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Blood
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August 15, 2000
Nonmyeloablative stem cell transplantation for congenital immunodeficiencies
P Amrolia, H B Gaspar, A Hassan, et al.
The Annals of Thoracic Surgery
|
April 25, 2006
Outcomes after late reoperation in patients with repaired tetralogy of Fallot: the impact of arrhythmia and arrhythmia surgery
Tara Karamlou, Ilana Silber, Robin Lao, et al.
Science (New York, N.Y.)
|
May 7, 2016
Uniform patchy and hollow rectangular platelet micelles from crystallizable polymer blends
Huibin Qiu, Yang Gao, Charlotte E Boott, et al.
Clinical Radiology
|
November 15, 2023
Evaluation of the current use of MRI to aid the diagnosis of axial spondyloarthritis in the UK: results from a freedom of information request
T J P Bray, J Eddison, J Hamilton, et al.
Antimicrobial Agents and Chemotherapy
|
June 1, 1993
Pharmacokinetics of 18F-labeled fluconazole in healthy human subjects by positron emission tomography
A J Fischman, N M Alpert, E Livni, et al.
The Patient
|
January 10, 2018
A Systematic Review of Discrete-Choice Experiments and Conjoint Analysis Studies in People with Multiple Sclerosis
Edward J D Webb, David Meads, Ieva Eskyte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2021
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly
Jennifer Morrison, Norah K Altuwaijri, Kirsten Brønstad, et al.
Leukemia
|
September 1, 1991
Near haploid acute lymphoblastic leukemia: seven new cases and a review of the literature
B Gibbons, P MacCallum, E Watts, et al.
Plos One
|
November 21, 2012
Biomarkers of whale shark health: a metabolomic approach
Alistair D M Dove, Johannes Leisen, Manshui Zhou, et al.
Clinical Genetics
|
August 10, 2013
A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population
B D Webb, T Brandt, L Liu, et al.
Page
of 82
Search research articles
Search
Showing results (711-720 of 812) with videos related to
Sort By:
Page
of 82
Blood
|
August 15, 2000
Nonmyeloablative stem cell transplantation for congenital immunodeficiencies
P Amrolia, H B Gaspar, A Hassan, et al.
The Annals of Thoracic Surgery
|
April 25, 2006
Outcomes after late reoperation in patients with repaired tetralogy of Fallot: the impact of arrhythmia and arrhythmia surgery
Tara Karamlou, Ilana Silber, Robin Lao, et al.
Science (New York, N.Y.)
|
May 7, 2016
Uniform patchy and hollow rectangular platelet micelles from crystallizable polymer blends
Huibin Qiu, Yang Gao, Charlotte E Boott, et al.
Clinical Radiology
|
November 15, 2023
Evaluation of the current use of MRI to aid the diagnosis of axial spondyloarthritis in the UK: results from a freedom of information request
T J P Bray, J Eddison, J Hamilton, et al.
Antimicrobial Agents and Chemotherapy
|
June 1, 1993
Pharmacokinetics of 18F-labeled fluconazole in healthy human subjects by positron emission tomography
A J Fischman, N M Alpert, E Livni, et al.
The Patient
|
January 10, 2018
A Systematic Review of Discrete-Choice Experiments and Conjoint Analysis Studies in People with Multiple Sclerosis
Edward J D Webb, David Meads, Ieva Eskyte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 7, 2021
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly
Jennifer Morrison, Norah K Altuwaijri, Kirsten Brønstad, et al.
Leukemia
|
September 1, 1991
Near haploid acute lymphoblastic leukemia: seven new cases and a review of the literature
B Gibbons, P MacCallum, E Watts, et al.
Plos One
|
November 21, 2012
Biomarkers of whale shark health: a metabolomic approach
Alistair D M Dove, Johannes Leisen, Manshui Zhou, et al.
Clinical Genetics
|
August 10, 2013
A founder mutation in COL4A3 causes autosomal recessive Alport syndrome in the Ashkenazi Jewish population
B D Webb, T Brandt, L Liu, et al.
Page
of 82