Search Results - Karaceper, Maria

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  1. 1
    Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening

    Health services use by children identified as heterozygous hemoglobinopathy mutation carriers via newborn screening by Khangura, Sara D, Potter, Beth K, Davies, Christine, Ducharme, Robin, Bota, A. Brianne, Hawken, Steven, Wilson, Kumanan, Karaceper, Maria D, Klaassen, Robert J, Little, Julian, Simpson, Ewurabena, Chakraborty, Pranesh

    Published in BMC pediatrics
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  2. 2
    Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada

    Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada 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, Prasad, Chitra, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Stockler, Sylvia, Ueda, Keiko, Vallance, Hilary, Wilson, Brenda J, Chakraborty, Pranesh, Potter, Beth K

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  3. 3
    The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

    The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study 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, Sparkes, Rebecca, Wilson, Brenda J, Potter, Beth K

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  4. 4
    Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease

    Scoping review of patient- and family-oriented outcomes and measures for chronic pediatric disease 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, Potter, Beth K

    Published in BMC pediatrics
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  5. 5
    An examination of sex differences in associations between cord blood adipokines and childhood adiposity

    An examination of sex differences in associations between cord blood adipokines and childhood adiposity by Ashley‐Martin, Jillian, Karaceper, Maria, Dodds, Linda, Arbuckle, Tye E., Ettinger, Adrienne S., Fraser, William D., Muckle, Gina, Monnier, Patricia, Fisher, Mandy, Kuhle, Stefan

    Published in Pediatric obesity
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  6. 6
    THE EPIDEMIOLOGY AND HEALTH SYSTEM IMPACT OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY AMONG AFFECTED CHILDREN AND THOSE WITH FALSE POSITIVE NEWBORN SCREENING RESULTS IN ONTARIO, CANADA

    THE EPIDEMIOLOGY AND HEALTH SYSTEM IMPACT OF MEDIUM-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY AMONG AFFECTED CHILDREN AND THOSE WITH FALSE POSITIVE NEWBORN SCREENING RESULTS IN ONTAR... by Karaceper, Maria D, Chakraborty, Pranesh, Coyle, Doug, Wilson, Kumanan, Potter, Beth K

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  7. 7
    Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–2014)

    Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information from newborn screening Ontario, Canada (2007–2014) by Gannavarapu, Srinitya, Prasad, Chitra, DiRaimo, Jennifer, Napier, Melanie, Goobie, Sharan, Potter, Murray, Chakraborty, Pranesh, Karaceper, Maria, Munoz, Tatiana, Schulze, Andreas, MacKenzie, Jennifer, Li, Lihua, Geraghty, Michael T., Al-Dirbashi, Osama Y., Rupar, C. Anthony

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  8. 8
    Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information—A pilot project

    Biotinidase deficiency: Spectrum of molecular, enzymatic and clinical information—A pilot project by Prasad, Chitra, DiRaimo, Jennifer, Napier, Melanie, Goobie, Sharan, Potter, Murray, Chakraborty, Pranesh, Karaceper, Maria, Schulze, Andreas, Rupar, Charles A.

    Published in Clinical biochemistry
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  9. 9
    Patient- and family-oriented outcomes for inborn errors of metabolism: A scoping review

    Patient- and family-oriented outcomes for inborn errors of metabolism: A scoping review by Khangura, Sara D., Chakraborty, Pranesh, Coyle, Doug, Karaceper, Maria D., Kronick, Jonathan B., Laberge, Anne-Marie, Little, Julian, Miller, Fiona, Mitchell, John J., Prasad, Chitra, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N., Stockler, Sylvia, Tingley, Kylie, Trakadis, Yannis, Wilson, Brenda, Wilson, Kumanan, Zayed, Reem, Potter, Beth K.

    Published in Clinical biochemistry
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  10. 10
    A REDCap database to support longitudinal follow-up of pediatric patients with inborn errors of metabolism

    A REDCap database to support longitudinal follow-up of pediatric patients with inborn errors of metabolism by Hernandez, Monica, Chakraborty, Pranesh, Kronick, Jonathan B., Potter, Beth K., Chan, Alicia K.J., Coyle, Doug, Dyack, Sarah, Feigenbaum, Annette, Geraghty, Michael T., Karaceper, Maria, Khan, Aneal, Little, Julian, MacKenzie, Jennifer, Maranda, Bruno, Mhanni, Aizeddin, Mitchell, Grant, Mitchell, John J., Potter, Murray, Prasad, Chitra, Siriwardena, Komudi, Stockler, Sylvia, Tingley, Kylie, Trakadis, Yannis, Turner, Lesley, Van Karnebeek, Clara, Vallance, Hilary, Wilson, Brenda, Wilson, Kumanan

    Published in Clinical biochemistry
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  11. 11
    The epidemiology and health service impact of medium-chain acyl-CoA dehydrogenase deficiency among affected children and those with false positive newborn screening results in Ontario

    The epidemiology and health service impact of medium-chain acyl-CoA dehydrogenase deficiency among affected children and those with false positive newborn screening results in Onta... by Karaceper, Maria D., Brownell, Marni, Casey, Robin, Chakraborty, Pranesh, Coyle, Doug, Dodds, Linda, Feigenbaum, Annette, Fell, Deshayne, Grosse, Scott, Guttmann, Astrid, Laberge, Anne-Marie, Mhanni, Aziz, Miller, Fiona, Nakhla, Meranda, Rockman-Greenberg, Cheryl, Sparkes, Rebecca, Vallance, Hilary, Wilson, Brenda, Wilson, Kumanan, Potter, Beth K.

    Published in Clinical biochemistry
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  12. 12
    Building a pan-Canadian practice-based research network for inherited metabolic diseases: The first two years of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN)

    Building a pan-Canadian practice-based research network for inherited metabolic diseases: The first two years of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN) by Potter, Beth K., Chakraborty, Pranesh, Coyle, Doug, Kronick, Jonathan B., Wilson, Kumanan, Brownell, Marni, Chan, Alicia, Dodd, Linda, Dyack, Sarah, Feigenbaum, Annette, Fell, Deshayne, Geraghty, Michael T., Gillis, Jane, Rockman-Greenberg, Cheryl, Guttmann, Astrid, Hernandez, Monica, Karaceper, Maria, Khan, Aneal, Khangura, Sara D., Laberge, Anne-Marie, Little, Julian, MacKenzie, Jennifer, Maranda, Bruno, Mhanni, Aizeddin, Miller, Fiona A., Mitchell, John J., Mitchell, Grant, Nakhla, Meranda, Potter, Murray, Prasad, Chitra, Siriwardena, Komudi, Sparkes, Rebecca, Speechley, Kathy N., Stockler, Sylvia, Tingley, Kylie, Trakadis, Yannis, Turner, Lesley, Vallance, Hilary, van Karnebeek, Clara, Wilson, Brenda J., Yuskiv, Nataliya

    Published in Clinical biochemistry
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