Wade A - Search Results

1

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

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 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

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

Fibromuscular dysplasia and childhood stroke.

Kirton A, Crone M, Benseler S, Mineyko A, Armstrong D, Wade A, Sebire G, Crous-Tsanaclis AM, deVeber G. Kirton A, et al. Among authors: wade a. Brain. 2013 Jun;136(Pt 6):1846-56. doi: 10.1093/brain/awt111. Epub 2013 May 28. Brain. 2013. PMID: 23715093 Review.

6

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.

7

Areal and volumetric bone mineral density changes after renal transplantation in children: a longitudinal study.

Hamiwka LA, Hanna M, Midgley JP, Wade AW, Grisaru S. Hamiwka LA, et al. Among authors: wade aw. Transplant Proc. 2008 Jun;40(5):1404-6. doi: 10.1016/j.transproceed.2008.03.098. Transplant Proc. 2008. PMID: 18589117

8

Substantial practice variation exists in the management of childhood nephrotic syndrome.

Samuel S, Morgan CJ, Bitzan M, Mammen C, Dart AB, Manns BJ, Alexander RT, Erickson RL, Grisaru S, Wade AW, Blydt-Hansen T, Feber J, Arora S, Licht C, Zappitelli M. Samuel S, et al. Pediatr Nephrol. 2013 Dec;28(12):2289-98. doi: 10.1007/s00467-013-2546-0. Epub 2013 Aug 6. Pediatr Nephrol. 2013. PMID: 23917450

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

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.

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