How to use thionamide anti-thyroid drug in the young– what’s new?

per Cheetham, Tim
Publicat a Thyroid Res (2021)

MON-LB050 Preliminary Results from the "Observational Study of Clinical Outcomes for Testosterone Treatment of Pubertal Delay in Duchenne Muscular Dystrophy (DMD) (NCT 02571205)"

per Wood, Claire, Straub, Volker, Guglieri, Michela, Cheetham, Tim
Publicat a J Endocr Soc (2019)

Congenital adrenal hyperplasia due to 21‐hydroxylase deficiency is associated with a prolonged gestational age

per O'Sullivan, Jackie, Iyer, Sriram, Taylor, Norman, Cheetham, Tim
Publicat 2007

Functional polymorphisms affecting the clinically important arginine-137 residue of AVPR2 do not influence serum sodium concentration at the population level

per Fu, Yi, Cheetham, Tim, Bourn, David, Orwoll, Eric, Cohen, David M.
Publicat 2013

New Therapeutic Horizons for Graves’ Hyperthyroidism

per Lane, Laura C, Cheetham, Tim D, Perros, Petros, Pearce, Simon H S
Publicat a Endocr Rev (2020)

Measurement of salivary testosterone in adolescents and young men with Duchenne muscular dystrophy

per Sahun, Yolanda Alins, Cheetham, Tim, Boot, Christopher, Straub, Volker, Wood, Claire L.
Publicat a BMC Endocr Disord (2021)

Space-time clustering analyses of type 1 diabetes in children from north-east England: support for an infectious aetiology?

per McNally, Richard JQ, Pollock, Raymond, Court, Simon, Begon, Mike, Cheetham, Tim D
Publicat 2009

Utility of genetic testing in suspected familial cranial diabetes insipidus

per Srinivasan, Ramesh, Ball, Stephen, Ward-Platt, Martin, Bourn, David, McAnulty, Ciaron, Cheetham, Tim
Publicat 2013

Increasing Incidence, but Lack of Seasonality, of Elevated TSH Levels, on Newborn Screening, in the North of England

per Pearce, Mark S., Korada, Murthy, Day, Julie, Turner, Steve, Allison, David, Kibirige, Mohammed, Cheetham, Tim D.
Publicat 2010

Safety and tolerability of one-year intramuscular testosterone regime to induce puberty in older men with CHH

per Pazderska, Agnieszka, Mamoojee, Yaasir, Artham, Satish, Miller, Margaret, Ball, Stephen G, Cheetham, Tim, Quinton, Richard
Publicat a Endocr Connect (2017)

The Lived Experience of Klinefelter Syndrome: A Narrative Review of the Literature

per Hanna, Esmée Sinéad, Cheetham, Tim, Fearon, Kristine, Herbrand, Cathy, Hudson, Nicky, McEleny, Kevin, Quinton, Richard, Stevenson, Eleanor, Wilkes, Scott
Publicat a Front Endocrinol (Lausanne) (2019)

Congenital Hypothyroidism: Space–Time Clustering of Thyroid Dysgenesis Indicates a Role for Environmental Factors in Disease Etiology

per McNally, Richard J.Q., Jones, Jeremy H., Shaikh, Mohamad Guftar, Donaldson, Malcolm D.C., Blakey, Karen, Cheetham, Tim D.
Publicat a Thyroid (2021)

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

per Farooqi, I. Sadaf, Yeo, Giles S.H., Keogh, Julia M., Aminian, Shiva, Jebb, Susan A., Butler, Gary, Cheetham, Tim, O’Rahilly, Stephen
Publicat 2000

Height as a Clinical Biomarker of Disease Burden in Adult Mitochondrial Disease

per Boal, Rachel L, Ng, Yi Shiau, Pickett, Sarah J, Schaefer, Andrew M, Feeney, Catherine, Bright, Alexandra, Taylor, Robert W, Turnbull, Doug M, Gorman, Grainne S, Cheetham, Tim, McFarland, Robert
Publicat a J Clin Endocrinol Metab (2018)

Adjuvant rituximab, a potential treatment for the young patient with Graves’ hyperthyroidism (RiGD): study protocol for a single-arm, single-stage, phase II trial

per Cole, Michael, Hynes, Ann Marie, Howel, Denise, Hall, Lesley, Abinun, Mario, Allahabadia, Amit, Barrett, Timothy, Boelaert, Kristien, Drake, Amanda J, Dimitri, Paul, Kirk, Jeremy, Zammitt, Nicola, Pearce, Simon, Cheetham, Tim
Publicat a BMJ Open (2019)

Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389

per Yau, Daphne, Laver, Thomas W., Dastamani, Antonia, Senniappan, Senthil, Houghton, Jayne A. L., Shaikh, Guftar, Cheetham, Tim, Mushtaq, Talat, Kapoor, Ritika R., Randell, Tabitha, Ellard, Sian, Shah, Pratik, Banerjee, Indraneel, Flanagan, Sarah E.
Publicat a PLoS One (2020)

Human SH2B1 mutations are associated with maladaptive behaviors and obesity

per Doche, Michael E., Bochukova, Elena G., Su, Hsiao-Wen, Pearce, Laura R., Keogh, Julia M., Henning, Elana, Cline, Joel M., Dale, Anne, Cheetham, Tim, Barroso, Inês, Argetsinger, Lawrence S., O’Rahilly, Stephen, Rui, Liangyou, Carter-Su, Christin, Farooqi, I. Sadaf
Publicat 2012

Human SH2B1 mutations are associated with maladaptive behaviors and obesity

per Doche, Michael E., Bochukova, Elena G., Su, Hsiao-Wen, Pearce, Laura R., Keogh, Julia M., Henning, Elana, Cline, Joel M., Saeed, Sadia, Dale, Anne, Cheetham, Tim, Barroso, Inês, Argetsinger, Lawrence S., O’Rahilly, Stephen, Rui, Liangyou, Carter-Su, Christin, Farooqi, I. Sadaf
Publicat 2013

Quality of Life in Children and Young People With Congenital Adrenal Hyperplasia in the United Kingdom - Nationwide Multicentre Assessment

per Lawrence, Neil Richard, Bacila, Irina-Alexandra, Mahdi, Sundus, Albi, Sabah, Cheetham, Tim D, Crowne, Elizabeth C, Das, Urmi, Dawson, Jeremy, Dattani, Mehul Tulsidas, Davies, Justin, Gevers, Eveline, Krone, Ruth, Kyriakou, Andreas, Patel, Leena, Randell, Tabitha, Ryan, Fiona, Keevil, Brian George, Ahmed, Syed Faisal, Krone, Nils Peter
Publicat a J Endocr Soc (2021)

Refinement of the critical genomic region for congenital hyperinsulinism in the Chromosome 9p deletion syndrome

per Banerjee, Indraneel, Senniappan, Senthil, Laver, Thomas W., Caswell, Richard, Zenker, Martin, Mohnike, Klaus, Cheetham, Tim, Wakeling, Matthew N., Ismail, Dunia, Lennerz, Belinda, Splitt, Miranda, Berberoğlu, Merih, Empting, Susann, Wabitsch, Martin, Pötzsch, Simone, Shah, Pratik, Siklar, Zeynep, Verge, Charles F., Weedon, Michael N., Ellard, Sian, Hussain, Khalid, Flanagan, Sarah E.
Publicat a Wellcome Open Res (2020)