Search research articles
Contact Us
Filters
Showing results (41-50 of 74) with videos related to
Page
of 8
Sort By:
Pediatric Blood & Cancer
|
December 7, 2020
Recommendation to reality: Closing the transcranial Doppler screening gap for children with sickle cell anemia
Ashima Singh, Vanaja Danda, Laura Van Swol, et al.
Plos One
|
April 16, 2024
Acute care utilization among individuals with sickle cell disease and related cardiopulmonary and renal complications
Ashima Singh, David C Brousseau, Mahua Dasgupta, et al.
Journal of Pediatric Hematology/Oncology
|
January 10, 2015
A Comparison of Pain Assessment Measures in Pediatric Sickle Cell Disease: Visual Analog Scale Versus Numeric Rating Scale
Matthew P Myrvik, Amy L Drendel, Amanda M Brandow, et al.
Blood Advances
|
April 14, 2023
Preliminary construct validity of patient-reported outcomes to assess chronic pain in adults with sickle cell disease
Lana Mucalo, Joshua J Field, Janelle Highland, et al.
Pediatric Blood & Cancer
|
June 19, 2013
Clinically meaningful measurement of pain in children with sickle cell disease
Matthew P Myrvik, Amanda M Brandow, Amy L Drendel, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Sickle cell disease patient plasma sensitizes iPSC-derived sensory neurons from sickle cell disease patients
Reilly L Allison, Anthony Burand, Damaris Nieves Torres, et al.
Pediatric Blood & Cancer
|
April 23, 2014
Do difficulties in swallowing medication impede the use of hydroxyurea in children?
ElShadey Bekele, Courtney D Thornburg, Amanda M Brandow, et al.
The Journal of School Health
|
July 10, 2013
Academic attainment findings in children with sickle cell disease
Amanda S Epping, Matthew P Myrvik, Robert F Newby, et al.
British Journal of Haematology
|
June 28, 2019
Gabapentin alleviates chronic spontaneous pain and acute hypoxia-related pain in a mouse model of sickle cell disease
Katelyn E Sadler, Sarah N Langer, Anthony D Menzel, et al.
British Journal of Haematology
|
August 20, 2016
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use
Amanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 74) with videos related to
Sort By:
Page
of 8
Pediatric Blood & Cancer
|
December 7, 2020
Recommendation to reality: Closing the transcranial Doppler screening gap for children with sickle cell anemia
Ashima Singh, Vanaja Danda, Laura Van Swol, et al.
Plos One
|
April 16, 2024
Acute care utilization among individuals with sickle cell disease and related cardiopulmonary and renal complications
Ashima Singh, David C Brousseau, Mahua Dasgupta, et al.
Journal of Pediatric Hematology/Oncology
|
January 10, 2015
A Comparison of Pain Assessment Measures in Pediatric Sickle Cell Disease: Visual Analog Scale Versus Numeric Rating Scale
Matthew P Myrvik, Amy L Drendel, Amanda M Brandow, et al.
Blood Advances
|
April 14, 2023
Preliminary construct validity of patient-reported outcomes to assess chronic pain in adults with sickle cell disease
Lana Mucalo, Joshua J Field, Janelle Highland, et al.
Pediatric Blood & Cancer
|
June 19, 2013
Clinically meaningful measurement of pain in children with sickle cell disease
Matthew P Myrvik, Amanda M Brandow, Amy L Drendel, et al.
Biorxiv : the Preprint Server for Biology
|
January 30, 2023
Sickle cell disease patient plasma sensitizes iPSC-derived sensory neurons from sickle cell disease patients
Reilly L Allison, Anthony Burand, Damaris Nieves Torres, et al.
Pediatric Blood & Cancer
|
April 23, 2014
Do difficulties in swallowing medication impede the use of hydroxyurea in children?
ElShadey Bekele, Courtney D Thornburg, Amanda M Brandow, et al.
The Journal of School Health
|
July 10, 2013
Academic attainment findings in children with sickle cell disease
Amanda S Epping, Matthew P Myrvik, Robert F Newby, et al.
British Journal of Haematology
|
June 28, 2019
Gabapentin alleviates chronic spontaneous pain and acute hypoxia-related pain in a mouse model of sickle cell disease
Katelyn E Sadler, Sarah N Langer, Anthony D Menzel, et al.
British Journal of Haematology
|
August 20, 2016
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide use
Amanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.
Page
of 8