Huculak C - Search Results

1

Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2.

Abdelfatah N, Chen R, Duff HJ, Seifer CM, Buffo I, Huculak C, Clarke S, Clegg R, Jassal DS, Gordon PMK, Ober C; Care4Rare Canada Consortium; Frosk P, Gerull B. Abdelfatah N, et al. Among authors: huculak c. JACC Basic Transl Sci. 2019 Apr 29;4(2):204-221. doi: 10.1016/j.jacbts.2018.12.001. eCollection 2019 Apr. JACC Basic Transl Sci. 2019. PMID: 31061923 Free PMC article.

2

Biallelic mutation in MYH7 and MYBPC3 leads to severe cardiomyopathy with left ventricular noncompaction phenotype.

Kolokotronis K, Kühnisch J, Klopocki E, Dartsch J, Rost S, Huculak C, Mearini G, Störk S, Carrier L, Klaassen S, Gerull B. Kolokotronis K, et al. Among authors: huculak c. Hum Mutat. 2019 Aug;40(8):1101-1114. doi: 10.1002/humu.23757. Epub 2019 Apr 24. Hum Mutat. 2019. PMID: 30924982

3

Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy.

Christian S, Atallah J, Clegg R, Giuffre M, Huculak C, Dzwiniel T, Parboosingh J, Taylor S, Somerville M. Christian S, et al. Among authors: huculak c. J Genet Couns. 2018 Feb;27(1):124-130. doi: 10.1007/s10897-017-0129-0. Epub 2017 Jul 11. J Genet Couns. 2018. PMID: 28699125

4

Early Death of 2 Siblings Related to Mutations in LMOD2, a Recently Discovered Cause of Neonatal Dilated Cardiomyopathy.

Greenway SC, Fruitman D, Ferrier R, Huculak C, Marcadier J, Sergi C, Bernier FP. Greenway SC, et al. Among authors: huculak c. CJC Open. 2021 Aug 1;3(10):1300-1302. doi: 10.1016/j.cjco.2021.07.017. eCollection 2021 Oct. CJC Open. 2021. PMID: 34888509 Free PMC article.

5

Practice Variation among an International Group of Genetic Counselors on when to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy.

Christian S, Somerville M, Huculak C, Atallah J. Christian S, et al. Among authors: huculak c. J Genet Couns. 2018 Aug 21. doi: 10.1007/s10897-018-0293-x. Online ahead of print. J Genet Couns. 2018. PMID: 30132189

6

Development and Evaluation of Decision Aids to Guide Families' Predictive Testing Choices for Children at Risk for Arrhythmia or Cardiomyopathy.

Christian S, Welsh A, Yetman J, Birch P, Bartels K, Burnell L, Curtis F, Huculak C, Zahavich L, Arbour L, Marcadier J, Atallah J. Christian S, et al. Among authors: huculak c. Can J Cardiol. 2021 Oct;37(10):1586-1592. doi: 10.1016/j.cjca.2021.05.018. Epub 2021 Jun 18. Can J Cardiol. 2021. PMID: 34147624 Review.

7

V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicity.

Huculak C, Bruyere H, Nelson TN, Kozak FK, Langlois S. Huculak C, et al. Am J Med Genet A. 2006 Nov 15;140(22):2394-400. doi: 10.1002/ajmg.a.31486. Am J Med Genet A. 2006. PMID: 17036313

8

Angiogenesis in the distal femoral chondroepiphysis of the rabbit during development of the secondary centre of ossification.

Doschak MR, Cooper DM, Huculak CN, Matyas JR, Hart DA, Hallgrimsson B, Zernicke RF, Bray RC. Doschak MR, et al. Among authors: huculak cn. J Anat. 2003 Aug;203(2):223-33. doi: 10.1046/j.1469-7580.2003.00198.x. J Anat. 2003. PMID: 12924822 Free PMC article.

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