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Clinical Genetics
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August 28, 2007
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families
M Hashemzadeh Chaleshtori, M A Simpson, E Farrokhi, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
March 1, 1995
Kidney transplantation in diabetic patients using cyclosporine. Five-year follow-up
D Shaffer, M A Simpson, P N Madras, et al.
Neurology
|
October 25, 2002
Diagnostic strategies in CADASIL
H S Markus, R J Martin, M A Simpson, et al.
The Journal of Biological Chemistry
|
March 30, 2001
Hyaluronan synthase elevation in metastatic prostate carcinoma cells correlates with hyaluronan surface retention, a prerequisite for rapid adhesion to bone marrow endothelial cells
M A Simpson, J Reiland, S R Burger, et al.
Transplantation
|
February 1, 1989
Sequential determinations of urinary cytology and plasma and urinary lymphokines in the management of renal allograft recipients
M A Simpson, P N Madras, A J Cornaby, et al.
Free Radical Biology & Medicine
|
July 27, 2019
Serum electrolytes can promote hydroxyl radical-initiated biomolecular damage from inflammation
Yukako Komaki, Adam M-A Simpson, Jong Kwon Choe, et al.
Cardiology
|
October 30, 2008
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair
M A Simpson, S Mansour, D Ahnood, et al.
Australian Veterinary Journal
|
May 1, 1988
Prevalence of bovine venereal disease in the Victoria River District of the Northern Territory: likely economic effects and practicable control measures
C J McCool, M P Townsend, S G Wolfe, et al.
Transplantation Proceedings
|
February 1, 1991
Sequential IL-2 and IL-2R levels predict rejection in liver allograft recipients
M A Simpson, T Young-Fadok, P N Madras, et al.
Neurology
|
May 9, 2008
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23
K J Dick, R Al-Mjeni, W Baskir, et al.
Page
of 16
Search research articles
Search
Showing results (111-120 of 153) with videos related to
Sort By:
Page
of 16
Clinical Genetics
|
August 28, 2007
Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families
M Hashemzadeh Chaleshtori, M A Simpson, E Farrokhi, et al.
Archives of Surgery (Chicago, Ill. : 1960)
|
March 1, 1995
Kidney transplantation in diabetic patients using cyclosporine. Five-year follow-up
D Shaffer, M A Simpson, P N Madras, et al.
Neurology
|
October 25, 2002
Diagnostic strategies in CADASIL
H S Markus, R J Martin, M A Simpson, et al.
The Journal of Biological Chemistry
|
March 30, 2001
Hyaluronan synthase elevation in metastatic prostate carcinoma cells correlates with hyaluronan surface retention, a prerequisite for rapid adhesion to bone marrow endothelial cells
M A Simpson, J Reiland, S R Burger, et al.
Transplantation
|
February 1, 1989
Sequential determinations of urinary cytology and plasma and urinary lymphokines in the management of renal allograft recipients
M A Simpson, P N Madras, A J Cornaby, et al.
Free Radical Biology & Medicine
|
July 27, 2019
Serum electrolytes can promote hydroxyl radical-initiated biomolecular damage from inflammation
Yukako Komaki, Adam M-A Simpson, Jong Kwon Choe, et al.
Cardiology
|
October 30, 2008
Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair
M A Simpson, S Mansour, D Ahnood, et al.
Australian Veterinary Journal
|
May 1, 1988
Prevalence of bovine venereal disease in the Victoria River District of the Northern Territory: likely economic effects and practicable control measures
C J McCool, M P Townsend, S G Wolfe, et al.
Transplantation Proceedings
|
February 1, 1991
Sequential IL-2 and IL-2R levels predict rejection in liver allograft recipients
M A Simpson, T Young-Fadok, P N Madras, et al.
Neurology
|
May 9, 2008
A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23
K J Dick, R Al-Mjeni, W Baskir, et al.
Page
of 16