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Steven Mumm

Showing results (41-50 of 85) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
Neonatal lethal osteochondrodysplasia with low serum levels of alkaline phosphatase and osteocalcinMyra H Wyckoff, Chirine El-Turk, Abbot Laptook, et al.
Bone|August 15, 2009
Effects of polymorphisms of the sex hormone-binding globulin (SHBG) gene on free estradiol and bone mineral densityNicola Napoli, Ana Varadharajan, Giovam Batista Rini, et al.
The Journal of Clinical Endocrinology and Metabolism|June 19, 2008
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvementDavid A Stevenson, John C Carey, Stephen P Coburn, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Lack of sustained response to teriparatide in a patient with adult hypophosphatasiaClaudia Gagnon, Natalie A Sims, Steven Mumm, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblastsRichard A Cahill, Deborah Wenkert, Sharon A Perlman, et al.
Bone|March 31, 2007
Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase geneSara Baumgartner-Sigl, Edda Haberlandt, Steven Mumm, et al.
Bone|August 6, 2018
Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature reviewMichael P Whyte, S Deepak Amalnath, William H McAlister, et al.
Bone|January 8, 2021
Non-endemic skeletal fluorosis: Causes and associated secondary hyperparathyroidism (case report and literature review)Fiona J Cook, Maighan Seagrove-Guffey, Steven Mumm, et al.
Bone|April 16, 2022
Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane "huffing"Nilton Salles Rosa Neto, Daniel Englert, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 2020
X-Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3'-UTR Mutation c.*231A>G (A Retrospective Case-Control Study)Pamela S Smith, Gary S Gottesman, Fan Zhang, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
Neonatal lethal osteochondrodysplasia with low serum levels of alkaline phosphatase and osteocalcinMyra H Wyckoff, Chirine El-Turk, Abbot Laptook, et al.
Bone|August 15, 2009
Effects of polymorphisms of the sex hormone-binding globulin (SHBG) gene on free estradiol and bone mineral densityNicola Napoli, Ana Varadharajan, Giovam Batista Rini, et al.
The Journal of Clinical Endocrinology and Metabolism|June 19, 2008
Autosomal recessive hypophosphatasia manifesting in utero with long bone deformity but showing spontaneous postnatal improvementDavid A Stevenson, John C Carey, Stephen P Coburn, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2010
Lack of sustained response to teriparatide in a patient with adult hypophosphatasiaClaudia Gagnon, Natalie A Sims, Steven Mumm, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Infantile hypophosphatasia: transplantation therapy trial using bone fragments and cultured osteoblastsRichard A Cahill, Deborah Wenkert, Sharon A Perlman, et al.
Bone|March 31, 2007
Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase geneSara Baumgartner-Sigl, Edda Haberlandt, Steven Mumm, et al.
Bone|August 6, 2018
Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature reviewMichael P Whyte, S Deepak Amalnath, William H McAlister, et al.
Bone|January 8, 2021
Non-endemic skeletal fluorosis: Causes and associated secondary hyperparathyroidism (case report and literature review)Fiona J Cook, Maighan Seagrove-Guffey, Steven Mumm, et al.
Bone|April 16, 2022
Periarticular calcifications containing giant pseudo-crystals of francolite in skeletal fluorosis from 1,1-difluoroethane "huffing"Nilton Salles Rosa Neto, Daniel Englert, William H McAlister, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 2020
X-Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3'-UTR Mutation c.*231A>G (A Retrospective Case-Control Study)Pamela S Smith, Gary S Gottesman, Fan Zhang, et al.
Pageof 9