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Teresa Campbell

Seattle Children's Hospital

9H-index
35Paper Count
194Citation Count
Published Papers 10
Publication Date
The Spectrum of Mosaic Double Aneuploidy of Monosomy X and Trisomy 18: Two New Cases and Review of the Literature
err2026-03-01
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PREAI
errCampbell, Teresa M.; Myers, Candace T.; Paschal, Cate R.; Bennett, James T.; Beck, Anita E.; Keefe, Alexandra C.
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The PRAGMATIC pathway - PRostate cancer diAGnosis and MAnagement Triage In Clinical care
err2026-02-26
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errOAAI
errAbhishek Sharma; Teresa Campbell; Sagar Kanabar; Hannah Soanes; Ganesh Sathanapally; Anthony Bates; Rincy John; Charlotte Adams; Aisling Brassill; Bryony Lennon; Sanjay Sinha; Louise Flaxman; Vanessa von Hasseln; Philip Camilleri; Ami Sabharwal; Philip Charlton; Gerard Andrade; Mark Tuthill; Andrew Protheroe; Alastair D. Lamb; Tom Leslie; Aaron Leiblich; Francisco Lopez; Clare Verrill; Fergus Gleeson; Ruth MacPherson; Freddie C. Hamdy; Richard Bell; Richard J. Bryant
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Ferroptosis is a novel pathogenic mechanism of FDXR-related disease via disruption of the NRF2 pathway
err2025-12-23
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errOAAI
errTeresa Campbell; Jesse Slone; Jimmy Vu; Wensheng Liu; Li Yang; Adam Dourson; Luis F. Queme; Michael P. Jankowski; Taosheng Huang
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Cost Effectiveness of Local Anaesthetic Transperineal Versus Transrectal Biopsy: Results from the TRANSLATE Study
err2025-12-12
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errOAAI
errMatthew Little; Jane Wolstenholme; Filipa Landeiro; Ioana R. Marian; Roxanne Williams; J. Francisco Lopez; Claudia Mercader; Mutie Raslan; Christopher Berridge; Jessica Whitburn; Teresa Campbell; Steve Tuck; Vicki S. Barber; Jessica Scaife; Aimi Hewitt; Amy Taylor; Alexander Ooms; Sukanya Ghosh; John M. Reynard; Freddie C. Hamdy
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FDXR variants cause adrenal insufficiency and atypical sexual development
err2024-06-17
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errOAAI
errPignatti, Emanuele; Slone, Jesse; Cano, Maria Angeles Gomez; Campbell, Teresa Margaret; Vu, Jimmy; Sauter, Kay-Sara; V. Pandey, Amit; Martinez-Azorin, Francisco; Alonso-Riano, Marina; Neilson, Derek E.; Longo, Nicola; du Toit, Therina; Voegel, Clarissa D.; Huang, Taosheng; Fluck, Christa E.
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Protocol for the TRANSLATE prospective, multicentre, randomised clinical trial of prostate biopsy technique
err2023-02-21
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errOAAI
errBryant, Richard J. J.; Yamamoto, Hide; Eddy, Ben; Kommu, Sashi; Narahari, Krishna; Omer, Altan; Leslie, Tom; Catto, James W. F.; Rosario, Derek J. J.; Good, Daniel W. W.; Gray, Rob; Liew, Matthew P. C.; Lopez, J. Francisco; Campbell, Teresa; Reynard, John M. M.; Tuck, Steve; Barber, Vicki S. S.; Medeghri, Nadjat; Davies, Lucy; Parkes, Matthew; Hewitt, Aimi; Landeiro, Filipa; Wolstenholme, Jane; Macpherson, Ruth; Verrill, Clare; Marian, Ioana R. R.; Williams, Roxanne; Hamdy, Freddie C. C.; Lamb, Alastair D. D.
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Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy
errCELLS
IF5.2
err2022-09-11
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errOAAI
errCampbell, Teresa; Slone, Jesse; Huang, Taosheng
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The effect of rapid exome sequencing on downstream health care utilization for infants with suspected genetic disorders in an intensive care unit
err2022-08-01
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errOAAI
errLlorian, Elisabet Rodriguez; Dragojlovic, Nick; Campbell, Teresa M.; Friedman, Jan M.; Osiovich, Horacio; Elliott, Alison M.; Lynd, Larry D.
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Utilization of telehealth in paediatric genome-wide sequencing: Health services implementation issues in the CAUSES Study
err2021-01-20
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PREAI
errElliott, Alison M.; Dragojlovic, Nick; Campbell, Teresa; Adam, Shelin; Souich, Christele du; Fryer, Michele; Lehman, Anna; Karnebeek, Clara van; Lynd, Larry D.; Friedman, Jan M.
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Mitochondrial genome variant m.3250T>C as a possible risk factor for mitochondrial cardiomyopathy
err2020-12-01
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errOAAI
errCampbell, Teresa; Lou, Xiaoting; Slone, Jesse; Brown, Jenice; Bromwell, Meghan; Liu, Jie; Bai, Renkui; Haude, Katrina; Balog, Amanda; Cui, Hong; Zou, Weiwei; Yang, Li; Al-Beshri, Ali; Huang, Taosheng
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