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March 1, 2020
Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia
Michael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 21, 2024
Pediatric hypophosphatasia: avoid diagnosis missteps!
Michael P Whyte, William H McAlister, Karen E Mack, 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.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
April 5, 2016
ADULT HYPOPHOSPHATASIA TREATED WITH TERIPARATIDE: REPORT OF 2 PATIENTS AND REVIEW OF THE LITERATURE
Pauline M Camacho, Alaleh M Mazhari, Cory Wilczynski, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 11, 2012
"Atypical femoral fractures" during bisphosphonate exposure in adult hypophosphatasia
Roger A L Sutton, Steven Mumm, Stephen P Coburn, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia
Steven Mumm, Jonathan Jones, Patrick Finnegan, 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.
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 Clinical Endocrinology and Metabolism
|
September 26, 2013
Acute severe hypercalcemia after traumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failure
Michael P Whyte, Rattana Leelawattana, William R Reinus, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 85) with videos related to
Sort By:
Page
of 9
Bone
|
March 1, 2020
Hyperphosphatemia with low FGF7 and normal FGF23 and sFRP4 levels in the circulation characterizes pediatric hypophosphatasia
Michael P Whyte, Fan Zhang, Deborah Wenkert, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 21, 2024
Pediatric hypophosphatasia: avoid diagnosis missteps!
Michael P Whyte, William H McAlister, Karen E Mack, 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.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
April 5, 2016
ADULT HYPOPHOSPHATASIA TREATED WITH TERIPARATIDE: REPORT OF 2 PATIENTS AND REVIEW OF THE LITERATURE
Pauline M Camacho, Alaleh M Mazhari, Cory Wilczynski, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
February 11, 2012
"Atypical femoral fractures" during bisphosphonate exposure in adult hypophosphatasia
Roger A L Sutton, Steven Mumm, Stephen P Coburn, et al.
Molecular Genetics and Metabolism
|
February 22, 2002
Denaturing gradient gel electrophoresis analysis of the tissue nonspecific alkaline phosphatase isoenzyme gene in hypophosphatasia
Steven Mumm, Jonathan Jones, Patrick Finnegan, 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.
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 Clinical Endocrinology and Metabolism
|
September 26, 2013
Acute severe hypercalcemia after traumatic fractures and immobilization in hypophosphatasia complicated by chronic renal failure
Michael P Whyte, Rattana Leelawattana, William R Reinus, et al.
Page
of 9