Patient Satisfaction with the Quality of Nursing Care in Public and Private Hospitals in Erbil City

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Background and Objectives: Patient satisfaction is an essential parameter in assessing the quality of care and healthcare facility performance and the most important competitive advantage of the government and private hospitals. The study aims to inv

Externí odkaz: https://doaj.org/article/49b89040b04a4e4e9f33743311ec00a9

Breast cancer patient’s knowledge about radiotherapy and physical side effects in Awat radiation oncology center.

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Publikováno v: Onkologia i Radioterapia; 2024, Vol. 18 Issue 6, p1-7, 7p

A qualitative investigation into the lived experiences of cancer patients receiving chemotherapy in the Kurdistan region of Iraq.

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Publikováno v: Journal of Research Development in Nursing & Midwifery; 2023, Vol. 20 Issue 2, p19-22, 4p

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Publikováno v: Human genetics 141 (2021): 147–173. doi:10.1007/s00439-021-02397-7
info:cnr-pdr/source/autori:Fallerini, Chiara; Picchiotti, Nicola; Baldassarri, Margherita; Zguro, Kristina; Daga, Sergio; Fava, Francesca; Benetti, Elisa; Amitrano, Sara; Bruttini, Mirella; Palmieril, Maria; Croci, Susanna; Lista, Mirjam; Beligni, Giada; Valentino, Floriana; Meloni, Ilaria; Tanfoni, Marco; Minnai, Francesca; Colombo, Francesca; Cabri, Enrico; Fratelli, Maddalena; Gabbi, Chiara; Mantovani, Stefania; Frullanti, Elisa; Gori, Marco; Crawley, Francis P.; Butler-Laporte, Guillaume; Richards, Brent; Zeberg, Hugo; Lipcsey, Miklos; Hultstrom, Michael; Ludwig, Kerstin U.; Schulte, Eva C.; Pairo-Castineira, Erola; Baillie, John Kenneth; Schmidt, Axel; Frithiof, Robert; Mari, Francesca; Renieri, Alessandra; Furini, Simone; GEN-COVID Multicenter Study (which includes Alessandra Stella and Filippo Biscarini)/titolo:Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity/doi:10.1007%2Fs00439-021-02397-7/rivista:Human genetics/anno:2021/pagina_da:147/pagina_a:173/intervallo_pagine:147–173/volume:141
Human genetics
Hum. Genet. 141, 147-173 (2022)
Human Genetics
2021, ' Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity ', Human Genetics . https://doi.org/10.1007/s00439-021-02397-7

The combined impact of common and rare exonic variants in COVID-19 host genetics is currently insufficiently understood. Here, common and rare variants from whole-exome sequencing data of about 4000 SARS-CoV-2-positive individuals were used to define

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4836dbe8027e2289c8e8ff11bfe68cc
https://doi.org/10.1101/2021.09.03.21262611