Intraventricular Hemorrhage and Multiple Intracranial Cysts Associated with Congenital Cytomegalovirus Infection

Por Suksumek, Nithipun, Scott, James N., Chadha, Rati, Yusuf, Kamran
Publicado em 2013

The ESC: The Dangerous By-Product of V(D)J Recombination

Por Smith, Alastair L., Scott, James N. F., Boyes, Joan
Publicado no Front Immunol (2019)

Effect of Atlas Vertebrae Realignment in Subjects with Migraine: An Observational Pilot Study

Por Woodfield, H. Charles, Hasick, D. Gordon, Becker, Werner J., Rose, Marianne S., Scott, James N.
Publicado no Biomed Res Int (2015)

MRI texture heterogeneity in the optic nerve predicts visual recovery after acute optic neuritis()

Por Zhang, Yunyan, Metz, Luanne M., Scott, James N., Trufyn, Jessie, Fick, Gordon H., Costello, Fiona
Publicado em 2014

Mutations in VLDLR as a Cause for Autosomal Recessive Cerebellar Ataxia with Mental Retardation (Dysequilibrium Syndrome)

Por Boycott, Kym M, Bonnemann, Carsten, Herz, Joachim, Neuert, Stephanie, Beaulieu, Chandree, Scott, James N, Venkatasubramanian, Anuradha, Parboosingh, Jillian S
Publicado em 2009

Intraventricular Hemorrhage: Risk Factors and Association With Patent Ductus Arteriosus Treatment in Extremely Preterm Neonates

Por Khanafer-Larocque, Ijab, Soraisham, Amuchou, Stritzke, Amelie, Al Awad, Essa, Thomas, Sumesh, Murthy, Prashanth, Kamaluddeen, Majeeda, Scott, James N., Mohammad, Khorshid
Publicado no Front Pediatr (2019)

Consensus Approach for Standardizing the Screening and Classification of Preterm Brain Injury Diagnosed With Cranial Ultrasound: A Canadian Perspective

Por Mohammad, Khorshid, Scott, James N., Leijser, Lara M., Zein, Hussein, Afifi, Jehier, Piedboeuf, Bruno, de Vries, Linda S., van Wezel-Meijler, Gerda, Lee, Shoo K., Shah, Prakesh S.
Publicado no Front Pediatr (2021)

Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification

Por Boycott, Kym M., Flavelle, Shauna, Bureau, Alexandre, Glass, Hannah C., Fujiwara, T. Mary, Wirrell, Elaine, Davey, Krista, Chudley, Albert E., Scott, James N., McLeod, D. Ross, Parboosingh, Jillian S.
Publicado em 2005

Validity of the diagnostic criteria for chronic cerebrospinal venous insufficiency and association with multiple sclerosis

Por Costello, Fiona, Modi, Jayesh, Lautner, David, Bhayana, Deepak, Scott, James N., Davenport, W. Jeptha, Trufyn, Jessie, Frayne, Richard, Ciura, Viesha A., Goyal, Mayank, Mah, Jean, Hill, Michael D.
Publicado em 2014

Cut-and-Run: A Distinct Mechanism by which V(D)J Recombination Causes Genome Instability

Por Kirkham, Christopher M., Scott, James N.F., Wang, Xiaoling, Smith, Alastair L., Kupinski, Adam P., Ford, Anthony M., Westhead, David R., Stockley, Peter G., Tuma, Roman, Boyes, Joan
Publicado no Mol Cell (2019)

Very early hypothermia induction in patients with severe brain injury (the National Acute Brain Injury Study: Hypothermia II): a randomised trial

Por Clifton, Guy L, Valadka, Alex, Zygun, David, Coffey, Christopher S, Drever, Pamala, Fourwinds, Sierra, Janis, L Scott, Wilde, Elizabeth, Taylor, Pauline, Harshman, Kathy, Conley, Adam, Puccio, Ava, Levin, Harvey S, McCauley, Stephen R, Bucholz, Richard D, Smith, Kenneth R, Schmidt, John H, Scott, James N, Yonas, Howard, Okonkwo, David O
Publicado em 2010

Neurological Outcome Scale for Traumatic Brain Injury: III. Criterion-Related Validity and Sensitivity to Change in the NABIS Hypothermia-II Clinical Trial

Por McCauley, Stephen R., Wilde, Elisabeth A., Moretti, Paolo, MacLeod, Marianne C., Pedroza, Claudia, Drever, Pamala, Fourwinds, Sierra, Frisby, Melisa L., Beers, Sue R., Scott, James N., Hunter, Jill V., Traipe, Elfrides, Valadka, Alex B., Okonkwo, David O., Zygun, David A., Puccio, Ava M., Clifton, Guy L.
Publicado em 2013

Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8

Por Boycott, Kym M., Beaulieu, Chandree L., Kernohan, Kristin D., Gebril, Ola H., Mhanni, Aziz, Chudley, Albert E., Redl, David, Qin, Wen, Hampson, Sarah, Küry, Sébastien, Tetreault, Martine, Puffenberger, Erik G., Scott, James N., Bezieau, Stéphane, Reis, André, Uebe, Steffen, Schumacher, Johannes, Hegele, Robert A., McLeod, D. Ross, Gálvez-Peralta, Marina, Majewski, Jacek, Ramaekers, Vincent T., Nebert, Daniel W., Innes, A. Micheil, Parboosingh, Jillian S., Abou Jamra, Rami
Publicado no Am J Hum Genet (2015)