Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Bruno, Michon"'
Autor:
Lye-Ann Robichaud, Julie Felipe, Michel Duval, Bruno Michon, Marianne Olivier-D’Avignon, Sébastien Perreault, Mathias Tyo-Gomez, Marc-Antoine Marquis, Serge Sultan
Publikováno v:
Current Oncology, Vol 31, Iss 4, Pp 2289-2304 (2024)
A recent measure was developed to assess the Quality of Life (QoL) of young people with advanced cancer and is available for parents and professionals (Advance QoL). The present study aimed to elaborate self-reported versions for children and adolesc
Externí odkaz:
https://doaj.org/article/fd29baa7e8af457f8842faa59d2c2892
Dieser Open-Access-Sammelband zeigt auf, welche Themen mit Blick auf das Handlungsfeld Soziale Arbeit und Stadtentwicklung besonders relevant sind und zurzeit im Vordergrund stehen. Marginalisierte Menschen und Quartiere sind typische Phänomene sozi
Autor:
Étienne Camiré-Bernier, Erwan Nidelet, Amel Baghdadli, Gabriel Demers, Marie-Christine Boulanger, Marie-Claude Brisson, Bruno Michon, Sophie Lauzier, Isabelle Laverdière
Publikováno v:
Current Oncology, Vol 28, Iss 6, Pp 4377-4391 (2021)
Acute lymphoblastic leukemia (ALL) is the most common type of cancer in children. Treatment includes home-based oral chemotherapies (OCs) (e.g., 6-mercaptopurine and dexamethasone) taken for 2 to 3 years. The management of OC can be challenging for c
Externí odkaz:
https://doaj.org/article/1feeb90c5afc41199bf028760d72baef
Autor:
Lynda M. Vrooman, Traci M. Blonquist, Marian H. Harris, Kristen E. Stevenson, Andrew E. Place, Sarah K. Hunt, Jane E. O'Brien, Barbara L. Asselin, Uma H. Athale, Luis A. Clavell, Peter D. Cole, Kara M. Kelly, Caroline Laverdiere, Jean-Marie Leclerc, Bruno Michon, Marshall A. Schorin, Maria Luisa Sulis, Jennifer J.G. Welch, Donna S. Neuberg, Stephen E. Sallan, Lewis B. Silverman
Publikováno v:
Blood Advances, Vol 2, Iss 12, Pp 1449-1458 (2018)
Abstract: Dana-Farber Cancer Institute (DFCI) ALL Consortium Protocol 05-001 tested a new risk stratification system in children and adolescents with newly diagnosed acute lymphoblastic leukemia (ALL). At study entry, B-ALL patients were classified a
Externí odkaz:
https://doaj.org/article/7fe5b025a97248a2bd7140b86b897665
Autor:
Thai Hoa Tran, Marian H. Harris, Jonathan V. Nguyen, Traci M. Blonquist, Kristen E. Stevenson, Eileen Stonerock, Barbara L. Asselin, Uma H. Athale, Luis A. Clavell, Peter D. Cole, Kara M. Kelly, Caroline Laverdiere, Jean-Marie Leclerc, Bruno Michon, Marshall A. Schorin, Jennifer J.G. Welch, Shalini C. Reshmi, Donna S. Neuberg, Stephen E. Sallan, Mignon L. Loh, Lewis B. Silverman
Publikováno v:
Blood Advances, Vol 2, Iss 5, Pp 529-533 (2018)
Abstract: Recurrent chromosomal rearrangements carry prognostic significance in pediatric B-lineage acute lymphoblastic leukemia (B-ALL). Recent genome-wide analyses identified a high-risk B-ALL subtype characterized by a diverse spectrum of genetic
Externí odkaz:
https://doaj.org/article/44b885b31a124a5584f54b008afc7fdf
Autor:
Nicolas Waespe, Santhosh Dhanraj, Manju Wahala, Elena Tsangaris, Tom Enbar, Bozana Zlateska, Hongbing Li, Robert J. Klaassen, Conrad V. Fernandez, Geoff D. E. Cuvelier, John K. Wu, Yves D. Pastore, Mariana Silva, Jeffrey H. Lipton, Joseé Brossard, Bruno Michon, Sharon Abish, MacGregor Steele, Roona Sinha, Mark J. Belletrutti, Vicky R. Breakey, Lawrence Jardine, Lisa Goodyear, Liat Kofler, Michaela Cada, Lillian Sung, Mary Shago, Stephen W. Scherer, Yigal Dror
Publikováno v:
npj Genomic Medicine, Vol 2, Iss 1, Pp 1-8 (2017)
Blood disorders: impact of genomic structural variation Copy number variation in patients with inherited bone marrow failure syndromes (IBMFSs) is associated with more severe clinical symptoms. In addition to persistently low levels of red blood cell
Externí odkaz:
https://doaj.org/article/fab055366f7246f79c31483ee2eaa142
Autor:
Kristine Karvonen, Puja Umaretiya, Victoria Koch, Yael Flamand, Rahela Aziz-Bose, Lenka Ilcisin, Ariana Valenzuela, Peter Cole, Lisa Gennarini, Justine Kahn, Kara Kelly, Thai Hoa Tran, Bruno Michon, Jennifer Welch, Joanne Wolfe, Lewis Silverman, Abby R. Rosenberg, Kira Bona
Black and Hispanic children with leukemia experience inferior survival compared to non-Hispanic White (NHW) children. Identifying modifiable social determinants of health can inform intervention targets to address inequities. We characterized the fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e7ebba2d4bfb1eba0cd5e5578e7545f
https://doi.org/10.22541/au.168018666.63114716/v1
https://doi.org/10.22541/au.168018666.63114716/v1
Autor:
Yeon Jung Lim, Omri A. Arbiv, Melanie E. Kalbfleisch, Robert J. Klaassen, Conrad Fernandez, Meera Rayar, MacGregor Steele, Jeffrey H. Lipton, Geoff Cuvelier, Yves D. Pastore, Mariana Silva, Josee Brossard, Bruno Michon, Sharon Abish, Roona Sinha, Catherine Corriveau‐Bourque, Vicky R. Breakey, Soumitra Tole, Lisa Goodyear, Lillian Sung, Bozana Zlateska, Michaela Cada, Yigal Dror
Publikováno v:
European Journal of Haematology. 108:278-287
Classification of inherited bone marrow failure syndromes (IBMFSs) according to clinical and genetic diagnoses enables proper adjustment of treatment. Unfortunately, 30% of patients enrolled in the Canadian Inherited Marrow Failure Registry (CIMFR) w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd138ab5e0106c0f7b2f018ff1282778
https://doi.org/10.1111/ejh.13733
https://doi.org/10.1111/ejh.13733
Publikováno v:
Quartiersforschung ISBN: 9783658373856
ZusammenfassungDer Beitrag widmet sich dem trinationalen und grenzüberschreitenden Forschungs- und Entwicklungsprojekt „MARGE – Einbindung marginalisierter Quartiere in die Oberrheinregion“ und diskutiert, wie sich die Effekte des grenzübersc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2837b119ab16694ac2ba9244cf1ad8ae
https://doi.org/10.1007/978-3-658-37386-3_11
https://doi.org/10.1007/978-3-658-37386-3_11
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:479-481
Idiopathic purpura fulminans (PF) is rare but has been reported in pediatric patients, commonly following infections. We present a case of a 5-year-old boy, heterozygous for factor V Leiden, with no history of recent infections, who presented with PF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff5ce076f3708a5e60bce9c0b4066d84
https://doi.org/10.1097/mph.0000000000002497
https://doi.org/10.1097/mph.0000000000002497