检索结果 - Cheetham, Tim

How to use thionamide anti-thyroid drug in the young– what’s new? 由 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)" 由 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 由 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 由 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 由 Fu, Yi, Cheetham, Tim, Bourn, David, Orwoll, Eric, Cohen, David M.

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New Therapeutic Horizons for Graves’ Hyperthyroidism 由 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 由 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? 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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 由 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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