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M Brandow

Showing results (41-50 of 74) with videos related to

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Pediatric Blood & Cancer|December 7, 2020
Recommendation to reality: Closing the transcranial Doppler screening gap for children with sickle cell anemiaAshima 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 complicationsAshima 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 ScaleMatthew 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 diseaseLana Mucalo, Joshua J Field, Janelle Highland, et al.
Pediatric Blood & Cancer|June 19, 2013
Clinically meaningful measurement of pain in children with sickle cell diseaseMatthew 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 patientsReilly 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 diseaseAmanda 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 diseaseKatelyn 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 useAmanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
Pediatric Blood & Cancer|December 7, 2020
Recommendation to reality: Closing the transcranial Doppler screening gap for children with sickle cell anemiaAshima 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 complicationsAshima 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 ScaleMatthew 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 diseaseLana Mucalo, Joshua J Field, Janelle Highland, et al.
Pediatric Blood & Cancer|June 19, 2013
Clinically meaningful measurement of pain in children with sickle cell diseaseMatthew 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 patientsReilly 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 diseaseAmanda 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 diseaseKatelyn 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 useAmanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.
Pageof 8