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Research Article

Caregiver burden and quality of life of patients with amyotrophic lateral sclerosis in India

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Pages 606-610 | Received 24 Jan 2018, Accepted 21 May 2018, Published online: 24 Jul 2018

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Zeliha Tülek, Aylin Özakgül, Naile Alankaya, Aynur Dik, Alper Kaya, Pemra C. Ünalan, Ayşe Nilüfer Özaydin & Halil Atilla İdrisoğlu. (2023) Care burden and related factors among informal caregivers of patients with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:1-2, pages 125-132.
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Andrea Carboni-Jiménez, Danielle B. Rice, Brooke Levis, Mara Cañedo-Ayala, Mahrukh Imran, Matthew Chiovitti, Andrea Benedetti & Brett D. Thombs. (2022) Intensity of care and perceived burden among informal caregivers to persons with chronic medical conditions: a systematic review and meta-analysis. Disability and Rehabilitation 44:21, pages 6230-6246.
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Manjusha G. Warrier, Priya Treesa Thomas, Arun Sadasivan, Bhuvaneshwari Balasubramaniam, Seena Vengalil, Saraswati Nashi, Veeramani Preethish-Kumar, Kiran Polavarapu, Niranjan Prakash Mahajan, Pradeep Chandra Reddy Chevula & Atchayaram Nalini. (2019) Family Caregivers’ Experiences with Dying and Bereavement of Individuals with Motor Neuron Disease in India. Journal of Social Work in End-of-Life & Palliative Care 15:2-3, pages 111-125.
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Shan Tang, Li Li, Hongxia Xue, Shuyan Cao, Chao Li, Kunjing Han & Binquan Wang. (2021) Caregiver burden and associated factors among primary caregivers of patients with ALS in home care: a cross-sectional survey study. BMJ Open 11:9, pages e050185.
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Anna Zinkevich, Johanna Sophie Lubasch, Sarah Anna Katharina Uthoff, Jens Boenisch, Stefanie Kalén Sachse, Tobias Bernasconi & Lena Ansmann. (2021) Caregiver burden and proxy-reported outcomes of people without natural speech: a cross-sectional survey study. BMJ Open 11:8, pages e048789.
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Merve Deniz PAK GÜRE & Cemre PAK. (2021) NADİR HASTALIĞI OLAN ÇOCUKLARIN AİLELERİNDE BAKIM YÜKÜNÜN İNCELENMESİEXAMINING THE CAREGIVER BURDEN IN THE FAMILIES OF CHILDREN WITH RARE DISEASES. Turkish Journal of Family Medicine and Primary Care 15:2, pages 269-277.
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Anna Markella Antoniadi, Miriam Galvin, Mark Heverin, Orla Hardiman & Catherine Mooney. (2021) Prediction of caregiver quality of life in amyotrophic lateral sclerosis using explainable machine learning. Scientific Reports 11:1.
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Meng‐Mei Yuan, Xi Peng, Tie‐Ying Zeng, Mei‐Li‐Yang Wu, Ye Chen, Ke Zhang & Xue‐Jun Wang. (2021) The illness experience for people with amyotrophic lateral sclerosis: A qualitative study. Journal of Clinical Nursing 30:9-10, pages 1455-1463.
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ManjushaG Warrier, Arun Sadasivan, Kiran Polavarapu, VeeramaniPreethish Kumar, NiranjanPrakash Mahajan, ChevulaPradeep Chandra Reddy, Seena Vengalil, Saraswati Nashi, Atchayaram Nalini & PriyaTreesa Thomas. (2020) Lived experience of spouses of persons with motor neuron disease: Preliminary findings through interpretative phenomenological analysis. Indian Journal of Palliative Care 26:1, pages 60.
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Jashelle Caga, Sharpley Hsieh, Patricia Lillo, Kaitlin Dudley & Eneida Mioshi. (2019) The Impact of Cognitive and Behavioral Symptoms on ALS Patients and Their Caregivers. Frontiers in Neurology 10.
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