Artykuły w czasopismach na temat „Male caregivers”
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Deskins, Barbara Pollard, Susan Letvak, Laurie Kennedy-Malone, Pamela Johnson Rowsey, Leandra Bedini i Denise Rhew. "The Experiences of African American Male Caregivers". Healthcare 10, nr 2 (28.01.2022): 252. http://dx.doi.org/10.3390/healthcare10020252.
Pełny tekst źródłaOpara, Józef, i W. Brola. "Quality of Life and Burden in caregivers of Multiple Sclerosis patients". Physiotherapy and Health Activity 25, nr 1 (1.03.2018): 9–16. http://dx.doi.org/10.1515/pha-2017-0002.
Pełny tekst źródłaRuisoto, Pablo, Marina Ramírez, Belén Paladines-Costa, Silvia Vaca i Vicente Javier Clemente-Suárez. "Predicting Caregiver Burden in Informal Caregivers for the Elderly in Ecuador". International Journal of Environmental Research and Public Health 17, nr 19 (8.10.2020): 7338. http://dx.doi.org/10.3390/ijerph17197338.
Pełny tekst źródłaFrias, Cindy E., Esther Cabrera i Adelaida Zabalegui. "Informal Caregivers’ Roles in Dementia: The Impact on Their Quality of Life". Life 10, nr 11 (23.10.2020): 251. http://dx.doi.org/10.3390/life10110251.
Pełny tekst źródłaWeinland, Jo Ann. "The Lived Experience of Informal African American Male Caregivers". American Journal of Men's Health 3, nr 1 (7.11.2007): 16–24. http://dx.doi.org/10.1177/1557988307305916.
Pełny tekst źródłaSmith, Matthew, Chung Lin Kew, Tiffany Washington, Caroline Bergeron, Ashley Merianos, Ledric Sherman i Kirby Goidel. "CAREGIVER STRAIN AMONG AFRICAN AMERICAN AND HISPANIC MALE CAREGIVERS WITH CHRONIC CONDITIONS". Innovation in Aging 6, Supplement_1 (1.11.2022): 100. http://dx.doi.org/10.1093/geroni/igac059.398.
Pełny tekst źródłaBuchanan, Robert J., Dagmar Radin i Chunfeng Huang. "Caregiver Burden Among Informal Caregivers Assisting People with Multiple Sclerosis". International Journal of MS Care 13, nr 2 (1.07.2011): 76–83. http://dx.doi.org/10.7224/1537-2073-13.2.76.
Pełny tekst źródłaLeung, Lai Ching, Kam Wah Chan i Kin Yuen Tam. "Reconstruction of Masculine Identities Through Caring Practices: The Experiences of Male Caregivers in Hong Kong". Journal of Family Issues 40, nr 6 (7.01.2019): 764–84. http://dx.doi.org/10.1177/0192513x18823820.
Pełny tekst źródłaSilva, Elton Gomes da, Karina Cuziol, Maura Aparecida Viana i Elizabeth Maria Aparecida Barasnevicius. "Quality of life in patients with Parkinson’s Disease and their caregivers’ stress levels". Revista Neurociências 16, nr 2 (30.04.1999): 113–17. http://dx.doi.org/10.34024/rnc.2008.v16.8647.
Pełny tekst źródłaMolitor, Fred, i Celeste Doerr. "Dietary Behaviors, Diet Quality, and Obesity among Children from Low-Income Households by Gender of Caregiver and Child: Results from the 2018 California Family Health Study". Current Developments in Nutrition 4, Supplement_2 (29.05.2020): 245. http://dx.doi.org/10.1093/cdn/nzaa043_096.
Pełny tekst źródłaHandi, Andrew, Dapot Parulian Gultom, Muhammad Surya Husada, Bahagia Loebis, Elmeida Effendy, Mustafa Mahmud Amin, Vita Camellia i Nazli Mahdinasari Nasution. "The Comparison of Hospital Anxiety and Depression Scale-Anxiety Scores between Female Caregivers of People with Schizophrenia According to Gender Difference". Open Access Macedonian Journal of Medical Sciences 7, nr 16 (25.08.2019): 2630–33. http://dx.doi.org/10.3889/oamjms.2019.472.
Pełny tekst źródłaWong, Ting-Hway, Timothy Xin Zhong Tan, Lynette Ma Loo, Wei Chong Chua, Philip Tsau Choong Iau, Arron Seng Hock Ang, Jerry Tiong Thye Goo i in. "Negative and positive experiences of caregiving among family caregivers of older blunt trauma patients". PLOS ONE 17, nr 10 (10.10.2022): e0275169. http://dx.doi.org/10.1371/journal.pone.0275169.
Pełny tekst źródłaMatolia, Riddhi R., Khadija Anandwala i Neha Verma. "A Study to Measure Caregiver Stress in Stroke Patients using Caregiver Strain Index". International Journal of Health Sciences and Research 12, nr 4 (19.04.2022): 276–82. http://dx.doi.org/10.52403/ijhsr.20220432.
Pełny tekst źródłaWilkes, Chelsey M., Karla T. Washington, William M. Palmer, Debra Parker Oliver, George Demiris i Kevin Craig. "Differential effects of patient symptom subtypes on informal hospice caregiver depression". Palliative and Supportive Care 16, nr 2 (31.01.2017): 127–36. http://dx.doi.org/10.1017/s1478951516001152.
Pełny tekst źródłaLopez–Anuarbe, Monika, i Priya Kohli. "Understanding Male Caregivers’ Emotional, Financial, and Physical Burden in the United States". Healthcare 7, nr 2 (22.05.2019): 72. http://dx.doi.org/10.3390/healthcare7020072.
Pełny tekst źródłaSwinkels, Joukje C., Marjolein I. Broese van Groenou, Alice de Boer i Theo G. van Tilburg. "Male and Female Partner-Caregivers’ Burden: Does It Get Worse Over Time?" Gerontologist 59, nr 6 (12.10.2018): 1103–11. http://dx.doi.org/10.1093/geront/gny132.
Pełny tekst źródłaBjørge, Heidi, Kari Kvaal i Ingun Ulstein. "309 - Quality of life in caregiver in a gender perspective". International Psychogeriatrics 32, S1 (październik 2020): 67. http://dx.doi.org/10.1017/s1041610220002094.
Pełny tekst źródłaRobinson, Carole A., Joan L. Bottorff, Barbara Pesut, John L. Oliffe i Jamie Tomlinson. "The Male Face of Caregiving". American Journal of Men's Health 8, nr 5 (9.01.2014): 409–26. http://dx.doi.org/10.1177/1557988313519671.
Pełny tekst źródłaFaqi-Rahid, Farida, i Shukir Hasan. "Caregiver’s Knowledge regarding Homecare Management of Spastic Cerebral Palsy Children Under 12 Years Old in Rapareen Province". Erbil Journal of Nursing and Midwifery 5, nr 2 (30.11.2022): 61–71. http://dx.doi.org/10.15218/ejnm.2022.07.
Pełny tekst źródłaWarapornmongkholkul, Anchalee, Nopporn Howteerakul, Nawarat Suwannapong i Nopadol Soparattanapaisarn. "Self-efficacy, social support, and quality of life among primary family-member caregivers of patients with cancer in Thailand". Journal of Health Research 32, nr 2 (12.03.2018): 111–22. http://dx.doi.org/10.1108/jhr-01-2018-012.
Pełny tekst źródłaBozkurt Zincir, Selma, Murat Sunbul, Serkan Zincir, Esra Aydin Sunbul, Mustafa Oguz, Fatma Feriha Cengiz, Erdal Durmus, Tarik Kivrak i Ibrahim Sari. "Burden and Depressive Symptoms Associated with Adult-Child Caregiving for Individuals with Heart Failure". Scientific World Journal 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/641817.
Pełny tekst źródłaEsezobor, Christopher I., Adaobi U. Solarin i Andrew T. Olagunju. "Significant Burden and Psychological Distress Among Caregivers of Children With Nephrotic Syndrome: A Cross-Sectional Study". Canadian Journal of Kidney Health and Disease 7 (styczeń 2020): 205435811989801. http://dx.doi.org/10.1177/2054358119898016.
Pełny tekst źródłaKenning, Heather, Yunjia Yang, Lisa O'Neill, Mindy Fain, Mark Wager i Amanda Sokan. "Caregiver Challenges of Older University Employees During the COVID-19 Pandemic". Innovation in Aging 5, Supplement_1 (1.12.2021): 65. http://dx.doi.org/10.1093/geroni/igab046.250.
Pełny tekst źródłaAccius, J. "BREAKING STEREOTYPES: MALE FAMILY CAREGIVERS". Innovation in Aging 2, suppl_1 (1.11.2018): 240. http://dx.doi.org/10.1093/geroni/igy023.894.
Pełny tekst źródłaGeiger, Jennifer R., Scott E. Wilks, Lauren L. Lovelace, Zibei Chen i Christina A. Spivey. "Burden Among Male Alzheimer’s Caregivers". American Journal of Alzheimer's Disease & Other Dementiasr 30, nr 3 (28.09.2014): 238–46. http://dx.doi.org/10.1177/1533317514552666.
Pełny tekst źródłaAu, Trang H., Hillevi Bauer, Jyothi Menon, Connor Willis, Eli Iacob, Junjie Ma, Alexandre Watanabe i in. "Impact of glioblastoma (GBM)-related cognitive dysfunction (CD) on caregiver burden: Preliminary results from multi-site study in the U.S." Journal of Clinical Oncology 36, nr 34_suppl (1.12.2018): 16. http://dx.doi.org/10.1200/jco.2018.36.34_suppl.16.
Pełny tekst źródłaTolea, Magdalena, Iris Cohen, Simone Camacho i James Galvin. "MINDFULNESS AND CAREGIVING EXPERIENCE IN ADRD CAREGIVERS". Innovation in Aging 6, Supplement_1 (1.11.2022): 454–55. http://dx.doi.org/10.1093/geroni/igac059.1772.
Pełny tekst źródłaVrettos, Ioannis, Konstantinos Kamposioras, Nick Kontodimopoulos, Evelina Pappa, Elissavet Georgiadou, Dionysios Haritos, Angelos A. Papadopoulos i Dimitris Niakas. "Comparing Health-Related Quality of Life of Cancer Patients under Chemotherapy and of Their Caregivers". Scientific World Journal 2012 (2012): 1–9. http://dx.doi.org/10.1100/2012/135283.
Pełny tekst źródłaKochhann, Renata, Ericksen Borba, Maria Otília Cerveira, Diego Onyszko, Alyne de Jesus, Letícia Forster, Luisa Franciscatto, Cláudia Godinho, Ana Luiza Camozzato i Márcia Lorena F. Chaves. "Neuropsychiatric symptoms as the main determinant of caregiver burden in Alzheimer's disease". Dementia & Neuropsychologia 5, nr 3 (wrzesień 2011): 203–8. http://dx.doi.org/10.1590/s1980-57642011dn05030008.
Pełny tekst źródłaFu, Wenhao, i Jiajia Li. "Explaining Gender Differences in Depressive Symptoms Among Caregivers of Older Patients With Critical Illness". Innovation in Aging 5, Supplement_1 (1.12.2021): 379. http://dx.doi.org/10.1093/geroni/igab046.1471.
Pełny tekst źródłaHendricks-Lalla, Abeedah, i Chrisma Pretorius. "The male familial caregiver experience of caring for persons with Alzheimer’s disease from low socio-economic status: A South African perspective". Dementia 19, nr 3 (18.06.2018): 618–39. http://dx.doi.org/10.1177/1471301218781372.
Pełny tekst źródłaSchaffler-Schaden, Dagmar, Simon Krutter, Alexander Seymer, Roland Eßl-Maurer, Maria Flamm i Jürgen Osterbrink. "Caring for a Relative with Dementia: Determinants and Gender Differences of Caregiver Burden in the Rural Setting". Brain Sciences 11, nr 11 (15.11.2021): 1511. http://dx.doi.org/10.3390/brainsci11111511.
Pełny tekst źródłaRaymond, Martha, i Margaret-Ann Simonetta. "The caregiver perspective: Advancing the understanding of cancer caregiving in the palliative care setting." Journal of Clinical Oncology 36, nr 34_suppl (1.12.2018): 17. http://dx.doi.org/10.1200/jco.2018.36.34_suppl.17.
Pełny tekst źródłaPrado, Lia, Rebecca Hadley i Dawn Rose. "Taking Time: A Mixed Methods Study of Parkinson’s Disease Caregiver Participation in Activities in Relation to Their Wellbeing". Parkinson's Disease 2020 (9.04.2020): 1–18. http://dx.doi.org/10.1155/2020/7370810.
Pełny tekst źródłaFulton Picot, Sandra J., JoAnne Youngblut i Richard Zeller. "Development and Testing of a Measure of Perceived Caregiver Rewards in Adults". Journal of Nursing Measurement 5, nr 1 (styczeń 1997): 33–52. http://dx.doi.org/10.1891/1061-3749.5.1.33.
Pełny tekst źródłaJabłoński, Marcin J., Francisco García-Torres, Paulina Zielińska, Alicja Bułat i Piotr Brandys. "Emotional Burden and Perceived Social Support in Male Partners of Women with Cancer". International Journal of Environmental Research and Public Health 17, nr 12 (12.06.2020): 4188. http://dx.doi.org/10.3390/ijerph17124188.
Pełny tekst źródłaBueno, Michael, i Jo-Ana Chase. "A DUTY TO CARE: MALE PERSPECTIVES ON THE CAREGIVER ROLE FOR PERSONS WITH ALZHEIMER’S OR RELATED DEMENTIA". Innovation in Aging 6, Supplement_1 (1.11.2022): 100. http://dx.doi.org/10.1093/geroni/igac059.397.
Pełny tekst źródłaNogueira, Douglas José, Ruth Minamisava, Sheila Araujo Teles, Sandra Maria Brunini de Souza, Jacqueline Andréia Bernardes Leão Cordeiro, Denise Soares de Cirqueira, Virginia Visconde Brasil i in. "Factors Associated with Marital Satisfaction and Quality of Life in Family Caregivers of Patients with Mental Disorders". International Journal of Environmental Research and Public Health 16, nr 16 (8.08.2019): 2825. http://dx.doi.org/10.3390/ijerph16162825.
Pełny tekst źródłaMirzaei, Abasat, Rasoul Raesi, Sam Saghari i Mehdi Raei. "Evaluation of Family Caregiver Burden among COVID-19 Patients". Open Public Health Journal 13, nr 1 (31.12.2020): 808–14. http://dx.doi.org/10.2174/1874944502013010808.
Pełny tekst źródłaSu, Jian-An, i Chih-Cheng Chang. "Association Between Family Caregiver Burden and Affiliate Stigma in the Families of People with Dementia". International Journal of Environmental Research and Public Health 17, nr 8 (17.04.2020): 2772. http://dx.doi.org/10.3390/ijerph17082772.
Pełny tekst źródłaLiang, Jiaming, i Maria Aranda. "The Role of Secondary Care Networks, Gender, and Race on Primary Caregiver Burden". Innovation in Aging 5, Supplement_1 (1.12.2021): 490–91. http://dx.doi.org/10.1093/geroni/igab046.1893.
Pełny tekst źródłaKovaleva, Mariya A., Melinda Higgins, Bonnie M. Jennings, Mi-Kyung Song, Carolyn Clevenger, Patricia C. Griffiths i Ken Hepburn. "PREDICTORS OF CHANGES IN WELL-BEING AMONG THE INTEGRATED MEMORY CARE CLINIC CLIENTS". Innovation in Aging 3, Supplement_1 (listopad 2019): S115. http://dx.doi.org/10.1093/geroni/igz038.425.
Pełny tekst źródłaKahn, Phoebe V., Heather A. Wishart, Jennifer S. Randolph i Robert B. Santulli. "Caregiver Stigma and Burden in Memory Disorders: An Evaluation of the Effects of Caregiver Type and Gender". Current Gerontology and Geriatrics Research 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/8316045.
Pełny tekst źródłaCoe, Maureen, i Anne Neufeld. "Male Caregivers’ Use of Formal Support". Western Journal of Nursing Research 21, nr 4 (sierpień 1999): 568–88. http://dx.doi.org/10.1177/01939459922044045.
Pełny tekst źródłaMays, Gloria Denise, i Carole Holden Lund. "Male Caregivers of Mentally Ill Relatives". Perspectives in Psychiatric Care 35, nr 2 (16.01.2009): 19–28. http://dx.doi.org/10.1111/j.1744-6163.1999.tb00571.x.
Pełny tekst źródłaKaye, Lenard W., i Jeffrey S. Applegate. "Family Support Groups for Male Caregivers:". Journal of Gerontological Social Work 20, nr 3-4 (4.02.1994): 167–85. http://dx.doi.org/10.1300/j083v20n03_08.
Pełny tekst źródłaPierce, Linda L., i Victoria Steiner. "What Are Male Caregivers Talking About?" Topics in Stroke Rehabilitation 11, nr 2 (kwiecień 2004): 77–83. http://dx.doi.org/10.1310/mhrl-nwl5-9xcg-jemc.
Pełny tekst źródłaSéguin, Lise, i Bilkis Vissandjee. "Les différences liées à la spécificité des genres dans la prise en charge d'un proche fragilisé". Canadian Journal on Aging / La Revue canadienne du vieillissement 22, nr 1 (2003): 109–25. http://dx.doi.org/10.1017/s0714980800003779.
Pełny tekst źródłaChen, Ya-Mei. "Differences in Outcomes of Caregiver Support Services for Male and Female Caregivers". SAGE Open 4, nr 3 (12.08.2014): 215824401454816. http://dx.doi.org/10.1177/2158244014548169.
Pełny tekst źródłaBédard, Michel, D. William Molloy, David Pedlar, Judith A. Lever i Michael J. Stones. "Associations Between Dysfunctional Behaviors, Gender, and Burden in Spousal Caregivers of Cognitively Impaired Older Adults". International Psychogeriatrics 9, nr 3 (wrzesień 1997): 277–90. http://dx.doi.org/10.1017/s1041610297004444.
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