Zobrazeno 1 - 10 of 114 pro vyhledávání: '"L. A. Clarkson"'
1
Adaptations to Support the Flint Water Task
Autor: Dana L. Grosser-Clarkson, Joanna S. Hung
Publikováno v: Mathematics Teacher Educator. 11:132-138
This Perspectives on Practice manuscript focuses on an innovation associated with “Engaging Teachers in the Powerful Combination of Mathematical Modeling and Social Justice: The Flint Water Task” from Volume 7, Issue 2 of MTE. The Flint Water Tas
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c290f742f826b57ef893e3f9f54acf53
https://doi.org/10.5951/mte.2022.0029
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2
Famine and Disease in Ireland
Autor: L. A. Clarkson, E. Margaret Crawford
Volume 1 Complete text: W R W Wilde, 'Table of cosmical phenomena, epizootics, epiphitics, famines, and pestilences in Ireland ', Census of Ireland for the Year 1851, part v (1856) Volume 2 Complete text: Sir Charles Trevelyan, The Irish Crisis (1847
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7326b918cd0b57c9141a5bb722c60171
https://doi.org/10.4324/9781003090403
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4
James Eadie Todd and the school of history at the Queen’s University of Belfast
Autor: L. A. Clarkson
Publikováno v: Irish Historical Studies. 41:22-40
James Eadie Todd was appointed to the chair of modern history in Queen’s University, Belfast in 1919, aged thirty-four, having previously held academic posts in Edinburgh, Montreal and Halifax, Nova Scotia. Todd published almost nothing but spent h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ca731389b8df3932479d65cce296c4dc
https://doi.org/10.1017/ihs.2017.2
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6
Clinical management of patients withASXL1mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance
Autor: Leslie G. Biesecker, William J. Rhead, Jennifer J. Johnston, Samantha A. Schrier Vergano, John M. Graham, Nancy Kramer, Bianca Russell, Benjamin M. Helm, Rachel Harrison, Amy Dobson, L. Kate Clarkson, Avi Z. Rosenberg, Catherine A. Brownstein, Angela Pickart, Wen-Hann Tan
Publikováno v: American Journal of Medical Genetics Part A. 167:2122-2131
Bohring-Opitz syndrome is a rare genetic condition characterized by distinctive facial features, variable microcephaly, hypertrichosis, nevus flammeus, severe myopia, unusual posture (flexion at the elbows with ulnar deviation, and flexion of the wri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea18a9922c70549e9aab551ac79bdd1c
https://doi.org/10.1002/ajmg.a.37131
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8
Unique Cerebrovascular Anomalies in Noonan Syndrome With RAF1 Mutation
Autor: M. Gisele Matheus, L. Kate Clarkson, Angie W. Lichty, Yuri A. Zarate, Kristen J. Champion, Kenton R. Holden
Publikováno v: Journal of Child Neurology. 29:NP13-NP17
Noonan syndrome is a common autosomal dominant neurodevelopmental disorder caused by gain-of-function germline mutations affecting components of the Ras-MAPK pathway. The authors present the case of a 6-year-old male with Noonan syndrome, Chiari malf
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e2c01b08d5ad24cbe76a6d3a1d159b9
https://doi.org/10.1177/0883073813492384
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