Works matching AU Laberge, Anne-Marie


Results: 38
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    The Serious Factor in Expanded Prenatal Genetic Testing.

    Published in:
    American Journal of Bioethics, 2022, v. 22, n. 2, p. 23, doi. 10.1080/15265161.2021.2013991
    By:
    • Kleiderman, Erika;
    • Rahimzadeh, Vasiliki;
    • Knoppers, Bartha;
    • Roy, Marie-Christine;
    • Laberge, Anne-Marie;
    • Ravitsky, Vardit
    Publication type:
    Article
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    Genome-wide profiling of circulating microRNAs in adolescent idiopathic scoliosis and their relation to spinal deformity severity, and disease pathophysiology.

    Published in:
    Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-88985-3
    By:
    • Khatami, Nasrin;
    • Caraus, Iurie;
    • Rahaman, Mahamuda;
    • Nepotchatykh, Evguenia;
    • Elbakry, Mohamed;
    • Elremaly, Wesam;
    • Franco, Anita;
    • Beauséjour, Marie;
    • Laberge, Anne-Marie;
    • Parent, Stefan;
    • Labelle, Hubert;
    • Aubin, Carl-Éric;
    • Lachaine, Jean;
    • Moreau, Alain
    Publication type:
    Article
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    Measuring severe obesity in pediatrics using body mass index-derived metrics from the Centers for Disease Control and Prevention and World Health Organization: a secondary analysis of CANadian Pediatric Weight management Registry (CANPWR) data.

    Published in:
    European Journal of Pediatrics, 2023, v. 182, n. 8, p. 3679, doi. 10.1007/s00431-023-05039-4
    By:
    • Ball, Geoff D. C.;
    • Sharma, Atul K.;
    • Moore, Sarah A.;
    • Metzger, Daniel L.;
    • Klein, Doug;
    • Morrison, Katherine M.;
    • on behalf of the CANadian Pediatric Weight management Registry (CANPWR) Investigators;
    • Buchholz, Annick;
    • Chanoine, J-P;
    • Hamilton, Jill;
    • Ho, Josephine;
    • Laberge, Anne-Marie;
    • Legault, Laurent;
    • Thabane, Lehana;
    • Tremblay, Mark S;
    • Zenlea, Ian
    Publication type:
    Article
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    Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.

    Published in:
    2016
    By:
    • Siddiq, Shabnaz;
    • Wilson, Brenda J;
    • Graham, Ian D;
    • Lamoureux, Monica;
    • Khangura, Sara D;
    • Tingley, Kylie;
    • Tessier, Laure;
    • Chakraborty, Pranesh;
    • Coyle, Doug;
    • Dyack, Sarah;
    • Gillis, Jane;
    • Greenberg, Cheryl;
    • Hayeems, Robin Z;
    • Jain-Ghai, Shailly;
    • Kronick, Jonathan B;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Mitchell, John J;
    • Prasad, Chitra;
    • Siriwardena, Komudi
    Publication type:
    journal article
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    Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.

    Published in:
    Orphanet Journal of Rare Diseases, 2016, v. 11, p. 1, doi. 10.1186/s13023-016-0548-2
    By:
    • Siddiq, Shabnaz;
    • Wilson, Brenda J.;
    • Graham, Ian D.;
    • Lamoureux, Monica;
    • Khangura, Sara D.;
    • Tingley, Kylie;
    • Tessier, Laure;
    • Chakraborty, Pranesh;
    • Coyle, Doug;
    • Dyack, Sarah;
    • Gillis, Jane;
    • Greenberg, Cheryl;
    • Hayeems, Robin Z.;
    • Jain-Ghai, Shailly;
    • Kronick, Jonathan B.;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Mitchell, John J.;
    • Prasad, Chitra;
    • Siriwardena, Komudi
    Publication type:
    Article
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    The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.

    Published in:
    2016
    By:
    • Karaceper, Maria D.;
    • Chakraborty, Pranesh;
    • Coyle, Doug;
    • Wilson, Kumanan;
    • Kronick, Jonathan B.;
    • Hawken, Steven;
    • Davies, Christine;
    • Brownell, Marni;
    • Dodds, Linda;
    • Feigenbaum, Annette;
    • Fell, Deshayne B.;
    • Grosse, Scott D.;
    • Guttmann, Astrid;
    • Laberge, Anne-Marie;
    • Mhanni, Aizeddin;
    • Miller, Fiona A.;
    • Mitchell, John J.;
    • Nakhla, Meranda;
    • Prasad, Chitra;
    • Rockman-Greenberg, Cheryl
    Publication type:
    journal article
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    Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease.

    Published in:
    BMC Pediatrics, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12887-015-0323-x
    By:
    • Khangura, Sara D.;
    • Karaceper, Maria D.;
    • Trakadis, Yannis;
    • Mitchell, John J.;
    • Chakraborty, Pranesh;
    • Tingley, Kylie;
    • Coyle, Doug;
    • Grosse, Scott D.;
    • Kronick, Jonathan B.;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Prasad, Chitra;
    • Sikora, Lindsey;
    • Siriwardena, Komudi;
    • Sparkes, Rebecca;
    • Speechley, Kathy N.;
    • Stockler, Sylvia;
    • Wilson, Brenda J.;
    • Wilson, Kumanan;
    • Zayed, Reem
    Publication type:
    Article
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    The CANadian Pediatric Weight Management Registry (CANPWR): Study protocol.

    Published in:
    BMC Pediatrics, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2431-14-161
    By:
    • Morrison, Katherine M.;
    • Damanhoury, Samah;
    • Buchholz, Annick;
    • Chanoine, Jean-Pierre;
    • Lambert, Marie;
    • Tremblay, Mark S.;
    • Berall, Glenn;
    • Hamilton, Jill;
    • Laberge, Anne Marie;
    • Legault, Laurent;
    • Thabane, Lehana;
    • Jakymyshyn, Monica;
    • Ambler, Kathryn A.;
    • Ball, Geoff D. C.
    Publication type:
    Article
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    Child and family experiences with inborn errors of metabolism: a qualitative interview study with representatives of patient groups.

    Published in:
    Journal of Inherited Metabolic Disease, 2016, v. 39, n. 1, p. 139, doi. 10.1007/s10545-015-9881-1
    By:
    • Khangura, Sara;
    • Tingley, Kylie;
    • Chakraborty, Pranesh;
    • Coyle, Doug;
    • Kronick, Jonathan;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Miller, Fiona;
    • Mitchell, John;
    • Prasad, Chitra;
    • Siddiq, Shabnaz;
    • Siriwardena, Komudi;
    • Sparkes, Rebecca;
    • Speechley, Kathy;
    • Stockler, Sylvia;
    • Trakadis, Yannis;
    • Wilson, Brenda;
    • Wilson, Kumanan;
    • Potter, Beth
    Publication type:
    Article
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    Family Experiences with Care for Children with Inherited Metabolic Diseases in Canada: A Cross-Sectional Survey.

    Published in:
    Patient, 2022, v. 15, n. 2, p. 171, doi. 10.1007/s40271-021-00538-8
    By:
    • Chow, Andrea J.;
    • Pugliese, Michael;
    • Tessier, Laure A.;
    • Chakraborty, Pranesh;
    • Iverson, Ryan;
    • Coyle, Doug;
    • Kronick, Jonathan B.;
    • Wilson, Kumanan;
    • Hayeems, Robin;
    • Al-Hertani, Walla;
    • Inbar-Feigenberg, Michal;
    • Jain-Ghai, Shailly;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Mitchell, John J.;
    • Prasad, Chitra;
    • Siriwardena, Komudi;
    • Sparkes, Rebecca;
    • Speechley, Kathy N.;
    • Stockler, Sylvia
    Publication type:
    Article
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    Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum.

    Published in:
    American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 386, doi. 10.1002/ajmg.a.61025
    By:
    • Alkhunaizi, Ebba;
    • Shuster, Shirley;
    • Shannon, Patrick;
    • Siu, Victoria Mok;
    • Darilek, Sandra;
    • Mohila, Carrie A;
    • Boissel, Sarah;
    • Ellezam, Benjamin;
    • Fallet‐Bianco, Catherine;
    • Laberge, Anne‐Marie;
    • Zandberg, Julianne;
    • Injeyan, Marie;
    • Hazrati, Lili‐Naz;
    • Hamdan, Fadi;
    • Chitayat, David
    Publication type:
    Article
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    The Experience of Parents of Children With Genetically Determined Leukoencephalopathies With the Health Care System: A Qualitative Study.

    Published in:
    Journal of Child Neurology, 2023, v. 38, n. 5, p. 329, doi. 10.1177/08830738231176672
    By:
    • Yazdani, Pouneh Amir;
    • St-Jean, Marie-Lou;
    • Matovic, Sara;
    • Spahr, Aaron;
    • Tran, Luan T.;
    • Boucher, Renée-Myriam;
    • Poulin, Chantal;
    • Osterman, Bradley;
    • Srour, Myriam;
    • Rosenblatt, Bernard;
    • Chénier, Sébastien;
    • Soucy, Jean-Francois;
    • Laberge, Anne-Marie;
    • D'Agostino, Maria Daniela;
    • Nguyen, Cam-Tu Emilie;
    • Morsa, Maxime;
    • Bernard, Geneviève
    Publication type:
    Article
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    Experience of Parents of Children with Genetically Determined Leukoencephalopathies Regarding the Adapted Health Care Services During the COVID-19 Pandemic.

    Published in:
    Journal of Child Neurology, 2022, v. 37, n. 4, p. 237, doi. 10.1177/08830738211065317
    By:
    • Amir Yazdani, Pouneh;
    • St-Jean, Marie-Lou;
    • Matovic, Sara;
    • Spahr, Aaron;
    • Tran, Luan T.;
    • Boucher, Renée-Myriam;
    • Poulin, Chantal;
    • Osterman, Bradley;
    • Srour, Myriam;
    • Rosenblatt, Bernard;
    • Chenier, Sébastien;
    • Soucy, Jean-Francois;
    • Laberge, Anne-Marie;
    • Braverman, Nancy;
    • D'Agostino, Maria Daniela;
    • Nguyen, Cam-Tu Emilie;
    • Morsa, Maxime;
    • Bernard, Geneviève
    Publication type:
    Article
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    Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.

    Published in:
    2019
    By:
    • Karaceper, Maria D.;
    • Khangura, Sara D.;
    • Wilson, Kumanan;
    • Coyle, Doug;
    • Brownell, Marni;
    • Davies, Christine;
    • Dodds, Linda;
    • Feigenbaum, Annette;
    • Fell, Deshayne B.;
    • Grosse, Scott D.;
    • Guttmann, Astrid;
    • Hawken, Steven;
    • Hayeems, Robin Z.;
    • Kronick, Jonathan B.;
    • Laberge, Anne-Marie;
    • Little, Julian;
    • Mhanni, Aizeddin;
    • Mitchell, John J.;
    • Nakhla, Meranda;
    • Potter, Murray
    Publication type:
    journal article
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    Metabolically healthy obesity in children enrolled in the CANadian Pediatric Weight management Registry (CANPWR): An exploratory secondary analysis of baseline data.

    Published in:
    Clinical Obesity, 2022, v. 12, n. 1, p. 1, doi. 10.1111/cob.12490
    By:
    • Damanhoury, Samah;
    • Morrison, Katherine M.;
    • Mian, Rajibul;
    • McPhee, Patrick G.;
    • Kozyrskyj, Anita L.;
    • Newton, Amanda S.;
    • Buchholz, Annick;
    • Chanoine, Jean‐Pierre;
    • Hamilton, Jill;
    • Ho, Josephine;
    • Laberge, Anne‐Marie;
    • Legault, Laurent;
    • Thabane, Lehana;
    • Tremblay, Mark S.;
    • Zenlea, Ian;
    • Ball, Geoff D. C.
    Publication type:
    Article
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