Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kheirie Issa"'
Autor:
Sara Long-Gagne, Danielle Arje, Natalie Weiser, Julia Orkin, Doug Miller, Tobey Audcent, Eyal Cohen, Anne Marie Sbrocchi, Nathalie Major, Derek Stephens, Kathleen Huth, Kheirie Issa
Publikováno v:
Academic Pediatrics. 20:282-289
Objective Children with medical complexity (CMC) are a growing population, yet training in complex care varies across pediatric residency programs. The purpose of this study was 1) to evaluate the effectiveness of a curriculum for pediatric residents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5989fbdeeccf091e23012549f44d01
https://doi.org/10.1016/j.acap.2019.09.002
https://doi.org/10.1016/j.acap.2019.09.002
Autor:
Hao Liu, Sarah L Sawyer, Monika Gos, David Grynspan, Kheirie Issa, Raveena Ramphal, Carmen Rotaru, FORGE Canada Consortium, Jacek Majewski, Kym M Boycott, Gail Graham, Matthew Bromwich
Publikováno v:
American Journal of Medical Genetics Part A. 167:1337-1341
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by congenital malformations of the great toes and progressive heterotopic ossification of connective tissue that begins during the first decade of life. Our patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e12f7b62794e1f4fde90e006122c4a5d
https://doi.org/10.1002/ajmg.a.36969
https://doi.org/10.1002/ajmg.a.36969
Autor:
Kheirie Issa, Margaret Boland, Michael T. Geraghty, C. Ronald Scott, Zaining Wu, Adam D. McIntyre, Robert A. Hegele, Matthew A. Lines, Julien L. Marcadier
Publikováno v:
Canadian Medical Association Journal. 187:102-107
Background Congenital sucrase-isomaltase deficiency is a rare hereditary cause of chronic diarrhea in children. People with this condition lack the intestinal brush-border enzyme required for digestion of di- and oligosaccharides, including sucrose a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c59eeb299adc66158115af294c64f9e
https://doi.org/10.1503/cmaj.140657
https://doi.org/10.1503/cmaj.140657
Autor:
Kathleen Huth, Tobey Audcent, Sara Long-Gagne, Anne Marie Sbrocchi, Natalie Weiser, Doug Miller, Danielle Arje, Nathalie Major, Kheirie Issa, Eyal Cohen, Julia Orkin
Publikováno v:
Academic Pediatrics. 18:e26-e27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68ae7d8335e02a3c1b023b612e5681c0
https://doi.org/10.1016/j.acap.2018.04.075
https://doi.org/10.1016/j.acap.2018.04.075
MG-107 Congenital sucrase-isomaltase deficiency: Identification of the common inuit founder mutation
Autor:
Julien L. Marcadier, Kheirie Issa, Robert A. Hegele, Matthew A. Lines, C. Ronald Scott, Michael T. Geraghty, Margaret Boland, Zaining Wu, Adam D. McIntyre
Publikováno v:
Journal of Medical Genetics. 52:A1.3-A2
Objective Congenital sucrase-isomaltase deficiency (CSID) is a rare hereditary cause of chronic diarrhoea in children. Persons with CSID lack the intestinal brush-border enzyme required for digestion of di- and oligosaccharides, including sucrose and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef1ddbbab6c4dcbfc16e140952494958
https://doi.org/10.1136/jmedgenet-2015-103577.3
https://doi.org/10.1136/jmedgenet-2015-103577.3