Chantal F Morel

Chantal F Morel

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Chantal F Morel

Chantal F Morel

Publications by authors named "Chantal F Morel"

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26Publications

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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 Aug 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.

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

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:

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

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

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

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.

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

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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.

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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.

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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.

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http://dx.doi.org/10.1517/14712590902902296 DOI 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.

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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.

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http://doi.wiley.com/10.1002/ajmg.a.31932
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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.

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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.

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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.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920500232
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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.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920500081
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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.

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