Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
2006.
Current awareness in geriatric psychiatry.
International Journal of Geriatric Psychiatry,
Vol. 21,
Issue. 5,
p.
500.
Williams, Janet K.
Hamilton, Rebekah
Nehl, Carissa
McGonigal‐Kenney, Meghan
Schutte, Debra L.
Sparbel, Kathleen
Birrer, Emily
Tripp‐Reimer, Toni
Friedrich, Rose
Penziner, Elizabeth
Jarmon, Lori
and
Paulsen, Jane
2007.
“No one else sees the difference: ”family members' perceptions of changes in persons with preclinical Huntington disease.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics,
Vol. 144B,
Issue. 5,
p.
636.
Cycyk, Lauren M.
and
Wright, Heather Harris
2008.
Frontotemporal dementia: Its definition, differential diagnosis, and management.
Aphasiology,
Vol. 22,
Issue. 4,
p.
422.
Milan, G.
Lamenza, F.
Iavarone, A.
Galeone, F.
Lorè, E.
de Falco, C.
Sorrentino, P.
and
Postiglione, A.
2008.
Frontal Behavioural Inventory in the differential diagnosis of dementia.
Acta Neurologica Scandinavica,
Vol. 117,
Issue. 4,
p.
260.
Williams, Janet K.
Skirton, Heather
Paulsen, Jane S.
Tripp‐Reimer, Toni
Jarmon, Lori
McGonigal Kenney, Meghan
Birrer, Emily
Hennig, Bonnie L.
and
Honeyford, Joann
2009.
The emotional experiences of family carers in Huntington disease.
Journal of Advanced Nursing,
Vol. 65,
Issue. 4,
p.
789.
Chemali, Z.
Withall, A.
and
Daffner, K.R.
2010.
The Plight of Caring for Young Patients With Frontotemporal Dementia.
American Journal of Alzheimer's Disease & Other Dementias®,
Vol. 25,
Issue. 2,
p.
109.
Williams, Janet K.
Erwin, Cheryl
Juhl, Andrew R.
Mengeling, Michelle
Bombard, Yvonne
Hayden, Michael R.
Quaid, Kimberly
Shoulson, Ira
Taylor, Sandra
and
Paulsen, Jane S.
2010.
In their own words: Reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND‐HD study.
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics,
Vol. 153B,
Issue. 6,
p.
1150.
Munro, Ian
and
Edward, Karen-Leigh
2010.
The Burden of Care of Gay Male Carers Caring for Men Living With HIV/AIDS.
American Journal of Men's Health,
Vol. 4,
Issue. 4,
p.
287.
Sousa, Valmi D.
Williams, Janet K.
Barnette, Jack J.
and
Reed, David A.
2010.
A new scale to measure family members' perception of community health care services for persons with Huntington disease.
Journal of Evaluation in Clinical Practice,
Vol. 16,
Issue. 3,
p.
470.
Nicolaou, Paula L.
Egan, Sarah J.
Gasson, Natalie
and
Kane, Robert T.
2010.
Identifying needs, burden, and distress of carers of people with Frontotemporal dementia compared to Alzheimer’s disease.
Dementia,
Vol. 9,
Issue. 2,
p.
215.
Williams, Janet K.
Skirton, Heather
Barnette, James Jackson
and
Paulsen, Jane S.
2012.
Family carer personal concerns in Huntington disease.
Journal of Advanced Nursing,
Vol. 68,
Issue. 1,
p.
137.
Cox, Marie
2012.
Quality of life among carers of people with Huntington’s disease.
British Journal of Neuroscience Nursing,
Vol. 8,
Issue. 5,
p.
288.
Mioshi, Eneida
Foxe, David
Leslie, Felicity
Savage, Sharon
Hsieh, Sharpley
Miller, Laurie
Hodges, John R.
and
Piguet, Olivier
2013.
The Impact of Dementia Severity on Caregiver Burden in Frontotemporal Dementia and Alzheimer Disease.
Alzheimer Disease & Associated Disorders,
Vol. 27,
Issue. 1,
p.
68.
O’Connor, Claire M.
Ahmed, Samrah
and
Mioshi, Eneida
2014.
Functional disability in primary progressive aphasia.
Aphasiology,
Vol. 28,
Issue. 8-9,
p.
1131.
O’Connell, Megan E
Crossley, Margaret
Cammer, Allison
Morgan, Debra
Allingham, Wendy
Cheavins, Betty
Dalziel, Donna
Lemire, Maurice
Mitchell, Sheri
and
Morgan, Ernie
2014.
Development and evaluation of a telehealth videoconferenced support group for rural spouses of individuals diagnosed with atypical early-onset dementias.
Dementia,
Vol. 13,
Issue. 3,
p.
382.
Barsuglia, Joseph P.
Nedjat-Haiem, Frances R.
Shapira, Jill S.
Velasco, Christina
Jimenez, Elvira E.
Mather, Michelle J.
and
Mendez, Mario F.
2014.
Observational themes of social behavioral disturbances in frontotemporal dementia.
International Psychogeriatrics,
Vol. 26,
Issue. 9,
p.
1475.
Kam, Jonathan S
van Keizerswaard, Jolanda
and
Piguet, Olivier
2015.
Diet and Nutrition in Dementia and Cognitive Decline.
p.
493.
Merrilees, Jennifer
Barton, Cynthia
Kuo, Amy
and
Ketelle, Robin
2016.
Non‐Alzheimer's and Atypical Dementia.
p.
202.
Takeuchi, Tomiko
Muraoka, Koko
Yamada, Megumi
Nishio, Yuri
and
Hozumi, Isao
2016.
Living with idiopathic basal ganglia calcification 3: a qualitative study describing the lives and illness of people diagnosed with a rare neurological disease.
SpringerPlus,
Vol. 5,
Issue. 1,
Gilhooly, K. J.
Gilhooly, M. L. M.
Sullivan, M. P.
McIntyre, A.
Wilson, L.
Harding, E.
Woodbridge, R.
and
Crutch, S.
2016.
A meta-review of stress, coping and interventions in dementia and dementia caregiving.
BMC Geriatrics,
Vol. 16,
Issue. 1,