Brundler MA - Search Results

1

Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy.

Brodehl A, Ferrier RA, Hamilton SJ, Greenway SC, Brundler MA, Yu W, Gibson WT, McKinnon ML, McGillivray B, Alvarez N, Giuffre M, Schwartzentruber J; FORGE Canada Consortium; Gerull B. Brodehl A, et al. Among authors: brundler ma. Hum Mutat. 2016 Mar;37(3):269-79. doi: 10.1002/humu.22942. Epub 2016 Jan 8. Hum Mutat. 2016. PMID: 26666891

2

Phenotype and pathology of the dilated cardiomyopathy with ataxia syndrome in children.

Machiraju P, Degtiarev V, Patel D, Hazari H, Lowry RB, Bedard T, Sinasac D, Brundler MA, Greenway SC, Khan A. Machiraju P, et al. Among authors: brundler ma. J Inherit Metab Dis. 2022 Mar;45(2):366-376. doi: 10.1002/jimd.12441. Epub 2021 Oct 7. J Inherit Metab Dis. 2022. PMID: 34580891

3

Polyglucosan Bodies in Placental Extravillious Trophoblast for the Diagnosis of Fatal Perinatal Neuromuscular-type Glycogen Storage Disease Type IV.

Yu W, Brundler MA, Wright JR Jr. Yu W, et al. Among authors: brundler ma. Pediatr Dev Pathol. 2018 Jul-Aug;21(4):423-427. doi: 10.1177/1093526617707852. Epub 2017 May 12. Pediatr Dev Pathol. 2018. PMID: 28497716

4

Characterization of vitelline vessel remnant circulation in the umbilical cord.

De Guzman JK, Yu W, Horn C, Brundler MA, Wright JR Jr. De Guzman JK, et al. Among authors: brundler ma. Placenta. 2021 Aug;111:97-104. doi: 10.1016/j.placenta.2021.06.009. Epub 2021 Jun 18. Placenta. 2021. PMID: 34225217

5

Molecular Alterations in Pediatric Fibroblastic/Myofibroblastic Tumors: An Appraisal of a Next Generation Sequencing Assay in a Retrospective Single Centre Study.

Slack JC, Bründler MA, Nohr E, McIntyre JB, Kurek KC. Slack JC, et al. Among authors: brundler ma. Pediatr Dev Pathol. 2021 Sep-Oct;24(5):405-421. doi: 10.1177/10935266211015558. Epub 2021 May 10. Pediatr Dev Pathol. 2021. PMID: 33970051

6

Bronchiolitis obliterans organising pneumonia associated with anticonvulsant hypersensitivity syndrome induced by lamotrigine.

Ghandourah H, Bhandal S, Brundler MA, Noseworthy M. Ghandourah H, et al. Among authors: brundler ma. BMJ Case Rep. 2016 Jan 29;2016:bcr2014207182. doi: 10.1136/bcr-2014-207182. BMJ Case Rep. 2016. PMID: 26825933 Free PMC article.

7

Workload Measurement in Subspecialty Placental Pathology in Canada.

Wright JR Jr, Chan S, Morgen EK, Maung RTA; and the Canadian Association of Pathologists’ Pan-Canadian Pediatric-Perinatal Pathology Workload Committee; Brundler MA, El Demellawy D, Fraser RB, Kurek KC, Magee F, Nizalik E, Oligny LL, Somers GR, Stefanovici C, Terry J. Wright JR Jr, et al. Among authors: brundler ma. Pediatr Dev Pathol. 2022 Nov-Dec;25(6):604-610. doi: 10.1177/10935266221118150. Epub 2022 Sep 8. Pediatr Dev Pathol. 2022. PMID: 36082400

8

Submucosal Colonic Lipoblastoma Presenting With Colo-colonic Intussusception in an Infant.

Brundler MA, Kurek KC, Patel K, Jester I. Brundler MA, et al. Pediatr Dev Pathol. 2018 Jul-Aug;21(4):401-405. doi: 10.1177/1093526617705271. Epub 2017 Apr 18. Pediatr Dev Pathol. 2018. PMID: 28420321

9

Bilateral Nephroblastic Tumors and a Complex Renal Vascular Anomaly in a Patient With a Mosaic RASopathy: Novel Histopathologic Features and Molecular Insights.

Slack JC, Bründler MA, Chang CA, Perrier R, Lafay-Cousin L, Kurek KC. Slack JC, et al. Among authors: brundler ma. Pediatr Dev Pathol. 2021 May-Jun;24(3):235-240. doi: 10.1177/1093526620986502. Epub 2021 Feb 4. Pediatr Dev Pathol. 2021. PMID: 33538228

10

Adipocyte-rich CTNNB1-mutated Intramuscular Gardner Fibroma Progressing to Desmoid Fibromatosis.

Bakker A, Slack JC, Caragea M, Kurek KC, Bründler MA. Bakker A, et al. Among authors: brundler ma. Pediatr Dev Pathol. 2021 Jan-Feb;24(1):62-67. doi: 10.1177/1093526620968807. Epub 2020 Oct 26. Pediatr Dev Pathol. 2021. PMID: 33104413

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