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Items: 1 to 50 of 51

1.

Central blood pressure and measures of early vascular disease in children with ADPKD.

Marlais M, Rajalingam S, Gu H, Savis A, Sinha MD, Winyard PJ.

Pediatr Nephrol. 2019 Jun 26. doi: 10.1007/s00467-019-04287-7. [Epub ahead of print]

PMID:
31243534
2.

International consensus statement on the diagnosis and management of autosomal dominant polycystic kidney disease in children and young people.

Gimpel C, Bergmann C, Bockenhauer D, Breysem L, Cadnapaphornchai MA, Cetiner M, Dudley J, Emma F, Konrad M, Harris T, Harris PC, König J, Liebau MC, Marlais M, Mekahli D, Metcalfe AM, Oh J, Perrone RD, Sinha MD, Titieni A, Torra R, Weber S, Winyard PJD, Schaefer F.

Nat Rev Nephrol. 2019 May 22. doi: 10.1038/s41581-019-0155-2. [Epub ahead of print] Review.

PMID:
31118499
3.

Imaging of Kidney Cysts and Cystic Kidney Diseases in Children: An International Working Group Consensus Statement.

Gimpel C, Avni EF, Breysem L, Burgmaier K, Caroli A, Cetiner M, Haffner D, Hartung EA, Franke D, König J, Liebau MC, Mekahli D, Ong ACM, Pape L, Titieni A, Torra R, Winyard PJD, Schaefer F.

Radiology. 2019 Mar;290(3):769-782. doi: 10.1148/radiol.2018181243. Epub 2019 Jan 1.

4.

Lithium induces mesenchymal-epithelial differentiation during human kidney development by activation of the Wnt signalling system.

Price KL, Kolatsi-Joannou M, Mari C, Long DA, Winyard PJD.

Cell Death Discov. 2018 Feb 7;4:13. doi: 10.1038/s41420-017-0021-6. eCollection 2018 Dec.

5.

DNAAF1 links heart laterality with the AAA+ ATPase RUVBL1 and ciliary intraflagellar transport.

Hartill VL, van de Hoek G, Patel MP, Little R, Watson CM, Berry IR, Shoemark A, Abdelmottaleb D, Parkes E, Bacchelli C, Szymanska K, Knoers NV, Scambler PJ, Ueffing M, Boldt K, Yates R, Winyard PJ, Adler B, Moya E, Hattingh L, Shenoy A, Hogg C, Sheridan E, Roepman R, Norris D, Mitchison HM, Giles RH, Johnson CA.

Hum Mol Genet. 2018 Feb 1;27(3):529-545. doi: 10.1093/hmg/ddx422.

6.

Perinatal Diagnosis, Management, and Follow-up of Cystic Renal Diseases: A Clinical Practice Recommendation With Systematic Literature Reviews.

Gimpel C, Avni FE, Bergmann C, Cetiner M, Habbig S, Haffner D, König J, Konrad M, Liebau MC, Pape L, Rellensmann G, Titieni A, von Kaisenberg C, Weber S, Winyard PJD, Schaefer F.

JAMA Pediatr. 2018 Jan 1;172(1):74-86. doi: 10.1001/jamapediatrics.2017.3938.

PMID:
29181500
7.

Loss of endogenous thymosin β4 accelerates glomerular disease.

Vasilopoulou E, Kolatsi-Joannou M, Lindenmeyer MT, White KE, Robson MG, Cohen CD, Sebire NJ, Riley PR, Winyard PJ, Long DA.

Kidney Int. 2016 Nov;90(5):1056-1070. doi: 10.1016/j.kint.2016.06.032. Epub 2016 Aug 26.

8.

Hypertension in autosomal dominant polycystic kidney disease: a meta-analysis.

Marlais M, Cuthell O, Langan D, Dudley J, Sinha MD, Winyard PJ.

Arch Dis Child. 2016 Dec;101(12):1142-1147. doi: 10.1136/archdischild-2015-310221. Epub 2016 Jun 10. Review.

PMID:
27288429
9.

The role of thymosin-β4 in kidney disease.

Vasilopoulou E, Winyard PJ, Riley PR, Long DA.

Expert Opin Biol Ther. 2015;15 Suppl 1:S187-90. doi: 10.1517/14712598.2015.1009891. Epub 2015 Jun 22.

PMID:
26096077
10.

Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases.

Huang JL, Woolf AS, Kolatsi-Joannou M, Baluk P, Sandford RN, Peters DJ, McDonald DM, Price KL, Winyard PJ, Long DA.

J Am Soc Nephrol. 2016 Jan;27(1):69-77. doi: 10.1681/ASN.2014090856. Epub 2015 Jun 2.

11.

Making your way as an academic paediatric trainee in the UK.

Brown CC, Apps JR, Davies G, Ware N, Fisher J, Winyard PJ.

Arch Dis Child Educ Pract Ed. 2014 Feb;99(1):13-4. doi: 10.1136/archdischild-2013-304675. Epub 2013 Dec 4.

PMID:
24306391
12.

Experimental renal progenitor cells: repairing and recreating kidneys?

Winyard PJ, Price KL.

Pediatr Nephrol. 2014 Apr;29(4):665-72. doi: 10.1007/s00467-013-2667-5. Epub 2013 Nov 13. Review.

PMID:
24221350
13.

A new generation of academic paediatricians.

Brown CC, Apps JR, Winyard PJ.

Lancet. 2013 Jul 6;382(9886):28. doi: 10.1016/S0140-6736(13)61527-5. No abstract available.

PMID:
23830340
14.

Low levels of knowledge on the assessment of underweight in children and adolescents among middle-grade doctors in England and Wales.

Hudson LD, Cumby C, Klaber RE, Nicholls DE, Winyard PJ, Viner RM.

Arch Dis Child. 2013 Apr;98(4):309-11. doi: 10.1136/archdischild-2012-303357. Epub 2013 Jan 31.

PMID:
23372059
15.

Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT).

Renkema KY, Winyard PJ, Skovorodkin IN, Levtchenko E, Hindryckx A, Jeanpierre C, Weber S, Salomon R, Antignac C, Vainio S, Schedl A, Schaefer F, Knoers NV, Bongers EM; EUCAKUT consortium.

Nephrol Dial Transplant. 2011 Dec;26(12):3843-51. doi: 10.1093/ndt/gfr655. Review.

PMID:
22121240
16.

Modified citrus pectin reduces galectin-3 expression and disease severity in experimental acute kidney injury.

Kolatsi-Joannou M, Price KL, Winyard PJ, Long DA.

PLoS One. 2011 Apr 8;6(4):e18683. doi: 10.1371/journal.pone.0018683.

17.

Corticosteroid-induced kidney dysmorphogenesis is associated with deregulated expression of known cystogenic molecules, as well as Indian hedgehog.

Chan SK, Riley PR, Price KL, McElduff F, Winyard PJ, Welham SJ, Woolf AS, Long DA.

Am J Physiol Renal Physiol. 2010 Feb;298(2):F346-56. doi: 10.1152/ajprenal.00574.2009. Epub 2009 Dec 9.

18.

HNF1B mutations associate with hypomagnesemia and renal magnesium wasting.

Adalat S, Woolf AS, Johnstone KA, Wirsing A, Harries LW, Long DA, Hennekam RC, Ledermann SE, Rees L, van't Hoff W, Marks SD, Trompeter RS, Tullus K, Winyard PJ, Cansick J, Mushtaq I, Dhillon HK, Bingham C, Edghill EL, Shroff R, Stanescu H, Ryffel GU, Ellard S, Bockenhauer D.

J Am Soc Nephrol. 2009 May;20(5):1123-31. doi: 10.1681/ASN.2008060633. Epub 2009 Apr 23.

19.

Mild fetal renal pelvis dilatation: much ado about nothing?

Hothi DK, Wade AS, Gilbert R, Winyard PJ.

Clin J Am Soc Nephrol. 2009 Jan;4(1):168-77. doi: 10.2215/CJN.00810208. Epub 2008 Nov 5. Review.

20.

Immunohistochemical analysis of Sonic hedgehog signalling in normal human urinary tract development.

Jenkins D, Winyard PJ, Woolf AS.

J Anat. 2007 Nov;211(5):620-9. Epub 2007 Sep 11.

21.

Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney disease.

Chiu MG, Johnson TM, Woolf AS, Dahm-Vicker EM, Long DA, Guay-Woodford L, Hillman KA, Bawumia S, Venner K, Hughes RC, Poirier F, Winyard PJ.

Am J Pathol. 2006 Dec;169(6):1925-38.

22.

Developing critical mass and growing our own academics.

Winyard PJ, Cass HD, Stephenson TJ, Wilkinson AR, Olver RE.

Arch Dis Child. 2006 Dec;91(12):1027-9.

23.

Microarray interrogation of human metanephric mesenchymal cells highlights potentially important molecules in vivo.

Price KL, Long DA, Jina N, Liapis H, Hubank M, Woolf AS, Winyard PJ.

Physiol Genomics. 2007 Jan 17;28(2):193-202. Epub 2006 Sep 19.

PMID:
16985006
24.

Perinatal renal venous thrombosis: presenting renal length predicts outcome.

Winyard PJ, Bharucha T, De Bruyn R, Dillon MJ, van't Hoff W, Trompeter RS, Liesner R, Wade A, Rees L.

Arch Dis Child Fetal Neonatal Ed. 2006 Jul;91(4):F273-8. Epub 2006 Feb 7.

25.

De novo Uroplakin IIIa heterozygous mutations cause human renal adysplasia leading to severe kidney failure.

Jenkins D, Bitner-Glindzicz M, Malcolm S, Hu CC, Allison J, Winyard PJ, Gullett AM, Thomas DF, Belk RA, Feather SA, Sun TT, Woolf AS.

J Am Soc Nephrol. 2005 Jul;16(7):2141-9. Epub 2005 May 11.

26.

OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.

Romio L, Fry AM, Winyard PJ, Malcolm S, Woolf AS, Feather SA.

J Am Soc Nephrol. 2004 Oct;15(10):2556-68.

27.

The P2X7 ATP receptor modulates renal cyst development in vitro.

Hillman KA, Woolf AS, Johnson TM, Wade A, Unwin RJ, Winyard PJ.

Biochem Biophys Res Commun. 2004 Sep 17;322(2):434-9.

PMID:
15325248
28.

Evolving concepts in human renal dysplasia.

Woolf AS, Price KL, Scambler PJ, Winyard PJ.

J Am Soc Nephrol. 2004 Apr;15(4):998-1007. Review.

29.

OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.

Romio L, Wright V, Price K, Winyard PJ, Donnai D, Porteous ME, Franco B, Giorgio G, Malcolm S, Woolf AS, Feather SA.

J Am Soc Nephrol. 2003 Mar;14(3):680-9.

30.

Effects of in utero bladder outflow obstruction on fetal sheep detrusor contractility, compliance and innervation.

Nyirady P, Thiruchelvam N, Fry CH, Godley ML, Winyard PJ, Peebles DM, Woolf AS, Cuckow PM.

J Urol. 2002 Oct;168(4 Pt 1):1615-20.

PMID:
12352467
31.

Molecular mechanisms of human embryogenesis: developmental pathogenesis of renal tract malformations.

Woolf AS, Winyard PJ.

Pediatr Dev Pathol. 2002 Mar-Apr;5(2):108-29. Review.

PMID:
11910506
32.

P2X(7) receptors are expressed during mouse nephrogenesis and in collecting duct cysts of the cpk/cpk mouse.

Hillman KA, Johnson TM, Winyard PJ, Burnstock G, Unwin RJ, Woolf AS.

Exp Nephrol. 2002;10(1):34-42.

PMID:
11803203
33.

Normal and abnormal development of the urogenital tract.

Cuckow PM, Nyirady P, Winyard PJ.

Prenat Diagn. 2001 Nov;21(11):908-16. Review.

PMID:
11746143
34.
35.

Multicystic dysplastic kidney and Kallmann's syndrome: a new association?

Deeb A, Robertson A, MacColl G, Bouloux PM, Gibson M, Winyard PJ, Woolf AS, Moghal NE, Cheetham TD.

Nephrol Dial Transplant. 2001 Jun;16(6):1170-5.

PMID:
11390716
36.

Galectin-3 modulates ureteric bud branching in organ culture of the developing mouse kidney.

Bullock SL, Johnson TM, Bao Q, Hughes RC, Winyard PJ, Woolf AS.

J Am Soc Nephrol. 2001 Mar;12(3):515-23.

37.

Potential biological role of transforming growth factor-beta1 in human congenital kidney malformations.

Yang SP, Woolf AS, Yuan HT, Scott RJ, Risdon RA, O'Hare MJ, Winyard PJ.

Am J Pathol. 2000 Nov;157(5):1633-47.

38.

Gene expression and cell turnover in human renal dysplasia.

Woolf AS, Winyard PJ.

Histol Histopathol. 2000 Jan;15(1):159-66. doi: 10.14670/HH-15.159. Review.

PMID:
10668206
39.

Inflammatory mediators in human renal dysplasia.

Cale CM, Klein NJ, Winyard PJ, Woolf AS.

Nephrol Dial Transplant. 2000 Feb;15(2):173-83.

PMID:
10648662
40.

Advances in the cell biology and genetics of human kidney malformations.

Woolf AS, Winyard PJ.

J Am Soc Nephrol. 1998 Jun;9(6):1114-25. Review. No abstract available.

41.

Short-term urinary flow impairment deregulates PAX2 and PCNA expression and cell survival in fetal sheep kidneys.

Attar R, Quinn F, Winyard PJ, Mouriquand PD, Foxall P, Hanson MA, Woolf AS.

Am J Pathol. 1998 May;152(5):1225-35.

42.

Epithelial galectin-3 during human nephrogenesis and childhood cystic diseases.

Winyard PJ, Bao Q, Hughes RC, Woolf AS.

J Am Soc Nephrol. 1997 Nov;8(11):1647-57.

43.
44.

Expression of hepatocyte growth factor/scatter factor and its receptor, MET, suggests roles in human embryonic organogenesis.

Kolatsi-Joannou M, Moore R, Winyard PJ, Woolf AS.

Pediatr Res. 1997 May;41(5):657-65.

PMID:
9128288
45.

The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformations.

Winyard PJ, Risdon RA, Sams VR, Dressler GR, Woolf AS.

J Clin Invest. 1996 Jul 15;98(2):451-9.

46.

Congenital enterocyte heparan sulphate deficiency with massive albumin loss, secretory diarrhoea, and malnutrition.

Murch SH, Winyard PJ, Koletzko S, Wehner B, Cheema HA, Risdon RA, Phillips AD, Meadows N, Klein NJ, Walker-Smith JA.

Lancet. 1996 May 11;347(9011):1299-301.

PMID:
8622507
47.

Deregulation of cell survival in cystic and dysplastic renal development.

Winyard PJ, Nauta J, Lirenman DS, Hardman P, Sams VR, Risdon RA, Woolf AS.

Kidney Int. 1996 Jan;49(1):135-46.

48.

KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development.

Duke VM, Winyard PJ, Thorogood P, Soothill P, Bouloux PM, Woolf AS.

Mol Cell Endocrinol. 1995 Apr 28;110(1-2):73-9.

PMID:
7545624
49.

Unravelling the pathogenesis of cystic kidney diseases.

Woolf AS, Winyard PJ.

Arch Dis Child. 1995 Feb;72(2):103-5. Review. No abstract available.

50.

The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone test.

Thornton PS, Alter CA, Katz LE, Gruccio DA, Winyard PJ, Moshang T Jr.

J Pediatr Endocrinol. 1994 Oct-Dec;7(4):317-24.

PMID:
7735369

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