Publications

 Millenaar J K, Bakker C, Koopmans R, Verhey F, Kurz A, de Vugt M E: The care needs and experiences with the use of services of people with young-onset dementia and their caregivers: a systematic review. In: International Journal of Geriatric Psychiatry, DOI: 10.1002/gps.4502, 2016.
Kurz A, Bakker C, Böhm M, Diehl-Schmid J, Dubois B, Ferreira C, Gage H, Graff C, Hergueta T, Jansen S, Jones B, Komar A, de Mendonça A, Metcalfe A, Milecka K, Millenaar J, Orrung Wallin A, Oyebode J, Saxl S, Schneider-Schelte H, and de Vugt M, on behalf of the RHAPSODY Study Group: RHAPSODY – Internet-based support for caregivers of people with young onset dementia: program design and methods of a pilot study. In: International Psychogeriatrics, doi:10.1017/S1041610216001186, 2016. Download
Griffin J, Oyebode JR, Allen J: Living with a diagnosis of bvFTD. In: Dementia: The International Journal of Social Research and Practice10.1177/1471301214568164, 2015.
Melo G, Maroco J, de Mendonça A.: Influence of personality on caregiver’s burden, depression and distress related to the BPSD. In: Int J Geriatr Psychiatry 2011 26, p. 1275-1282. 2014.
LaFontaine J, & Oyebode JR : Family relationships and dementia: a synthesis of qualitative research including the person with dementia. In: Ageing & Society. 34, (7), p. 1243-1272. 2014.
Gage H, Cheynel J, Williams P, Mitchell K, Stinton C, Katz J, Holland C, Sheehan B: Formal and informal caring of people with dementia: a cohort study in England, forthcoming. In: International Journal of Geriatric Psychiatry, 2014.
Riedl L, Last D, Danek A, Diehl-Schmid J: Long-term follow-up in primary progressive aphasia: clinical course and health care utilization. In: Aphasiology 8-9, p. 981-992. 2014.
Riley G, Fisher G, Hagger B, Elliott A, LeServe H, & Oyebode JR : The Birmingham Relationship Continuity Measure: The Development and Evaluation of a Measure of the Perceived Continuity of Spousal Relationships in Dementia. In: International Psychogeriatrics, 25. DOI: 10.1017/S1041610212001743, p. 263-274. 2013.
Freitag, K, Zimmermann, V: Massive open online courses. In: Information Management 28, p. 52–57. 2013.
Sheehan B, Lall R, Gage H, Holland C, Katz J, Mitchell K: A 12 month follow-up study of people with dementia referred to general hospital liaison psychiatry services. In: Age and Ageing 42, p. 786-790. 2013.
Bakker C, de Vugt M. E.: Unmet needs and health related quality of life in young-onset dementia. Am J Geriatr Psychiatry, 2013.
Katz J, Holland C, Mitchell K, Gage H, Thein N, Sheehan B: Carers' perspectives on choosing a care home for a relative with dementia. In: Families, Relationships and Societies, DOI: 10.1332/204674313X664905, 2013.
Trivedi D, Goodman C, Dickinson A, Gage H, McLaughlin J, Manthorpe J, Ashaye K, Iliffe S: A protocol for a systematic review of research on managing Behavioural and Psychological Symptoms in Dementia for community dwelling older people: evidence mapping and syntheses. In: Systematic Reviews 2. DOI: 10.1186/2046-4053-2-70, p. 70. 2013.
Bárrios H, Narciso S, Guerreiro M, Maroco J, Logsdon R, de Mendonça A: Quality of life in patients with Mild Cognitive Impairment. In: Aging Ment Health 2013 17, p. 287-292. 2013.
Diehl-Schmid J, Schmidt EM, Nunnemann S, Riedl L, Kurz A, Förstl H, Wagenpfeil S, Cramer B: Caregiver burden and needs in frontotemporal dementia. In: J Geriatr Psychiatry Neurol 26, p. 221-229. 2013.
Chiang HH, Forsell C, Lilius L, Öijerstedt L, Thordardottir S, Shanmugarajan K, Westerlund M, Nennesmo I, Thonberg H, Graff C: Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal dementia. In: European Journal of Human Genetics, 2013.
Diehl-Schmid J, Last D, Schuster T, Förstl H, Schneider-Schelte H, Kurz A: Health care utilization in frontotemporal lobar degeneration. In: Alzheimer Dis Assoc Disord. 26, p. 166-170. 2012.
Nunnemann S, Kurz A, Leucht S, Diehl-Schmid J: Caregivers of patients with frontotemporal lobar degeneration: a review of burden, problems, needs, and interventions. In: Int Psychogeriatr 24, p. 1368-1386. 2012.
Schermann M, Wiesche M, Krcmar, H: The role of information systems in supporting exploitative and exploratory management control activities. In: JMAR 24, p. 31–59. 2012.
Schöll M, Wall A, Thordardottir S, Ferreira D, Bogdanovic N, Långström B, Almkvist O, Graff C, Nordberg A: Low PIB PET retention in presence of pathological CSF biomarkers in Arctic APP mutation carriers. In: Neurology 79, p. 229-236. 2012.
Sheenan B, Lall R, Stinton C, Mitchell K, Gage H, Holland C, Katz J: Patient and Proxy measurement of quality of life among general hospital in-patients with dementia. In: Ageing and Mental Health 16(5), p. 603-7. 2012.
Jansen S: Demenz auf nationaler Ebene begegnen. In: ersatzkasse magazin. 01./02: 34, 2012.
Bakker C, de Vugt M. E. et al.: Determinants of the use of formal and informal care in early onset dementia: The NeedYD study. Am J Geriatr Psychiatry, 2012.
Bakker C, de Vugt M. E. et al.: Predictors of institutionalization in young onset dementia versus late onset dementia. In: Journal of the American Medical Directors Association, 2012.
Van Vliet D, de Vugt M. E. et al.: Awareness and its association with affective symptoms in young-onset and late-onset Alzheimer's disease: A prospective study. In: Alzheimer Dis Assoc Disord, Sep 18, 2012.
Van Vliet D, de Vugt M. E. et al.: Predictors of time to diagnosis in early onset dementia: a comparison with late onset dementia. In: Psychol Med, May 28, p. 1-10. 2012.
Lilja Andersson P, Juth N, Petersén Å, Graff C, Edberg AK: Ethical aspects of undergoing a predictive genetic testing for Huntington's disease. In: Nursing Ethics DOI: 10.1177/0969733012452686, 2012.
Oyebode J, Bradley, P & Allen J: Relatives’ Experiences of Frontal-variant Frontotemporal Dementia. In: Qualitative Health Research. E-publication ahead of print, DOI: 10.1177/1049732312466294, 2012.
Deutsche Alzheimer Gesellschaft (ed): Miteinander – Füreinander. Menschen mit Demenz und ihre Angehörigen in der Gemeinschaft. 2012.
Maruta C, Guerreiro M, de Mendonça A, Hort J, Scheltens P: The Use of Neuropsychological Tests across Europe: The Need for a Consensus in the Use of Assessment Tools for Dementia. In: Eur J Neurol 2011 18, p. 279-285. 2011.
Negovanska V, Hergueta T, Guichart-Gomez E, Dubois B et al.: Beneficial effect of a cognitive behavioral and multidisciplinary program in Alzheimer Disease on spouse caregiver anxiety: French study ELMMA. In: Rev Neurol 167, p. 114-122. 2011.
Funkiewiez A, Bertoux M, de Souza LC, Lévy R, Dubois B: The SEA (social cognition and emotional assessment): A clinical neuropsychological tool for early diagnosis of frontal variant of frontotemporal lobar degeneration. In: Neuropsychology Sep 5, 2011.
Jansen S: Gesichter der Demenz. Eine Demenzerkrankung hat viele Aspekte. In: Forum Sozialarbeit und Gesundheit 3, p. 11-14. 2011.
Thonberg H, Fallström M, Björkström J, Schoumans J, Nennesmo I, Graff C: Mutation screening of patients with Alzheimer disease identifies APP locus duplication in a Swedish patient. In: BMC Research Notes 4, p. 476. 2011.
Aisen PS, Andrieu S, Sampaio C, Carrillo M, Khachaturian ZS, Dubois B et al.: Report of the task force on designing clinical trials in early (predementia) AD. In: Neurology.76, p. 280-286. 2011.
Haman J, Bronner K, Margull J, Mendel R, Diehl-Schmid J,Bühner M, Klein R, Schneider A, Kurz A, Perneczky R: Patient participation in medical and social decisions in Alzheimer's disease. In: J AM Geriatr Soc, 59, p. 2045-52. 2011.
Dubois B, Feldman HH, Jacova C, et al.: Revising the definition of Alzheimer's disease: a new lexicon. In: Lancet Neurol 9, p. 1118-1127. 2010.
Pedrosa H, de Sá A, Guerreiro M, Maroco J, Simões MR, Galasko D, de Mendonça A: Functional Evaluation distinguishes MCI patients from healthy elderly people - the ADCS/MCI/ADL scale. In: J Nutr Health Aging 2010 14, p. 703-709. 2010.
Ginó S, Mendes T, Maroco J, Ribeiro F, Schmand BA, de Mendonça A, Guerreiro M: Memory complaints are frequent but qualitatively different in young and old healthy people. In: Gerontology, p. 272-277. 2010.
Keller L, Welander H, Chiang H-H, Tjernberg LO, Nennesmo I, Wallin ÅK, Graff C: The PSEN1 I143T mutation in a Swedish family with Alzheimer disease: Clinical report and quantification of Aβ in different brain regions. In: Eur J Hum Genet 18, p. 1202-1208. 2010.
Deutsche Alzheimer Gesellschaft (ed): Allein leben mit Demenz. Herausforderung für Kommunen. 2010.
Küchler T, Thissen D, Zimmermann V: Into the great wide open: responsive learning environments for personalised learning. In: Technology-supported environment for personalised learning: methods and case studies, IGI Global, London, 2009.
Küchler T, Pawlowski J M, Zimmermann V: Social tagging and open content: a concept for the future of e-learning and knowledge management. In: Good tags – bad tags: social tagging in der Wissensorganisation. Medien in der Wissenschaft Vol. 47, p. 131-140. Waxmann-Verlag, Muenster, 2008.
Dubois B, Feldman HH, Jacova C, Dekosky ST, Barberger-Gateau P, Cummings J, Delacourte A, Galasko D, Gauthier S, Jicha G, Meguro K, O'brien J, Pasquier F, Robert P, Rossor M, Salloway S, Stern Y, Visser PJ, Scheltens P: Research criteria for the diagnosis of Alzheimer's disease: revising the NINCDS-ADRDA criteria. In: Lancet Neurol 6, p. 734-746. 2007.