Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sarah Goodman"'
Publikováno v:
Palliative Care, Vol 12 (2019)
Background: A Rapid Response Team can respond to critically ill patients in hospital to prevent further deterioration and unexpected deaths. However, approximately one-third of reviews involve a patient approaching the end-of-life. It is not well und
Externí odkaz:
https://doaj.org/article/95a86f85e58543eeb360a851d7712586
Publikováno v:
Disability and Rehabilitation. :1-9
This study explored the experience of adolescents with brain injuries and their caregivers who participated in the Program for the Education and Enrichment of Relational Skills (PEERS®) in Australia. Twenty-seven adolescents and 31 caregivers, who c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47aaedff37dd5cc784fa8f790b639543
https://doi.org/10.1080/09638288.2023.2167008
https://doi.org/10.1080/09638288.2023.2167008
Publikováno v:
Human Genetics.
Pathogenic variants in genes that encode epigenetic regulators are the cause for more than 100 rare neurodevelopmental syndromes also termed “chromatinopathies”. DNA methylation signatures, syndrome-specific patterns of DNA methylation alteration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e11d7bbd6be417e23b6cfca9bc8421ea
https://doi.org/10.1007/s00439-023-02544-2
https://doi.org/10.1007/s00439-023-02544-2
Autor:
Zain, Awamleh, Sarah, Goodman, Prajkta, Kallurkar, Wendy, Wu, Kevin, Lu, Sanaa, Choufani, Andrei L, Turinsky, Rosanna, Weksberg
Publikováno v:
Current Protocols. 2
There are more than 700 genes that encode proteins that function in epigenetic regulation and chromatin modification. Germline variants in these genes (typically heterozygous) are associated with rare neurodevelopmental disorders (NDDs) characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f1349af051877d38d398093f9b6caa2
https://doi.org/10.1002/cpz1.597
https://doi.org/10.1002/cpz1.597
Publikováno v:
Clinical Infectious Diseases. 73:521-523
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06f87edc6c621a8dbe57384bc98e7a5c
https://doi.org/10.1093/cid/ciaa357
https://doi.org/10.1093/cid/ciaa357
Publikováno v:
Research in developmental disabilities. 125
Group social skills interventions (GSSIs) are offered to youth with Autism Spectrum Disorder (ASD) to improve social functioning. This systematic review focused on the adolescent population, including a wider range of disabilities.To evaluate effecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f65e561e2c006aeedb9365997963bb3
https://pubmed.ncbi.nlm.nih.gov/35306461
https://pubmed.ncbi.nlm.nih.gov/35306461
Autor:
Sachin Jambawalikar, Peter Chang, Kevin Kalinsky, Michael Z. Liu, Elyse Blum, Simukayi Mutasa, Sarah Goodman, Richard Ha, Jenika Karcich
Publikováno v:
Journal of Magnetic Resonance Imaging. 49:518-524
BACKGROUND Oncotype Dx is a validated genetic analysis that provides a recurrence score (RS) to quantitatively predict outcomes in patients who meet the criteria of estrogen receptor positive / human epidermal growth factor receptor-2 negative (ER+/H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e873b8d0dedaebdc7e31f61e264b940
https://doi.org/10.1002/jmri.26244
https://doi.org/10.1002/jmri.26244
Autor:
Richard Ha, Sarah Goodman, Victoria L. Mango, Hanina Hibshoosh, Kim Clarkin, Lauren Friedlander, Ralph Wynn
Publikováno v:
Clinical Imaging. 50:78-85
Male breast disease is uncommon. Men presenting with breast symptoms may represent unique diagnostic challenges for the radiologist, particularly if imaging findings are not classic for gynecomastia or carcinoma. In this paper we review 10 unusual ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dafa2913bd20b654f14e242098d9d316
https://doi.org/10.1016/j.clinimag.2017.12.012
https://doi.org/10.1016/j.clinimag.2017.12.012
Autor:
Sarah Goodman
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2595926498e30ff043dd7a86b7a2ea17
https://doi.org/10.2139/ssrn.4228603
https://doi.org/10.2139/ssrn.4228603
Publikováno v:
Cureus
Central nervous system (CNS) histoplasmosis is a rare manifestation of disease, often misdiagnosed due to the wide spectrum of neurological presentation. We present a rare case of CNS histoplasmosis in a 62-year-old male with untreated myeloprolifera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d294f72831b1fa3d75b37453a33a15a
https://doi.org/10.7759/cureus.4238
https://doi.org/10.7759/cureus.4238