Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 46

1.

Liraglutide in Children and Adolescents with Type 2 Diabetes.

Tamborlane WV, Barrientos-Pérez M, Fainberg U, Frimer-Larsen H, Hafez M, Hale PM, Jalaludin MY, Kovarenko M, Libman I, Lynch JL, Rao P, Shehadeh N, Turan S, Weghuber D, Barrett T; Ellipse Trial Investigators.

N Engl J Med. 2019 Aug 15;381(7):637-646. doi: 10.1056/NEJMoa1903822. Epub 2019 Apr 28.

PMID:
31034184
2.

Causes, patterns and severity of androgen excess in 487 consecutively recruited pre- and post-pubertal children.

Idkowiak J, Elhassan YS, Mannion P, Smith K, Webster R, Saraff V, Barrett TG, Shaw NJ, Krone N, Dias RP, Kershaw M, Kirk JM, Högler W, Krone RE, O'Reilly MW, Arlt W.

Eur J Endocrinol. 2019 Mar 1;180(3):213-221. doi: 10.1530/EJE-18-0854.

3.

Empowering youth sport environments: Implications for daily moderate-to-vigorous physical activity and adiposity.

Fenton SAM, Duda JL, Appleton PR, Barrett TG.

J Sport Health Sci. 2017 Dec;6(4):423-433. doi: 10.1016/j.jshs.2016.03.006. Epub 2016 Mar 31.

4.

Treatment adherence and BMI reduction are key predictors of HbA1c 1 year after diagnosis of childhood type 2 diabetes in the United Kingdom.

Candler TP, Mahmoud O, Lynn RM, Majbar AA, Barrett TG, Shield JPH.

Pediatr Diabetes. 2018 Dec;19(8):1393-1399. doi: 10.1111/pedi.12761. Epub 2018 Oct 11.

PMID:
30175430
5.

Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes.

Skinner TC, Lange KS, Hoey H, Mortensen HB, Aanstoot HJ, Castaňo L, Skovlund S, Swift PG, Cameron FJ, Dorchy HR, Palmert MR, Kaprio E, Robert JJ, Danne T, Neu A, Shalitin S, Chiarelli F, Chiari G, Urakami T, Njølstad PR, Jarosz-Chobot PK, Roche EF, Castro-Correia CG, Kocova M, Åman J, Schönle E, Barrett TG, Fisher L, de Beaufort CE; Hvidoere Study Group.

Pediatr Diabetes. 2018 May;19(3):559-565. doi: 10.1111/pedi.12606. Epub 2017 Nov 20.

PMID:
29159931
6.

Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model.

Chen JH, Goh KJ, Rocha N, Groeneveld MP, Minic M, Barrett TG, Savage D, Semple RK.

Dis Model Mech. 2017 Dec 19;10(12):1411-1420. doi: 10.1242/dmm.030981.

7.

Microstructural abnormalities in white and gray matter in obese adolescents with and without type 2 diabetes.

Nouwen A, Chambers A, Chechlacz M, Higgs S, Blissett J, Barrett TG, Allen HA.

Neuroimage Clin. 2017 Jul 5;16:43-51. doi: 10.1016/j.nicl.2017.07.004. eCollection 2017.

8.

Refining genotype-phenotype correlation in Alström syndrome through study of primary human fibroblasts.

Chen JH, Geberhiwot T, Barrett TG, Paisey R, Semple RK.

Mol Genet Genomic Med. 2017 May 15;5(4):390-404. doi: 10.1002/mgg3.296. eCollection 2017 Jul.

9.

Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia.

Astuti D, Sabir A, Fulton P, Zatyka M, Williams D, Hardy C, Milan G, Favaretto F, Yu-Wai-Man P, Rohayem J, López de Heredia M, Hershey T, Tranebjaerg L, Chen JH, Chaussenot A, Nunes V, Marshall B, McAfferty S, Tillmann V, Maffei P, Paquis-Flucklinger V, Geberhiwot T, Mlynarski W, Parkinson K, Picard V, Bueno GE, Dias R, Arnold A, Richens C, Paisey R, Urano F, Semple R, Sinnott R, Barrett TG.

Hum Mutat. 2017 Jul;38(7):764-777. doi: 10.1002/humu.23233. Epub 2017 Jun 1.

10.

Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty.

Idkowiak J, Taylor AE, Subtil S, O'Neil DM, Vijzelaar R, Dias RP, Amin R, Barrett TG, Shackleton CH, Kirk JM, Moss C, Arlt W.

J Clin Endocrinol Metab. 2016 Jun;101(6):2545-53. doi: 10.1210/jc.2015-4101. Epub 2016 Mar 22.

11.

A truncating TPO mutation (Y55X) in patients with hypothyroidism and total iodide organification defect.

Cangul H, Darendeliler F, Saglam Y, Kucukemre B, Kendall M, Boelaert K, Barrett TG, Maher ER.

Endocr Res. 2015;40(3):146-50. doi: 10.3109/07435800.2014.967354. Epub 2014 Oct 20.

PMID:
25328990
12.

Sarco(endo)plasmic reticulum ATPase is a molecular partner of Wolfram syndrome 1 protein, which negatively regulates its expression.

Zatyka M, Da Silva Xavier G, Bellomo EA, Leadbeater W, Astuti D, Smith J, Michelangeli F, Rutter GA, Barrett TG.

Hum Mol Genet. 2015 Feb 1;24(3):814-27. doi: 10.1093/hmg/ddu499. Epub 2014 Sep 30.

13.

One Base Deletion (c.2422delT) in the TPO Gene Causes Severe Congenital Hypothyroidism.

Cangül H, Doğan M, Sağlam Y, Kendall M, Boelaert K, Barrett TG, Maher ER.

J Clin Res Pediatr Endocrinol. 2014 Sep;6(3):169-73. doi: 10.4274/Jcrpe.1404.

14.

A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.

Cangul H, Bas VN, Saglam Y, Kendall M, Barrett TG, Maher ER, Aycan Z.

J Pediatr Endocrinol Metab. 2014 Nov;27(11-12):1101-5. doi: 10.1515/jpem-2014-0025.

PMID:
24945425
15.

An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesis.

Cangul H, Saglam H, Saglam Y, Eren E, Dogan D, Kendall M, Tarim O, Maher ER, Barrett TG.

J Pediatr Endocrinol Metab. 2014 Sep;27(9-10):1021-5. doi: 10.1515/jpem-2014-0048.

PMID:
24859513
16.

A deletion including exon 2 of the TSHR gene is associated with thyroid dysgenesis and severe congenital hypothyroidism.

Cangul H, Schoenmakers NA, Saglam H, Doganlar D, Saglam Y, Eren E, Kendall M, Tarim O, Barrett TG, Chatterjee K, Maher ER.

J Pediatr Endocrinol Metab. 2014 Jul;27(7-8):731-5. doi: 10.1515/jpem-2014-0011.

PMID:
24690939
17.

A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.

Cangul H, Aycan Z, Kendall M, Bas VN, Saglam Y, Barrett TG, Maher ER.

J Pediatr Endocrinol Metab. 2014 Mar;27(3-4):323-7. doi: 10.1515/jpem-2013-0314.

PMID:
24127536
18.

EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome.

Farmer A, Aymé S, de Heredia ML, Maffei P, McCafferty S, Młynarski W, Nunes V, Parkinson K, Paquis-Flucklinger V, Rohayem J, Sinnott R, Tillmann V, Tranebjaerg L, Barrett TG.

BMC Pediatr. 2013 Aug 27;13:130. doi: 10.1186/1471-2431-13-130.

19.

Novel truncating thyroglobulin gene mutations associated with congenital hypothyroidism.

Cangul H, Boelaert K, Dogan M, Saglam Y, Kendall M, Barrett TG, Maher ER.

Endocrine. 2014 Mar;45(2):206-12. doi: 10.1007/s12020-013-0027-7. Epub 2013 Aug 15.

PMID:
23949896
20.

Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing.

Dias RP, Nightingale P, Hardy C, Kirby G, Tee L, Price S, Macdonald F, Barrett TG, Maher ER.

J Med Genet. 2013 Sep;50(9):635-9. doi: 10.1136/jmedgenet-2013-101693. Epub 2013 Jun 28.

PMID:
23812911
21.

Do eating behaviors in the general population account for country variance in glycemic control among adolescents with diabetes: the Hvidoere Study Group and the Health Behaviour in School-Aged Children study.

Due P, de Beaufort C, Damsgaard MT, Mortensen HB, Rasmussen M, Ahluwalia N, Skinner T, Swift P; HSG and HBSC consortia.

Pediatr Diabetes. 2013 Dec;14(8):554-61. doi: 10.1111/pedi.12038. Epub 2013 Jun 17.

PMID:
23773782
22.

Clinical utility gene card for: Alström Syndrome - update 2013.

Marshall JD, Maffei P, Beck S, Barrett TG, Paisey R, Naggert JK.

Eur J Hum Genet. 2013 Nov;21(11). doi: 10.1038/ejhg.2013.61. Epub 2013 Apr 24. No abstract available.

23.

Home urine C-peptide creatinine ratio (UCPCR) testing can identify type 2 and MODY in pediatric diabetes.

Besser RE, Shields BM, Hammersley SE, Colclough K, McDonald TJ, Gray Z, Heywood JJ, Barrett TG, Hattersley AT.

Pediatr Diabetes. 2013 May;14(3):181-8. doi: 10.1111/pedi.12008. Epub 2013 Jan 4.

PMID:
23289766
24.

Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community.

Cangul H, Aycan Z, Olivera-Nappa A, Saglam H, Schoenmakers NA, Boelaert K, Cetinkaya S, Tarim O, Bober E, Darendeliler F, Bas V, Demir K, Aydin BK, Kendall M, Cole T, Högler W, Chatterjee VK, Barrett TG, Maher ER.

Clin Endocrinol (Oxf). 2013 Aug;79(2):275-81. doi: 10.1111/cen.12127. Epub 2013 May 6.

PMID:
23236987
25.

Vacuolar-type H+-ATPase V1A subunit is a molecular partner of Wolfram syndrome 1 (WFS1) protein, which regulates its expression and stability.

Gharanei S, Zatyka M, Astuti D, Fenton J, Sik A, Nagy Z, Barrett TG.

Hum Mol Genet. 2013 Jan 15;22(2):203-17. doi: 10.1093/hmg/dds400. Epub 2012 Oct 3.

PMID:
23035048
26.

TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis.

Cangul H, Aycan Z, Saglam H, Forman JR, Cetinkaya S, Tarim O, Bober E, Cesur Y, Kurtoglu S, Darendeliler F, Bas V, Eren E, Demir K, Kiraz A, Aydin BK, Karthikeyan A, Kendall M, Boelaert K, Shaw NJ, Kirk J, Högler W, Barrett TG, Maher ER.

J Pediatr Endocrinol Metab. 2012;25(5-6):419-26.

PMID:
22876533
27.

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility.

Haghighi A, Haghighi A, Setoodeh A, Saleh-Gohari N, Astuti D, Barrett TG.

Eur J Hum Genet. 2013 Mar;21(3):347-51. doi: 10.1038/ejhg.2012.154. Epub 2012 Jul 11.

28.

Premature adrenarche: novel lessons from early onset androgen excess.

Idkowiak J, Lavery GG, Dhir V, Barrett TG, Stewart PM, Krone N, Arlt W.

Eur J Endocrinol. 2011 Aug;165(2):189-207. doi: 10.1530/EJE-11-0223. Epub 2011 May 26. Review.

PMID:
21622478
29.

Clinical utility gene card for: Alström syndrome.

Marshall JD, Maffei P, Beck S, Barrett TG, Paisey RB.

Eur J Hum Genet. 2011 Oct;19(10). doi: 10.1038/ejhg.2011.72. Epub 2011 Apr 27. No abstract available.

30.

Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism.

Cangul H, Morgan NV, Forman JR, Saglam H, Aycan Z, Yakut T, Gulten T, Tarim O, Bober E, Cesur Y, Kirby GA, Pasha S, Karkucak M, Eren E, Cetinkaya S, Bas V, Demir K, Yuca SA, Meyer E, Kendall M, Hogler W, Barrett TG, Maher ER.

Clin Endocrinol (Oxf). 2010 Nov;73(5):671-7. doi: 10.1111/j.1365-2265.2010.03849.x.

PMID:
20718767
31.

Design and validation of a metabolic disorder resequencing microarray (BRUM1).

Bruce CK, Smith M, Rahman F, Liu ZF, McMullan DJ, Ball S, Hartley J, Kroos MA, Heptinstall L, Reuser AJ, Rolfs A, Hendriksz C, Kelly DA, Barrett TG, MacDonald F, Maher ER, Gissen P.

Hum Mutat. 2010 Jul;31(7):858-65. doi: 10.1002/humu.21261.

PMID:
20578233
32.

Adolescent type 1 Diabetes Cardio-renal Intervention Trial (AdDIT).

Adolescent type 1 Diabetes cardio-renal Intervention Trial Research Group.

BMC Pediatr. 2009 Dec 17;9:79. doi: 10.1186/1471-2431-9-79.

33.

Psychosocial factors are associated with metabolic control in adolescents: research from the Hvidoere Study Group on Childhood Diabetes.

Hoey H; Hvidoere Study Group on Childhood Diabetes.

Pediatr Diabetes. 2009 Dec;10 Suppl 13:9-14. doi: 10.1111/j.1399-5448.2009.00609.x. Review. No abstract available.

PMID:
19930221
34.

Maternal but not paternal association of ambulatory blood pressure with albumin excretion in young offspring with type 1 diabetes.

Marcovecchio ML, Tossavainen PH, Acerini CL, Barrett TG, Edge J, Neil A, Shield J, Widmer B, Dalton RN, Dunger DB.

Diabetes Care. 2010 Feb;33(2):366-71. doi: 10.2337/dc09-1152. Epub 2009 Nov 16.

35.

Prevalence of abnormal lipid profiles and the relationship with the development of microalbuminuria in adolescents with type 1 diabetes.

Marcovecchio ML, Dalton RN, Prevost AT, Acerini CL, Barrett TG, Cooper JD, Edge J, Neil A, Shield J, Widmer B, Todd JA, Dunger DB.

Diabetes Care. 2009 Apr;32(4):658-63. doi: 10.2337/dc08-1641. Epub 2009 Jan 26.

36.

Hearing impairment in genotyped Wolfram syndrome patients.

Plantinga RF, Pennings RJ, Huygen PL, Bruno R, Eller P, Barrett TG, Vialettes B, Paquis-Fluklinger V, Lombardo F, Cremers CW.

Ann Otol Rhinol Laryngol. 2008 Jul;117(7):494-500.

PMID:
18700423
37.

Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress.

Zatyka M, Ricketts C, da Silva Xavier G, Minton J, Fenton S, Hofmann-Thiel S, Rutter GA, Barrett TG.

Hum Mol Genet. 2008 Jan 15;17(2):190-200. Epub 2007 Oct 18.

38.

Functional analysis of monocarboxylate transporter 8 mutations identified in patients with X-linked psychomotor retardation and elevated serum triiodothyronine.

Jansen J, Friesema EC, Kester MH, Milici C, Reeser M, Grüters A, Barrett TG, Mancilla EE, Svensson J, Wemeau JL, Busi da Silva Canalli MH, Lundgren J, McEntagart ME, Hopper N, Arts WF, Visser TJ.

J Clin Endocrinol Metab. 2007 Jun;92(6):2378-81. Epub 2007 Mar 13.

PMID:
17356046
39.

Rising incidence of type 2 diabetes in children in the U.K.

Haines L, Wan KC, Lynn R, Barrett TG, Shield JP.

Diabetes Care. 2007 May;30(5):1097-101. Epub 2007 Jan 26.

PMID:
17259470
40.

The Birmingham Registry for Twin and Heritability Studies (BiRTHS).

Krone RE, Ewer AK, Barrett TG, Moy RJ, Bakour S, Maher ER, Thangaratinam S, Cox P, Martin B, Khan KS, Zeegers MP.

Twin Res Hum Genet. 2006 Dec;9(6):907-12.

PMID:
17254429
41.

Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.

Ricketts CJ, Minton JA, Samuel J, Ariyawansa I, Wales JK, Lo IF, Barrett TG.

Acta Paediatr. 2006 Jan;95(1):99-104.

PMID:
16373304
42.

Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation.

Friesema EC, Grueters A, Biebermann H, Krude H, von Moers A, Reeser M, Barrett TG, Mancilla EE, Svensson J, Kester MH, Kuiper GG, Balkassmi S, Uitterlinden AG, Koehrle J, Rodien P, Halestrap AP, Visser TJ.

Lancet. 2004 Oct 16-22;364(9443):1435-7.

PMID:
15488219
43.

Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.

Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C.

Diabetes. 2004 Jul;53(7):1876-83.

44.

The emergence of type 2 diabetes in childhood.

Ehtisham S, Barrett TG.

Ann Clin Biochem. 2004 Jan;41(Pt 1):10-6. Review.

PMID:
14713381
45.

[Report of a Brazilian patient with Wolfram Syndrome].

Zen PR, Pinto LL, Schwartz IV, Barrett TG, Paskulin G.

J Pediatr (Rio J). 2002 Nov-Dec;78(6):529-32. Portuguese.

46.

Wolfram syndrome.

Minton JA, Rainbow LA, Ricketts C, Barrett TG.

Rev Endocr Metab Disord. 2003 Mar;4(1):53-9. Review. No abstract available.

PMID:
12618560

Supplemental Content

Loading ...
Support Center