Dawn Cordeiro

Dawn Cordeiro

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Dawn Cordeiro

Dawn Cordeiro

Publications by authors named "Dawn Cordeiro"

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Clinical Application of Targeted Next-Generation Sequencing Panels and Whole Exome Sequencing in Childhood Epilepsy.

Neuroscience 2019 Oct 2;418:291-310. Epub 2019 Sep 2.

Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.neuroscience.2019.08.016DOI Listing
October 2019

DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis.

Eur J Hum Genet 2018 12 23;26(12):1867-1870. Epub 2018 Aug 23.

Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8, Canada.

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http://dx.doi.org/10.1038/s41431-018-0237-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244406PMC
December 2018

Genetic landscape of pediatric movement disorders and management implications.

Neurol Genet 2018 Oct 26;4(5):e265. Epub 2018 Sep 26.

Division of Clinical and Metabolic Genetics (D.C., G.B., R.D.C., S.M.-A.), Department of Pediatrics, Toronto, Ontario, Canada; Department of Medical Genetics (K.S.), University of Alberta, Edmonton, Canada; Department of Pediatrics (A.E., J.K., R.D.C., S.M.-A.), University of Toronto; the Emergency Medicine Division (A.E.), Department of Paediatrics, The Hospital for Sick Children; Division of Neurology (J.K.), Department of Paediatrics, The Hospital for Sick Children,; Genetics and Genome Biology Program (R.D.C., S.M.-A.), Research Institute, The Hospital for Sick Children; and Institute of Medical Sciences (S.M.-A.), University of Toronto, Toronto, Ontario, Canada.

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http://ng.neurology.org/lookup/doi/10.1212/NXG.0000000000000
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http://dx.doi.org/10.1212/NXG.0000000000000265DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167181PMC
October 2018

Outcome of Patients With Inherited Neurotransmitter Disorders.

Can J Neurol Sci 2018 09 15;45(5):571-576. Epub 2018 Aug 15.

1Department of Pediatrics,Division of Clinical and Metabolic Genetics,University of Toronto,Toronto,Ontario,Canada.

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https://www.cambridge.org/core/product/identifier/S031716711
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http://dx.doi.org/10.1017/cjn.2018.266DOI Listing
September 2018

Riboflavin transporter deficiency mimicking mitochondrial myopathy caused by complex II deficiency.

Am J Med Genet A 2018 02 30;176(2):399-403. Epub 2017 Nov 30.

Division of Clinical and Metabolic Genetics, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.38530DOI Listing
February 2018

A New Patient With Intermediate Severe Salla Disease With Hypomyelination: A Literature Review for Salla Disease.

Pediatr Neurol 2017 Sep 1;74:87-91.e2. Epub 2017 Jun 1.

Division of Neurology, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, Toronto, Ontario, Canada; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Pediatrics, University of Toronto, Toronto, Ontario Canada; Institute of Medical Sciences, University of Toronto, Toronto, Ontario Canada. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2017.05.022DOI Listing
September 2017

Phenotype, biochemical features, genotype and treatment outcome of pyridoxine-dependent epilepsy.

Metab Brain Dis 2017 04 23;32(2):443-451. Epub 2016 Nov 23.

Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Canada.

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http://dx.doi.org/10.1007/s11011-016-9933-8DOI Listing
April 2017

Phenotypic and genotypic spectrum of congenital disorders of glycosylation type I and type II.

Mol Genet Metab 2017 03 3;120(3):235-242. Epub 2017 Jan 3.

Division of Clinical and Metabolic Genetics, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, Toronto, Ontario, Canada; Genetics and Genome Biology Program, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada; Institute of Medical Sciences, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2016.12.014DOI Listing
March 2017

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy.

Am J Hum Genet 2016 06 26;98(6):1249-1255. Epub 2016 May 26.

Children's Health Research Center, Sanford Research, Sioux Falls, SD 57104, USA; Department of Child Health, University of Arizona College of Medicine, Phoenix, AZ 85004, USA; Neurogenetics Research Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA; Program in Neuroscience, Arizona State University, Tempe, AZ 85287, USA; Pediatric Movement Disorders Center, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2016.04.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908178PMC
June 2016

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood.

Epilepsia 2015 May 25;56(5):707-16. Epub 2015 Mar 25.

Division of Neurology, Department of Paediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1111/epi.12954DOI Listing
May 2015

Novel therapy for pyridoxine dependent epilepsy due to ALDH7A1 genetic defect: L-arginine supplementation alternative to lysine-restricted diet.

Eur J Paediatr Neurol 2014 Nov 27;18(6):741-6. Epub 2014 Jul 27.

Department of Psychology, The Hospital for Sick Children, Toronto, ON, Canada.

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http://dx.doi.org/10.1016/j.ejpn.2014.07.001DOI Listing
November 2014