Caro-Lyne DesRoches
Overview
Explore the profile of Caro-Lyne DesRoches including associated specialties, affiliations and a list of published articles.
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5
Citations
46
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Recent Articles
1.
Luo K, DesRoches C, Johnston A, Harris L, Zhao H, Ouellet T
Can J Microbiol
. 2017 Sep;
63(11):921-927.
PMID: 28926717
Fusarium graminearum is a plant pathogen that can cause the devastating cereal grain disease fusarium head blight in temperate regions of the world. Previous studies have shown that F. graminearum...
2.
Bruun T, DesRoches C, Wilson D, Chau V, Nakagawa T, Yamasaki M, et al.
Genet Med
. 2017 Aug;
20(5):486-494.
PMID: 28817111
PurposeNeonatal encephalopathy, which is characterized by a decreased level of consciousness, occurs in 1-7/1,000 live-term births. In more than half of term newborns, there is no identifiable etiological factor. To...
3.
DesRoches C, Bruun T, Wang P, Marshall C, Mercimek-Mahmutoglu S
Hum Mutat
. 2016 May;
37(9):926-32.
PMID: 27233232
Arginine-glycine amidinotransferase (GATM) deficiency is an autosomal-recessive disorder caused by pathogenic variants in GATM. Clinical features include intellectual disability, hypotonia, and myopathy. Due to normal neurodevelopment in asymptomatic individuals on...
4.
DesRoches C, Patel J, Wang P, Minassian B, Marshall C, Salomons G, et al.
Mol Genet Genomics
. 2015 May;
290(6):2163-71.
PMID: 26003046
Guanidinoacetate methyltransferase (GAMT) deficiency is a neurodegenerative disease. Although no symptomatic patients on treatment achieved normal neurodevelopment, three asymptomatic newborns were reported with normal neurodevelopmental outcome on neonatal treatment. GAMT...
5.
DesRoches C, Patel J, Wang P, Minassian B, Salomons G, Marshall C, et al.
Gene
. 2015 Apr;
565(2):187-91.
PMID: 25861866
Creatine transporter deficiency (CRTR-D) is an X-linked inherited disorder of creatine transport. All males and about 50% of females have intellectual disability or cognitive dysfunction. Creatine deficiency on brain proton...