Works by Mitchell, John J.

Results: 37

Ethics in Business Today.

Published in:

Journal of Education for Business, 1980, v. 56, n. 2, p. 61, doi. 10.1080/08832323.1980.10117193

By:

Mitchell, John J.

Publication type:

Article

Current Advances and Material Innovations in the Search for Novel Treatments of Phenylketonuria.

Published in:

Advanced Healthcare Materials, 2024, v. 13, n. 26, p. 1, doi. 10.1002/adhm.202401353

By:

Delbreil, Philippe;
Dhondt, Sofie;
Kenaan El Rahbani, Rita Maria;
Banquy, Xavier;
Mitchell, John J.;
Brambilla, Davide

Publication type:

Article

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

Does cardiorespiratory fitness mediate or moderate the association between mid-life physical activity frequency and cognitive function? findings from the 1958 British birth cohort study.

Published in:

PLoS ONE, 2024, v. 19, n. 6, p. 1, doi. 10.1371/journal.pone.0295092

By:

Norris, Tom;
Mitchell, John J.;
Blodgett, Joanna M.;
Hamer, Mark;
Pinto Pereira, Snehal M.

Publication type:

Article

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

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

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

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

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

Published in:

2015

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:

journal article

Safety and Efficacy of DTX401, an AAV8‐Mediated Liver‐Directed Gene Therapy, in Adults With Glycogen Storage Disease Type I a (GSDIa).

Published in:

Journal of Inherited Metabolic Disease, 2025, v. 48, n. 2, p. 1, doi. 10.1002/jimd.70014

By:

Weinstein, David A.;
Derks, Terry G.;
Rodriguez‐Buritica, David F.;
Ahmad, Ayesha;
Couce, María‐Luz;
Mitchell, John J.;
Riba‐Wolman, Rebecca;
Mount, Malaya;
Sallago, Julieta Bonvin;
Ross, Katalin M.;
van der Klauw, Melanie M.;
de Boer, Foekje;
van der Schaaf, Caroline;
Saavedra, Heather;
Martínez‐Olmos, Miguel;
Atanga, Elvis;
Hosseini, Asad;
Mitragotri, Deepali;
Crombez, Eric

Publication type:

Article

Online Module for Carrier Screening in Ashkenazi Jewish Individuals Compared with In-Person Genetics Education: A Randomized Controlled Trial.

Published in:

Journal of Genetic Counseling, 2018, v. 27, n. 2, p. 426, doi. 10.1007/s10897-017-0133-4

By:

Fan, Chia Wei;
Castonguay, Lysanne;
Rummell, Sonja;
Lévesque, Sébastien;
Mitchell, John J.;
Sillon, Guillaume

Publication type:

Article

Review of clinical trials and guidelines for children and youth with mucopolysaccharidosis: outcome selection and measurement.

Published in:

Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03364-x

By:

Howie, Alison H.;
Tingley, Kylie;
Inbar-Feigenberg, Michal;
Mitchell, John J.;
Angel, Kim;
Gentle, Jenifer;
Smith, Maureen;
Offringa, Martin;
Butcher, Nancy J.;
Campeau, Philippe M.;
Chakraborty, Pranesh;
Chan, Alicia;
Fergusson, Dean;
Mamak, Eva;
McClelland, Peyton;
Mercimek-Andrews, Saadet;
Mhanni, Aizeddin;
Moazin, Zeinab;
Rockman-Greenberg, Cheryl;
Rupar, C. Anthony

Publication type:

Article

Book reviews.

Published in:

1990

By:

Mitchell Jr., John J.

Publication type:

Book Review

Case report: maternal mosaicism resulting in inheritance of a novel GATA6 mutation causing pancreatic agenesis and neonatal diabetes mellitus.

Published in:

2017

By:

Yau, Daphne;
De Franco, Elisa;
Flanagan, Sarah E.;
Ellard, Sian;
Blumenkrantz, Miriam;
Mitchell, John J.

Publication type:

Case Study

Reforming Welfare: Lessons from the WIN Experience.

Published in:

Public Administration Review, 1981, v. 41, n. 3, p. 372, doi. 10.2307/975798

By:

Chadwin, Mark Lincoln;
Mitchell, John J.;
Nightingale, Demetra Smith

Publication type:

Article

THE WORTH OF PERSONS: SOME COMMENTS.

Published in:

Journal of Humanistic Psychology, 1975, v. 15, n. 1, p. 79, doi. 10.1177/002216787501500112

By:

Mitchell, John J.

Publication type:

Article

Social Custom and Psychological Health.

Published in:

Journal of Humanistic Psychology, 1974, v. 14, n. 2, p. 49, doi. 10.1177/002216787401400206

By:

Mitchell, John J.

Publication type:

Article

Impact of COVID-19 Pandemic on Weight and BMI among UK Adults: A Longitudinal Analysis of Data from the HEBECO Study.

Published in:

Nutrients, 2021, v. 13, n. 9, p. 2911, doi. 10.3390/nu13092911

By:

Dicken, Samuel J.;
Mitchell, John J.;
Newberry Le Vay, Jessica;
Beard, Emma;
Kale, Dimitra;
Herbec, Aleksandra;
Shahab, Lion

Publication type:

Article

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.

Published in:

Human Mutation, 2011, v. 32, n. 1, p. E1976, doi. 10.1002/humu.21399

By:

Ho, Gladys;
Yonezawa, Atsushi;
Masuda, Satohiro;
Inui, Ken-ichi;
Sim, Keow G.;
Carpenter, Kevin;
Olsen, Rikke K.J.;
Mitchell, John J.;
Rhead, William J.;
Peters, Gregory;
Christodoulou, John

Publication type:

Article

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.

Published in:

Human Mutation, 2008, v. 29, n. 12, p. 1435, doi. 10.1002/humu.20799

By:

Baldridge, Dustin;
Schwarze, Ulrike;
Morello, Roy;
Lennington, Jennifer;
Bertin, Terry K.;
Pace, James M.;
Pepin, Melanie G.;
Weis, MaryAnn;
Eyre, David R.;
Walsh, Jennifer;
Lambert, Deborah;
Green, Andrew;
Robinson, Haynes;
Michelson, Melonie;
Houge, Gunnar;
Lindman, Carl;
Martin, Judith;
Ward, Jewell;
Lemyre, Emmanuelle;
Mitchell, John J.

Publication type:

Article

Recommendations for the management of MPS IVA: systematic evidence- and consensus-based guidance.

Published in:

2019

By:

Akyol, Mehmet Umut;
Alden, Tord D.;
Amartino, Hernan;
Ashworth, Jane;
Belani, Kumar;
Berger, Kenneth I.;
Borgo, Andrea;
Braunlin, Elizabeth;
Eto, Yoshikatsu;
Gold, Jeffrey I.;
Jester, Andrea;
Jones, Simon A.;
Karsli, Cengiz;
Mackenzie, William;
Marinho, Diane Ruschel;
McFadyen, Andrew;
McGill, Jim;
Mitchell, John J.;
Muenzer, Joseph;
Okuyama, Torayuki

Publication type:

journal article

Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance.

Published in:

2019

By:

Akyol, Mehmet Umut;
Alden, Tord D.;
Amartino, Hernan;
Ashworth, Jane;
Belani, Kumar;
Berger, Kenneth I.;
Borgo, Andrea;
Braunlin, Elizabeth;
Eto, Yoshikatsu;
Gold, Jeffrey I.;
Jester, Andrea;
Jones, Simon A.;
Karsli, Cengiz;
Mackenzie, William;
Marinho, Diane Ruschel;
McFadyen, Andrew;
McGill, Jim;
Mitchell, John J.;
Muenzer, Joseph;
Okuyama, Torayuki

Publication type:

journal article

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

Using a meta-narrative literature review and focus groups with key stakeholders to identify perceived challenges and solutions for generating robust evidence on the effectiveness of treatments for rare diseases.

Published in:

2018

By:

Tingley, Kylie;
Coyle, Doug;
Graham, Ian D.;
Sikora, Lindsey;
Chakraborty, Pranesh;
Wilson, Kumanan;
Mitchell, John J.;
Stockler-Ipsiroglu, Sylvia;
Potter, Beth K.;
in collaboration with the Canadian Inherited Metabolic Diseases Research Network;
Canadian Inherited Metabolic Diseases Research Network

Publication type:

journal article

Longitudinal changes in physical activity during and after the first national lockdown due to the COVID-19 pandemic in England.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97065-1

By:

Bu, Feifei;
Bone, Jessica K.;
Mitchell, John J.;
Steptoe, Andrew;
Fancourt, Daisy

Publication type:

Article

Longitudinal changes and correlates of meeting WHO recommended levels of physical activity in the UK during the COVID-19 pandemic: Findings from the HEBECO study.

Published in:

PLoS ONE, 2022, v. 17, n. 8, p. 1, doi. 10.1371/journal.pone.0273530

By:

Mitchell, John J.;
Dicken, Samuel J.;
Kale, Dimitra;
Herbec, Aleksandra;
Beard, Emma;
Shahab, Lion

Publication type:

Article

Correction to: Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys.

Published in:

2021

By:

Howie, Alison H.;
Tingley, Kylie;
Inbar-Feigenberg, Michal;
Mitchell, John J.;
Butcher, Nancy J.;
Offringa, Martin;
Smith, Maureen;
Angel, Kim;
Gentle, Jenifer;
Wyatt, Alexandra;
Campeau, Philippe M.;
Chan, Alicia;
Chakraborty, Pranesh;
El Turk, Farah;
Mamak, Eva;
Mhanni, Aizeddin;
Skidmore, Becky;
Sparkes, Rebecca;
Stockler, Sylvia;
Potter, Beth K.

Publication type:

corrected article

Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys.

Published in:

2021

By:

Howie, Alison H.;
Tingley, Kylie;
Inbar-Feigenberg, Michal;
Mitchell, John J.;
Butcher, Nancy J.;
Offringa, Martin;
Smith, Maureen;
Angel, Kim;
Gentle, Jenifer;
Wyatt, Alexandra;
Campeau, Philippe M.;
Chan, Alicia;
Chakraborty, Pranesh;
El Turk, Farah;
Mamak, Eva;
Mhanni, Aizeddin;
Skidmore, Becky;
Sparkes, Rebecca;
Stockler, Sylvia;
Potter, Beth K.

Publication type:

Literature Review

Establishing a core outcome set for mucopolysaccharidoses (MPS) in children: study protocol for a rapid literature review, candidate outcomes survey, and Delphi surveys.

Published in:

2021

By:

Howie, Alison H.;
Tingley, Kylie;
Inbar-Feigenberg, Michal;
Mitchell, John J.;
Butcher, Nancy J.;
Offringa, Martin;
Smith, Maureen;
Angel, Kim;
Gentle, Jenifer;
Wyatt, Alexandra;
Campeau, Philippe M.;
Chan, Alicia;
Chakraborty, Pranesh;
El Turk, Farah;
Mamak, Eva;
Mhanni, Aizeddin;
Skidmore, Becky;
Sparkes, Rebecca;
Stockler, Sylvia;
Potter, Beth K.

Publication type:

journal article

Clinical characteristics of patients from Quebec, Canada, with Morquio A syndrome: a longitudinal observational study.

Published in:

2020

By:

Moisan, Lina;
Iannuzzi, David;
Maranda, Bruno;
Campeau, Philippe M.;
Mitchell, John J.

Publication type:

journal article

Cytomatrix synthesis in MDCK epithelial cells.

Published in:

Journal of Cellular Physiology, 1990, v. 143, n. 3, p. 501, doi. 10.1002/jcp.1041430315

By:

Mitchell, John J.;
Low, Robert B.;
Woodcock-Mitchell, Janet L.

Publication type:

Article

Establishing core outcome sets for phenylketonuria (PKU) and medium-chain Acyl-CoA dehydrogenase (MCAD) deficiency in children: study protocol for systematic reviews and Delphi surveys.

Published in:

2017

By:

Potter, Beth K.;
Hutton1,2, Brian;
Clifford, Tammy J.;
Pallone, Nicole;
Smith, Maureen;
Stockler, Sylvia;
Chakraborty, Pranesh;
Barbeau, Pauline;
Garritty, Chantelle M.;
Pugliese, Michael;
Rahman, Alvi;
Skidmore, Becky;
Tessier, Laure;
Tingley, Kylie;
Coyle, Doug;
Greenberg, Cheryl R.;
Korngut, Lawrence;
MacKenzie, Alex;
Mitchell, John J.;
Nicholls, Stuart

Publication type:

journal article

Hematopoietic stem cell transplant does not prevent neurological deterioration in infants with Farber disease: Case report and literature review.

Published in:

Journal of Inherited Metabolic Disease Reports, 2019, v. 46, n. 1, p. 46, doi. 10.1002/jmd2.12008

By:

Goudie, Catherine;
Alayoubi, Abdulfatah M.;
Tibout, Pauline;
Duval, Michel;
Maranda, Bruno;
Mitchell, David;
Mitchell, John J.

Publication type:

Article

Longitudinal associations between physical activity and other health behaviours during the COVID-19 pandemic: a fixed effects analysis.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-20196-6

By:

Mitchell, John J.;
Bu, Feifei;
Fancourt, Daisy;
Steptoe, Andrew;
Bone, Jessica K.

Publication type:

Article

Safety and physiological effects of two different doses of elosulfase alfa in patients with morquio a syndrome: A randomized, double-blind, pilot study.

Published in:

American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 10, p. 2272, doi. 10.1002/ajmg.a.37172

By:

Burton, Barbara K.;
Berger, Kenneth I.;
Lewis, Gregory D.;
Tarnopolsky, Mark;
Treadwell, Marsha;
Mitchell, John J.;
Muschol, Nicole;
Jones, Simon A.;
Sutton, V. Reid;
Pastores, Gregory M.;
Lau, Heather;
Sparkes, Rebecca;
Genter, Fred;
Shaywitz, Adam J.;
Harmatz, Paul

Publication type:

Article

Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease).

Published in:

2019

By:

Zapata-Aldana, Eugenio;
McMillan, Hugh J;
Rupar, Tony;
Brunel-Guitton, Catherine;
Chakraborty, Pranesh;
Mitchell, John J;
Roth, Johannes;
Tarnopolsky, Mark A;
Turner, Lesley;
Campbell, Craig

Publication type:

Case Study

Insulin-Induced Insulin Receptor Substrate-1 Degradation is mediated by the Proteasome Degradation Pathway.

Published in:

Diabetes, 1999, v. 48, n. 7, p. 1359, doi. 10.2337/diabetes.48.7.1359

By:

Xiao Jian Sun;
Goldberg, Jonathan L.;
Li-ya Qiao;
Mitchell, John J.

Publication type:

Article