormone receptor mutation.

Published in:

European Journal of Endocrinology, 2018, v. 178, n. 5, p. 481, doi. 10.1530/EJE-18-0042

By:

Chatterjee, Sumana;
Shapiro, Lucy;
Rose, Stephen J.;
Mushtaq, Talat;
Clayton, Peter E.;
Ten, Svetlana B.;
Bhangoo, Amrit;
Kumbattae, Uma;
Dias, Renuka;
Savage, Martin O.;
Metherel, Louise A.;
Storr, Helen L.

Publication type:

Article

The neuroendocrine sequelae of paediatric craniopharyngioma: a 40-year meta-data analysis of 185 cases from three UK centres.

Published in:

European Journal of Endocrinology, 2017, v. 176, n. 3, p. 359, doi. 10.1530/EJE-16-0812

By:

Ern Tan, Timothy Shao;
Patel, Leena;
Gopal-Kothandapani, Jaya Sujatha;
Ehtisham, Sarah;
Ikazoboh, Esieza Clare;
Hayward, Richard;
Aquilina, Kristian;
Skae, Mars;
Thorp, Nicky;
Pizer, Barry;
Didi, Mohammed;
Mallucci, Conor;
Blair, Joanne C.;
Gaze, Mark N.;
Kamaly-Asl, Ian;
Spoudeas, Helen;
Clayton, Peter E.

Publication type:

Article

Insulinoma in childhood: clinical, radiological, molecular and histological aspects of nine patients.

Published in:

European Journal of Endocrinology, 2014, v. 170, n. 5, p. 741, doi. 10.1530/EJE-13-1008

By:

Padidela, Raja;
Fiest, Miriam;
Arya, Ved;
Smith, Virpi V.;
Ashworth, Michael;
Rampling, Dyanne;
Newbould, Melanie;
Batra, Gauri;
James, Jacqueline;
Wright, Neville B.;
Dunne, Mark J.;
Clayton, Peter E.;
Banerjee, Indraneel;
Hussain, Khalid

Publication type:

Article

The association of cardiac ventricular hypertrophy with congenital hyperinsulinism.

Published in:

European Journal of Endocrinology, 2012, v. 167, n. 5, p. 619, doi. 10.1530/EJE-12-0632

By:

Banerjee, Indraneel;
Avatapalle, Bindu;
Petkar, Anjali;
Skae, Mars;
Padidela, Raja;
Ehtisham, Sarah;
Patel, Leena;
Rigby, Lindsey;
Flanagan, Sarah;
Ellard, Sian;
Jones, Caroline;
Ciotti, Giovanna;
Malaiya, Nilima;
Clayton, Peter E.

Publication type:

Article

Phenotypic variation in constitutional delay of growth and puberty: relationship to specific leptin and leptin receptor gene polymorphisms.

Published in:

European Journal of Endocrinology, 2006, v. 155, n. 1, p. 121, doi. 10.1530/eje.1.02184

By:

Banerjee, Indraneel;
Trueman, Julie A.;
Hall, Catherine M.;
Price, David A.;
Patel, Leena;
Whatmore, Andrew J.;
Hirschhorn, Joel N.;
Read, Andrew P.;
Palmert, Mark R.;
Clayton, Peter E.

Publication type:

Article

A new missense mutation in the growth hormone-releasing hormone receptor gene in familial isolated GH deficiency.

Published in:

European Journal of Endocrinology, 2003, v. 148, n. 1, p. 25, doi. 10.1530/eje.0.1480025

By:

Carakushansky, Mauri;
Whatmore, Andrew J.;
Clayton, Peter E.;
Shalet, Stephen M.;
Gleeson, Helena K.;
Price, David A.;
Levine, Michael A.;
Salvatori, Roberto

Publication type:

Article

Rare variants in single-minded 1 (SIM1) are associated with severe obesity.

Published in:

Journal of Clinical Investigation, 2013, v. 123, n. 7, p. 3042, doi. 10.1172/JCI68016

By:

Ramachandrappa, Shwetha;
Raimondo, Anne;
Cali, Anna M. G.;
Keogh, Julia M.;
Henning, Elana;
Saeed, Sadia;
Thompson, Amanda;
Garg, Sumedha;
Bochukova, Elena G.;
Brage, Soren;
Trowse, Victoria;
Wheeler, Eleanor;
Sullivan, Adrienne E.;
Dattani, Mehul;
Clayton, Peter E.;
Datta, Vippan;
Bruning, John B.;
Wareham, Nick J.;
O’Rahilly, Stephen;
Peet, Daniel J.

Publication type:

Article

Endocrine Control of Growth.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 2, p. 1, doi. 10.1002/ajmg.c.31357

By:

MURRAY, PHILIP G.;
CLAYTON, PETER E.

Publication type:

Article

Can network biology unravel the aetiology of congenital hyperinsulinism?

Published in:

Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-21

By:

Stevens, Adam;
Cosgrove, Karen E.;
Padidela, Raja;
Skae, Mars S.;
Clayton, Peter E.;
Banerjee, Indraneel;
Dunne, Mark J.

Publication type:

Article

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".

Published in:

2023

By:

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

Publication type:

Letter to the Editor

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

Published in:

Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 12, p. 3287, doi. 10.1210/clinem/dgac517

By:

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.;
Reiko Horikawa;
Toshiaki Tanaka;
Dörr, Helmuth-Günther;
Albertsson-Wikland, Kerstin;
Polak, Michel

Publication type:

Article

Gonadotrophin-Independent Precocious Puberty and Dyschondrosteosis.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 1994, v. 7, n. 3, p. 265, doi. 10.1515/jpem.1994.7.3.265

By:

Patel, Leena;
Clayton, Peter E.;
Super, Maurice;
Price, David A.

Publication type:

Article

Adiponectin and lipid profiles compared with insulins in relation to early growth of British South Asian and European children: the Manchester children's growth and vascular health study.

Published in:

2011

By:

Bansal, Narinder;
Anderson, Simon G;
Vyas, Avni;
Gemmell, Isla;
Charlton-Menys, Valentine;
Oldroyd, John;
Pemberton, Philip;
Durrington, Paul N;
Clayton, Peter E;
Cruickshank, J Kennedy

Publication type:

journal article

Serum leptin and IGF-I during growth hormone treatment in chronic renal failure.

Published in:

Pediatric Nephrology, 2002, v. 17, n. 8, p. 643, doi. 10.1007/s00467-002-0883-5

By:

Patel, Leena;
Webb, Nicholas A.;
Bradbury, Mark G.;
Zaman, Nasra;
Smith, Patricia;
Lewis, Malcolm A.;
Postlethwaite, Robert J.;
Price, David A.;
Clayton, Peter E.

Publication type:

Article

Feeding Problems are Persistent in children with severe congenital hyperinsulinism.

Published in:

Frontiers in Endocrinology, 2016, p. 1, doi. 10.3389/fendo.2016.00008

By:

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.;
Jääskeläinen, Jarmo;
Saenger, Paul;
Garibaldi, Luigi R.

Publication type:

Article

Reduced glycemic variability in diazoxide-responsive children with congenital hyperinsulinism using supplemental omega-3-polyunsaturated fatty acids; a pilot trial with MaxEPA<sup>R</sup>\.

Published in:

Frontiers in Endocrinology, 2014, v. 5, p. 1, doi. 10.3389/fendo.2014.00031

By:

Skae, Mars;
Bindu Avatapalle, Hima;
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.

Publication type:

Article

Abnormal neurodevelopmental outcomes are common in children with transient congenital hyperinsulinism.

Published in:

Frontiers in Endocrinology, 2013, v. 4, p. 1, doi. 10.3389/fendo.2013.00060

By:

Bindu Avatapalle, Hima;
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.

Publication type:

Article

The Genetics of 3-M Syndrome: Unravelling a Potential New Regulatory Growth Pathway.

Published in:

Hormone Research in Paediatrics, 2011, v. 76, n. 6, p. 369, doi. 10.1159/000334392

By:

Hanson, Dan;
Murray, Philip G.;
Black, Graeme C.M.;
Clayton, Peter E.

Publication type:

Article

Serum Insulin-Like Growth Factor-I, IGF Binding Protein-3 and IGFBP-3 Protease Activity after Cranial Irradiation.

Published in:

Hormone Research in Paediatrics, 1998, v. 50, n. 2, p. 71, doi. 10.1159/000023237

By:

Tillmann, Vallo;
Shalet, Stephen M.;
Price, David A.;
Wales, Jeremy K.H.;
Pennells, Louise;
Soden, Joanne;
Gill, Matthew S.;
Whatmore, Andy J.;
Clayton, Peter E.

Publication type:

Article

Variability in anterior pituitary size within members of a family with GH deficiency due to a new splice mutation in the GHRH receptor gene.

Published in:

Clinical Endocrinology, 2004, v. 60, n. 4, p. 470, doi. 10.1111/j.1365-2265.2004.02003.x

By:

Alba, Maria;
Hall, Catherine M.;
Whatmore, Andrew J.;
Clayton, Peter E.;
Price, David A.;
Salvatori, Roberto

Publication type:

Article

Leptin measurement in urine in children and its relationship to other growth peptides in serum and urine.

Published in:

Clinical Endocrinology, 2003, v. 58, n. 1, p. 78, doi. 10.1046/j.1365-2265.2003.01677.x

By:

Zaman, Nasra;
Hall, Catherine M.;
Gill, Matthew S.;
Jones, Julie;
Tillmann, Vallo;
Westwood, Melissa;
Whatmore, Andrew J.;
Clayton, Peter E.

Publication type:

Article

Suppression of puberty with long-acting goserelin (Zoladex-LA): effect on gonadotrophin response to GnRH in the first treatment cycle.

Published in:

Clinical Endocrinology, 2002, v. 57, n. 2, p. 223, doi. 10.1046/j.1365-2265.2002.01571.x

By:

Trueman, Julie A.;
Tillmann, Vallo;
Cusick, Colin F.;
Foster, Peter;
Patel, Leena;
Hall, Catherine M.;
Price, David A.;
Clayton, Peter E.

Publication type:

Article

Lipid profiles in untreated severe congenital isolated growth hormone deficiency through the lifespan.

Published in:

Clinical Endocrinology, 2002, v. 57, n. 1, p. 89, doi. 10.1046/j.1365-2265.2002.01568.x

By:

Gleeson, Helena K.;
Souza, Anita H. O.;
Gill, Matthew S.;
Wieringa, Gilbert E.;
de A. Barretto, Elenilde S.;
Barretto-Filho, J. A. S.;
Shalet, Stephen M.;
Aguiar-Oliveira, Manuel H.;
Clayton, Peter E.

Publication type:

Article

Tall stature in familial glucocorticoid deficiency.

Published in:

Clinical Endocrinology, 2000, v. 53, n. 4, p. 423, doi. 10.1046/j.1365-2265.2000.01122.x

By:

Elias, Lucila L. K.;
Huebner, Angela;
Metherell, Louise A.;
Canas, Atilio;
Warne, Gary L.;
Bitti, Maria L Manca;
Cianfarani, Stefano;
Clayton, Peter E.;
Savage, Martin O.;
Clark, Adrian J. L.

Publication type:

Article

Serum leptin and body composition in children with familial GH deficiency (GHD) due to a mutation in the growth hormone-releasing hormone (GHRH) receptor.

Published in:

Clinical Endocrinology, 1999, v. 51, n. 5, p. 559, doi. 10.1046/j.1365-2265.1999.00837.x

By:

de A. Barretto, Elenilde S.;
Gill, Matthew S.;
de Freitas, Maria E. S.;
Magalhães, Marta M. G.;
Souza, Anita H. O.;
Aguiar-Oliveira, Manuel H.;
Clayton, Peter E.

Publication type:

Article

Constitutional delay in growth and puberty (CDGP) is associated with hypoleptinaemia.

Published in:

Clinical Endocrinology, 1999, v. 50, n. 6, p. 721, doi. 10.1046/j.1365-2265.1999.00736.x

By:

Gill, Matthew S.;
Hall, Catherine M.;
Tillmann, Vallo;
Clayton, Peter E.

Publication type:

Article

Relationship between growth hormone (GH) status, serum leptin and body composition in healthy and GH deficient elderly subjects.

Published in:

Clinical Endocrinology, 1997, v. 47, n. 2, p. 161, doi. 10.1046/j.1365-2265.1997.2291056.x

By:

Gill, Matthew S.;
Toogood, Andrew A.;
O'Neill, Paul A.;
Adams, Judith E.;
Thorner, Michael O.;
Shalet, Stephen M.;
Clayton, Peter E.

Publication type:

Article

Serum leptin through childhood and adolescence.

Published in:

Clinical Endocrinology, 1997, v. 46, n. 6, p. 727, doi. 10.1046/j.1365-2265.1997.2081026.x

By:

Clayton, Peter E.;
Gill, Matthew S.;
Hall, Catherine M.;
Tillmann, Vallo;
Whatmore, Andrew J.;
Price, David A.

Publication type:

Article

Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis.

Published in:

2012

By:

Renehan, Andrew G.;
Solomon, Mattea;
Zwahlen, Marcel;
Morjaria, Reena;
Whatmore, Andrew;
Audí, Laura;
Binder, Gerhard;
Blum, Werner;
Bougnères, Pierre;
Santos, Christine Dos;
Carrascosa, Antonio;
Hokken-Koelega, Anita;
Jorge, Alexander;
Mullis, Primus E.;
Tauber, Maïthé;
Patel, Leena;
Clayton, Peter E.

Publication type:

Journal Article