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Steven Mumm

Showing results (1-10 of 85) with videos related to

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Journal of Musculoskeletal & Neuronal Interactions|December 24, 2004
Heritable disorders of the RANKL/OPG/RANK signaling pathwayMichael P Whyte, Steven Mumm
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Adult hypophosphatasia treated with teriparatideMichael P Whyte, Steven Mumm, Chad Deal
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 19, 2007
Low serum alkaline phosphatase activity and pathologic fracture: case report and brief review of hypophosphatasia diagnosed in adulthoodHasnain M Khandwala, Steven Mumm, Michael P Whyte
The Journal of Pediatrics|June 14, 2006
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestryMichael P Whyte, Kevan Essmyer, Michael Geimer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Pregnancy-associated osteoporosis with a heterozygous deactivating LDL receptor-related protein 5 (LRP5) mutation and a homozygous methylenetetrahydrofolate reductase (MTHFR) polymorphismFiona J Cook, Steven Mumm, Michael P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 13, 2005
Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutationMichael R Rickels, Xiafang Zhang, Steven Mumm, et al.
Bone|March 3, 2019
No vascular calcification on cardiac computed tomography spanning asfotase alfa treatment for an elderly woman with hypophosphatasiaMichael P Whyte, William H McAlister, Steven Mumm, et al.
JBJS Case Connector|July 16, 2020
A Case Report of a 44-Year-Old Woman With Camurati-Englemann Disease: A Case ReportRebisi A Owhonda, Joel E Wells, Eric W Lloyd, et al.
Clinical Orthopaedics and Related Research|June 15, 2007
Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathyDeborah Wenkert, Steven Mumm, Stefanie M Wiegand, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 17, 2013
Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutationForough Saki, Zohreh Karamizadeh, Shiva Nasirabadi, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Journal of Musculoskeletal & Neuronal Interactions|December 24, 2004
Heritable disorders of the RANKL/OPG/RANK signaling pathwayMichael P Whyte, Steven Mumm
The Journal of Clinical Endocrinology and Metabolism|January 11, 2007
Adult hypophosphatasia treated with teriparatideMichael P Whyte, Steven Mumm, Chad Deal
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|January 19, 2007
Low serum alkaline phosphatase activity and pathologic fracture: case report and brief review of hypophosphatasia diagnosed in adulthoodHasnain M Khandwala, Steven Mumm, Michael P Whyte
The Journal of Pediatrics|June 14, 2006
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestryMichael P Whyte, Kevan Essmyer, Michael Geimer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2013
Pregnancy-associated osteoporosis with a heterozygous deactivating LDL receptor-related protein 5 (LRP5) mutation and a homozygous methylenetetrahydrofolate reductase (MTHFR) polymorphismFiona J Cook, Steven Mumm, Michael P Whyte, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 13, 2005
Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutationMichael R Rickels, Xiafang Zhang, Steven Mumm, et al.
Bone|March 3, 2019
No vascular calcification on cardiac computed tomography spanning asfotase alfa treatment for an elderly woman with hypophosphatasiaMichael P Whyte, William H McAlister, Steven Mumm, et al.
JBJS Case Connector|July 16, 2020
A Case Report of a 44-Year-Old Woman With Camurati-Englemann Disease: A Case ReportRebisi A Owhonda, Joel E Wells, Eric W Lloyd, et al.
Clinical Orthopaedics and Related Research|June 15, 2007
Absence of MMP2 mutation in idiopathic multicentric osteolysis with nephropathyDeborah Wenkert, Steven Mumm, Stefanie M Wiegand, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 17, 2013
Juvenile paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutationForough Saki, Zohreh Karamizadeh, Shiva Nasirabadi, et al.
Pageof 9