Nicholls K - Search Results

1

Clinical impact of genomic testing in patients with suspected monogenic kidney disease.

Jayasinghe K, Stark Z, Kerr PG, Gaff C, Martyn M, Whitlam J, Creighton B, Donaldson E, Hunter M, Jarmolowicz A, Johnstone L, Krzesinski E, Lunke S, Lynch E, Nicholls K, Patel C, Prawer Y, Ryan J, See EJ, Talbot A, Trainer A, Tytherleigh R, Valente G, Wallis M, Wardrop L, West KH, White SM, Wilkins E, Mallett AJ, Quinlan C. Jayasinghe K, et al. Among authors: nicholls k. Genet Med. 2021 Jan;23(1):183-191. doi: 10.1038/s41436-020-00963-4. Epub 2020 Sep 17. Genet Med. 2021. PMID: 32939031 Free PMC article.

2

Clinical features of Fabry's disease in Australian patients.

Galanos J, Nicholls K, Grigg L, Kiers L, Crawford A, Becker G. Galanos J, et al. Among authors: nicholls k. Intern Med J. 2002 Dec;32(12):575-84. doi: 10.1046/j.1445-5994.2002.00291.x. Intern Med J. 2002. PMID: 12512750

3

Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

KDIGO Conference Participants. KDIGO Conference Participants. Kidney Int. 2022 Jun;101(6):1126-1141. doi: 10.1016/j.kint.2022.03.019. Epub 2022 Apr 20. Kidney Int. 2022. PMID: 35460632 Free PMC article.

4

Reduced hip bone mineral density is associated with high levels of calciprotein particles in patients with Fabry disease.

Bruell S, Nicholls KM, Hewitson TD, Talbot AS, Holt SG, Smith ER, Ruderman I. Bruell S, et al. Among authors: nicholls km. Osteoporos Int. 2022 Aug;33(8):1783-1794. doi: 10.1007/s00198-022-06420-z. Epub 2022 May 16. Osteoporos Int. 2022. PMID: 35575807 Free PMC article.

5

Absence of renal phenotype in hereditary haemorrhagic telangiectasia.

Healy L, Nicholls K, Gibson R, Stella D, Bogwitz M, Taylor J, Walsh M, Donaldson L, Winship I. Healy L, et al. Among authors: nicholls k. Intern Med J. 2018 Oct;48(10):1255-1257. doi: 10.1111/imj.14059. Intern Med J. 2018. PMID: 30288899

6

Ethnicity and lupus nephritis: an Australian single centre study.

Ong C, Nicholls K, Becker G. Ong C, et al. Among authors: nicholls k. Intern Med J. 2011 Mar;41(3):270-8. doi: 10.1111/j.1445-5994.2009.02159.x. Intern Med J. 2011. PMID: 21426464

7

Retinal disease in the C3 glomerulopathies and the risk of impaired vision.

Savige J, Amos L, Ierino F, Mack HG, Symons RC, Hughes P, Nicholls K, Colville D. Savige J, et al. Among authors: nicholls k. Ophthalmic Genet. 2016 Dec;37(4):369-376. doi: 10.3109/13816810.2015.1101777. Epub 2016 Feb 25. Ophthalmic Genet. 2016. PMID: 26915021 Review.

8

Safety and efficacy of a novel short occlusive regimen of imiquimod for selected non-melanotic skin lesions in renal transplant patients.

Das G, Tan B, Nicholls K. Das G, et al. Among authors: nicholls k. Intern Med J. 2016 Mar;46(3):352-5. doi: 10.1111/imj.13004. Intern Med J. 2016. PMID: 26968597

9

Treatable lysosomal storage diseases in the advent of disease-specific therapy.

Peters H, Ellaway C, Nicholls K, Reardon K, Szer J. Peters H, et al. Among authors: nicholls k. Intern Med J. 2020 Nov;50 Suppl 4:5-27. doi: 10.1111/imj.15100. Intern Med J. 2020. PMID: 33210402

10

The significance of focal and segmental hyalinosis and sclerosis (FSHS) and nephrotic range proteinuria in IgA nephropathy.

Packham DK, Yan HD, Hewitson TD, Nicholls KM, Fairley KF, Kincaid-Smith P, Becker GJ. Packham DK, et al. Among authors: nicholls km. Clin Nephrol. 1996 Oct;46(4):225-9. Clin Nephrol. 1996. PMID: 8905206

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