Improvements in patient blood management for pediatric craniosynostosis surgery using a ROTEM®-assisted strategy – feasibility and costs

Por Haas, Thorsten, Goobie, Susan, Spielmann, Nelly, Weiss, Markus, Schmugge, Markus
Publicado em 2014

Malignancies in Systemic Lupus Erythematosus – a 2015 Update

Por Goobie, Gillian C, Bernatsky, Sasha, Ramsey-Goldman, Rosalind, Clarke, Ann E.
Publicado no Curr Opin Rheumatol (2015)

Segregation Analysis in Shwachman-Diamond Syndrome: Evidence for Recessive Inheritance

Por Ginzberg, H., Shin, J., Ellis, L., Goobie, S., Morrison, J., Corey, M., Durie, P. R., Rommens, J. M.
Publicado em 2000

YouTube-videos for patient education in lymphangioleiomyomatosis?

Por Finn M. Wilkens, Claudia Ganter, Katharina Kriegsmann, Heinrike Wilkens, Nicolas Kahn, Gillian C. Goobie, Christopher J. Ryerson, Michael Kreuter
Publicado em 2022-04-01

Infantile Muscular Dystrophy in Canadian Aboriginals is an αB-Crystallinopathy

Por Del Bigio, Marc R., Chudley, Albert E., Sarnat, Harvey B., Campbell, Craig, Goobie, Sharan, Chodirker, Bernard N., Selcen, Duygu
Publicado em 2011

Tranexamic Acid Use in US Children’s Hospitals

Por Nishijima, Daniel K., Monuteaux, Michael C., Faraoni, David, Goobie, Susan M., Lee, Lois, Galante, Joseph, Holmes, James F., Kuppermann, Nathan
Publicado no J Emerg Med (2016)

Lessons from lung transplantation: Cause for redefining the pathophysiology of pulmonary hypertension in gaucher disease

Por Gillian C. Goobie, Sandra M. Sirrs, John Yee, John C. English, Celine Bergeron, Roland Nador, John R. Swiston, Pramod K. Mistry, Wendy Paquin, Robert D. Levy
Publicado em 2019-01-01

Shwachman-Diamond Syndrome with Exocrine Pancreatic Dysfunction and Bone Marrow Failure Maps to the Centromeric Region of Chromosome 7

Por Goobie, Sharan, Popovic, Maja, Morrison, Jodi, Ellis, Lynda, Ginzberg, Hedy, Boocock, Graeme R. B., Ehtesham, Nadia, Bétard, Christine, Brewer, Carl G., Roslin, Nicole M., Hudson, Thomas J., Morgan, Kenneth, Fujiwara, T. Mary, Durie, Peter R., Rommens, Johanna M.
Publicado em 2001

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting

Por Goobie, S., Knijnenburg, J., FitzPatrick, D., Sharkey, F.H., Lionel, A.C., Marshall, C.R., Azam, T., Shago, M., Chong, K., Mendoza-Londono, R., den Hollander, N.S., Ruivenkamp, C., Maher, E., Tanke, H.J., Szuhai, K., Wintle, R.F., Scherer, S.W.
Publicado em 2009

VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families

Por Bourassa, Cynthia V., Meijer, Inge A., Merner, Nancy D., Grewal, Kanwal K., Stefanelli, Mark G., Hodgkinson, Kathleen, Ives, Elizabeth J., Pryse-Phillips, William, Jog, Mandar, Boycott, Kym, Grimes, David A., Goobie, Sharan, Leckey, Richard, Dion, Patrick A., Rouleau, Guy A.
Publicado em 2012

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression

Por Lowther, Chelsea, Speevak, Marsha, Armour, Christine M., Goh, Elaine S., Graham, Gail E., Li, Chumei, Zeesman, Susan, Nowaczyk, Malgorzata J.M., Schultz, Lee-Anne, Morra, Antonella, Nicolson, Rob, Bikangaga, Peter, Samdup, Dawa, Zaazou, Mostafa, Boyd, Kerry, Jung, Jack H., Siu, Victoria, Rajguru, Manjulata, Goobie, Sharan, Tarnopolsky, Mark A., Prasad, Chitra, Dick, Paul T., Hussain, Asmaa S., Walinga, Margreet, Reijenga, Renske G., Gazzellone, Matthew, Lionel, Anath C., Marshall, Christian R., Scherer, Stephen W., Stavropoulos, Dimitri J., McCready, Elizabeth, Bassett, Anne S.
Publicado no Genet Med (2016)