Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Christine A. Martin"'
Autor:
Kaitlyn Easson, Guillaume Gilbert, Claudine Gauthier, Charles V. Rohlicek, Christine Saint‐Martin, Marie Brossard‐Racine
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 12 (2023)
Background Lower cerebral blood flow (CBF) has previously been documented preoperatively in neonates with congenital heart disease (CHD). However, it remains unclear if these CBF deficits persist over the life span of CHD survivors following heart su
Externí odkaz:
https://doaj.org/article/1362c1ab89e44201960998bd92b1d86f
Autor:
Kaitlyn Easson, May Khairy, Charles V. Rohlicek, Christine Saint-Martin, Guillaume Gilbert, Kim-Anh Nguyen, Thuy Mai Luu, Élise Couture, Anne-Monique Nuyt, Pia Wintermark, Sean C. L. Deoni, Maxime Descoteaux, Marie Brossard-Racine
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
IntroductionAlterations to white matter microstructure as detected by diffusion tensor imaging have been documented in both individuals born with congenital heart disease (CHD) and individuals born preterm. However, it remains unclear if these distur
Externí odkaz:
https://doaj.org/article/931809a7bc8e48d6b1e207979a9000a5
Autor:
Yarab Al Bulushi, Christine Saint-Martin, Nikesh Muthukrishnan, Farhad Maleki, Caroline Reinhold, Reza Forghani
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Non-tuberculous mycobacterial (NTM) infection is an emerging infectious entity that often presents as lymphadenitis in the pediatric age group. Current practice involves invasive testing and excisional biopsy to diagnose NTM lymphadenitis. I
Externí odkaz:
https://doaj.org/article/d414c0fc5feb4dbab0944969aaf2d76f
Autor:
Anna L. Buczak, Benjamin D. Baugher, Christine S. Martin, Meg W. Keiley-Listermann, James Howard, Nathan H. Parrish, Anton Q. Stalick, Daniel S. Berman, Mark H. Dredze
Publikováno v:
Applied Artificial Intelligence, Vol 36, Iss 1 (2022)
Disruptive events within a country can have global repercussions, creating a need for the anticipation and planning of these events. Crystal Cube (CC) is a novel approach to forecasting disruptive political events at least one month into the future.
Externí odkaz:
https://doaj.org/article/4360a353004f448eaa73015ed8788c44
Autor:
Najmah Almuhsen, Simon‐pierre Guay, Marie Lefrancois, Cheryl Gauvin, AL Qasim Al Bahlani, Najma Ahmed, Christine Saint‐Martin, Tommy Gagnon, Paula Waters, Nancy Braverman, D. Buhas
Publikováno v:
JIMD Reports, Vol 61, Iss 1, Pp 52-59 (2021)
Abstract Adenosine kinase (ADK) deficiency is a rare autosomal recessive inborn error of metabolism involving the methionine and purine metabolic pathways. Prior reports show that most patients present in infancy with jaundice, hypotonia, development
Externí odkaz:
https://doaj.org/article/e77a685162f34ca1891ed887702aeba9
Autor:
Isabelle Buard, Natalie Lopez-Esquibel, Finnuella J. Carey, Mark S. Brown, Luis D. Medina, Eugene Kronberg, Christine S. Martin, Sarah Rogers, Samantha K. Holden, Michael R. Greher, Benzi M. Kluger
Publikováno v:
Frontiers in Human Neuroscience, Vol 16 (2022)
IntroductionCognitive impairment is a highly prevalent non-motor feature of Parkinson’s disease (PD). A better understanding of the underlying pathophysiology may help in identifying therapeutic targets to prevent or treat dementia. This study soug
Externí odkaz:
https://doaj.org/article/c21581b9e4214ab2ace90cd8a6278b7d
Autor:
Vincente Enguix, Kaitlyn Easson, Guillaume Gilbert, Christine Saint-Martin, Charles Rohlicek, David Luck, Gregory Anton Lodygensky, Marie Brossard-Racine
Publikováno v:
PLoS ONE, Vol 17, Iss 4 (2022)
Congenital heart disease (CHD) has been associated with structural brain growth and long-term developmental impairments, including deficits in learning, memory, and executive functions. Altered functional connectivity has been shown to be altered in
Externí odkaz:
https://doaj.org/article/ef746d9485d54241b99e820c9344f4bb
Publikováno v:
Children, Vol 10, Iss 4, p 647 (2023)
Holoprosencephaly (HPE) is the most common malformation of the prosencephalon in humans. It is characterized by a continuum of structural brain anomalies resulting from the failure of midline cleavage of the prosencephalon. The three classic subtypes
Externí odkaz:
https://doaj.org/article/9dd0f7400f944c0098b3e619c9d477da
Autor:
Tenzin Gayden, Gabriel Crevier-Sorbo, Wajih Jawhar, Christine Saint-Martin, Robert Eveleigh, Mirko S. Gilardino, Natascia Anastasio, Yannis Trakadis, Angelia V. Bassenden, Albert M. Berghuis, Nada Jabado, Roy W. R. Dudley
Publikováno v:
Journal of Neurosurgery: Pediatrics. :1-9
OBJECTIVE The aim of this study was to characterize a novel pathogenic variant in the transient receptor potential vanilloid 4 (TRPV4) gene, causing familial nonsyndromic craniosynostosis (CS) with complete penetrance and variable expressivity. METHO
Autor:
Kaitlyn Easson, Charles V. Rohlicek, Jean-Christophe Houde, Guillaume Gilbert, Christine Saint-Martin, Kimberly Fontes, Annette Majnemer, Ariane Marelli, Pia Wintermark, Maxime Descoteaux, Marie Brossard-Racine
Publikováno v:
NeuroImage, Vol 205, Iss , Pp 116255- (2020)
Background: White matter alterations have previously been demonstrated in adolescents born with congenital heart disease (CHD) using diffusion tensor imaging (DTI). However, due to the non-specific nature of DTI metrics, it is difficult to interpret
Externí odkaz:
https://doaj.org/article/20157d2a56014257a8ba7a14b94b53a5