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The American Journal of Medicine
|
October 1, 1992
Painful diffuse osteosclerosis after intravenous drug abuse
D T Villareal, W A Murphy, S L Teitelbaum, et al.
Medicine
|
September 1, 1979
Adult hypophosphatasia. Clinical, laboratory, and genetic investigation of a large kindred with review of the literature
M P Whyte, S L Teitelbaum, W A Murphy, et al.
Journal of Occupational Medicine and Toxicology (London, England)
|
March 1, 2008
The effects of a graduated aerobic exercise programme on cardiovascular disease risk factors in the NHS workplace: a randomised controlled trial
Jennifer A Hewitt, Gregory P Whyte, Michelle Moreton, et al.
Oncogene
|
August 20, 2013
Bmi1 is required for tumorigenesis in a mouse model of intestinal cancer
M A Maynard, R Ferretti, K I Hilgendorf, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 1, 1992
X-linked hypophosphatemic rickets: a study (with literature review) of linear growth response to calcitriol and phosphate therapy
D J Petersen, A M Boniface, F W Schranck, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1988
Anti-oncogenes and the negative regulation of cell growth
J M Horowitz, S H Friend, R A Weinberg, et al.
The American Journal of Pathology
|
December 24, 1997
Matrix vesicles in osteomalacic hypophosphatasia bone contain apatite-like mineral crystals
H C Anderson, H H Hsu, D C Morris, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 5, 2011
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand
Michael P Whyte, William G Totty, Deborah V Novack, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification
W S Sly, D Hewett-Emmett, M P Whyte, et al.
Thorax
|
October 18, 2005
Mid-expiratory flow versus FEV1 measurements in the diagnosis of exercise induced asthma in elite athletes
J W Dickinson, G P Whyte, A K McConnell, et al.
Page
of 52
Search research articles
Search
Showing results (281-290 of 515) with videos related to
Sort By:
Page
of 52
The American Journal of Medicine
|
October 1, 1992
Painful diffuse osteosclerosis after intravenous drug abuse
D T Villareal, W A Murphy, S L Teitelbaum, et al.
Medicine
|
September 1, 1979
Adult hypophosphatasia. Clinical, laboratory, and genetic investigation of a large kindred with review of the literature
M P Whyte, S L Teitelbaum, W A Murphy, et al.
Journal of Occupational Medicine and Toxicology (London, England)
|
March 1, 2008
The effects of a graduated aerobic exercise programme on cardiovascular disease risk factors in the NHS workplace: a randomised controlled trial
Jennifer A Hewitt, Gregory P Whyte, Michelle Moreton, et al.
Oncogene
|
August 20, 2013
Bmi1 is required for tumorigenesis in a mouse model of intestinal cancer
M A Maynard, R Ferretti, K I Hilgendorf, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 1, 1992
X-linked hypophosphatemic rickets: a study (with literature review) of linear growth response to calcitriol and phosphate therapy
D J Petersen, A M Boniface, F W Schranck, et al.
Cold Spring Harbor Symposia on Quantitative Biology
|
January 1, 1988
Anti-oncogenes and the negative regulation of cell growth
J M Horowitz, S H Friend, R A Weinberg, et al.
The American Journal of Pathology
|
December 24, 1997
Matrix vesicles in osteomalacic hypophosphatasia bone contain apatite-like mineral crystals
H C Anderson, H H Hsu, D C Morris, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 5, 2011
Camurati-Engelmann disease: unique variant featuring a novel mutation in TGFβ1 encoding transforming growth factor beta 1 and a missense change in TNFSF11 encoding RANK ligand
Michael P Whyte, William G Totty, Deborah V Novack, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 1, 1983
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification
W S Sly, D Hewett-Emmett, M P Whyte, et al.
Thorax
|
October 18, 2005
Mid-expiratory flow versus FEV1 measurements in the diagnosis of exercise induced asthma in elite athletes
J W Dickinson, G P Whyte, A K McConnell, et al.
Page
of 52