Resultats de la cerca - Cheetham, Tim

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

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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

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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

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Processing of Positive Newborn Screening Results for Congenital Hypothyroidism: A Qualitative Exploration of Current Practice in England per Holder, Pru, Cheetham, Tim, Cocca, Alessandra, Chinnery, Holly, Chudleigh, Jane

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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.

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New Therapeutic Horizons for Graves’ Hyperthyroidism per Lane, Laura C, Cheetham, Tim D, Perros, Petros, Pearce, Simon H S

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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.

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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

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Utility of genetic testing in suspected familial cranial diabetes insipidus per Srinivasan, Ramesh, Ball, Stephen, Ward-Platt, Martin, Bourn, David, McAnulty, Ciaron, Cheetham, Tim

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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.

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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

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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

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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.

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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

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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

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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

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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.

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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

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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

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Adjuvant Rituximab—Exploratory Trial in Young People With Graves Disease per Cheetham, Tim D, Cole, Michael, Abinun, Mario, Allahabadia, Amit, Barratt, Tim, Davies, Justin H, Dimitri, Paul, Drake, Amanda, Mohamed, Zainaba, Murray, Robert D, Steele, Caroline A, Zammitt, Nicola, Carnell, Sonya, Prichard, Jonathan, Watson, Gillian, Hambleton, Sophie, Matthews, John N S, Pearce, Simon H S

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