Cheryl Rockman-Greenberg
Cheryl Rockman-Greenberg (born September 26, 1950) is a Canadian physician and educator. She was inducted into the Canadian Medical Hall of Fame in 2018. Cheryl has two children, Matthew and Michelle.She was born in Montreal and received a MDCM from McGill University in 1974. In 1979, she began work as a clinical and metabolic geneticist for the Winnipeg Regional Health Authority. She was director of the Metabolic Service in the Program of Genetics and Metabolism there from 1992 to 2015. From 2004 to 2014, she was head of the Department of Pediatrics and Child Health at the University of Manitoba and Medical Director for the Child Health Program at the Winnipeg Regional Health Authority. She is a clinician scientist at the Children's Hospital Research Institute of Manitoba and holds the title of Distinguished Professor at the University of Manitoba.
Rockman-Greenberg is the leading Canadian researcher in the treatment of hypophosphatasia. She also developed targeted DNA-based screening programs for newborns in Manitoba for a number of rare conditions including glutaric aciduria type 1 in the Oji-Cree and carnitine palmitoyltransferase I deficiency in Hutterites; these screening programs were aimed at groups with higher incidence of these conditions than the general population.
In 2012, she was named one of the Top 100 Most Powerful Women in Canada by the Toronto-based Women's Executive Network.
She was appointed to the Order of Canada as an Officer of the Order in the December 2019 New Year's list. Provided by Wikipedia
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Generation of new human iPSC cell line (UOMi008-A) from a Hypophosphatasia patient by Abhay Srivastava, Elika Verma, Cheryl Rockman-Greenberg, Sanjiv Dhingra
Published 2022-10-01
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Mass Spectrometry Evaluation of Biomarkers in the Vitreous Fluid in Gaucher Disease Type 3 with Disease Progression Despite Long-Term Treatment by Aizeddin Mhanni, Michel Boutin, Frank Stockl, Janine Johnston, Jeff Barnes, Donald Duerksen, Leanne Zimmer, Christiane Auray-Blais, Cheryl Rockman-Greenberg
Published 2020-01-01
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Diagnostic delay is common among patients with hypophosphatasia: initial findings from a longitudinal, prospective, global registry by Wolfgang Högler, Craig Langman, Hugo Gomes da Silva, Shona Fang, Agnès Linglart, Keiichi Ozono, Anna Petryk, Cheryl Rockman-Greenberg, Lothar Seefried, Priya S. Kishnani
Published 2019-02-01
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P494: An analysis of ALPL gene variants in patients with hypophosphatasia from the Global Hypophosphatasia Registry by Priya Kishnani, Kathryn Dahir, Gabriel Martos-Moreno, Agnès Linglart, Anna Petryk, William Mowrey, Shona Fang, Cheryl Rockman-Greenberg, Keiichi Ozono, Wolfgang Högler, Lothar Seefried
Published 2023-01-01
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Effectiveness of asfotase alfa for treatment of adults with hypophosphatasia: results from a global registry by Priya S. Kishnani, Gabriel Ángel Martos-Moreno, Agnès Linglart, Anna Petryk, Andrew Messali, Shona Fang, Cheryl Rockman-Greenberg, Keiichi Ozono, Wolfgang Högler, Lothar Seefried, Kathryn M. Dahir
Published 2024-03-01
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Does specialist physician supply affect pediatric asthma health outcomes? by Guido Filler, Tom Kovesi, Erik Bourdon, Sarah Ann Jones, Laurentiu Givelichian, Cheryl Rockman-Greenberg, Jason Gilliland, Marion Williams, Elaine Orrbine, Bruno Piedboeuf, The Paediatric Chairs of Canada Mark Bernstein
Published 2018-04-01
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Impact of muscular symptoms and/or pain on disease characteristics, disability, and quality of life in adult patients with hypophosphatasia: A cross-sectional analysis from the Glo... by Kathryn M. Dahir, Priya S. Kishnani, Gabriel Ángel Martos-Moreno, Gabriel Ángel Martos-Moreno, Gabriel Ángel Martos-Moreno, Agnès Linglart, Anna Petryk, Cheryl Rockman-Greenberg, Samantha E. Martel, Keiichi Ozono, Wolfgang Högler, Lothar Seefried
Published 2023-03-01
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Review of clinical trials and guidelines for children and youth with mucopolysaccharidosis: outcome selection and measurement by Alison H. Howie, Kylie Tingley, Michal Inbar-Feigenberg, John J. Mitchell, Kim Angel, Jenifer Gentle, Maureen Smith, Martin Offringa, Nancy J. Butcher, Philippe M. Campeau, Pranesh Chakraborty, Alicia Chan, Dean Fergusson, Eva Mamak, Peyton McClelland, Saadet Mercimek-Andrews, Aizeddin Mhanni, Zeinab Moazin, Cheryl Rockman-Greenberg, C. Anthony Rupar, Becky Skidmore, Sylvia Stockler, Kednapa Thavorn, Alexandra Wyatt, Beth K. Potter, INFORM RARE Network
Published 2024-10-01
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P480: Parent and healthcare personnel perspectives on challenges to family-centered care for children with inherited metabolic diseases: A qualitative analysis by Andrea Chow, Guylaine D'Amours, Isabel Jordan, Nicole Pallone, Maureen Smith, Pranesh Chakraborty, Zobaida Al-Baldawi, Julie Paradis, Jamie Brehaut, Alicia Chan, Eyal Cohen, Sarah Dyack, Jane Gillis, Sharan Goobie, Ian Graham, Cheryl Rockman-Greenberg, Jeremy Grimshaw, Robin Hayeems, Michal Inbar-Feigenberg, Shailly Jain-Ghai, Sara Khangura, Jennifer MacKenzie, Nathalie Major, John Mitchell, Stuart Nicholls, Amy Pender, Murray Potter, Chitra Prasad, Natalya Karp, Andreas Schulze, Komudi Siriwardena, Kathy Speechley, Sylvia Stockler, Yannis Trakadis, Clara van Karnebeek, Jagdeep Walia, Kumanan Wilson, Brenda Wilson, Andrea Yu, Beth Potter
Published 2024-01-01
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