Search research articles
Contact Us
Filters
Showing results (1-10 of 44) with videos related to
Page
of 5
Sort By:
The American Journal of Pediatric Hematology/Oncology
|
January 1, 1983
A decade of screening in the hemoglobinopathies: is a national program to prevent sickle cell anemia possible?
D L Rucknagel
Pediatric Pathology & Molecular Medicine
|
April 4, 2003
The role of rib infarcts in the acute chest syndrome of sickle cell diseases
D L Rucknagel
Progress in Clinical and Biological Research
|
January 1, 1987
Painful crisis and dense echinocytes: effects of hydration and vasodilators
J A Warth, D L Rucknagel
The American Journal of Medicine
|
July 1, 1975
A heterozygote for Hb S beta, Hb C beta and Hb G Philadelphia beta in a family presenting evidence for heterogeneity of hemoglobin alpha chain loci
D L Rucknagel, J A Rising
The Medical Clinics of North America
|
July 1, 1980
Clinical implications of recent advances in hemoglobin disorders
S M Hanash, D L Rucknagel
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1978
Proteolytic activity in erythrocyte precursors
S M Hanash, D L Rucknagel
Hemoglobin
|
January 1, 1981
The proportion of Hb A2 is higher in sickle cell trait than in normal homozygotes
W J Whitten, D L Rucknagel
Radiology
|
June 1, 1978
Increased bone marrow blood flow in sickle cell anemia demonstrated by thallium-201 and Tc-99m human albumin microspheres
J H Thrall, D L Rucknagel
Blood
|
August 1, 1984
Density ultracentrifugation of sickle cells during and after pain crisis: increased dense echinocytes in crisis
J A Warth, D L Rucknagel
American Journal of Hematology
|
May 1, 1995
Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-->Ser in a newborn with cyanosis
M Kohli-Kumar, T Zwerdling, D L Rucknagel
Page
of 5
Search research articles
Search
Showing results (1-10 of 44) with videos related to
Sort By:
Page
of 5
The American Journal of Pediatric Hematology/Oncology
|
January 1, 1983
A decade of screening in the hemoglobinopathies: is a national program to prevent sickle cell anemia possible?
D L Rucknagel
Pediatric Pathology & Molecular Medicine
|
April 4, 2003
The role of rib infarcts in the acute chest syndrome of sickle cell diseases
D L Rucknagel
Progress in Clinical and Biological Research
|
January 1, 1987
Painful crisis and dense echinocytes: effects of hydration and vasodilators
J A Warth, D L Rucknagel
The American Journal of Medicine
|
July 1, 1975
A heterozygote for Hb S beta, Hb C beta and Hb G Philadelphia beta in a family presenting evidence for heterogeneity of hemoglobin alpha chain loci
D L Rucknagel, J A Rising
The Medical Clinics of North America
|
July 1, 1980
Clinical implications of recent advances in hemoglobin disorders
S M Hanash, D L Rucknagel
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1978
Proteolytic activity in erythrocyte precursors
S M Hanash, D L Rucknagel
Hemoglobin
|
January 1, 1981
The proportion of Hb A2 is higher in sickle cell trait than in normal homozygotes
W J Whitten, D L Rucknagel
Radiology
|
June 1, 1978
Increased bone marrow blood flow in sickle cell anemia demonstrated by thallium-201 and Tc-99m human albumin microspheres
J H Thrall, D L Rucknagel
Blood
|
August 1, 1984
Density ultracentrifugation of sickle cells during and after pain crisis: increased dense echinocytes in crisis
J A Warth, D L Rucknagel
American Journal of Hematology
|
May 1, 1995
Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-->Ser in a newborn with cyanosis
M Kohli-Kumar, T Zwerdling, D L Rucknagel
Page
of 5