Morand M - Search Results

1

The day-to-day experiences of caring for children with Osteogenesis Imperfecta: A qualitative descriptive study.

Castro AR, Marinello J, Chougui K, Morand M, Bilodeau C, Tsimicalis A. Castro AR, et al. Among authors: morand m. J Clin Nurs. 2020 Aug;29(15-16):2999-3011. doi: 10.1111/jocn.15310. Epub 2020 May 22. J Clin Nurs. 2020. PMID: 32350946

2

Use of Netnography to Understand GoFundMe^® Crowdfunding Profiles Posted for Individuals and Families of Children with Osteogenesis Imperfecta.

Tsimicalis A, Gasse M, Morand M, Rauch F. Tsimicalis A, et al. Among authors: morand m. Healthcare (Basel). 2022 Aug 2;10(8):1451. doi: 10.3390/healthcare10081451. Healthcare (Basel). 2022. PMID: 36011107 Free PMC article.

3

Expanded prenatal phenotype of ALG12-associated congenital disorder of glycosylation including bilateral multicystic kidneys.

Shanmugasundaram M, Wang A, Morand M, Bixler C, Jain S, Ray J. Shanmugasundaram M, et al. Among authors: morand m. Am J Med Genet A. 2024 May 8:e63660. doi: 10.1002/ajmg.a.63660. Online ahead of print. Am J Med Genet A. 2024. PMID: 38717015

4

Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females.

Bier C, Dickey K, Bibb B, Crutcher A, Sponberg R, Chang R, Boyer M, Davis-Keppen L, Matthes C, Tharp M, Vice D, Cooney E, Morand M, Ray J, Lah M, McNutt M, Andersson HC. Bier C, et al. Among authors: morand m. Mol Genet Metab. 2024 Mar;141(3):108152. doi: 10.1016/j.ymgme.2024.108152. Epub 2024 Feb 3. Mol Genet Metab. 2024. PMID: 38367583 Free article.

5

Top 10 research priorities for cutaneous squamous cell carcinoma: results of the Skin Investigation Network of Canada Priority Setting Initiative.

Lefrançois P, Doueidari Z, Kleiner O, Manion R, Dutz J, Philip A, Chan AW; Skin Investigation Network of Canada Priority Setting Collaborative. Lefrançois P, et al. Br J Dermatol. 2024 Feb 16;190(3):431-432. doi: 10.1093/bjd/ljad387. Br J Dermatol. 2024. PMID: 38114099

6

Repair of a Large Infraorbital Cheek Defect.

Mistry B, Morand M, Liu M, Chan AW. Mistry B, et al. Among authors: morand m. Dermatol Surg. 2024 May 1;50(5):477-479. doi: 10.1097/DSS.0000000000004021. Epub 2023 Nov 10. Dermatol Surg. 2024. PMID: 37962123 No abstract available.

7

Novel mosaic TRAF7 likely pathogenic variant in an African American family.

Colleran JA, Daykin EC, Hernandez C, Ray J, Morand M. Colleran JA, et al. Among authors: morand m. Am J Med Genet A. 2023 Jul;191(7):1990-1993. doi: 10.1002/ajmg.a.63214. Epub 2023 Apr 17. Am J Med Genet A. 2023. PMID: 37067385

8

Serpentine Supravenous Hyperpigmentation.

Maalouf NS, Morand M. Maalouf NS, et al. Among authors: morand m. N Engl J Med. 2022 Dec 22;387(25):e67. doi: 10.1056/NEJMicm2207158. N Engl J Med. 2022. PMID: 36546629 No abstract available.

9

GABRG1 variant as a potential novel cause of epileptic encephalopathy, hypotonia, and global developmental delay.

Williams A, Cooney E, Segal G, Narayanan S, Morand M, Agadi S. Williams A, et al. Among authors: morand m. Am J Med Genet A. 2022 Dec;188(12):3546-3549. doi: 10.1002/ajmg.a.62969. Epub 2022 Sep 19. Am J Med Genet A. 2022. PMID: 36121006

10

Factors impacting adolescent and young adult cancer patients' decision to pursue genetic counseling and testing.

Morand M, Roth M, Peterson SK, Bednar EM, Ramdaney A, Livingston JA, Yarbrough A, Corredor J. Morand M, et al. Support Care Cancer. 2022 Jun;30(6):5481-5489. doi: 10.1007/s00520-022-06974-y. Epub 2022 Mar 19. Support Care Cancer. 2022. PMID: 35306607 Free PMC article.

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