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British Journal of Clinical Pharmacology
|
October 26, 2018
Genetic approaches to metabolic bone diseases
Fadil M Hannan, Paul J Newey, Michael P Whyte, et al.
Skeletal Radiology
|
January 1, 1981
Mixed-sclerosing-bone-dystrophy: report of a case and review of the literature
M P Whyte, W A Murphy, M D Fallon, et al.
The American Journal of Medicine
|
December 1, 1981
Axial osteomalacia. Clinical, laboratory and genetic investigation of an affected mother and son
M P Whyte, M D Fallon, W A Murphy, et al.
Clinical Chemistry
|
June 1, 1980
Hypophosphatasia (adult form): quantitation of serum alkaline phosphatase isoenzyme activity in a large kindred
J L Millán, M P Whyte, L V Avioli, et al.
American Journal of Medical Genetics
|
May 30, 1998
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasia
M C Eddy, R D Steiner, W H McAlister, et al.
International Review of Physiology
|
January 1, 1981
Hormonal regulation of mineral metabolism
S J Birge, T J Hahn, M P Whyte, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1982
Normal cortical bone mass in patients after long term coumadin therapy
L D Piro, M P Whyte, W A Murphy, et al.
Thorax
|
August 3, 2005
Impact of changes in the IOC-MC asthma criteria: a British perspective
J W Dickinson, G P Whyte, A K McConnell, et al.
Medicine
|
February 17, 1999
X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature
M P Whyte, G S Gottesman, M C Eddy, et al.
European Journal of Applied Physiology
|
March 1, 2006
The effects of intensive, moderate and downhill treadmill running on human blood lymphocytes expressing the adhesion/activation molecules CD54 (ICAM-1), CD18 (beta2 integrin) and CD53
Richard J Simpson, Geraint D Florida-James, Greg P Whyte, et al.
Page
of 52
Search research articles
Search
Showing results (191-200 of 515) with videos related to
Sort By:
Page
of 52
British Journal of Clinical Pharmacology
|
October 26, 2018
Genetic approaches to metabolic bone diseases
Fadil M Hannan, Paul J Newey, Michael P Whyte, et al.
Skeletal Radiology
|
January 1, 1981
Mixed-sclerosing-bone-dystrophy: report of a case and review of the literature
M P Whyte, W A Murphy, M D Fallon, et al.
The American Journal of Medicine
|
December 1, 1981
Axial osteomalacia. Clinical, laboratory and genetic investigation of an affected mother and son
M P Whyte, M D Fallon, W A Murphy, et al.
Clinical Chemistry
|
June 1, 1980
Hypophosphatasia (adult form): quantitation of serum alkaline phosphatase isoenzyme activity in a large kindred
J L Millán, M P Whyte, L V Avioli, et al.
American Journal of Medical Genetics
|
May 30, 1998
Bilateral radial ray hypoplasia with multiple epiphyseal dysplasia
M C Eddy, R D Steiner, W H McAlister, et al.
International Review of Physiology
|
January 1, 1981
Hormonal regulation of mineral metabolism
S J Birge, T J Hahn, M P Whyte, et al.
The Journal of Clinical Endocrinology and Metabolism
|
February 1, 1982
Normal cortical bone mass in patients after long term coumadin therapy
L D Piro, M P Whyte, W A Murphy, et al.
Thorax
|
August 3, 2005
Impact of changes in the IOC-MC asthma criteria: a British perspective
J W Dickinson, G P Whyte, A K McConnell, et al.
Medicine
|
February 17, 1999
X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature
M P Whyte, G S Gottesman, M C Eddy, et al.
European Journal of Applied Physiology
|
March 1, 2006
The effects of intensive, moderate and downhill treadmill running on human blood lymphocytes expressing the adhesion/activation molecules CD54 (ICAM-1), CD18 (beta2 integrin) and CD53
Richard J Simpson, Geraint D Florida-James, Greg P Whyte, et al.
Page
of 52