| scholarly article | Q13442814 |
| P50 | author | Alessandra Lugaresi | Q41721881 |
| Maria Pia Amato | Q56451881 | ||
| Erika Pietrolongo | Q57040760 | ||
| Marta Bassi | Q57076865 | ||
| Benedetta Goretti | Q114425902 | ||
| P2093 | author name string | Francesco Patti | |
| Antonella Delle Fave | |||
| Eleonora Minacapelli | |||
| Monica Falautano | |||
| Manuela Valsecchi | |||
| Marianna Pattini | |||
| Monica Grobberio | |||
| Sabina Cilia | |||
| Beatrice Allegri | |||
| P2860 | cites work | Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS) | Q22241644 |
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| Residents of poor nations have a greater sense of meaning in life than residents of wealthy nations | Q30457228 | ||
| Factorial and construct validity of the Italian Positive and Negative Affect Schedule (PANAS) | Q33844318 | ||
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| Intolerance of Uncertainty: Shaping an Agenda for Research on Coping with Multiple Sclerosis | Q35974817 | ||
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| Use of the International Classification of Functioning, Disability and Health (ICF) to identify preliminary comprehensive and brief core sets for multiple sclerosis | Q36761639 | ||
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| If, Why, and When Subjective Well-Being Influences Health, and Future Needed Research | Q38657750 | ||
| Caregiving in multiple sclerosis and quality of life: A meta-synthesis of qualitative research | Q38689605 | ||
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| Promoting and protecting mental health as flourishing: a complementary strategy for improving national mental health | Q39271886 | ||
| The relationship between burden and well-being among caregivers of Italian people diagnosed with severe neuromotor and cognitive disorders | Q39274029 | ||
| Impaired health-related quality of life predicts progression of disability in multiple sclerosis | Q39595351 | ||
| A qualitative investigation of adaptation in older individuals with multiple sclerosis | Q40001240 | ||
| Illness Perception and Well-Being Among Persons with Multiple Sclerosis and Their Caregivers | Q40689536 | ||
| Integrating the ICF with positive psychology: Factors predicting role participation for mothers with multiple sclerosis | Q40787058 | ||
| Using the International Classification of Functioning, Disability and Health (ICF) to address facilitators and barriers to participation at work | Q41121554 | ||
| The coexistence of well- and ill-being in persons with multiple sclerosis, their caregivers and health professionals. | Q46007408 | ||
| A systematic approach to analyse health-related quality of life in multiple sclerosis: the GEDMA study | Q47221401 | ||
| Re-examining the psychology of spinal cord injury: a meaning centered approach from a cultural perspective | Q47619359 | ||
| Goal disengagement and goal re-engagement among multiple sclerosis patients: relationship to well-being and illness representation | Q48226685 | ||
| Unmet needs of severely affected multiple sclerosis patients: the health professionals' view | Q48678810 | ||
| The dimensional structure of benefit finding in multiple sclerosis and relations with positive and negative adjustment: A longitudinal study | Q48870876 | ||
| Burden and health-related quality of life of Spanish caregivers of persons with multiple sclerosis | Q49011583 | ||
| Adversarial growth in patients with multiple sclerosis and their partners: relationships with illness perceptions, disability and distress. | Q50606247 | ||
| Caregiver quality of life in multiple sclerosis: a multicentre Italian study. | Q50903977 | ||
| The Multiple Sclerosis impact Profile (MSIP). Development and testing psychometric properties of an ICF-based health measure. | Q51899456 | ||
| Predictors of life satisfaction among caregivers of individuals with multiple sclerosis. | Q53133243 | ||
| The nature of benefit finding in multiple sclerosis (MS). | Q53200996 | ||
| Happy People Live Longer: Subjective Well-Being Contributes to Health and Longevity | Q53983390 | ||
| Patient and public involvement in chronic illness: beyond the expert patient | Q57270497 | ||
| Using the ICF and psychological models of behavior to predict mobility limitations | Q57700459 | ||
| Sources and motives for personal meaning in adulthood | Q58050994 | ||
| The Eudaimonic and Hedonic Components of Happiness: Qualitative and Quantitative Findings | Q58051022 | ||
| Health-related quality of life and depression in an Italian sample of multiple sclerosis patients | Q73438110 | ||
| Predictors of quality of life among patients with multiple sclerosis: an Italian cross-sectional study | Q79450565 | ||
| Predictors of subjective well-being among individuals with multiple sclerosis | Q80206854 | ||
| Making sense of illness or disability: the nature of sense making in multiple sclerosis (MS) | Q80216618 | ||
| Promoting well-being: time for a paradigm shift in health and human services1 | Q81330491 | ||
| Making sense of caregiving for persons with multiple sclerosis (MS): the dimensional structure of sense making and relations with positive and negative adjustment | Q81771665 | ||
| Consequences of chronic obstructive pulmonary disease and chronic heart failure: the relationship between objective and subjective health | Q81801667 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | happiness | Q8 |
| P304 | page(s) | 2216 | |
| P577 | publication date | 2017-12-20 | |
| P1433 | published in | Frontiers in Psychology | Q2794477 |
| P1476 | title | Beyond Disease: Happiness, Goals, and Meanings among Persons with Multiple Sclerosis and Their Caregivers | |
| P478 | volume | 8 |
| Q95661710 | Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions |
| Q64068257 | In Patients With Multiple Sclerosis, Both Objective and Subjective Sleep, Depression, Fatigue, and Paresthesia Improved After 3 Weeks of Regular Exercise |
| Q89067401 | Quality of life and psychological well-being in the early stages of multiple sclerosis (MS): Importance of adopting a biopsychosocial model |
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