Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Prunty, Martine C.
Sharpe, Louise
Butow, Phyllis
and
Fulcher, Gary
2008.
The motherhood choice: A decision aid for women with multiple sclerosis.
Patient Education and Counseling,
Vol. 71,
Issue. 1,
p.
108.
Kaptein, Ad A.
Hughes, Brian M.
Scharloo, Margreet
Fischer, Maarten J.
Snoei, Lucia
Weinman, John
and
Rabe, Klaus F.
2008.
Illness Perceptions About Asthma Are Determinants of Outcome.
Journal of Asthma,
Vol. 45,
Issue. 6,
p.
459.
Philip, Errol J.
Lindner, Helen
and
Lederman, Leah
2009.
Relationship of illness perceptions with depression among individuals diagnosed with lupus.
Depression and Anxiety,
Vol. 26,
Issue. 6,
p.
575.
Hale, Elizabeth D.
and
Treharne, Gareth J.
2010.
Rheumatology.
p.
151.
Fischer, Maarten
Scharloo, Margreet
Abbink, Jannie
van 't Hul, Alex
van Ranst, Dirk
Rudolphus, Arjan
Weinman, John
Rabe, Klaus
and
Kaptein, Ad A.
2010.
The dynamics of illness perceptions: Testing assumptions of Leventhal's common‐sense model in a pulmonary rehabilitation setting.
British Journal of Health Psychology,
Vol. 15,
Issue. 4,
p.
887.
Karademas, Evangelos C.
Kynigopoulou, Eleftheria
Aghathangelou, Eleni
and
Anestis, Dimitrios
2011.
The relation of illness representations to the ‘end-stage’ appraisal of outcomes through health status, and the moderating role of optimism.
Psychology & Health,
Vol. 26,
Issue. 5,
p.
567.
Sperry, Len
2011.
Systemic Lupus Erythematosus: The Impact of Individual, Couple, and Family Dynamics.
The Family Journal,
Vol. 19,
Issue. 3,
p.
328.
Kaptein, Ad A.
Yamaoka, Kazue
Snoei, Lucia
Kobayashi, Kunihiko
Uchida, Yuka
van der Kloot, Willem A.
Tabei, Toshio
Kleijn, Wim Chr.
Koster, Mariska
Wijnands, Giel
Kaajan, Hans
Tran, Tommy
Inoue, Kenichi
van Klink, Rik
van Dooren-Coppens, Eva
Dik, Hans
Hayashi, Fumi
Willems, Luuk
Annema-Schmidt, Dunja
Annema, Jouke
van der Maat, Bas
van Kralingen, Klaas
Meirink, Corrie
Ogoshi, Kyoji
Aaronson, Neil
Nortier, Hans
and
Rabe, Klaus
2011.
Illness perceptions and quality of life in Japanese and Dutch patients with non-small-cell lung cancer.
Lung Cancer,
Vol. 72,
Issue. 3,
p.
384.
Daleboudt, Gabriëlle M.N.
Berger, Stefan P.
Broadbent, Elizabeth
and
Kaptein, Ad A.
2011.
Health-related quality of life in patients with systemic lupus erythematosus and proliferative lupus nephritis.
Psychology, Health & Medicine,
Vol. 16,
Issue. 4,
p.
393.
Daleboudt, GMN
Broadbent, E
Berger, SP
and
Kaptein, AA
2011.
Illness perceptions in patients with systemic lupus erythematosus and proliferative lupus nephritis.
Lupus,
Vol. 20,
Issue. 3,
p.
290.
Beckerman, N. L.
and
Sarracco, Michele
2012.
Listening to Lupus Patients and Families: Fine Tuning the Assessment.
Social Work in Health Care,
Vol. 51,
Issue. 7,
p.
597.
Daleboudt, Gabriëlle M.N.
Broadbent, Elizabeth
McQueen, Fiona
and
Kaptein, Ad A.
2013.
The impact of illness perceptions on sexual functioning in patients with systemic lupus erythematosus.
Journal of Psychosomatic Research,
Vol. 74,
Issue. 3,
p.
260.
Baines, Tineke
Wittkowski, Anja
and
Wieck, Angelika
2013.
Illness perceptions in mothers with postpartum depression.
Midwifery,
Vol. 29,
Issue. 7,
p.
779.
Valencia-Toro, Paula A.
Claudia, Mora K.
Ana Milena, Arbeláez S.
Jaimes, Diego Alejandro
Yahira, Guzmán R.
Plazas, Merideidy
Romero-Sánchez, María Consuelo
Valle-Oñate, Rafael
and
John, Londoño P.
2014.
¿Cuál es la percepción de enfermedad de pacientes colombianos con lupus eritematoso sistémico? Aplicación del Revised Illness Perceptions Questionnaire (IPQ-R).
Revista Colombiana de Reumatología,
Vol. 21,
Issue. 1,
p.
4.
Lamiani, G.
Strada, I.
Mancuso, M. E.
Coppola, A.
Vegni, E.
and
Moja, E. A.
2015.
Factors influencing illness representations and perceived adherence in haemophilic patients: a pilot study.
Haemophilia,
Vol. 21,
Issue. 5,
p.
598.
Israel, Jared I.
White, Kamila S.
and
Gervino, Ernest V.
2015.
Illness Perceptions, Negative Emotions, and Pain in Patients with Noncardiac Chest Pain.
Journal of Clinical Psychology in Medical Settings,
Vol. 22,
Issue. 1,
p.
77.
Nowicka-Sauer, Katarzyna
Pietrzykowska, Małgorzata
Banaszkiewicz, Dorota
Hajduk, Adam
Czuszyńska, Zenobia
and
Smoleńska, Żaneta
2016.
How do patients and doctors-to-be perceive systemic lupus erythematosus?.
Rheumatology International,
Vol. 36,
Issue. 5,
p.
725.
del Pino‐Sedeño, Tasmania
Trujillo‐Martín, María M.
Ruiz‐Irastorza, Guillermo
Cuellar‐Pompa, Leticia
de Pascual‐Medina, Ana M.
and
Serrano‐Aguilar, Pedro
2016.
Effectiveness of Nonpharmacologic Interventions for Decreasing Fatigue in Adults With Systemic Lupus Erythematosus: A Systematic Review.
Arthritis Care & Research,
Vol. 68,
Issue. 1,
p.
141.
Valencia, Paula
Mora, Claudia
Rossinni, Yahira
Arbeláez, Ana Milena
Plazas, Merideidy
and
Londoño, John
2017.
Análisis de grupos focales en pacientes colombianos con lupus eritematoso sistémico: una mirada cualitativa a las representaciones de la enfermedad.
Revista Colombiana de Reumatología,
Vol. 24,
Issue. 1,
p.
11.
Valencia, Paula
Mora, Claudia
Rossinni, Yahira
Arbeláez, Ana Milena
Plazas, Merideidy
and
Londoño, John
2017.
Analysis of focus groups of Colombian patients with systemic lupus erythematosus: A qualitative look at representations of the disease.
Revista Colombiana de Reumatología (English Edition),
Vol. 24,
Issue. 1,
p.
11.