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BMJ Open
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June 20, 2019
Individualised screening for diabetic retinopathy: the ISDR study-rationale, design and methodology for a randomised controlled trial comparing annual and individualised risk-based variable-interval screening
Deborah M Broadbent, Christopher J Sampson, Amu Wang, et al.
Environmental Health Perspectives
|
March 14, 2003
Measurement of p-nitrophenol in the urine of residents whose homes were contaminated with methyl parathion
Dana B Barr, Wayman E Turner, Emily DiPietro, et al.
The New England Journal of Medicine
|
March 5, 2005
Family-based association between Alzheimer's disease and variants in UBQLN1
Lars Bertram, Mikko Hiltunen, Michele Parkinson, et al.
Journal of Medical Genetics
|
January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex
R Vrtel, S Verhoef, K Bouman, et al.
Circulation Research
|
March 28, 2013
Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation
Ling Xiao, Tamara T Koopmann, Balázs Ördög, et al.
Cell Stem Cell
|
September 15, 2020
Reengineering an Antiarrhythmic Drug Using Patient hiPSC Cardiomyocytes to Improve Therapeutic Potential and Reduce Toxicity
Wesley L McKeithan, Dries A M Feyen, Arne A N Bruyneel, et al.
Clinical Chemistry
|
January 24, 1998
Development and validation of sensitive method for determination of serum cotinine in smokers and nonsmokers by liquid chromatography/atmospheric pressure ionization tandem mass spectrometry
J T Bernert, W E Turner, J L Pirkle, et al.
QJM : Monthly Journal of the Association of Physicians
|
September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)
D Trump, B Farren, C Wooding, et al.
Journal of Medical Genetics
|
February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3
S Olschwang, D Markie, S Seal, et al.
Journal of the National Cancer Institute
|
August 17, 2000
Randomized trial of a specialist genetic assessment service for familial breast cancer
K Brain, J Gray, P Norman, et al.
Page
of 42
Search research articles
Search
Showing results (391-400 of 411) with videos related to
Sort By:
Page
of 42
BMJ Open
|
June 20, 2019
Individualised screening for diabetic retinopathy: the ISDR study-rationale, design and methodology for a randomised controlled trial comparing annual and individualised risk-based variable-interval screening
Deborah M Broadbent, Christopher J Sampson, Amu Wang, et al.
Environmental Health Perspectives
|
March 14, 2003
Measurement of p-nitrophenol in the urine of residents whose homes were contaminated with methyl parathion
Dana B Barr, Wayman E Turner, Emily DiPietro, et al.
The New England Journal of Medicine
|
March 5, 2005
Family-based association between Alzheimer's disease and variants in UBQLN1
Lars Bertram, Mikko Hiltunen, Michele Parkinson, et al.
Journal of Medical Genetics
|
January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complex
R Vrtel, S Verhoef, K Bouman, et al.
Circulation Research
|
March 28, 2013
Unique cardiac Purkinje fiber transient outward current β-subunit composition: a potential molecular link to idiopathic ventricular fibrillation
Ling Xiao, Tamara T Koopmann, Balázs Ördög, et al.
Cell Stem Cell
|
September 15, 2020
Reengineering an Antiarrhythmic Drug Using Patient hiPSC Cardiomyocytes to Improve Therapeutic Potential and Reduce Toxicity
Wesley L McKeithan, Dries A M Feyen, Arne A N Bruyneel, et al.
Clinical Chemistry
|
January 24, 1998
Development and validation of sensitive method for determination of serum cotinine in smokers and nonsmokers by liquid chromatography/atmospheric pressure ionization tandem mass spectrometry
J T Bernert, W E Turner, J L Pirkle, et al.
QJM : Monthly Journal of the Association of Physicians
|
September 1, 1996
Clinical studies of multiple endocrine neoplasia type 1 (MEN1)
D Trump, B Farren, C Wooding, et al.
Journal of Medical Genetics
|
February 25, 1998
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3
S Olschwang, D Markie, S Seal, et al.
Journal of the National Cancer Institute
|
August 17, 2000
Randomized trial of a specialist genetic assessment service for familial breast cancer
K Brain, J Gray, P Norman, et al.
Page
of 42