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Neurological Research
A Journal of Progress in Neurosurgery, Neurology and Neurosciences
Volume 39, 2017 - Issue 1
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Original Research Paper

Predicting caregiving status and caregivers’ burden in multiple sclerosis. A short report

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Pages 13-15 | Received 05 Apr 2016, Accepted 14 Oct 2016, Published online: 09 Nov 2016

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María Granados-Santiago, Ramón Romero-Fernández, Andrés Calvache-Mateo, Alejandro Heredia-Ciuro, Javier Martin-Nuñez, Laura López-López & Marie Carmen Valenza. (2023) Relationship between patient functionality impairment and caregiver burden: is there a cut off point for the severe COPD patient?. Expert Review of Respiratory Medicine 17:3, pages 247-253.
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Jose M García-Domínguez, María L Martínez-Ginés, Olga Carmona, Ana B Caminero, Daniel Prefasi, Jorge Maurino & Javier Ballesteros. (2019) Measuring burden in caregivers of people with multiple sclerosis: psychometric properties of the CSI questionnaire. Patient Preference and Adherence 13, pages 101-106.
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Articles from other publishers (17)

Katherine L. Cardwell, Taylor A. Hume, Odessa J. McKenna, Lara A. Pilutti & Afolasade Fakolade. (2023) Symptom Management Among Multiple Sclerosis Care Partners in Canada. International Journal of MS Care 25:6, pages 281-287.
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Caroline K. Geiger, Danny Sheinson, Tu My To, David Jones & Nicole G. Bonine. (2023) Real-World Clinical and Economic Outcomes Among Persons With Multiple Sclerosis Initiating First- Versus Second- or Later-Line Treatment With Ocrelizumab. Neurology and Therapy 12:5, pages 1709-1728.
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Stefan Braune, Sandra Bluemich, Carola Bruns, Petra Dirks, Jeanette Hoffmann, Yanic Heer, Erwan Muros-Le Rouzic, Arnfin Bergmann, Walter Albrecht, Felix Bischof, Foroogh Bittkau, Simon Bittkau, Kin-Arno Bohr, Bettina Borries, Bernd Brockmeier, Dagmar Brummer, Bernhard Bühler, Wolfgang Butz, Lukas Cepek, Lars Claassen, Jürgen Dee, Lienhard Dieterle, Eckehard Drees, Christoph Engelmann, Michael Ernst, Oliver Fasold, Johannes Fischer, Michael Flach, Robert Fleischer, Lea Friedrich, Anke Friedrich, Michael Fritzinger, Klaus Gehring, Stephanie Gierer, Stephan Gierer, Jens Gößling, Eva Grips, Andreas Hans-Joachim Haldenwanger, Andreas Harth, Rolf Hartmann, Roland Helm, Heinz-Peter Herbst, Christian Hofer, Werner Erwin Hofmann, Alexander Hoge, Sibylla Hummel, Benno Ikenberg, Heike Israel-Willner, Ralf Jankovits, Boris-Alexander Kallmann, Ulrich Kausch, Marc Keppler, Kirn Kessler, Ulrike Kirchhöfer, Jürgen Kirchmeier, Rupert Knoblich, Thomas Knoll, Philipp Knorn, Monika Köchling, Anselm Wolfgang Kornhuber, Bernd Kramer, Michaela Krause, Martin Krauß, Ralf Kubalek, Jürgen Kunz, Harald Landefeld, Thomas Lange, Klaus Lehmann-Horn, Esther Lippert, Karla Lippmann, Walter Maier-Janson, Martin Märkl, Said Masri, Christof Moser, Clemens Neusch, Julius Niemann, Tilmann Paschke, Anna Sybilla Peikert, Andreas Peikert, Henning Peters, Robert Pfister, Gerd Reifschneider, Stefan Ries, Christoph Rieth, Holger Roick, Gerhard Dieter Roth, Roland Roth, Ali Safavi, Joachim Saur, Brigitte Schmitt-Roth, Erich Franz Scholz, Herbert Schreiber, Klaus Schreiber, Christoph Schrey, Carsten Schumann, Martin Seiler, Karl-Otto Sigel, Viola Sikora, Nikolaos Sotiriadis, Stefanie Spiegel, Detlef Städt, Torsten Sühnel, Klaus Tiel-Wilck, Jochen Christoph Ulzheimer, Barbara Sofie Unsorg, Silvia Voith, Achim Stephan Wannenmacher, Hildegund Weber, Markus Weih, Bernd Wendtland, Andreas Wiborg, Martin Wimmer, Thomas Winker, Isaak Wontroba & Monika Wüstenhagen. (2023) The natural history of primary progressive multiple sclerosis: insights from the German NeuroTransData registry. BMC Neurology 23:1.
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Stefano Benini, Erika Pellegrini, Carlo Descovich & Alessandra Lugaresi. (2023) Burden and resources in caregivers of people with multiple sclerosis: A qualitative study. PLOS ONE 18:4, pages e0265297.
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Aleksandra Kołtuniuk, Beata Pawlak, Dorota Krówczyńska & Justyna Chojdak-Łukasiewicz. (2023) The quality of life in patients with multiple sclerosis – Association with depressive symptoms and physical disability: A prospective and observational study. Frontiers in Psychology 13.
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Soheila BANITALEBI, Shahram ETEMADIFAR, Soleiman KHEIRI & Reza MASOUDI. (2022) The Effect of a Self-Management Program on Care Burden and Self-Efficacy in Family Caregivers of People With Multiple Sclerosis. Journal of Nursing Research 30:5, pages e234.
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Abdallah A. Sarhan, Khaled A. El-Sharkawy, Ahmed M. Mahmoudy & Noha A. Hashim. (2022) Burden of multiple sclerosis: impact on the patient, family and society. Multiple Sclerosis and Related Disorders 63, pages 103864.
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Gogem Topcu, Heather Buchanan, Aimee Aubeeluck & Hatice Ülsever. (2020) Informal carers’ experiences of caring for someone with Multiple Sclerosis: A photovoice investigation. British Journal of Health Psychology 26:2, pages 360-384.
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Leili Rabiei, Masoud Lotfizadeh, Zahra Karimi & Reza Masoudi. (2020) The effects of the Fordyce’s 14 fundamentals for happiness program on happiness and caregiver burden among the family caregivers of patients with epilepsy: A randomized controlled trial. Seizure 83, pages 124-131.
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Rebecca Maguire & Phil Maguire. (2020) Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions. Current Neurology and Neuroscience Reports 20:7.
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Joy Williams, Marina Moldavskiy, Katie Bauer, Grace Reed, Alexis Theuring, Jayme Zedrow, W. Mark Sweatman & Deborah Backus. (2020) Safety and Feasibility of Various Functional Electrical Stimulation Cycling Protocols in Individuals With Multiple Sclerosis Who Are Nonambulatory. Archives of Rehabilitation Research and Clinical Translation 2:2, pages 100045.
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A. Ochoa-Morales, T. Hernández-Mojica, F. Paz-Rodríguez, A. Jara-Prado, Z. Trujillo-De Los Santos, M.A. Sánchez-Guzmán, J.L. Guerrero-Camacho, T. Corona-Vázquez, J. Flores, A. Camacho-Molina, V. Rivas-Alonso & D.J. Dávila-Ortiz de Montellano. (2019) Quality of life in patients with multiple sclerosis and its association with depressive symptoms and physical disability. Multiple Sclerosis and Related Disorders 36, pages 101386.
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K. van der Hiele, D.A.M. van Gorp, M.A.P. Heerings, P.J. Jongen, J.J.L. van der Klink, E.A.C. Beenakker, J.J.J. van Eijk, S.T.F.M. Frequin, B.M. van Geel, G.J.D. Hengstman, E. Hoitsma, J.P. Mostert, W.I.M. Verhagen, K. de Gans, D. Zemel, H.A.M. Middelkoop & L.H. Visser. (2019) Caregiver strain among life partners of persons with mild disability due to relapsing-remitting multiple sclerosis. Multiple Sclerosis and Related Disorders 31, pages 5-11.
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Petros PetrikisAnastasia BaldoumaAristeidis H. KatsanosSpyridon KonitsiotisSotirios Giannopoulos. (2019) Quality of Life and Emotional Strain in Caregivers of Patients with Multiple Sclerosis. Journal of Clinical Neurology 15:1, pages 77.
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Timothy S. Sannes & Benzi M. Kluger. 2019. Neuropalliative Care. Neuropalliative Care 279 292 .
Markus Ebke, Andreas Koch, Kim Dillen, Ingrid Becker, Raymond Voltz & Heidrun Golla. (2018) The “Surprise Question” in Neurorehabilitation—Prognosis Estimation by Neurologist and Palliative Care Physician; a Longitudinal, Prospective, Observational Study. Frontiers in Neurology 9.
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Matthias Seibl-Leven, Christian von Reeken, Roland Goldbrunner, Stefan Grau, Maximilian Ingolf Ruge, Norbert Galldiks, Veronika Dunkl, Martin Kocher, Raymond Voltz & Heidrun Golla. (2018) Clinical routine assessment of palliative care symptoms and concerns and caregiver burden in glioblastoma patients: an explorative field study. Journal of Neuro-Oncology 138:2, pages 321-333.
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