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Plos One
|
February 8, 2011
Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9
Vanessa R Paixão-Côrtes, Diogo Meyer, Tiago V Pereira, et al.
Haematologica
|
July 14, 2011
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
Danitza Nebor, Andre Bowers, Marie-Dominique Hardy-Dessources, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2005
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency
Mohammed Tredano, David N Cooper, Manfred Stuhrmann, et al.
British Journal of Haematology
|
January 6, 2016
Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study
Julie Sommet, Corinne Alberti, Nathalie Couque, et al.
Clinical Hemorheology and Microcirculation
|
March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control study
Jennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB
Mohammed Tredano, Matthias Griese, Jacques de Blic, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Newborn Screening for Sickle Cell Disease in Europe
Yvonne Daniel, Jacques Elion, Bichr Allaf, et al.
British Journal of Haematology
|
November 29, 2020
Cell-derived microparticles and sickle cell disease chronic vasculopathy in sub-Saharan Africa: A multinational study
Abdoul K Dembélé, Claudine Lapoumeroulie, Mor Diaw, et al.
Annals of Hematology
|
April 4, 2014
Hydroxycarbamide modulates components involved in the regulation of adenosine levels in blood cells from sickle-cell anemia patients
Ana C Silva-Pinto, Carolina Dias-Carlos, Felipe Saldanha-Araujo, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2012
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene
Andrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 69) with videos related to
Sort By:
Page
of 7
Plos One
|
February 8, 2011
Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9
Vanessa R Paixão-Côrtes, Diogo Meyer, Tiago V Pereira, et al.
Haematologica
|
July 14, 2011
Frequency of pain crises in sickle cell anemia and its relationship with the sympatho-vagal balance, blood viscosity and inflammation
Danitza Nebor, Andre Bowers, Marie-Dominique Hardy-Dessources, et al.
American Journal of Medical Genetics. Part A
|
December 8, 2005
Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency
Mohammed Tredano, David N Cooper, Manfred Stuhrmann, et al.
British Journal of Haematology
|
January 6, 2016
Clinical and haematological risk factors for cerebral macrovasculopathy in a sickle cell disease newborn cohort: a prospective study
Julie Sommet, Corinne Alberti, Nathalie Couque, et al.
Clinical Hemorheology and Microcirculation
|
March 31, 2012
Relationship between acute chest syndrome and the sympatho-vagal balance in adults with hemoglobin SS disease; a case control study
Jennifer M Knight-Madden, Philippe Connes, Andre Bowers, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB
Mohammed Tredano, Matthias Griese, Jacques de Blic, et al.
International Journal of Neonatal Screening
|
October 19, 2020
Newborn Screening for Sickle Cell Disease in Europe
Yvonne Daniel, Jacques Elion, Bichr Allaf, et al.
British Journal of Haematology
|
November 29, 2020
Cell-derived microparticles and sickle cell disease chronic vasculopathy in sub-Saharan Africa: A multinational study
Abdoul K Dembélé, Claudine Lapoumeroulie, Mor Diaw, et al.
Annals of Hematology
|
April 4, 2014
Hydroxycarbamide modulates components involved in the regulation of adenosine levels in blood cells from sickle-cell anemia patients
Ana C Silva-Pinto, Carolina Dias-Carlos, Felipe Saldanha-Araujo, et al.
American Journal of Medical Genetics. Part A
|
August 21, 2012
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene
Andrée Delahaye, Suonavy Khung-Savatovsky, Azzedine Aboura, et al.
Page
of 7