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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 26, 2010
Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders
Michael P Whyte, Lydia G Kempa, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 2, 2011
Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1
Michael P Whyte, Deborah Wenkert, Jennifer L Demertzis, et al.
The Journal of Rheumatology
|
June 18, 2013
Rheumatoid arthritis disease activity and disability affect the risk of serious infection events in RADIUS 1
Arthur Weaver, Orrin Troum, Michele Hooper, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 8, 2006
Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis
Steven Mumm, Deborah Wenkert, Xiafang Zhang, et al.
Therapeutic Innovation & Regulatory Science
|
December 10, 2022
Why are There not More Bayesian Clinical Trials? Ability to Interpret Bayesian and Conventional Statistics Among Medical Researchers
, Ross Bray, Andrew Hartley, et al.
Therapeutic Innovation & Regulatory Science
|
January 3, 2022
Why are not There More Bayesian Clinical Trials? Perceived Barriers and Educational Preferences Among Medical Researchers Involved in Drug Development
, Jennifer Clark, Natalia Muhlemann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 29, 2008
Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases
Michael P Whyte, William H McAlister, Deborah V Novack, et al.
Bone
|
January 10, 2016
Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9
Voraluck Phatarakijnirund, Steven Mumm, William H McAlister, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
April 30, 2008
Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2007 Pediatric Official Positions
Frank Rauch, Horacio Plotkin, Linda DiMeglio, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2016
Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease
Gary S Gottesman, Katherine L Madson, William H McAlister, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 26, 2010
Elevated serum lactate dehydrogenase isoenzymes and aspartate transaminase distinguish Albers-Schönberg disease (Chloride Channel 7 Deficiency Osteopetrosis) among the sclerosing bone disorders
Michael P Whyte, Lydia G Kempa, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
December 2, 2011
Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1
Michael P Whyte, Deborah Wenkert, Jennifer L Demertzis, et al.
The Journal of Rheumatology
|
June 18, 2013
Rheumatoid arthritis disease activity and disability affect the risk of serious infection events in RADIUS 1
Arthur Weaver, Orrin Troum, Michele Hooper, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 8, 2006
Deactivating germline mutations in LEMD3 cause osteopoikilosis and Buschke-Ollendorff syndrome, but not sporadic melorheostosis
Steven Mumm, Deborah Wenkert, Xiafang Zhang, et al.
Therapeutic Innovation & Regulatory Science
|
December 10, 2022
Why are There not More Bayesian Clinical Trials? Ability to Interpret Bayesian and Conventional Statistics Among Medical Researchers
, Ross Bray, Andrew Hartley, et al.
Therapeutic Innovation & Regulatory Science
|
January 3, 2022
Why are not There More Bayesian Clinical Trials? Perceived Barriers and Educational Preferences Among Medical Researchers Involved in Drug Development
, Jennifer Clark, Natalia Muhlemann, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
May 29, 2008
Bisphosphonate-induced osteopetrosis: novel bone modeling defects, metaphyseal osteopenia, and osteosclerosis fractures after drug exposure ceases
Michael P Whyte, William H McAlister, Deborah V Novack, et al.
Bone
|
January 10, 2016
Congenital insensitivity to pain: Fracturing without apparent skeletal pathobiology caused by an autosomal dominant, second mutation in SCN11A encoding voltage-gated sodium channel 1.9
Voraluck Phatarakijnirund, Steven Mumm, William H McAlister, et al.
Journal of Clinical Densitometry : the Official Journal of the International Society for Clinical Densitometry
|
April 30, 2008
Fracture prediction and the definition of osteoporosis in children and adolescents: the ISCD 2007 Pediatric Official Positions
Frank Rauch, Horacio Plotkin, Linda DiMeglio, et al.
American Journal of Medical Genetics. Part A
|
January 15, 2016
Auricular ossification: A newly recognized feature of osteoprotegerin-deficiency juvenile Paget disease
Gary S Gottesman, Katherine L Madson, William H McAlister, et al.
Page
of 4