Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Patrick Lawson"'
Autor:
Carole Samango-Sprouse, Eser Kırkızlar, Megan P Hall, Patrick Lawson, Zachary Demko, Susan M Zneimer, Kirsten J Curnow, Susan Gross, Andrea Gropman
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161045 (2016)
X&Y chromosomal aneuploidies are among the most common human whole-chromosomal copy number changes, but the population-based incidence and prevalence in the child-bearing population is unclear.This retrospective analysis of prospectively collected da
Externí odkaz:
https://doaj.org/article/d12ae733980340c5ad68455cfc4b9385
Autor:
Catherine Deveney, Patrick Lawson
Publikováno v:
Counselling and Psychotherapy Research. 22:292-300
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e035629caf03d0bafa726995982a981
https://doi.org/10.1002/capr.12435
https://doi.org/10.1002/capr.12435
Publikováno v:
Applied ergonomics. 86
Phishing is a social engineering tactic where a malicious actor impersonates a trustworthy third party with the intention of tricking the user into divulging sensitive information. Previous social engineering research in a real-world setting has show
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4049e7eb5bb0777c80d1282a2619489
https://pubmed.ncbi.nlm.nih.gov/32174448
https://pubmed.ncbi.nlm.nih.gov/32174448
Publikováno v:
Proceedings of the Human Factors and Ergonomics Society Annual Meeting. 61:1331-1333
Phishing is a social engineering tactic where a malicious actor impersonates a trustworthy third party with the intention of tricking the user into divulging sensitive information. Previous social engineering research has shown an interaction between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee3d7cbc01e772eeec22f5da03079cf
https://doi.org/10.1177/1541931213601815
https://doi.org/10.1177/1541931213601815
Autor:
Patrick Lawson, Chris Cappello, Carole A. Samango-Sprouse, Emily Stapleton, Sophie van Rijn, Leo M. J. de Sonneville, Teresa Sadeghin, Selena Chea
Publikováno v:
American Journal of Medical Genetics
American Journal of Medical Genetics, 176(4), 877-885
American Journal of Medical Genetics, 176(4), 877-885
47,XXY (KS) occurs in 1:650 male births, though less than 25% are ever identified. We assessed stability of neurocognitive features across diverse populations and quantified factors mediating outcome. Forty‐four boys from the Netherlands (NL) and 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7764294b41e6211b31a501496696a1e9
https://hdl.handle.net/1887/74289
https://hdl.handle.net/1887/74289
Autor:
Eser Kirkizlar, Patrick Lawson, Carole A. Samango-Sprouse, Susan J. Gross, Zachary Demko, Susan Zneimer, Kirsten J. Curnow, Megan P. Hall, Andrea L. Gropman
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161045 (2016)
PLoS ONE
PLoS ONE
Background X&Y chromosomal aneuploidies are among the most common human whole-chromosomal copy number changes, but the population-based incidence and prevalence in the child-bearing population is unclear. Methods This retrospective analysis of prospe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567408d4e1c6c040d0fc6ec58cc82a15
http://europepmc.org/articles/PMC4981345?pdf=render
http://europepmc.org/articles/PMC4981345?pdf=render
Autor:
Sherida Powell, Teresa Sadeghin, Carole A. Samango-Sprouse, Patrick Lawson, Francie L. Mitchell, Andrea L. Gropman, Emily Stapleton
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics. 169(2)
47, XXY occurs in up to 1 in 650 male births and is associated with androgen deficiency, neurodevelopmental delays, and atypical social-behaviors. Previously, we showed that young boys with 47, XXY who received early hormonal therapy (EHT) had signif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a139c629b17d70c59ec119c3a1397ec
https://pubmed.ncbi.nlm.nih.gov/25939399
https://pubmed.ncbi.nlm.nih.gov/25939399
Autor:
Carole A. Samango-Sprouse, Andrea L. Gropman, Teresa Sadeghin, Patrick Lawson, Emily Stapleton, Courtney Sprouse
Publikováno v:
American journal of medical genetics. Part A. (5)
Kleefstra syndrome (KS) is a rare neurogenetic disorder most commonly caused by deletion in the 9q34.3 chromosomal region and is associated with intellectual disabilities, severe speech delay, and motor planning deficits. To our knowledge, this is th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::838a133656ebeaa871228dfa74f92aa7
https://pubmed.ncbi.nlm.nih.gov/26833960
https://pubmed.ncbi.nlm.nih.gov/26833960
Autor:
Riad Khatib, Patrick Lawson, Marilyn S. Held, Kathleen Riederer, Laurence E. Briski, Karen Petrylka
Publikováno v:
Canadian Journal of Microbiology. 41:88-91
Latex agglutination and the enzyme immunoassays Cytoclone (EIA-C) and VIDAS (EIA-V) were compared with a cytotoxicity assay for the diagnosis of Clostridium difficile associated diarrhea. Among patients with discrepant results, the cytotoxicity assay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b0f19fd66869e457a5ab7a48e4a4db9
https://doi.org/10.1139/m95-011
https://doi.org/10.1139/m95-011
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