about
Presence of pain on three or more days of the week is associated with worse patient reported outcomes in adults with sickle cell disease.Association of genetic variation in COMT gene with pain related to sickle cell disease in patients from the walk-PHaSST study.Quantitative sensory testing is feasible and is well-tolerated in patients with sickle cell disease following a vaso-occlusive episode.Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease.From trust to skepticism: An in-depth analysis across age groups of adults with sickle cell disease on their perspectives regarding hydroxyurea.Bone marrow transplantation for adolescents and young adults with sickle cell disease: Results of a prospective multicenter pilot studyHow I treat sickle cell disease with hematopoietic cell transplantationComparative Effectiveness of a Web-Based Patient Decision Aid for Therapeutic Options for Sickle Cell Disease: Randomized Controlled TrialSafety and Feasibility of Hematopoietic Progenitor Stem Cell Collection by Mobilization with Plerixafor Followed by Apheresis vs Bone Marrow Harvest in Patients with Sickle Cell Disease in the Multi-center HGB-206 Trial
P50
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P50
description
researcher ORCID ID = 0000-0003-3242-0037
@en
wetenschapper
@nl
name
Lakshmanan Krishnamurti
@ast
Lakshmanan Krishnamurti
@en
Lakshmanan Krishnamurti
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Lakshmanan Krishnamurti
@nl
type
label
Lakshmanan Krishnamurti
@ast
Lakshmanan Krishnamurti
@en
Lakshmanan Krishnamurti
@es
Lakshmanan Krishnamurti
@nl
prefLabel
Lakshmanan Krishnamurti
@ast
Lakshmanan Krishnamurti
@en
Lakshmanan Krishnamurti
@es
Lakshmanan Krishnamurti
@nl
P106
P31
P496
0000-0003-3242-0037