Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Beatrix Wong"'
Publikováno v:
IDCases, Vol 13, Iss , Pp - (2018)
An 85-year-old man with a history of aortic valve replacement presented with lower limb cramps. He was initially diagnosed with degenerative disc disease, but was found to have Lactococcus garvieae infective endocarditis with septic embolic strokes c
Externí odkaz:
https://doaj.org/article/71ceb91068c345b48a949e8fa0b48295
Autor:
Charu Venkatesan, Elizabeth Countee, Beatrix Wong, Christine Spaeth, Beth M. Kline-Fath, Usha D. Nagaraj
Publikováno v:
Journal of Child Neurology. 38:31-37
Prenatal identification by magnetic resonance imaging (MRI) of callosal anomalies, particularly with accompanying intracranial abnormalities, poses a challenge for accurate prognostication and fetal counseling as outcome can vary widely depending on
Publikováno v:
Prenatal Diagnosis. 42:27-36
To determine factors influencing patients to choose prenatal or postnatal repair of their child's myelomeningocele (MMC) when both treatment options are offered.We distributed a retrospective survey via email and social media to parents of children w
Autor:
Bobby K, Brar, Marisa Gilstrop, Thompson, Neeta L, Vora, Kelly, Gilmore, Karin, Blakemore, Kristen A, Miller, Jessica, Giordano, Andreas, Dufke, Beatrix, Wong, Samantha, Stover, Billie, Lianoglou, Ignatia, Van den Veyver, Esther, Dempsey, Mara, Rosner, Karen, Chong, David, Chitayat, Teresa N, Sparks, Mary E, Norton, Ronald, Wapner, Kristin, Baranano, Angie C, Jelin
Publikováno v:
Prenatal diagnosisREFERENCES. 42(13)
Tubulinopathies refer to conditions caused by genetic variants in isotypes of tubulin resulting in defective neuronal migration. Historically, diagnosis was primarily via postnatal imaging. Our objective was to establish the prenatal phenotype/genoty
Publikováno v:
Obstetrical & Gynecological Survey. 76:663-664
Publikováno v:
Genetics in Medicine
Purpose Previous studies have reported that prenatal exome sequencing (pES) can detect monogenic diseases in fetuses with congenital anomalies with diagnostic yields ranging from 6% to 81%, but there are few reports of its clinical utility. Methods W
Autor:
Samantha Stover, Angie C. Jelin, Mary E. Norton, Ronald J. Wapner, Marisa Gilstrop Thompson, Jessica L. Giordano, Billie R. Lianoglou, Beatrix Wong, Ignatia B. Van den Veyver, Andreas Dufke
Publikováno v:
American Journal of Obstetrics and Gynecology. 224:S190-S191
Autor:
Melyssa Aronson, George S. Charames, Ashton A. Connor, Kara Semotiuk, Marina Wang, Beatrix Wong, Tahsin Khan, Kate Mcnamara, Jordan Lerner-Ellis, Sam Khalouei, Aaron Pollett, Zane Cohen, Steve Gallinger, Spring Holter, Saud H. AlDubayan
Publikováno v:
Cancer. 122:1672-1679
BACKGROUND In November 2001, genetic testing for Lynch syndrome (LS) was introduced by the Ministry of Health and Long-Term Care (MOH) in Ontario for individuals at high risk for LS cancers according to either tumor immunohistochemistry staining or t
Autor:
Matthew S. Lebo, Kathleen-Rose Zakoor, Kathy Chun, Marsha D. Speevak, John S. Waye, Elizabeth McCready, Jillian S. Parboosingh, Ryan E. Lamont, Harriet Feilotter, Ian Bosdet, Tracy Tucker, Sean Young, Aly Karsan, George S. Charames, Ronald Agatep, Elizabeth L. Spriggs, Caitlin Chisholm, Nasim Vasli, Hussein Daoud, Olga Jarinova, Robert Tomaszewski, Stacey Hume, Sherryl Taylor, Mohammad R. Akbari, Jordan Lerner-Ellis, Ron Agatep, Peter Ainsworth, Melyssa Aronson, Raveen Basran, Andre Blavier, Andrea Blumenthal, Kym Boycott, Michael Brudno, Kathleen Buckley, Jodi Campbell, Philippe M. Campeau, Melanie Care, Nancy Carson, Ronald Carter, George Charames, David Chitayat, George Chong, Edmond Chouinard, Kenneth J. Craddock, Rod Docking, Andrea Eisen, Hanna Faghfoury, Sandra Farrell, Bridget Fernandez, Marc Fiume, Cynthia Forster-Gibson, Jan Friedman, William Foulkes, Peter Goodhand, Jessica Gu, Robert Hegele, Spring Holter, Sheri Horsburgh, Lauren Hughes, Franny Jewett, Anne Junker, Sam Khalouei, Joan Knoll, Elena Kolomeitz, Bartha Knoppers, Ryan Lamont, Matthew Lebo, Georges Maire, Christian Marshall, Grant Mitchell, Michael J Moorhouse, Chantal Morel, Tanya Nelson, Abdul Noor, Brian O'Connor, Darren O'Rielly, Francis Ouellette, Jillian Parboosingh, Hilary Racher, Peter Ray, Heidi Rehm, Christie Riddell, Jean-Baptiste Riviere, David S. Rosenblatt, Guy Rouleau, Andrea Ruchon, Peter Sabatini, Bekim Sadikovic, Kara Semotiuk, Stephen W. Scherer, Cheryl Shuman, Josh Silver, Katherine Siminovitch, Lesley Solomon-Izsak, Jean-Francois Soucy, Marsha Speevak, James Stavropoulos, Lincoln Stein, Rhonda Tannenbaum, Deborah Terespolsky, Richard F. Wintle, Beatrix Wong, Nora Wong, Marina Wang, Nicholas Watkins, Shana White, Michael O. Woods, Philip Wyatt
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 20(3)
PurposeThe purpose of this study was to develop a national program for Canadian diagnostic laboratories to compare DNA-variant interpretations and resolve discordant-variant classifications using the BRCA1 and BRCA2 genes as a case study.MethodsBRCA1
Autor:
Marina, Wang, Saud, Aldubayan, Ashton A, Connor, Beatrix, Wong, Kate, Mcnamara, Tahsin, Khan, Kara, Semotiuk, Sam, Khalouei, Spring, Holter, Melyssa, Aronson, Zane, Cohen, Steve, Gallinger, George, Charames, Aaron, Pollett, Jordan, Lerner-Ellis
Publikováno v:
Cancer. 122(11)
In November 2001, genetic testing for Lynch syndrome (LS) was introduced by the Ministry of Health and Long-Term Care (MOH) in Ontario for individuals at high risk for LS cancers according to either tumor immunohistochemistry staining or their family