Publications by authors named "Chantal F Morel"

33Publications

Increased Spread of Native T1 Assessed by MRI is a Marker of Cardiac Involvement in Fabry Disease.

AJR Am J Roentgenol 2020 Jul 8. Epub 2020 Jul 8.

Toronto Joint Department of Medical Imaging, Toronto General Hospital, Peter Munk Cardiac Centre, University Health Network, University of Toronto, 585 University Avenue, Toronto, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2214/AJR.20.23102DOI Listing
July 2020

Genetic Testing for Diagnosis of Hypertrophic Cardiomyopathy Mimics: Yield and Clinical Significance.

Circ Genom Precis Med 2020 04 9;13(2):e002748. Epub 2020 Mar 9.

Division of Cardiology, Peter Munk Cardiac Centre (S.H., M.H., R.H.C., M.H.G., H.R., A.A.), Toronto General Hospital, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCGEN.119.002748DOI Listing
April 2020

A case of secondary acute myeloid leukemia on a background of glycogen storage disease with chronic neutropenia treated with granulocyte colony stimulating factor.

JIMD Rep 2019 Sep 23;49(1):37-42. Epub 2019 Jul 23.

Department of Medical Oncology and Hematology, Princess Margaret Hospital Cancer Centre University Health Network Toronto Ontario Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/jmd2.12069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875697PMC
September 2019

Left Ventricular Hypertrophy and Late Gadolinium Enhancement at Cardiac MRI Are Associated with Adverse Cardiac Events in Fabry Disease.

Radiology 2020 01 29;294(1):42-49. Epub 2019 Oct 29.

From the Toronto Joint Department of Medical Imaging, Toronto General Hospital, Peter Munk Cardiac Centre, University Health Network, University of Toronto, 585 University Ave, 1 PMB-298, Toronto, ON, Canada M5G 2N2 (K.H., G.R.K., R.M.W.); Fred A. Litwin Centre in Genetic Medicine, University Health Network & Mount Sinai Hospital, University of Toronto, Toronto, Canada (S.W., C.F.M.); and Division of Cardiology, Peter Munk Cardiac Centre, University Health Network, University of Toronto, Toronto, Canada (R.M.W., R.M.I.).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1148/radiol.2019191385DOI Listing
January 2020

Loss of base-to-apex circumferential strain gradient assessed by cardiovascular magnetic resonance in Fabry disease: relationship to T1 mapping, late gadolinium enhancement and hypertrophy.

J Cardiovasc Magn Reson 2019 08 1;21(1):45. Epub 2019 Aug 1.

Toronto Joint Department of Medical Imaging, Toronto General Hospital, University of Toronto, 585 University Avenue, 1PMB-298, Toronto, ON, M5G 2N2, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12968-019-0557-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6670217PMC
August 2019

Prognostic Significance of Cardiac Magnetic Resonance Imaging Late Gadolinium Enhancement in Fabry Disease.

Circulation 2018 11;138(22):2579-2581

Division of Cardiology, Peter Munk Cardiac Centre, University Health Network (R.M.I.), University of Toronto, Toronto, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1161/CIRCULATIONAHA.118.037103DOI Listing
November 2018

Characterization of VHL promoter variants in patients suspected of Von Hippel-Lindau disease.

Eur J Med Genet 2019 Mar 10;62(3):177-181. Epub 2018 Jul 10.

Fred A Litwin Family Centre in Genetic Medicine, University Health Network, Canada; Division of Medical Oncology and Hematology, Department of Medicine, University of Toronto, Toronto, Canada. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S17697212173088
Publisher Site
http://dx.doi.org/10.1016/j.ejmg.2018.07.006DOI Listing
March 2019

Renal thrombotic microangiopathy and pulmonary arterial hypertension in a patient with late-onset cobalamin C deficiency.

Clin Kidney J 2018 Jun 26;11(3):310-314. Epub 2017 Oct 26.

Division of Nephrology, University Hospital Network, Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/ckj/sfx119DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007252PMC
June 2018

Use of Myocardial T1 Mapping at 3.0 T to Differentiate Anderson-Fabry Disease from Hypertrophic Cardiomyopathy.

Radiology 2018 08 24;288(2):398-406. Epub 2018 Apr 24.

From the Toronto Joint Department of Medical Imaging, Toronto General Hospital, University of Toronto, 585 University Ave, 1 PMB-298, Toronto, ON, Canada M5G 2N2 (G.R.K., S.R., P.T., E.T.N., S.M., K.H.); Division of Cardiology, Peter Munk Cardiac Centre, University Health Network, University of Toronto, Toronto, ON, Canada (R.M.I., A.M.C., P.T.); and Fred A. Litwin Centre in Genetic Medicine, University Health Network & Mount Sinai Hospital, University of Toronto, Toronto, ON, Canada (C.F.M., S.W.).

View Article

Download full-text PDF

Source
http://pubs.rsna.org/doi/10.1148/radiol.2018172613
Publisher Site
http://dx.doi.org/10.1148/radiol.2018172613DOI Listing
August 2018

The Expanding Clinical Spectrum of Extracardiovascular and Cardiovascular Manifestations of Heritable Thoracic Aortic Aneurysm and Dissection.

Can J Cardiol 2016 Jan 14;32(1):86-99. Epub 2015 Nov 14.

Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.cjca.2015.11.007DOI Listing
January 2016

Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association.

Virchows Arch 2015 Jun 24;466(6):727-32. Epub 2015 Mar 24.

Department of Medicine, University Health Network, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00428-015-1755-2DOI Listing
June 2015

Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.

Pediatr Neurol 2009 Jul;41(1):27-33

Division of Neurology and Pediatric Emergency Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.pediatrneurol.2009.02.010DOI Listing
July 2009

The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry disease.

Expert Opin Biol Ther 2009 May;9(5):631-9

Department of Medicine, University Health Network and Mount Sinai Hospital, University of Toronto, Toronto, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1517/14712590902902296DOI Listing
May 2009

Ocular phenotype in patients with methylmalonic aciduria and homocystinuria, cobalamin C type.

J AAPOS 2008 Dec 10;12(6):591-6. Epub 2008 Oct 10.

Department of Ophthalmology and Vision Sciences, The Hospital for Sick Children, Toronto, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jaapos.2008.06.008DOI Listing
December 2008

Late-onset combined homocystinuria and methylmalonic aciduria (cblC) and neuropsychiatric disturbance.

Am J Med Genet A 2007 Oct;143A(20):2430-4

Division of Clinical Genetics and Metabolism, The Children's Hospital, University of Colorado School of Medicine, Denver, Colorado 80218, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.31932
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.31932DOI Listing
October 2007

Combined methylmalonic aciduria and homocystinuria (cblC): phenotype-genotype correlations and ethnic-specific observations.

Mol Genet Metab 2006 Aug 22;88(4):315-21. Epub 2006 May 22.

Department of Human Genetics and Division of Medical Genetics, Department of Medicine, McGill University, Montreal, Que., Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ymgme.2006.04.001DOI Listing
August 2006

A LMNA splicing mutation in two sisters with severe Dunnigan-type familial partial lipodystrophy type 2.

J Clin Endocrinol Metab 2006 Jul 24;91(7):2689-95. Epub 2006 Apr 24.

Blackburn Cardiovascular Genetics Laboratory, Robarts Research Institute, London, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2005-2746DOI Listing
July 2006

Prenatal diagnosis for methylmalonic acidemia and inborn errors of vitamin B12 metabolism and transport.

Mol Genet Metab 2005 Sep-Oct;86(1-2):160-71

Department of Human Genetics, McGill University, Montreal, Que., Canada.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S109671920500232
Publisher Site
http://dx.doi.org/10.1016/j.ymgme.2005.07.018DOI Listing
January 2006

Prenatal diagnosis for severe methylenetetrahydrofolate reductase deficiency by linkage analysis and enzymatic assay.

Mol Genet Metab 2005 Jun 1;85(2):115-20. Epub 2005 Apr 1.

Department of Human Genetics, McGill University, Montreal, Que., Canada.

View Article

Download full-text PDF

Source
http://linkinghub.elsevier.com/retrieve/pii/S109671920500081
Publisher Site
http://dx.doi.org/10.1016/j.ymgme.2005.03.001DOI Listing
June 2005

A fragile site at 10q23 (FRA10A) in a phenytoin-exposed fetus: a case report and review of the literature.

Prenat Diagn 2005 Apr;25(4):318-21

F. Clarke Fraser Clinical Genetics Unit, Division of Medical Genetics, Department of Pediatrics, Montreal Children's Hospital, Montreal, Québec H3H 1P3, Canada.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/pd.1134
Publisher Site
http://dx.doi.org/10.1002/pd.1134DOI Listing
April 2005