Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Aaron Spahr"'
Autor:
Aaron Spahr, Zaliqa Rosli, Mélanie Legault, Luan T. Tran, Simon Fournier, Helia Toutounchi, Lama Darbelli, Cécile Madjar, Cassandra Lucia, Marie-Lou St-Jean, Samir Das, Alan C. Evans, Geneviève Bernard
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Rare diseases are estimated to affect 150–350 million people worldwide. With advances in next generation sequencing, the number of known disease-causing genes has increased significantly, opening the door for therapy development
Externí odkaz:
https://doaj.org/article/458e89caa53041649c3cf15c4c13ae3b
Autor:
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, Aaron Spahr, Luan T. Tran, Renée-Myriam Boucher, Chantal Poulin, Bradley Osterman, Myriam Srour, Bernard Rosenblatt, Sébastien Chénier, Jean-Francois Soucy, Anne-Marie Laberge, Maria Daniela D’Agostino, Cam-Tu Emilie Nguyen, Maxime Morsa, Geneviève Bernard
Publikováno v:
Journal of Child Neurology. :088307382311766
Parents of children with genetically determined leukoencephalopathies play a major role in their children's health care. We sought to gain a better understanding of their experience with the public health care system in Quebec, Canada, to obtain sugg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::225d6ffdf414239d4f027f04a6fedeb2
https://doi.org/10.1177/08830738231176672
https://doi.org/10.1177/08830738231176672
Autor:
Aaron Spahr, E. Malvey-Dorn, S. Chandratre, F Pelletier, B. Osterman, M. Desmeules, G. Roedde, Marie Emmanuelle Dilenge, S. Chenier, Albert Larbrisseau, P. Marois, A Mirchi, Luan Tran, Elsa Rossignol, K. Y. Lim, Nancy Braverman, E. Dermer, Michael Shevell, J. Reggin, Mark A. Tarnopolsky, Guillaume Sébire, J. Laflamme, Kether Guerrero, Catalina Maftei, Geneviève Legault, Soad M. Ahmed, Sunita Venkateswaran, Daniela Pohl, Daniela Buhas, Philippe Major, I. Paradis, John J. Mitchell, Geneviève Bernard, M. Sullivan, Bernard Brais, Nicolas Chrestian, Myriam Srour, Michel Sylvain, EM Riou, A. Nadeau
Publikováno v:
Journal of Child Neurology. 35:901-907
Genetically determined leukoencephalopathies comprise a group of rare inherited white matter disorders. The majority are progressive diseases resulting in early death. We performed a cross-sectional pilot study including 55 parents from 36 families t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f960a9c3c06818684c86c6b2dd83c196
https://doi.org/10.1177/0883073820938645
https://doi.org/10.1177/0883073820938645
Autor:
Pouneh Amir Yazdani, Marie-Lou St-Jean, Sara Matovic, Aaron Spahr, Luan T. Tran, Renée-Myriam Boucher, Chantal Poulin, Bradley Osterman, Myriam Srour, Bernard Rosenblatt, Sébastien Chenier, Jean-Francois Soucy, Anne-Marie Laberge, Nancy Braverman, Maria Daniela D’Agostino, Cam-Tu Emilie Nguyen, Maxime Morsa, Geneviève Bernard
Publikováno v:
Journal of child neurology. 37(4)
Parents of children with genetically determined leukoencephalopathies play a major role in their children's health care. Because of the COVID-19 pandemic, many health care services were suspended, delayed or delivered remotely with telemedicine. We s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15682a82cf0691d2d566a87f5c213c80
https://pubmed.ncbi.nlm.nih.gov/34986037
https://pubmed.ncbi.nlm.nih.gov/34986037
Autor:
Geneviève Bernard, Aaron Spahr, Mélanie Legault, Marie-Lou St-Jean, Alan C. Evans, Helia Toutounchi, Samir Das, Cassandra Lucia, Lama Darbelli, Luan Tran, Zaliqa Rosli, Cécile Madjar, Simon Fournier
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Rare diseases are estimated to affect 150–350 million people worldwide. With advances in next generation sequencing, the number of known disease-causing genes has increased significantly, opening the door for therapy development. Rare di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b862fc4df92b0af9831f83d1f2899e2
https://doi.org/10.21203/rs.3.rs-491571/v1
https://doi.org/10.21203/rs.3.rs-491571/v1
Publikováno v:
Journal of Child Neurology. 36:245-246
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3def4d2d93fd728fdfcc6c5adc99466d
https://doi.org/10.1177/0883073820960984
https://doi.org/10.1177/0883073820960984
Autor:
Yazdani, Pouneh Amir, St-Jean, Marie-Lou, Matovic, Sara, Spahr, Aaron, Tran, Luan T., Boucher, Renée-Myriam, Poulin, Chantal, Osterman, Bradley, Srour, Myriam, Rosenblatt, Bernard, Chénier, Sébastien, Soucy, Jean-Francois, Laberge, Anne-Marie, D'Agostino, Maria Daniela, Nguyen, Cam-Tu Emilie, Morsa, Maxime, Bernard, Geneviève
Publikováno v:
Journal of Child Neurology; Apr2023, Vol. 38 Issue 5, p329-335, 7p
Publikováno v:
Journal of Child Neurology; Mar2021, Vol. 36 Issue 3, p245-246, 2p
Autor:
Amir Yazdani, Pouneh, St-Jean, Marie-Lou, Matovic, Sara, Spahr, Aaron, Tran, Luan T., Boucher, Renée-Myriam, Poulin, Chantal, Osterman, Bradley, Srour, Myriam, Rosenblatt, Bernard, Chenier, Sébastien, Soucy, Jean-Francois, Laberge, Anne-Marie, Braverman, Nancy, D'Agostino, Maria Daniela, Nguyen, Cam-Tu Emilie, Morsa, Maxime, Bernard, Geneviève
Publikováno v:
Journal of Child Neurology; Mar2022, Vol. 37 Issue 4, p237-245, 9p