Wade A - Search Results

1

A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders.

Innes AM, Boycott KM, Puffenberger EG, Redl D, MacDonald IM, Chudley AE, Beaulieu C, Perrier R, Gillan T, Wade A, Parboosingh JS. Innes AM, et al. Among authors: wade a. Clin Genet. 2010 Nov;78(5):424-31. doi: 10.1111/j.1399-0004.2010.01481.x. Clin Genet. 2010. PMID: 20618352

2

Meckel syndrome in the Hutterite population is actually a Joubert-related cerebello-oculo-renal syndrome.

Boycott KM, Parboosingh JS, Scott JN, McLeod DR, Greenberg CR, Fujiwara TM, Mah JK, Midgley J, Wade A, Bernier FP, Chodirker BN, Bunge M, Innes AM. Boycott KM, et al. Among authors: wade a. Am J Med Genet A. 2007 Aug 1;143A(15):1715-25. doi: 10.1002/ajmg.a.31832. Am J Med Genet A. 2007. PMID: 17603801

3

A relatively mild skeletal ciliopathy phenotype consistent with cranioectodermal dysplasia is associated with a homozygous nonsynonymous mutation in WDR35.

Smith C, Lamont RE, Wade A, Bernier FP, Parboosingh JS, Innes AM. Smith C, et al. Among authors: wade a. Am J Med Genet A. 2016 Mar;170(3):760-5. doi: 10.1002/ajmg.a.37514. Epub 2015 Dec 22. Am J Med Genet A. 2016. PMID: 26691894

4

Genome sequencing identifies biallelic variants in SCLT1 in a patient with syndromic nephronophthisis: Reflections on the SCLT1-related ciliopathy spectrum.

Gillesse E, Wade A, Parboosingh JS, Au PYB, Bernier FP; C4R Consortium; Lamont RE, Innes AM. Gillesse E, et al. Among authors: wade a. Am J Med Genet A. 2024 Nov;194(11):e63789. doi: 10.1002/ajmg.a.63789. Epub 2024 Jun 25. Am J Med Genet A. 2024. PMID: 38924217

5

Invasive Streptococcus pneumoniae infection causing hemolytic uremic syndrome in children: Two recent cases.

Vanderkooi OG, Kellner JD, Wade AW, Jadavji T, Midgley JP, Louie T, Tyrell GJ. Vanderkooi OG, et al. Can J Infect Dis. 2003 Nov;14(6):339-43. doi: 10.1155/2003/219027. Can J Infect Dis. 2003. PMID: 18159477 Free PMC article.

6

Outcomes of kidney transplantation in children with nephronophthisis: an analysis of the North American Pediatric Renal Trials and Collaborative Studies (NAPRTCS) Registry.

Hamiwka LA, Midgley JP, Wade AW, Martz KL, Grisaru S. Hamiwka LA, et al. Among authors: wade aw. Pediatr Transplant. 2008 Dec;12(8):878-82. doi: 10.1111/j.1399-3046.2008.00942.x. Pediatr Transplant. 2008. PMID: 19000067

7

Diarrhea-associated hemolytic uremic syndrome in southern Alberta: A long-term single-centre experience.

Grisaru S, Midgley JP, Hamiwka LA, Wade AW, Samuel SM. Grisaru S, et al. Among authors: wade aw. Paediatr Child Health. 2011 Jun;16(6):337-40. doi: 10.1093/pch/16.6.337. Paediatr Child Health. 2011. PMID: 22654544 Free PMC article.

8

Acute renal replacement therapy in children with diarrhea-associated hemolytic uremic syndrome: a single center 16 years of experience.

Grisaru S, Morgunov MA, Samuel SM, Midgley JP, Wade AW, Tee JB, Hamiwka LA. Grisaru S, et al. Among authors: wade aw. Int J Nephrol. 2011;2011:930539. doi: 10.4061/2011/930539. Epub 2011 May 26. Int J Nephrol. 2011. PMID: 21716936 Free PMC article.

9

Glomerular Filtration Rate Trends During Follow-up in Children With Steroid-Sensitive Nephrotic Syndrome.

Alsaidi S, Wagner D, Grisaru S, Midgley J, Hamiwka L, Wade A, Nettel-Aguirre A, Samuel S. Alsaidi S, et al. Among authors: wade a. Can J Kidney Health Dis. 2017 May 29;4:2054358117709496. doi: 10.1177/2054358117709496. eCollection 2017. Can J Kidney Health Dis. 2017. PMID: 28607687 Free PMC article.

10

The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methods.

Samuel S, Scott S, Morgan C, Dart A, Mammen C, Parekh R, Nettel-Aguirre A, Eddy A, Flynn R, Pinsk M, Wade A, Arora S, Benoit G, Bitzan M, Erickson R, Feber J, Filler G, Geier P, Girardin C, Grisaru S, Tee J, Kemp K, Zappitelli M. Samuel S, et al. Among authors: wade a. Can J Kidney Health Dis. 2014 Jul 22;1:17. doi: 10.1186/2054-3581-1-17. eCollection 2014. Can J Kidney Health Dis. 2014. PMID: 25960884 Free PMC article.

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