N. Kraeva

Exome analysis identifies Brody myopathy in a family diagnosed with malignant hyperthermia susceptibility

B. Brandom, O. Sizova, D. Maclennan, 2014, Molecular genetics & genomic medicine.

Ryanodine receptor type 1 gene mutations found in the Canadian malignant hyperthermia population

D. Maclennan, S. Riazi, A. Kraev, 2011, Canadian journal of anaesthesia = Journal canadien d'anesthesie.

Ca2+ dysregulation in Ryr1I4895T/wt mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

J. Seidman, C. Seidman, D. Maclennan, 2009, Proceedings of the National Academy of Sciences.

An Ryr1I4895T mutation abolishes Ca2+ release channel function and delays development in homozygous offspring of a mutant mouse line

J. Seidman, A. Gramolini, C. Seidman, 2007, Proceedings of the National Academy of Sciences.

Mutations in ryr1 gene associated with malignant hyperthermia and a non-anaesthetic phenotype

D. Maclennan, J. Loke, N. Kraeva, 2007 .

Genetic variation and cognitive dysfunction one year after cardiac surgery

V. Rao, G. Djaiani, J. Carroll, 2013, Anaesthesia.

Ryanodine receptor type 1 gene mutations found in the Canadian malignant hyperthermia population Observation de mutations genetiques des recepteurs de la ryanodine de type 1 chez les patients canadiens atteints d'hyperthermie maligne

W. Frodis, N. Kraeva, Lou Crossan, 2011 .