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Indian Pacing and Electrophysiology Journal, 2006 Andersen-Tawil syndrome (ATS) is a rare condition consisting of ventricular arrhythmias, periodic paralysis, and dysmorphic features. In 2001, mutations in KCNJ2, which encodes the α subunit of the potassium channel Kir2.1, were identified in patients ...
Andrew H. Smith +2 more
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Creator and Art in Hans Christian Andersen’s Novels [PDF]
Studia Litterarum, 2021 The article deals with three novels by Danish writer Hans Christian Andersen, who is known worldwide as an author of fairy tales. In his novels The Improviser (1835), Only a Fiddler (1837) and Lucky Peer (1870) the main plot is built on the issue of ...
Andrey V. Korovin
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Andersen Tawil syndrome – a case study
Journal of Education, Health and Sport, 2021 The first case of a patient with periodic paralysis of muscles accompanied by ventricular arrhythmias was described in 1963 by Klein and colleagues[1]. In 1971, the team led by E.D.
Joanna Mroczek +2 more
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Славянский мир в третьем тысячелетии, 2022 This article examines the artistic specifi city of the images and motifs of the works of Evgeny Lvovich Schwartz (1896–1958), in whose dramaturgical and prose fairy tales the infl uence of the romantic literary tradition is traced.
Darya Zavelskaya
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“You paint when you speak”: On the creative process of Hans Christian Andersen
Acta Universitatis Lodziensis. Folia Litteraria Polonica, 2022 The article analyses the creative process of Hans Christian Andersen. The author focuses on the writer’s early years and then juxtaposes them with his mature creative period.
Magdalena Kuczaba-Flisak
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Journal of Education and Health Promotion, 2021 BACKGROUND: This study aimed to identify the quality of life (QoL) and its predictive factors based on the Andersen's behavioral model among the elderly in Iran. MATERIALS AND METHODS: A quantitative cross-sectional study was conducted on 400 people aged
Soghra Nazari +2 more
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Cardiology in Review, 2020 Andersen–Tawil syndrome (ATS) is a very rare orphan genetic multisystem channelopathy without structural heart disease (with rare exceptions). ATS type 1 is inherited in an autosomal dominant fashion and is caused by mutations in the KCNJ2 gene, which encodes the α subunit of the K+ channel protein Kir2.1 (in ≈ 50–60% of cases).
Pérez-Riera, Andrés Ricardo +8 more
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Revista de Dialectología y Tradiciones Populares, 2005 Con frecuencia las autoridades académicas hablan de la importancia que, para los estudiantes, posee la lectura y de la necesidad de su aprendizaje en la enseñanza primaría, con carácter obligatorio en nuestra sociedad.
Gustavo Martín Garzo
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Immunity, Inflammation and Disease, 2022 Background Surfactant Protein D (SP‐D) is a pattern recognition molecule belonging to the family of collectins expressed in multiple human organ systems, including the lungs.
Benjamin Hoffmann‐Petersen +8 more
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Stereotactic Radiosurgery for Brain Metastases in Patients With Small Cell Lung Cancer
Advances in Radiation Oncology, 2023 Purpose: Treatment of small cell lung cancer (SCLC) with brain metastatic disease has traditionally involved whole brain radiation therapy (WBRT). The role of stereotactic radiosurgery (SRS) is unclear.
Victoria H. Wang, BS +8 more
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