M. Galushko

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Feeling severely affected by Multiple Sclerosis: What does this mean?

H. Golla, H. Pfaff, J. Strupp, 2012, Palliative medicine.

End-of-life research on patients’ attitudes in Germany: a feasibility study

L. Radbruch, H. Pfaff, M. Galushko, 2010, Supportive Care in Cancer.

Severely Affected by Parkinson Disease: The Patient’s View and Implications for Palliative Care

H. Golla, J. Strupp, M. Galushko, 2018, The American journal of hospice & palliative care.

Analysing the impact of a case management model on the specialised palliative care multi-professional team

H. Golla, H. Pfaff, N. Ernstmann, 2018, Supportive Care in Cancer.

Self-rating makes the difference: Identifying palliative care needs of patients feeling severely affected by multiple sclerosis

H. Golla, H. Pfaff, N. Ernstmann, 2014, Palliative and Supportive Care.

Unmet needs of patients feeling severely affected by multiple sclerosis in Germany: a qualitative study.

H. Golla, H. Pfaff, N. Ernstmann, 2014, Journal of palliative medicine.

Risk Factors for Suicidal Ideation in Patients Feeling Severely Affected by Multiple Sclerosis.

H. Golla, K. Perrar, H. Pfaff, 2016, Journal of palliative medicine.

The desire to die in palliative care: a sequential mixed methods study to develop a semi-structured clinical approach

K. Perrar, H. Pfaff, M. Galushko, 2020, BMC Palliative Care.

The Desire to Die in Palliative Care: A sequential mixed methods study to develop a semi-structured clinical guideline

K. Perrar, H. Pfaff, M. Galushko, 2020 .

The DEsire to DIe in Palliative care: Optimization of Management (DEDIPOM) – a study protocol

H. Pfaff, M. Galushko, R. Voltz, 2018, BMC Palliative Care.

Validation of the German version of the Schedule of Attitudes Toward Hastened Death (SAHD–D) with patients in palliative care

L. Radbruch, H. Pfaff, N. Ernstmann, 2014, Palliative and Supportive Care.

“It’s Not that Easy”—Medical Students’ Fears and Barriers in End-of-Life Communication

M. Galushko, C. Ostgathe, V. Romotzky, 2014, Journal of Cancer Education.

Patients feeling severely affected by multiple sclerosis: how do patients want to communicate about end-of-life issues?

H. Golla, H. Pfaff, N. Ernstmann, 2012, Patient education and counseling.

Complexity in Non-Pharmacological Caregiving Activities at the End of Life: An International Qualitative Study

Guido Miccinesi, Carina Lundh Hagelin, Carl Johan Fürst, 2012, PLoS medicine.

Challenges in end-of-life communication

M. Galushko, R. Voltz, V. Romotzky, 2012, Current opinion in supportive and palliative care.

A palliative care hotline for multiple sclerosis: A pilot feasibility study

H. Golla, J. Strupp, M. Galushko, 2014, Palliative and Supportive Care.

Palliative care for severely affected patients with multiple sclerosis: when and why? Results of a Delphi survey of health care professionals.

H. Golla, J. Strupp, M. Galushko, 2014, Journal of palliative medicine.

Communication about the desire to die: Development and evaluation of a first needs-oriented training concept — A pilot study

H. Golla, K. Perrar, J. Strupp, 2020, Palliative and Supportive Care.

Desire for hastened death: how do professionals in specialized palliative care react?

L. Radbruch, H. Golla, K. Perrar, 2016, Psycho-oncology.

Determinants and implications of cancer patients’ psychosocial needs

M. Wirtz, M. Hallek, O. Ommen, 2009, Supportive Care in Cancer.

Barriers to using psycho-oncology services: a qualitative research into the perspectives of users, their relatives, non-users, physicians, and nurses

M. Wirtz, O. Ommen, H. Pfaff, 2010, Supportive Care in Cancer.

Issues of “life” and “death” for patients receiving palliative care—comments when confronted with a research tool

L. Radbruch, H. Pfaff, N. Ernstmann, 2011, Supportive Care in Cancer.

Multiple sclerosis and palliative care - perceptions of severely affected multiple sclerosis patients and their health professionals: a qualitative study

H. Golla, H. Pfaff, M. Galushko, 2014, BMC Palliative Care.

Unmet needs of caregivers of severely affected multiple sclerosis patients: A qualitative study

H. Golla, H. Pfaff, M. Galushko, 2015, Palliative and Supportive Care.

Glioblastoma multiforme from diagnosis to death: a prospective, hospital-based, cohort, pilot feasibility study of patient reported symptoms and needs

Martin Hellmich, Michael Schroeter, Raymond Voltz, 2014, Supportive Care in Cancer.

Palliative care needs of chronically ill nursing home residents in Germany: focusing on living, not dying.

M. Galushko, R. Voltz, Barbara Strohbuecker, 2011, International journal of palliative nursing.

Patients Feeling Severely Affected by Multiple Sclerosis

H. Golla, H. Pfaff, U. Karbach, 2016 .

Unmet needs of severely affected multiple sclerosis patients: The health professionals’ view

H. Golla, H. Pfaff, M. Galushko, 2012, Palliative medicine.

Quality indicators for care of cancer patients in their last days of life: literature update and experts' evaluation.

M. Galushko, J. Ellershaw, N. Raijmakers, 2012, Journal of palliative medicine.

Identifying patients suitable for palliative care - a descriptive analysis of enquiries using a Case Management Process Model approach

M. Galushko, R. Voltz, C. Ostgathe, 2012, BMC Research Notes.

“It’s Not that Easy”—Medical Students’ Fears and Barriers in End-of-Life Communication

M. Galushko, A. Düsterdiek, R. Obliers, 2015, Journal of Cancer Education.

Advance care planning and the parental geographical background in pediatric palliative home care: a retrospective chart review

M. Galushko, G. Janssen, L. Trocan, 2022, European Journal of Pediatrics.