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Health Education Research
|
May 11, 2013
Structural issues affecting creation of a community action and advocacy board
M R Weeks, M Abbott, H Hilario, et al.
European Journal of Haematology
|
August 1, 1987
Intravenous gammaglobulin treatment for thrombocytopenic purpura in patients with human immunodeficiency virus (HIV) infection
G Tertian, N Risler, P Le Bras, et al.
BMJ Open Diabetes Research & Care
|
January 31, 2023
Major malformations risk following early pregnancy exposure to metformin: a systematic review and meta-analysis
Nazanin Abolhassani, Ursula Winterfeld, Yusuf C Kaplan, et al.
Rheumatology (Oxford, England)
|
October 7, 2020
Mendelian randomization provides evidence for a causal effect of higher serum IGF-1 concentration on risk of hip and knee osteoarthritis
April Hartley, Eleanor Sanderson, Lavinia Paternoster, et al.
Human Genetics
|
March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene
J J Pernelle, P Chafey, J Chelly, et al.
British Journal of Haematology
|
July 1, 1996
Low incidence of specific anti-platelet antibodies detected by the MAIPA assay in the serum of thrombocytopenic MDS patients and lack of correlation between platelet autoantibodies, platelet lifespan and response to danazol therapy
M Hebbar, C Kaplan, M T Caulier, et al.
Molecular and Cellular Probes
|
June 1, 1992
Comparison of spot-blot and microtitre plate methods for the detection of HIV-1 PCR products
B Conway, L J Bechtel, K A Adler, et al.
British Journal of Haematology
|
January 1, 1989
PL2-49, a monoclonal antibody against glycoprotein IIb which is a platelet activator
M C Morel, T Lecompte, P Champeix, et al.
Prenatal Diagnosis
|
January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases
C Junien, A Leroux, D Lostanlen, et al.
Human Heredity
|
January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait
C Junien, A Chaventré, Y Fofana, et al.
Page
of 119
Search research articles
Search
Showing results (551-560 of 1,185) with videos related to
Sort By:
Page
of 119
Health Education Research
|
May 11, 2013
Structural issues affecting creation of a community action and advocacy board
M R Weeks, M Abbott, H Hilario, et al.
European Journal of Haematology
|
August 1, 1987
Intravenous gammaglobulin treatment for thrombocytopenic purpura in patients with human immunodeficiency virus (HIV) infection
G Tertian, N Risler, P Le Bras, et al.
BMJ Open Diabetes Research & Care
|
January 31, 2023
Major malformations risk following early pregnancy exposure to metformin: a systematic review and meta-analysis
Nazanin Abolhassani, Ursula Winterfeld, Yusuf C Kaplan, et al.
Rheumatology (Oxford, England)
|
October 7, 2020
Mendelian randomization provides evidence for a causal effect of higher serum IGF-1 concentration on risk of hip and knee osteoarthritis
April Hartley, Eleanor Sanderson, Lavinia Paternoster, et al.
Human Genetics
|
March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene
J J Pernelle, P Chafey, J Chelly, et al.
British Journal of Haematology
|
July 1, 1996
Low incidence of specific anti-platelet antibodies detected by the MAIPA assay in the serum of thrombocytopenic MDS patients and lack of correlation between platelet autoantibodies, platelet lifespan and response to danazol therapy
M Hebbar, C Kaplan, M T Caulier, et al.
Molecular and Cellular Probes
|
June 1, 1992
Comparison of spot-blot and microtitre plate methods for the detection of HIV-1 PCR products
B Conway, L J Bechtel, K A Adler, et al.
British Journal of Haematology
|
January 1, 1989
PL2-49, a monoclonal antibody against glycoprotein IIb which is a platelet activator
M C Morel, T Lecompte, P Champeix, et al.
Prenatal Diagnosis
|
January 1, 1981
Prenatal diagnosis of congenital enzymopenic methaemoglobinaemia with mental retardation due to generalized cytochrome b5 reductase deficiency: first report of two cases
C Junien, A Leroux, D Lostanlen, et al.
Human Heredity
|
January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait
C Junien, A Chaventré, Y Fofana, et al.
Page
of 119