Výsledky vyhledávání - "Christine A Sabapathy"

Cerebral Sinovenous Thrombosis in Infants and Children: A Practical Approach to Management

Autor: Noa Mandel-Shorer, Christine A. Sabapathy, Pradeep Krishnan, Mukta Sharma, Neil A. Goldenberg, Leonardo R. Brandão, Mahendranath D. Moharir

Publikováno v: Seminars in pediatric neurology. 44

Cerebral sinovenous thrombosis (CSVT) is a rare, yet potentially devastating disorder, associated with acute complications and long-term neurologic sequelae. Consensus-based international pediatric CSVT treatment guidelines emphasize early clinical-r

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816732b84460675e36aff8a14be214eb
https://pubmed.ncbi.nlm.nih.gov/36456034

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Cost-Effectiveness of Extended Thromboprophylaxis in Patients Undergoing Colorectal Surgery from a Canadian Health Care System Perspective

Autor: Maude Trepanier, Barry Stein, Lawrence Lee, A. Sender Liberman, Liane S. Feldman, Christine A Sabapathy, Noura Alhassan, Patrick Charlebois

Publikováno v: Diseases of the Colon & Rectum. 62:1381-1389

There is increasing evidence to support extended thromboprophylaxis after colorectal surgery to minimize the incidence of postdischarge venous thromboembolic events. However, the absolute number of events is small, and extended thromboprophylaxis req

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78699aa771a11284c950b8d189d1ee7c
https://doi.org/10.1097/dcr.0000000000001438

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Megalencephaly–Capillary Malformation–Polymicrogyria with Cerebral Venous Thrombosis

Autor: Olivier Fortin, Kenneth A. Myers, Christine A. Sabapathy, Caroline Lacroix, Mohammed Ashour

Publikováno v: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 47:828-829

Megalencephaly–capillary malformation–polymicrogyria (MCAP) syndrome (OMIM #602501) is characterized by megalencephaly, midline capillary malformations, and cortical malformations. This genetic overgrowth syndrome is associated with mosaic gain-o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43073de5ebb6230d9f0fcb5861f5ea45
https://doi.org/10.1017/cjn.2020.127

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Lateral Medullary Syndrome Due to Left Vertebral Artery Occlusion in a Boy Postflexion Neck Injury

Autor: Guillaume Sébire, Michael Shevell, Abdulla Alawadhi, Christine A. Sabapathy, Christine Saint-Martin

Publikováno v: Child Neurology Open, Vol 6 (2019)
Child Neurology Open

Lateral medullary syndrome is rare in pediatrics. It is characterized by neurological deficits due to an ischemic lesion in the lateral medulla. The authors describe a 17-year-old boy who developed lateral medullary syndrome in the context of a hyper

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd28e0a9c8deb36c7e3c6012534cf4c
https://doaj.org/article/6a29d8aa40014588b574600630ea1d47

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Thromboembolism Incidence and Risk Factors in Children with Cancer: A Population-Based Cohort Study

Autor: David Stammers, Leonardo R. Brandão, Jason D. Pole, Uma H. Athale, Christine A. Sabapathy, Marie-Claude Pelland-Marcotte, Jessica Halparin, Lillian Sung, Ketan Kulkarni

Publikováno v: Thrombosis and haemostasis. 118(9)

There is conflicting information about the epidemiology of thromboembolism (TE) in paediatric oncology. Objectives were to describe the incidence and risk factors of TE in children with cancer. We included all children with cancer less than 15 years

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e1bafe5c660a17016353e3d5a096fd3
https://pubmed.ncbi.nlm.nih.gov/30103249

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A prospective surveillance study of inhibitor development in haemophilia A patients following a population switch to a third-generation B-domain-deleted recombinant factor VIII

Autor: Clémence Merlen, Stéphanie Cloutier, Christine Demers, Evemie Dubé, Jean-François Castilloux, M. Warner, J. St-Louis, Arnaud Bonnefoy, Georges-Etienne Rivard, Catherine Vézina, Christine A. Sabapathy

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 24(2)

Introduction Following a provincial tender, most subjects with haemophilia A in Quebec switched their treatment to a third-generation recombinant B-domain-deleted factor VIII (FVIII). Aim Our objective was to evaluate the incidence of inhibitor devel

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac90d54d8200c1b7813353ca980ee7f9
https://pubmed.ncbi.nlm.nih.gov/29388742

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