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L Styles

Showing results (11-20 of 26) with videos related to

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Annals of the New York Academy of Sciences|July 21, 1998
Preliminary report: hydroxyurea produces significant clinical response in thalassemia intermediaL Styles, B Lewis, D Foote, et al.
Infection Control and Hospital Epidemiology|March 1, 1994
The 'roving team': employee health service in the workplaceR Wurtz, P Bush, L Styles, et al.
The Journal of Biological Chemistry|October 25, 1979
The characteristics and significance of sulfonamides as substrates for Escherichia coli dihydropteroate synthaseS Roland, R Ferone, R J Harvey, et al.
Journal of Pediatric Hematology/Oncology|August 26, 2000
Use of hydroxyurea in children ages 2 to 5 years with sickle cell diseaseC Hoppe, E Vichinsky, K Quirolo, et al.
Annals of the New York Academy of Sciences|July 21, 1998
The hemoglobin E syndromesD C Rees, L Styles, E P Vichinsky, et al.
Journal of Pediatric Hematology/Oncology|December 29, 2000
Changing outcome of homozygous alpha-thalassemia: cautious optimismS T Singer, L Styles, J Bojanowski, et al.
Journal of the American Society for Mass Spectrometry|August 11, 2000
The fragmentation pathways of protonated glycine: a computational studyR A O'Hair, P S Broughton, M L Styles, et al.
Healthcare (Basel, Switzerland)|May 14, 2025
Family-Centered Care in Adolescent Intensive Outpatient Mental Health Treatment in the United States: A Case StudyHenry W Kietzman, Willem L Styles, Liese Franklin-Zitzkat, et al.
British Journal of Haematology|September 13, 2001
A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anaemiaC Hoppe, S Cheng, M Grow, et al.
The Journal of Pediatrics|December 18, 2001
Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemiaS T Miller, E Wright, M Abboud, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Annals of the New York Academy of Sciences|July 21, 1998
Preliminary report: hydroxyurea produces significant clinical response in thalassemia intermediaL Styles, B Lewis, D Foote, et al.
Infection Control and Hospital Epidemiology|March 1, 1994
The 'roving team': employee health service in the workplaceR Wurtz, P Bush, L Styles, et al.
The Journal of Biological Chemistry|October 25, 1979
The characteristics and significance of sulfonamides as substrates for Escherichia coli dihydropteroate synthaseS Roland, R Ferone, R J Harvey, et al.
Journal of Pediatric Hematology/Oncology|August 26, 2000
Use of hydroxyurea in children ages 2 to 5 years with sickle cell diseaseC Hoppe, E Vichinsky, K Quirolo, et al.
Annals of the New York Academy of Sciences|July 21, 1998
The hemoglobin E syndromesD C Rees, L Styles, E P Vichinsky, et al.
Journal of Pediatric Hematology/Oncology|December 29, 2000
Changing outcome of homozygous alpha-thalassemia: cautious optimismS T Singer, L Styles, J Bojanowski, et al.
Journal of the American Society for Mass Spectrometry|August 11, 2000
The fragmentation pathways of protonated glycine: a computational studyR A O'Hair, P S Broughton, M L Styles, et al.
Healthcare (Basel, Switzerland)|May 14, 2025
Family-Centered Care in Adolescent Intensive Outpatient Mental Health Treatment in the United States: A Case StudyHenry W Kietzman, Willem L Styles, Liese Franklin-Zitzkat, et al.
British Journal of Haematology|September 13, 2001
A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anaemiaC Hoppe, S Cheng, M Grow, et al.
The Journal of Pediatrics|December 18, 2001
Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemiaS T Miller, E Wright, M Abboud, et al.
Pageof 3