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Assessing Preferences for Rare Disease Treatment: Qualitative Development of the Paroxysmal Nocturnal Hemoglobinuria Patient Preference Questionnaire (PNH-PPQ©)

Overview of attention for article published in Patient preference and adherence, April 2020
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Title
Assessing Preferences for Rare Disease Treatment: Qualitative Development of the Paroxysmal Nocturnal Hemoglobinuria Patient Preference Questionnaire (PNH-PPQ©)
Published in
Patient preference and adherence, April 2020
DOI 10.2147/ppa.s233830
Pubmed ID
Authors

Karen Kaiser, Susan E Yount, Christa E Martens, Kimberly A Webster, Sara Shaunfield, Amy Sparling, John Devin Peipert, David Cella, Scott T Rottinghaus, Bonnie M K Donato, Richard Wells, Ioannis Tomazos

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 46 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 46 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 10 22%
Student > Bachelor 4 9%
Student > Master 3 7%
Student > Ph. D. Student 2 4%
Student > Doctoral Student 1 2%
Other 5 11%
Unknown 21 46%
Readers by discipline Count As %
Social Sciences 7 15%
Medicine and Dentistry 5 11%
Nursing and Health Professions 3 7%
Pharmacology, Toxicology and Pharmaceutical Science 3 7%
Agricultural and Biological Sciences 2 4%
Other 5 11%
Unknown 21 46%