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Annals of Clinical Biochemistry
|
November 30, 2006
Comparison of Bayer Advia Centaur immunoassay results obtained on samples collected in four different Becton Dickinson Vacutainer tubes
A Morovat, T S James, S D Cox, et al.
Pflugers Archiv : European Journal of Physiology
|
November 16, 2019
The role of WNK in modulation of KCl cotransport activity in red cells from normal individuals and patients with sickle cell anaemia
David C-Y Lu, Anke Hannemann, Rasiqh Wadud, et al.
American Journal of Hematology
|
July 11, 2008
Hydroxyurea therapy lowers circulating DNA levels in sickle cell anemia
Pinar Ulug, Nisha Vasavda, Rohan Kumar, et al.
British Journal of Haematology
|
February 22, 2011
Soluble CD163 levels in children with sickle cell disease
Holger Jon Moller, Marianne Jensby Nielsen, Jack Bartram, et al.
Pediatric Neurology
|
June 13, 2006
Trials in sickle cell disease
Fenella J Kirkham, Norma B Lerner, Michael Noetzel, et al.
Acta Crystallographica. Section D, Biological Crystallography
|
July 1, 1994
Crystallization and X-ray structure determination of cytochrome c2 from Rhodobacter sphaeroides in three crystal forms
H L Axelrod, G Feher, J P Allen, et al.
Hemoglobin
|
May 1, 1996
Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies
P J Ho, J Rochette, D C Rees, et al.
Cancer Immunity
|
January 12, 2010
HAGE, a cancer/testis antigen expressed at the protein level in a variety of cancers
Morgan G Mathieu, Adam J Linley, Stephen P Reeder, et al.
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society
|
May 13, 1999
Prevalence of high-risk behaviors and obesity among low-income patients attending primary care clinics in Louisiana
P J Brantley, I C Scarinci, C L Carmack, et al.
Health Technology Assessment (Winchester, England)
|
November 13, 2012
The clinical effectiveness and cost-effectiveness of primary stroke prevention in children with sickle cell disease: a systematic review and economic evaluation
M G Cherry, J Greenhalgh, L Osipenko, et al.
Page
of 96
Search research articles
Search
Showing results (721-730 of 960) with videos related to
Sort By:
Page
of 96
Annals of Clinical Biochemistry
|
November 30, 2006
Comparison of Bayer Advia Centaur immunoassay results obtained on samples collected in four different Becton Dickinson Vacutainer tubes
A Morovat, T S James, S D Cox, et al.
Pflugers Archiv : European Journal of Physiology
|
November 16, 2019
The role of WNK in modulation of KCl cotransport activity in red cells from normal individuals and patients with sickle cell anaemia
David C-Y Lu, Anke Hannemann, Rasiqh Wadud, et al.
American Journal of Hematology
|
July 11, 2008
Hydroxyurea therapy lowers circulating DNA levels in sickle cell anemia
Pinar Ulug, Nisha Vasavda, Rohan Kumar, et al.
British Journal of Haematology
|
February 22, 2011
Soluble CD163 levels in children with sickle cell disease
Holger Jon Moller, Marianne Jensby Nielsen, Jack Bartram, et al.
Pediatric Neurology
|
June 13, 2006
Trials in sickle cell disease
Fenella J Kirkham, Norma B Lerner, Michael Noetzel, et al.
Acta Crystallographica. Section D, Biological Crystallography
|
July 1, 1994
Crystallization and X-ray structure determination of cytochrome c2 from Rhodobacter sphaeroides in three crystal forms
H L Axelrod, G Feher, J P Allen, et al.
Hemoglobin
|
May 1, 1996
Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies
P J Ho, J Rochette, D C Rees, et al.
Cancer Immunity
|
January 12, 2010
HAGE, a cancer/testis antigen expressed at the protein level in a variety of cancers
Morgan G Mathieu, Adam J Linley, Stephen P Reeder, et al.
The Journal of the Louisiana State Medical Society : Official Organ of the Louisiana State Medical Society
|
May 13, 1999
Prevalence of high-risk behaviors and obesity among low-income patients attending primary care clinics in Louisiana
P J Brantley, I C Scarinci, C L Carmack, et al.
Health Technology Assessment (Winchester, England)
|
November 13, 2012
The clinical effectiveness and cost-effectiveness of primary stroke prevention in children with sickle cell disease: a systematic review and economic evaluation
M G Cherry, J Greenhalgh, L Osipenko, et al.
Page
of 96