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

Por Cheetham, Tim
Publicado no 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)"

Por Wood, Claire, Straub, Volker, Guglieri, Michela, Cheetham, Tim
Publicado no J Endocr Soc (2019)

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

Por O'Sullivan, Jackie, Iyer, Sriram, Taylor, Norman, Cheetham, Tim
Publicado em 2007

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

Por Fu, Yi, Cheetham, Tim, Bourn, David, Orwoll, Eric, Cohen, David M.
Publicado em 2013

New Therapeutic Horizons for Graves’ Hyperthyroidism

Por Lane, Laura C, Cheetham, Tim D, Perros, Petros, Pearce, Simon H S
Publicado no Endocr Rev (2020)

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

Por Sahun, Yolanda Alins, Cheetham, Tim, Boot, Christopher, Straub, Volker, Wood, Claire L.
Publicado no BMC Endocr Disord (2021)

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

Por McNally, Richard JQ, Pollock, Raymond, Court, Simon, Begon, Mike, Cheetham, Tim D
Publicado em 2009

Utility of genetic testing in suspected familial cranial diabetes insipidus

Por Srinivasan, Ramesh, Ball, Stephen, Ward-Platt, Martin, Bourn, David, McAnulty, Ciaron, Cheetham, Tim
Publicado em 2013

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

Por Pearce, Mark S., Korada, Murthy, Day, Julie, Turner, Steve, Allison, David, Kibirige, Mohammed, Cheetham, Tim D.
Publicado em 2010

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

Por Pazderska, Agnieszka, Mamoojee, Yaasir, Artham, Satish, Miller, Margaret, Ball, Stephen G, Cheetham, Tim, Quinton, Richard
Publicado no Endocr Connect (2017)

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

Por Hanna, Esmée Sinéad, Cheetham, Tim, Fearon, Kristine, Herbrand, Cathy, Hudson, Nicky, McEleny, Kevin, Quinton, Richard, Stevenson, Eleanor, Wilkes, Scott
Publicado no Front Endocrinol (Lausanne) (2019)

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

Por McNally, Richard J.Q., Jones, Jeremy H., Shaikh, Mohamad Guftar, Donaldson, Malcolm D.C., Blakey, Karen, Cheetham, Tim D.
Publicado no Thyroid (2021)

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

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

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

Por 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
Publicado no 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

Por 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
Publicado no 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

Por 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.
Publicado no PLoS One (2020)

Human SH2B1 mutations are associated with maladaptive behaviors and obesity

Por 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
Publicado em 2012

Human SH2B1 mutations are associated with maladaptive behaviors and obesity

Por 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
Publicado em 2013

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

Por 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
Publicado no J Endocr Soc (2021)

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

Por 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.
Publicado no Wellcome Open Res (2020)