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Autor:
CHRIST, CAROL P.
Publikováno v:
Literature and Theology, 2016 Jun 01. 30(2), 248-249.
Externí odkaz:
https://www.jstor.org/stable/44490846
Autor:
Keller, Mary L.
Publikováno v:
Journal of the American Academy of Religion, 2014 Jun 01. 82(2), 555-558.
Externí odkaz:
https://www.jstor.org/stable/24488168
Autor:
Løøv, Margrethe
Publikováno v:
Numen, 2014 Jan 01. 61(4), 441-443.
Externí odkaz:
https://www.jstor.org/stable/24644797
Autor:
Engel, Manfred
Publikováno v:
Journal of Cultural Poetics / KulturPoetik: Zeitschrift für Kulturgeschichtliche Literaturwissenschaft; Oct2023, Vol. 23 Issue 2, p226-247, 22p
Autor:
Vernon-Yorke, Suzanne
Publikováno v:
Religion and Gender; January 2022, Vol. 12 Issue: 1 p113-115, 3p
Autor:
Konrad W. Walek, Sabina Stefan, Jang-Hoon Lee, Pooja Puttigampala, Anna H. Kim, Seong Wook Park, Paul J. Marchand, Frederic Lesage, Tao Liu, Yu-Wen Alvin Huang, David A. Boas, Christopher Moore, Jonghwan Lee
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-13 (2023)
Abstract In age-related neurodegenerative diseases, pathology often develops slowly across the lifespan. As one example, in diseases such as Alzheimer’s, vascular decline is believed to onset decades ahead of symptomology. However, challenges inher
Externí odkaz:
https://doaj.org/article/6b19c683424f47f4a5c50b789dfd06bb
Autor:
Anastasiya Aleksandrovna Kozina, Guria Kurbanovna Kanaeva, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Anastasia Vladimirovna Erofeeva, Nadezhda Andreevna Pogodina, Jamilya Payzutdinova Gadzhiyeva, Ekaterina Ivanovna Surkova, Valery Vladimirovich Ilinsky
Publikováno v:
Journal of International Medical Research, Vol 51 (2023)
Joubert syndrome (JS) is a recessive disorder that is characterized by midbrain-hindbrain malformation and shows the “molar tooth sign” on magnetic resonance imaging. Mutations in 40 genes, including Abelson helper integration site 1 ( AHI1 ), in
Externí odkaz:
https://doaj.org/article/cb3fbf99cefa4d37beaa01d6e0d4d25b
Autor:
Anastasiya Aleksandrovna Kozina, Natalia Vladimirovna Baryshnikova, Anna Yurievna Ilinskaya, Anna Alexandrovna Kim, Nikolay Alekseevich Plotnikov, Nadezhda Andreevna Pogodina, Ekaterina Ivanovna Surkova, Peter Alekseevich Shatalov, Valery Vladimirovich Ilinsky
Publikováno v:
Journal of International Medical Research, Vol 50 (2022)
Charcot–Marie–Tooth disease (CMT) is a genetically heterogeneous group of peripheral neuropathies most of which are associated with mutations in four genes including peripheral myelin protein-22 ( PMP22) , myelin protein zero ( MPZ ), gap junctio
Externí odkaz:
https://doaj.org/article/811cc3bc9dd0483f85523d089e326669
Autor:
Mar Griera
Publikováno v:
Social Anthropology. 22:497-498